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Nereo Bresolin
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104
Comi, Giacomo
58
Scarlato, Guglielmo
56
Moggio, Maurizio
48
Prelle, Alessandro
45
Del Bo, Roberto
42
Scarpini, Elio
41
Fortunato, Francesco
40
Bordoni, Andreina
36
Galimberti, Daniela
32
Corti, Stefania
29
Fenoglio, Chiara
27
Sironi, Manuela
27
Torrente, Yvan
27
Venturelli, Eliana
25
Cagliani, Rachele
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All Publications
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2009: Braghin Elisa; Galimberti Daniela; Scarpini Elio; Bresolin Nereo; Baron Pierluigi
Alpha1-antichymotrypsin induces TNF-alpha production and NF-kappaB activation in the murine N9 microglial cell line.
Neuroscience letters 2009;467(1):40-2.
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2009: Carecchio Miryam; Fenoglio Chiara; De Riz Milena; Guidi Ilaria; Comi Cristoforo; Cortini Francesca; Venturelli Eliana; Restelli Ilaria; Cantoni Claudia; Bresolin Nereo; Monaco Francesco; Scarpini Elio; Galimberti Daniela
Progranulin plasma levels as potential biomarker for the identification of GRN deletion carriers. A case with atypical onset as clinical amnestic Mild Cognitive Impairment converted to Alzheimer's disease.
Journal of the neurological sciences 2009;287(1-2):291-3.
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2009: Lanfranconi Silvia; Corti Stefania; Bersano Anna; Costa Antonella; Prelle Alessandro; Sciacco Monica; Bresolin Nereo; Ghione Isabella
Aphasic and visual aura with increased vasogenic leakage: an atypical migrainosus status.
Journal of the neurological sciences 2009;285(1-2):227-9.
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2009: Corti Stefania; Nizzardo Monica; Nardini Martina; Donadoni Chiara; Salani Sabrina; Del Bo Roberto; Papadimitriou Dimitra; Locatelli Federica; Mezzina Nicoletta; Gianni Francesca; Bresolin Nereo; Comi Giacomo P
Motoneuron transplantation rescues the phenotype of SMARD1 (spinal muscular atrophy with respiratory distress type 1).
The Journal of neuroscience : the official journal of the Society for Neuroscience 2009;29(38):11761-71.
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2009: Bersano A; Del Bo R; Ballabio E; Cinnante C; Lanfranconi S; Comi G P; Baron P; Bresolin N; Candelise L
Transthyretin asn90 variant: amyloidogenic or non-amyloidogenic role.
Journal of the neurological sciences 2009;284(1-2):113-5.
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2009: Losito Luciana; De Rinaldis Marta; Gennaro Leonarda; Priori Silvia G; Bloise Raffaella; Bassi Maria Teresa; Bresolin Nereo; Trabacca Antonio
Charcot-Marie-Tooth type 1a in a child with Long QT syndrome.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2009;13(5):459-62.
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2009: Deponti Daniela; Buono Roberta; Catanzaro Giuseppina; De Palma Clara; Longhi Renato; Meneveri Raffaella; Bresolin Nereo; Bassi Maria Teresa; Cossu Giulio; Clementi Emilio; Brunelli Silvia
The low-affinity receptor for neurotrophins p75NTR plays a key role for satellite cell function in muscle repair acting via RhoA.
Molecular biology of the cell 2009;20(16):3620-7.
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2009: Villa Chiara; Venturelli Eliana; Fenoglio Chiara; Clerici Francesca; Marcone Alessandra; Benussi Luisa; Ghidoni Roberta; Gallone Salvatore; Cortini Francesca; Scalabrini Diego; Serpente Maria; Binetti Giuliano; Cappa Stefano; Mariani Claudio; Rainero Innocenzo; Bresolin Nereo; Scarpini Elio; Galimberti Daniela
CCL8/MCP-2 association analysis in patients with Alzheimer's disease and frontotemporal lobar degeneration.
Journal of neurology 2009;256(8):1379-81.
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2009: Del Bo Roberto; Ghezzi Serena; Scarpini Elio; Bresolin Nereo; Comi Giacomo Pietro
VEGF genetic variability is associated with increased risk of developing Alzheimer's disease.
Journal of the neurological sciences 2009;283(1-2):66-8.
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2009: Cagliani Rachele; Fumagalli Matteo; Pozzoli Uberto; Riva Stefania; Comi Giacomo P; Torri Federica; Macciardi Fabio; Bresolin Nereo; Sironi Manuela
Diverse evolutionary histories for beta-adrenoreceptor genes in humans.
American journal of human genetics 2009;85(1):64-75.
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2009: Villa C; Venturelli E; Fenoglio C; Clerici F; Marcone A; Benussi L; Gallone S; Scalabrini D; Cortini F; Serpente M; Martinelli Boneschi F; Cappa S; Binetti G; Mariani C; Rainero I; Giordana M T; Bresolin N; Scarpini E; Galimberti D
DCUN1D1 is a risk factor for frontotemporal lobar degeneration.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2009;16(7):870-3.
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2009: Vantaggiato Chiara; Redaelli Francesca; Falcone Sestina; Perrotta Cristiana; Tonelli Alessandra; Bondioni Sara; Morbin Michela; Riva Daria; Saletti Veronica; Bonaglia Maria C; Giorda Roberto; Bresolin Nereo; Clementi Emilio; Bassi Maria Teresa
A novel CLN8 mutation in late-infantile-onset neuronal ceroid lipofuscinosis (LINCL) reveals aspects of CLN8 neurobiological function.
Human mutation 2009;30(7):1104-16.
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2009: Fumagalli Matteo; Pozzoli Uberto; Cagliani Rachele; Comi Giacomo P; Riva Stefania; Clerici Mario; Bresolin Nereo; Sironi Manuela
Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions.
The Journal of experimental medicine 2009;206(6):1395-408.
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2009: Virgilio Roberta; Ronchi Dario; Bordoni Andreina; Fassone Elisa; Bonato Sara; Donadoni Chiara; Torgano Giuseppe; Moggio Maurizio; Corti Stefania; Bresolin Nereo; Comi Giacomo P
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study.
Journal of the neurological sciences 2009;281(1-2):85-92.
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2009: Del Bo R; Ghezzi S; Corti S; Pandolfo M; Ranieri M; Santoro D; Ghione I; Prelle A; Orsetti V; Mancuso M; Sorarù G; Briani C; Angelini C; Siciliano G; Bresolin N; Comi G P
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2009;16(6):727-32.
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2009: Galimberti Daniela; Venturelli Eliana; Villa Chiara; Fenoglio Chiara; Clerici Francesca; Marcone Alessandra; Benussi Luisa; Cortini Francesca; Scalabrini Diego; Perini Luca; Restelli Ilaria; Binetti Giuliano; Cappa Stefano; Mariani Claudio; Bresolin Nereo; Scarpini Elio
MCP-1 A-2518G polymorphism: effect on susceptibility for frontotemporal lobar degeneration and on cerebrospinal fluid MCP-1 levels.
Journal of Alzheimer's disease : JAD 2009;17(1):125-33.
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2009: Tonelli A; Lanfranconi S; Bersano A; Corti S; Bassi M T; Bresolin N
Aberrant splicing due to a silent nucleotide change in CCM2 gene in a family with cerebral cavernous malformation.
Clinical genetics 2009;75(5):494-7.
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2009: Bresolin N; Zucca C; Pecori A
Efficacy and tolerability of eperisone and baclofen in spastic palsy: a double-blind randomized trial.
Advances in therapy 2009;26(5):563-73.
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2009: Di Fonzo Alessio; Ronchi Dario; Lodi Tiziana; Fassone Elisa; Tigano Marco; Lamperti Costanza; Corti Stefania; Bordoni Andreina; Fortunato Francesco; Nizzardo Monica; Napoli Laura; Donadoni Chiara; Salani Sabrina; Saladino Francesca; Moggio Maurizio; Bresolin Nereo; Ferrero Iliana; Comi Giacomo P
The mitochondrial disulfide relay system protein GFER is mutated in autosomal-recessive myopathy with cataract and combined respiratory-chain deficiency.
American journal of human genetics 2009;84(5):594-604.
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2009: Brighina Erika; Bresolin Nereo; Pardi Giorgio; Rango Mario
Human fetal brain chemistry as detected by proton magnetic resonance spectroscopy.
Pediatric neurology 2009;40(5):327-42.
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2009: Fenoglio Chiara; Scalabrini Diego; Piccio Laura; De Riz Milena; Venturelli Eliana; Cortini Francesca; Villa Chiara; Serpente Maria; Parks Becky; Rinker John; Cross Anne H; Bresolin Nereo; Scarpini Elio; Galimberti Daniela
Candidate gene analysis of selectin cluster in patients with multiple sclerosis.
Journal of neurology 2009;256(5):832-3.
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2009: Bersano Anna; Del Bo Roberto; Lamperti Costanza; Ghezzi Serena; Fagiolari Gigliola; Fortunato Francesco; Ballabio Elena; Moggio Maurizio; Candelise Livia; Galimberti Daniela; Virgilio Roberta; Lanfranconi Silvia; Torrente Yvan; Carpo Marinella; Bresolin Nereo; Comi Giacomo P; Corti Stefania
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation.
Neurobiology of aging 2009;30(5):752-8.
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2009: Ghezzi Serena; Del Bo Roberto; Scarlato Marina; Nardini Martina; Carlesi Cecilia; Prelle Alessandro; Corti Stefania; Mancuso Michelangelo; Briani Chiara; Siciliano Gabriele; Murri Luigi; Bresolin Nereo; Comi Giacomo Pietro
Is erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?
Neurobiology of aging 2009;30(5):842-4.
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2009: Fruguglietti M E; Napoli L; Sciacco M; Ripolone M; Serafini M; Grimoldi N; Bresolin N; Moggio M; Prelle A
Severe acute multineuropathy in Churg-Strauss syndrome in a patient with a history of melanoma.
Clinical neuropathology 2009;28(2):125-8.
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2009: Parolini D; Meregalli M; Belicchi M; Razini P; Lopa R; Del Carlo B; Farini A; Maciotta S; Bresolin N; Porretti L; Pellegrino M; Torrente Y
CD20-related signaling pathway is differently activated in normal and dystrophic circulating CD133(+) stem cells.
Cellular and molecular life sciences : CMLS 2009;66(4):697-710.
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2009: Fumagalli Matteo; Cagliani Rachele; Pozzoli Uberto; Riva Stefania; Comi Giacomo P; Menozzi Giorgia; Bresolin Nereo; Sironi Manuela
Widespread balancing selection and pathogen-driven selection at blood group antigen genes.
Genome research 2009;19(2):199-212.
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2009: Corti Stefania; Donadoni Chiara; Ronchi Dario; Bordoni Andreina; Fortunato Francesco; Santoro Domenico; Del Bo Roberto; Lucchini Valeria; Crugnola Veronica; Papadimitriou Dimitra; Salani Sabrina; Moggio Maurizio; Bresolin Nereo; Comi Giacomo P
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction.
Journal of the neurological sciences 2009;276(1-2):170-4.
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2009: Cagliani Rachele; Fumagalli Matteo; Pozzoli Uberto; Riva Stefania; Cereda Matteo; Comi Giacomo P; Pattini Linda; Bresolin Nereo; Sironi Manuela
A complex selection signature at the human AVPR1B gene.
BMC evolutionary biology 2009;9():123.
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2008: Del Bo R; Moggio M; Rango M; Bonato S; D'Angelo M G; Ghezzi S; Airoldi G; Bassi M T; Guglieri M; Napoli L; Lamperti C; Corti S; Federico A; Bresolin N; Comi G P
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction.
Neurology 2008;71(24):1959-66.
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2008: Lucchiari S; Pagliarani S; Corti S; Mancinelli E; Servida M; Fruguglietti E; Sansone V; Moggio M; Bresolin N; Comi G P; Meola G
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion.
Journal of the neurological sciences 2008;275(1-2):159-63.
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2008: Del Bo Roberto; Ghezzi Serena; Scarlato Marina; Albani Diego; Galimberti Daniela; Lucca Ugo; Tettamanti Mauro; Scarpini Elio; Forloni Gianluigi; Bresolin Nereo; Comi Giacomo Pietro
Role of VEGF gene variability in longevity: a lesson from the Italian population.
Neurobiology of aging 2008;29(12):1917-22.
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2008: Corti Stefania; Nizzardo Monica; Nardini Martina; Donadoni Chiara; Salani Sabrina; Ronchi Dario; Saladino Francesca; Bordoni Andreina; Fortunato Francesco; Del Bo Roberto; Papadimitriou Dimitra; Locatelli Federica; Menozzi Giorgia; Strazzer Sandra; Bresolin Nereo; Comi Giacomo P
Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy.
The Journal of clinical investigation 2008;118(10):3316-30.
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2008: Cortini F; Fenoglio C; Guidi I; Venturelli E; Pomati S; Marcone A; Scalabrini D; Villa C; Clerici F; Dalla Valle E; Mariani C; Cappa S; Bresolin N; Scarpini E; Galimberti D
Novel exon 1 progranulin gene variant in Alzheimer's disease.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2008;15(10):1111-7.
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2008: Gallanti Andrea; Tonelli Alessandra; Cardin Veronica; Bussone Gennaro; Bresolin Nereo; Bassi Maria Teresa
A novel de novo nonsense mutation in ATP1A2 associated with sporadic hemiplegic migraine and epileptic seizures.
Journal of the neurological sciences 2008;273(1-2):123-6.
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2008: Virgilio Roberta; Ronchi Dario; Hadjigeorgiou Georgios M; Bordoni Andreina; Saladino Francesca; Moggio Maurizio; Adobbati Laura; Kafetsouli Demetra; Tsironi Evangelia; Previtali Stefano; Papadimitriou Alexandros; Bresolin Nereo; Comi Giacomo P
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia.
Journal of neurology 2008;255(9):1384-91.
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2008: Galimberti Daniela; Scarpini Elio; Venturelli Eliana; Strobel Alexander; Herterich Sabine; Fenoglio Chiara; Guidi Ilaria; Scalabrini Diego; Cortini Francesca; Bresolin Nereo; Lesch Klaus-Peter; Reif Andreas
Association of a NOS1 promoter repeat with Alzheimer's disease.
Neurobiology of aging 2008;29(9):1359-65.
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2008: Sforza Chiarella; Rango Mario; Galante Domenico; Bresolin Nereo; Ferrario Virgilio F
Spontaneous blinking in healthy persons: an optoelectronic study of eyelid motion.
Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) 2008;28(4):345-53.
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2008: Bersano A; Ballabio E; Bresolin N; Candelise L
Genetic polymorphisms for the study of multifactorial stroke.
Human mutation 2008;29(6):776-95.
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2008: Galimberti D; Fenoglio C; Comi C; Scalabrini D; De Riz M; Leone M; Venturelli E; Cortini F; Piola M; Monaco F; Bresolin N; Scarpini E
MDC/CCL22 intrathecal levels in patients with multiple sclerosis.
Multiple sclerosis (Houndmills, Basingstoke, England) 2008;14(4):547-9.
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2008: Zucca Claudio; Redaelli Francesca; Epifanio Roberta; Zanotta Nicoletta; Romeo Antonino; Lodi Monica; Veggiotti Pierangelo; Airoldi Giovanni; Panzeri Chris; Romaniello Romina; De Polo Gianni; Bonanni Paolo; Cardinali Simonetta; Baschirotto Cinzia; Martorell Loreto; Borgatti Renato; Bresolin Nereo; Bassi Maria Teresa
Cryptogenic epileptic syndromes related to SCN1A: twelve novel mutations identified.
Archives of neurology 2008;65(4):489-94.
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2008: Galimberti Daniela; Venturelli Eliana; Fenoglio Chiara; Guidi Ilaria; Villa Chiara; Bergamaschini Luigi; Cortini Francesca; Scalabrini Diego; Baron Pierluigi; Vergani Carlo; Bresolin Nereo; Scarpini Elio
Intrathecal levels of IL-6, IL-11 and LIF in Alzheimer's disease and frontotemporal lobar degeneration.
Journal of neurology 2008;255(4):539-44.
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2008: Arnoldi Alessia; Tonelli Alessandra; Crippa Francesca; Villani Gaetano; Pacelli Consiglia; Sironi Manuela; Pozzoli Uberto; D'Angelo Maria Grazia; Meola Giovanni; Martinuzzi Andrea; Crimella Claudia; Redaelli Francesca; Panzeri Chris; Renieri Alessandra; Comi Giacomo Pietro; Turconi Anna Carla; Bresolin Nereo; Bassi Maria Teresa
A clinical, genetic, and biochemical characterization of SPG7 mutations in a large cohort of patients with hereditary spastic paraplegia.
Human mutation 2008;29(4):522-31.
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2008: Galimberti Daniela; Scalabrini Diego; Fenoglio Chiara; De Riz Milena; Comi Cristoforo; Venturelli Eliana; Cortini Francesca; Piola Mirko; Leone Maurizio; Dianzani Umberto; D'Alfonso Sandra; Monaco Francesco; Bresolin Nereo; Scarpini Elio
Gender-specific influence of the chromosome 16 chemokine gene cluster on the susceptibility to Multiple Sclerosis.
Journal of the neurological sciences 2008;267(1-2):86-90.
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2008: Butera Gianfranco; Agostoni Elio; Biondi-Zoccai Giuseppe; Bresolin Nereo; Fumagalli Lorenzo; Chessa Massimo; Gallanti Andrea; Scacciatela Paolo; Carminati Mario
Migraine, stroke and patent foramen ovale: a dangerous trio?
Journal of cardiovascular medicine (Hagerstown, Md.) 2008;9(3):233-8.
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2008: Corti S; Bordoni A; Ronchi D; Musumeci O; Aguennouz M; Toscano A; Lamperti C; Bresolin N; Comi G P
Clinical features and new molecular findings in Carnitine Palmitoyltransferase II (CPT II) deficiency.
Journal of the neurological sciences 2008;266(1-2):97-103.
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2008: Guglieri Michela; Magri Francesca; D'Angelo Maria Grazia; Prelle Alessandro; Morandi Lucia; Rodolico Carmelo; Cagliani Rachele; Mora Marina; Fortunato Francesco; Bordoni Andreina; Del Bo Roberto; Ghezzi Serena; Pagliarani Serena; Lucchiari Sabrina; Salani Sabrina; Zecca Chiara; Lamperti Costanza; Ronchi Dario; Aguennouz Mohammed; Ciscato Patrizia; Di Blasi Claudia; Ruggieri Alessandra; Moroni Isabella; Turconi Anna; Toscano Antonio; Moggio Maurizio; Bresolin Nereo; Comi Giacomo P
Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients.
Human mutation 2008;29(2):258-66.
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2008: Del Bo Roberto; Scarlato Marina; Ghezzi Serena; Martinelli-Boneschi Filippo; Corti Stefania; Locatelli Federica; Santoro Domenico; Prelle Alessandro; Briani Chiara; Nardini Martina; Siciliano Gabriele; Mancuso Michelangelo; Murri Luigi; Bresolin Nereo; Comi Giacomo Pietro
Absence of angiogenic genes modification in Italian ALS patients.
Neurobiology of aging 2008;29(2):314-6.
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2008: Benchaouir Rachid; Meregalli Mirella; Farini Andrea; D'Antona Giuseppe; Belicchi Marzia; Goyenvalle Aurélie; Battistelli Maurizio; Bresolin Nereo; Bottinelli Roberto; Garcia Luis; Torrente Yvan
[Restoration of human dystrophin following transplantation of exon-skipping-engineered DMD patient stem cells into dystrophic mice]
Médecine sciences : M/S 2008;24(1):99-101.
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2008: Venturelli E; Villa C; Scarpini E; Fenoglio C; Guidi I; Lovati C; Marcone A; Cortini F; Scalabrini D; Clerici F; Bresolin N; Mariani C; Cappa S; Galimberti D
Neuronal nitric oxide synthase C276T polymorphism increases the risk for frontotemporal lobar degeneration.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2008;15(1):77-81.
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2008: Cagliani Rachele; Fumagalli Matteo; Riva Stefania; Pozzoli Uberto; Comi Giacomo P; Menozzi Giorgia; Bresolin Nereo; Sironi Manuela
The signature of long-standing balancing selection at the human defensin beta-1 promoter.
Genome biology 2008;9(9):R143.
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2008: Marchesi Chiara; Belicchi Marzia; Meregalli Mirella; Farini Andrea; Cattaneo Alessandra; Parolini Daniele; Gavina Manuela; Porretti Laura; D'Angelo Maria Grazia; Bresolin Nereo; Cossu Giulio; Torrente Yvan
Correlation of circulating CD133+ progenitor subclasses with a mild phenotype in Duchenne muscular dystrophy patients.
PloS one 2008;3(5):e2218.
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2008: Pozzoli Uberto; Menozzi Giorgia; Fumagalli Matteo; Cereda Matteo; Comi Giacomo P; Cagliani Rachele; Bresolin Nereo; Sironi Manuela
Both selective and neutral processes drive GC content evolution in the human genome.
BMC evolutionary biology 2008;8():99.
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2007: Benchaouir Rachid; Meregalli Mirella; Farini Andrea; D'Antona Giuseppe; Belicchi Marzia; Goyenvalle Aurélie; Battistelli Maurizio; Bresolin Nereo; Bottinelli Roberto; Garcia Luis; Torrente Yvan
Restoration of human dystrophin following transplantation of exon-skipping-engineered DMD patient stem cells into dystrophic mice.
Cell stem cell 2007;1(6):646-57.
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2007: Tonelli A; Gallanti A; Bersano A; Cardin V; Ballabio E; Airoldi G; Redaelli F; Candelise L; Bresolin N; Bassi M T
Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraine.
Clinical genetics 2007;72(6):517-23.
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2007: Del Bo Roberto; Di Fonzo Alessio; Ghezzi Serena; Locatelli Federica; Stevanin Giovanni; Costa Antonella; Corti Stefania; Bresolin Nereo; Comi Giacomo Pietro
SPG11: a consistent clinical phenotype in a family with homozygous spatacsin truncating mutation.
Neurogenetics 2007;8(4):301-5.
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2007: Tavano Alessandro; Grasso Rita; Gagliardi Chiara; Triulzi Fabio; Bresolin Nereo; Fabbro Franco; Borgatti Renato
Disorders of cognitive and affective development in cerebellar malformations.
Brain : a journal of neurology 2007;130(Pt 10):2646-60.
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2007: Scalabrini Diego; Fenoglio Chiara; Scarpini Elio; De Riz Milena; Comi Cristoforo; Venturelli Eliana; Cortini Francesca; Piola Mirko; Villa Chiara; Naldi Paola; Monaco Francesco; Bresolin Nereo; Galimberti Daniela
Candidate gene analysis of SPARCL1 gene in patients with multiple sclerosis.
Neuroscience letters 2007;425(3):173-6.
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2007: Ballabio E; Bersano A; Bresolin N; Candelise L
Monogenic vessel diseases related to ischemic stroke: a clinical approach.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2007;27(10):1649-62.
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2007: Locatelli Federica; Corti Stefania; Papadimitriou Dimitra; Fortunato Francesco; Del Bo Roberto; Donadoni Chiara; Nizzardo Monica; Nardini Martina; Salani Sabrina; Ghezzi Serena; Strazzer Sandra; Bresolin Nereo; Comi Giacomo Pietro
Fas small interfering RNA reduces motoneuron death in amyotrophic lateral sclerosis mice.
Annals of neurology 2007;62(1):81-92.
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2007: Marini A; Lorusso M L; D'Angelo M G; Civati F; Turconi A C; Fabbro F; Bresolin N
Evaluation of narrative abilities in patients suffering from Duchenne Muscular Dystrophy.
Brain and language 2007;102(1):1-12.
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2007: Corti Stefania; Nizzardo Monica; Nardini Martina; Donadoni Chiara; Locatelli Federica; Papadimitriou Dimitra; Salani Sabrina; Del Bo Roberto; Ghezzi Serena; Strazzer Sandra; Bresolin Nereo; Comi Giacomo P
Isolation and characterization of murine neural stem/progenitor cells based on Prominin-1 expression.
Experimental neurology 2007;205(2):547-62.
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2007: Corti Stefania; Locatelli Federica; Papadimitriou Dimitra; Del Bo Roberto; Nizzardo Monica; Nardini Martina; Donadoni Chiara; Salani Sabrina; Fortunato Francesco; Strazzer Sandra; Bresolin Nereo; Comi Giacomo P
Neural stem cells LewisX+ CXCR4+ modify disease progression in an amyotrophic lateral sclerosis model.
Brain : a journal of neurology 2007;130(Pt 5):1289-305.
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2007: Ghione Isabella; Di Fonzo Alessio; Saladino Francesca; Del Bo Roberto; Bresolin Nereo; Comi Giacomo Pietro; Rango Mario
Parkin polymorphisms and environmental exposure: decrease in age at onset of Parkinson's disease.
Neurotoxicology 2007;28(3):698-701.
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2007: Rango Mario; Arighi Andrea; Biondetti Piero; Barberis Barbara; Bonifati Cristiana; Blandini Fabio; Pacchetti Claudio; Martignoni Emilia; Bresolin Nereo; Nappi Giuseppe
Magnetic resonance spectroscopy in Parkinson's disease and parkinsonian syndromes.
Functional neurology 2007;22(2):75-9.
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2007: Fabbro F; Marini A; Felisari G; Comi G P; D'Angelo M G; Turconi A C; Bresolin N
Language disturbances in a group of participants suffering from Duchenne muscular dystrophy: a pilot study.
Perceptual and motor skills 2007;104(2):663-76.
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2007: Pisati Federica; Belicchi Marzia; Acerbi Francesco; Marchesi Chiara; Giussani Carlo; Gavina Manuela; Javerzat Sophie; Hagedorn Martin; Carrabba Giorgio; Lucini Valeria; Gaini Sergio Maria; Bresolin Nereo; Bello Lorenzo; Bikfalvi Andreas; Torrente Yvan
Effect of human skin-derived stem cells on vessel architecture, tumor growth, and tumor invasion in brain tumor animal models.
Cancer research 2007;67(7):3054-63.
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2007: Galimberti D; Venturelli E; Fenoglio C; Lovati C; Guidi I; Scalabrini D; Mariani C; Bresolin N; Scarpini E
IP-10 serum levels are not increased in mild cognitive impairment and Alzheimer's disease.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2007;14(4):e3-4.
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2007: Marchesi C; Pluderi M; Colleoni F; Belicchi M; Meregalli M; Farini A; Parolini D; Draghi L; Fruguglietti M E; Gavina M; Porretti L; Cattaneo A; Battistelli M; Prelle A; Moggio M; Borsa S; Bello L; Spagnoli D; Gaini S M; Tanzi M C; Bresolin N; Grimoldi N; Torrente Y
Skin-derived stem cells transplanted into resorbable guides provide functional nerve regeneration after sciatic nerve resection.
Glia 2007;55(4):425-38.
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2007: Galimberti D; Scalabrini D; Fenoglio C; Comi C; De Riz M; Venturelli E; Lovati C; Mariani C; Monaco F; Bresolin N; Scarpini E
CXCL10 haplotypes and multiple sclerosis: association and correlation with clinical course.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2007;14(2):162-7.
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2007: Fenoglio Chiara; Galimberti Daniela; Piccio Laura; Scalabrini Diego; Panina Paola; Buonsanti Cecilia; Venturelli Eliana; Lovati Carlo; Forloni Gianluigi; Mariani Claudio; Bresolin Nereo; Scarpini Elio
Absence of TREM2 polymorphisms in patients with Alzheimer's disease and Frontotemporal Lobar Degeneration.
Neuroscience letters 2007;411(2):133-7.
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2007: Pozzoli Uberto; Menozzi Giorgia; Comi Giacomo P; Cagliani Rachele; Bresolin Nereo; Sironi Manuela
Intron size in mammals: complexity comes to terms with economy.
Trends in genetics : TIG 2007;23(1):20-4.
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2007: Pisati Federica; Bossolasco Patrizia; Meregalli Mirella; Cova Lidia; Belicchi Marzia; Gavina Manuela; Marchesi Chiara; Calzarossa Cinzia; Soligo Davide; Lambertenghi-Deliliers Giorgio; Bresolin Nereo; Silani Vincenzo; Torrente Yvan; Polli Elio
Induction of neurotrophin expression via human adult mesenchymal stem cells: implication for cell therapy in neurodegenerative diseases.
Cell transplantation 2007;16(1):41-55.
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2006: Galimberti Daniela; Fenoglio Chiara; Lovati Carlo; Venturelli Eliana; Guidi Ilaria; Corrà Barbara; Scalabrini Diego; Clerici Francesca; Mariani Claudio; Bresolin Nereo; Scarpini Elio
Serum MCP-1 levels are increased in mild cognitive impairment and mild Alzheimer's disease.
Neurobiology of aging 2006;27(12):1763-8.
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2006: D'Adda Elisabetta; Sciacco Monica; Fruguglietti Maria Elisa; Crugnola Veronica; Lucchini Valeria; Martinelli-Boneschi Filippo; Zecca Chiara; Lamperti Costanza; Comi Giacomo Pietro; Bresolin Nereo; Moggio Maurizio; Prelle Alessandro
Follow-up of a large population of asymptomatic/oligosymptomatic hyperckemic subjects.
Journal of neurology 2006;253(11):1399-403.
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2006: Torrente Y; Gavina M; Belicchi M; Fiori F; Komlev V; Bresolin N; Rustichelli F
High-resolution X-ray microtomography for three-dimensional visualization of human stem cell muscle homing.
FEBS letters 2006;580(24):5759-64.
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2006: Gavina Manuela; Belicchi Marzia; Rossi Barbara; Ottoboni Linda; Colombo Fabio; Meregalli Mirella; Battistelli Maurizio; Forzenigo Laura; Biondetti Piero; Pisati Federica; Parolini Daniele; Farini Andrea; Issekutz Andrew C; Bresolin Nereo; Rustichelli Franco; Constantin Gabriela; Torrente Yvan
VCAM-1 expression on dystrophic muscle vessels has a critical role in the recruitment of human blood-derived CD133+ stem cells after intra-arterial transplantation.
Blood 2006;108(8):2857-66.
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2006: Sironi Manuela; Pozzoli Uberto; Comi Giacomo P; Riva Stefania; Bordoni Andreina; Bresolin Nereo; Nag Dilip K
A region in the dystrophin gene major hot spot harbors a cluster of deletion breakpoints and generates double-strand breaks in yeast.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2006;20(11):1910-2.
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2006: Venturelli Eliana; Galimberti Daniela; Fenoglio Chiara; Lovati Carlo; Finazzi Dario; Guidi Ilaria; Corrà Barbara; Scalabrini Diego; Clerici Francesca; Mariani Claudio; Forloni Gianluigi; Bresolin Nereo; Scarpini Elio
Candidate gene analysis of IP-10 gene in patients with Alzheimer's disease.
Neuroscience letters 2006;404(1-2):217-21.
-
2006: Panzeri Chris; De Palma Clara; Martinuzzi Andrea; Daga Andrea; De Polo Gianni; Bresolin Nereo; Miller Christopher C; Tudor Elizabeth L; Clementi Emilio; Bassi Maria T
The first ALS2 missense mutation associated with JPLS reveals new aspects of alsin biological function.
Brain : a journal of neurology 2006;129(Pt 7):1710-9.
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2006: D'Angelo Maria Grazia; Bresolin Nereo
Cognitive impairment in neuromuscular disorders.
Muscle & nerve 2006;34(1):16-33.
-
2006: Lucchiari S; Pagliarani S; Salani S; Filocamo M; Di Rocco M; Melis D; Rodolico C; Musumeci O; Toscano A; Bresolin N; Comi G P
Hepatic and neuromuscular forms of glycogenosis type III: nine mutations in AGL.
Human mutation 2006;27(6):600-1.
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2006: Crippa Francesca; Panzeri Chris; Martinuzzi Andrea; Arnoldi Alessia; Redaelli Francesca; Tonelli Alessandra; Baschirotto Cinzia; Vazza Giovanni; Mostacciuolo Maria Luisa; Daga Andrea; Orso Genny; Profice Paolo; Trabacca Antonio; D'Angelo Maria Grazia; Comi Giacomo Pietro; Galbiati Sara; Lamperti Costanza; Bonato Sara; Pandolfo Massimo; Meola Giovanni; Musumeci Olimpia; Toscano Antonio; Trevisan Carlo Pietro; Bresolin Nereo; Bassi Maria Teresa
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia.
Archives of neurology 2006;63(5):750-5.
-
2006: Del Bo Roberto; Scarlato Marina; Ghezzi Serena; Martinelli-Boneschi Filippo; Fenoglio Chiara; Galimberti Gloria; Galbiati Sara; Virgilio Roberta; Galimberti Daniela; Ferrarese Carlo; Scarpini Elio; Bresolin Nereo; Comi Giacomo Pietro
Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis.
Neurobiology of aging 2006;27(5):770.e1-770.e5.
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2006: Galimberti Daniela; Schoonenboom Niki; Scheltens Philip; Fenoglio Chiara; Bouwman Femke; Venturelli Eliana; Guidi Ilaria; Blankenstein Marinus A; Bresolin Nereo; Scarpini Elio
Intrathecal chemokine synthesis in mild cognitive impairment and Alzheimer disease.
Archives of neurology 2006;63(4):538-43.
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2006: Del Bo Roberto; Scarlato Marina; Ghezzi Serena; Maestroni Anna; Sjölind Lisa; Forsblom Carol; Wessman Maija; Groop Per-Henrik; Comi Giacomo Pietro; Bresolin Nereo; Luzi Livio; Zerbini Gianpaolo
VEGF gene variability and type 1 diabetes: evidence for a protective role.
Immunogenetics 2006;58(2-3):107-12.
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2006: Lamperti Costanza; Cagliani Rachele; Ciscato Patrizia; Moroni Isabella; Viri Maurizio; Romeo Antonio; Fagiolari Gigliola; Prelle Alessandro; Comi Giacomo Pietro; Bresolin Nereo; Moggio Maurizio
Congenital muscular dystrophy with muscle inflammation alpha dystroglycan glycosylation defect and no mutation in FKRP gene.
Journal of the neurological sciences 2006;243(1-2):47-51.
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2006: Corti Stefania; Locatelli Federica; Papadimitriou Dimitra; Donadoni Chiara; Salani Sabrina; Del Bo Roberto; Strazzer Sandra; Bresolin Nereo; Comi Giacomo P
Identification of a primitive brain-derived neural stem cell population based on aldehyde dehydrogenase activity.
Stem cells (Dayton, Ohio) 2006;24(4):975-85.
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2006: Del Bo R; Locatelli F; Corti S; Scarlato M; Ghezzi S; Prelle A; Fagiolari G; Moggio M; Carpo M; Bresolin N; Comi G P
Coexistence of CMT-2D and distal SMA-V phenotypes in an Italian family with a GARS gene mutation.
Neurology 2006;66(5):752-4.
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2006: Bedeschi Maria Francesca; Bonaglia Maria Clara; Grasso Rita; Pellegri Alda; Garghentino Rosaria Rita; Battaglia Maria Amalia; Panarisi Anna Maria; Di Rocco Maja; Balottin Umberto; Bresolin Nereo; Bassi Maria Teresa; Borgatti Renato
Agenesis of the corpus callosum: clinical and genetic study in 63 young patients.
Pediatric neurology 2006;34(3):186-93.
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2006: Galbiati Sara; Bordoni Andreina; Papadimitriou Dimitra; Toscano Antonio; Rodolico Carmelo; Katsarou Efi; Sciacco Monica; Garufi Anastasia; Prelle Alessandro; Aguennouz M 'hammed; Bonsignore Maria; Crimi Marco; Martinuzzi Andrea; Bresolin Nereo; Papadimitriou Alex; Comi Giacomo P
New mutations in TK2 gene associated with mitochondrial DNA depletion.
Pediatric neurology 2006;34(3):177-85.
-
2006: Zanotta Nicoletta; Raggi M Elisabetta; Radice Lucia; Degrate Alessandro; Bresolin Nereo; Zucca Claudio
Clinical experience with topiramate dosing and serum levels in patients with epilepsy.
Seizure : the journal of the British Epilepsy Association 2006;15(2):86-92.
-
2006: Rango M; Canesi M; Ghione I; Farabola M; Righini A; Bresolin N; Antonini A; Pezzoli G
Parkinson's disease, chronic hydrocarbon exposure and striatal neuronal damage: a 1-H MRS study.
Neurotoxicology 2006;27(2):164-8.
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2006: Guidi Ilaria; Galimberti Daniela; Lonati Silvia; Novembrino Cristina; Bamonti Fabrizia; Tiriticco Marco; Fenoglio Chiara; Venturelli Eliana; Baron Pierluigi; Bresolin Nereo; Scarpini Elio
Oxidative imbalance in patients with mild cognitive impairment and Alzheimer's disease.
Neurobiology of aging 2006;27(2):262-9.
-
2006: Tonelli Alessandra; D'Angelo Maria Grazia; Salati Roberto; Villa Laura; Germinasi Chiara; Frattini Tiziano; Meola Giovanni; Turconi Anna Carla; Bresolin Nereo; Bassi Maria Teresa
Early onset, non fluctuating spinocerebellar ataxia and a novel missense mutation in CACNA1A gene.
Journal of the neurological sciences 2006;241(1-2):13-7.
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2006: Fenoglio Chiara; Galimberti Daniela; Ban Maria; Maranian Mel; Scalabrini Diego; Venturelli Eliana; Piccio Laura; De Riz Milena; Yeo Tai Wai; Goris An; Gray Julia; Bresolin Nereo; Scarpini Elio; Compston Alastair; Sawcer Stephen
SELPLG and SELP single-nucleotide polymorphisms in multiple sclerosis.
Neuroscience letters 2006;394(2):92-6.
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2006: Rango Mario; Bonifati Cristiana; Bresolin Nereo
Parkinson's disease and brain mitochondrial dysfunction: a functional phosphorus magnetic resonance spectroscopy study.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2006;26(2):283-90.
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2006: Galimberti D; Schoonenboom N; Scheltens P; Fenoglio C; Venturelli E; Pijnenburg Y A L; Bresolin N; Scarpini E
Intrathecal chemokine levels in Alzheimer disease and frontotemporal lobar degeneration.
Neurology 2006;66(1):146-7.
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2006: Corti Stefania; Locatelli Federica; Papadimitriou Dimitra; Donadoni Chiara; Del Bo Roberto; Crimi Marco; Bordoni Andreina; Fortunato Francesco; Strazzer Sandra; Menozzi Giorgia; Salani Sabrina; Bresolin Nereo; Comi Giacomo P
Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1.
Human molecular genetics 2006;15(2):167-87.
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2006: Scarpini Elio; Galimberti Daniela; Guidi Ilaria; Bresolin Nereo; Scheltens Philip
Progressive, isolated language disturbance: its significance in a 65-year-old-man. A case report with implications for treatment and review of literature.
Journal of the neurological sciences 2006;240(1-2):45-51.
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2006: Sironi Manuela; Menozzi Giorgia; Comi Giacomo P; Cereda Matteo; Cagliani Rachele; Bresolin Nereo; Pozzoli Uberto
Gene function and expression level influence the insertion/fixation dynamics of distinct transposon families in mammalian introns.
Genome biology 2006;7(12):R120.
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2005: Bassi Maria T; Balottin Umberto; Panzeri Chris; Piccinelli Paolo; Castaldo Pasqualina; Barrese Vincenzo; Soldovieri Maria V; Miceli Francesco; Colombo Maria; Bresolin Nereo; Borgatti Renato; Taglialatela Maurizio
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC).
Neurogenetics 2005;6(4):185-93.
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2005: Sciacco Monica; Prelle Alessandro; Fagiolari Gigliola; Bordoni Andreina; Crimi Marco; Di Fonzo Alessio; Ciscato Patrizia; Lamperti Costanza; D'Adda Elisabetta; Jann Stefano; Bresolin Nereo; Comi Giacomo P; Moggio Maurizio
A case of CPT deficiency, homoplasmic mtDNA mutation and ragged red fibers at muscle biopsy.
Journal of the neurological sciences 2005;239(1):21-4.
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2005: Lamperti Costanza; Naini Ali B; Lucchini Valeria; Prelle Alessandro; Bresolin Nereo; Moggio Maurizio; Sciacco Monica; Kaufmann Petra; DiMauro Salvatore
Muscle coenzyme Q10 level in statin-related myopathy.
Archives of neurology 2005;62(11):1709-12.
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2005: Corti Stefania; Locatelli Federica; Papadimitriou Dimitra; Donadoni Chiara; Del Bo Roberto; Fortunato Francesco; Strazzer Sandra; Salani Sabrina; Bresolin Nereo; Comi Giacomo P
Multipotentiality, homing properties, and pyramidal neurogenesis of CNS-derived LeX(ssea-1)+/CXCR4+ stem cells.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2005;19(13):1860-2.
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2005: Scalabrini Diego; Galimberti Daniela; Fenoglio Chiara; Comi Cristoforo; De Riz Milena; Venturelli Eliana; Castelli Luca; Piccio Laura; Ronzoni Marco; Lovati Carlo; Mariani Claudio; Monaco Francesco; Bresolin Nereo; Scarpini Elio
P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis.
Neuroscience letters 2005;388(3):149-52.
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2005: Baron Pierluigi; Bussini Simona; Cardin Veronica; Corbo Massimo; Conti Giancarlo; Galimberti Daniela; Scarpini Elio; Bresolin Nereo; Wharton Stephen B; Shaw Pamela J; Silani Vincenzo
Production of monocyte chemoattractant protein-1 in amyotrophic lateral sclerosis.
Muscle & nerve 2005;32(4):541-4.
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2005: Cagliani Rachele; Magri Francesca; Toscano Antonio; Merlini Luciano; Fortunato Francesco; Lamperti Costanza; Rodolico Carmelo; Prelle Alessandro; Sironi Manuela; Aguennouz Mohammed; Ciscato Patrizia; Uncini Antonino; Moggio Maurizio; Bresolin Nereo; Comi Giacomo P
Mutation finding in patients with dysferlin deficiency and role of the dysferlin interacting proteins annexin A1 and A2 in muscular dystrophies.
Human mutation 2005;26(3):283.
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2005: Sironi Manuela; Menozzi Giorgia; Comi Giacomo P; Cagliani Rachele; Bresolin Nereo; Pozzoli Uberto
Analysis of intronic conserved elements indicates that functional complexity might represent a major source of negative selection on non-coding sequences.
Human molecular genetics 2005;14(17):2533-46.
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2005: Sironi Manuela; Menozzi Giorgia; Comi Giacomo P; Bresolin Nereo; Cagliani Rachele; Pozzoli Uberto
Fixation of conserved sequences shapes human intron size and influences transposon-insertion dynamics.
Trends in genetics : TIG 2005;21(9):484-8.
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2005: Galimberti Daniela; Fenoglio Chiara; Clerici Raffaella; Comi Cristoforo; De Riz Milena; Rottoli Mariarosa; Piccio Laura; Ronzoni Marco; Venturelli Eliana; Monaco Francesco; Poloni Marco; Bresolin Nereo; Scarpini Elio
E-selectin A561C and G98T polymorphisms influence susceptibility and course of multiple sclerosis.
Journal of neuroimmunology 2005;165(1-2):201-5.
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2005: Galimberti Daniela; Venturelli Eliana; Gatti Alberto; Lovati Carlo; Fenoglio Chiara; Mariani Claudio; Forloni Gianluigi; Bresolin Nereo; Scarpini Elio
Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's disease.
Journal of neurology 2005;252(8):985-6.
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2005: Bussini Simona; Meda Lucia; Scarpini Elio; Clementi Emilio; Conti Giancarlo; Tiriticco Marco; Bresolin Nereo; Baron Pierluigi
Heparan sulfate proteoglycan induces the production of NO and TNF-alpha by murine microglia.
Immunity & ageing : I & A 2005;2():11.
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2005: Venturelli Eliana; Galimberti Daniela; Lovati Carlo; Fenoglio Chiara; Scalabrini Diego; Mariani Claudio; Forloni Gianluigi; Bresolin Nereo; Scarpini Elio
The T-786C NOS3 polymorphism in Alzheimer's disease: association and influence on gene expression.
Neuroscience letters 2005;382(3):300-3.
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2005: Guidi Ilaria; Galimberti Daniela; Venturelli Eliana; Lovati Carlo; Del Bo Roberto; Fenoglio Chiara; Gatti Alberto; Dominici Roberto; Galbiati Sara; Virgilio Roberta; Pomati Simone; Comi Giacomo P; Mariani Claudio; Forloni Gianluigi; Bresolin Nereo; Scarpini Elio
Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients.
Neurobiology of aging 2005;26(6):789-94.
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2005: Crimi Marco; Bordoni Andreina; Menozzi Giorgia; Riva Laura; Fortunato Francesco; Galbiati Sara; Del Bo Roberto; Pozzoli Uberto; Bresolin Nereo; Comi Giacomo Pietro
Skeletal muscle gene expression profiling in mitochondrial disorders.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2005;19(7):866-8.
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2005: Basilisco Guido; Gebbia Carlotta; Peracchi Maddalena; Velio Pietro; Conte Dario; Bresolin Nereo; Nobile-Orazio Eduardo
Cerebellar degeneration and hearing loss in a patient with idiopathic myenteric ganglionitis.
European journal of gastroenterology & hepatology 2005;17(4):449-52.
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2005: Del Bo Roberto; Scarlato Marina; Ghezzi Serena; Martinelli Boneschi Filippo; Fenoglio Chiara; Galbiati Sara; Virgilio Roberta; Galimberti Daniela; Galimberti Gloria; Crimi Marco; Ferrarese Carlo; Scarpini Elio; Bresolin Nereo; Comi Giacomo P
Vascular endothelial growth factor gene variability is associated with increased risk for AD.
Annals of neurology 2005;57(3):373-80.
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2004: Scalabrino Giuseppe; Carpo Marinella; Bamonti Fabrizia; Pizzinelli Simona; D'Avino Carla; Bresolin Nereo; Meucci Giuseppe; Martinelli Vittorio; Comi Gian Carlo; Peracchi Maddalena
High tumor necrosis factor-alpha [corrected] levels in cerebrospinal fluid of cobalamin-deficient patients.
Annals of neurology 2004;56(6):886-90.
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2004: Galimberti Daniela; Fenoglio Chiara; Lovati Carlo; Gatti Alberto; Guidi Ilaria; Venturelli Eliana; Cutter Gary R; Mariani Claudio; Forloni Gianluigi; Pettenati Carla; Baron Pierluigi; Conti Giancarlo; Bresolin Nereo; Scarpini Elio
CCR2-64I polymorphism and CCR5Delta32 deletion in patients with Alzheimer's disease.
Journal of the neurological sciences 2004;225(1-2):79-83.
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2004: Fenoglio Chiara; Galimberti Daniela; Lovati Carlo; Guidi Ilaria; Gatti Alberto; Fogliarino Sergio; Tiriticco Marco; Mariani Claudio; Forloni Gianluigi; Pettenati Carla; Baron Pierluigi; Conti Giancarlo; Bresolin Nereo; Scarpini Elio
MCP-1 in Alzheimer's disease patients: A-2518G polymorphism and serum levels.
Neurobiology of aging 2004;25(9):1169-73.
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2004: Pozzoli Uberto; Riva Laura; Menozzi Giorgia; Cagliani Rachele; Comi Giacomo P; Bresolin Nereo; Giorda Roberto; Sironi Manuela
Over-representation of exonic splicing enhancers in human intronless genes suggests multiple functions in mRNA processing.
Biochemical and biophysical research communications 2004;322(2):470-6.
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2004: Salani Sabrina; Lucchiari Sabrina; Fortunato Francesco; Crimi Marco; Corti Stefania; Locatelli Federica; Bossolasco Patrizia; Bresolin Nereo; Comi Giacomo Pietro
Developmental and tissue-specific regulation of a novel dysferlin isoform.
Muscle & nerve 2004;30(3):366-74.
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2004: Belicchi Marzia; Pisati Federica; Lopa Raffaella; Porretti Laura; Fortunato Francesco; Sironi Manuela; Scalamogna Mario; Parati Eugenio A; Bresolin Nereo; Torrente Yvan
Human skin-derived stem cells migrate throughout forebrain and differentiate into astrocytes after injection into adult mouse brain.
Journal of neuroscience research 2004;77(4):475-86.
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2004: Borgatti Renato; Piccinelli Paolo; Montirosso Rosario; Donati Gemma; Rampani Alessandra; Molteni Laura; Tofani Annalisa; Nicoli Francesca; Zucca Claudio; Bresolin Nereo; Balottin Umberto
Study of attentional processes in children with idiopathic epilepsy by Conners' Continuous Performance Test.
Journal of child neurology 2004;19(7):509-15.
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2004: Torrente Yvan; Belicchi Marzia; Sampaolesi Maurilio; Pisati Federica; Meregalli Mirella; D'Antona Giuseppe; Tonlorenzi Rossana; Porretti Laura; Gavina Manuela; Mamchaoui Kamel; Pellegrino Maria Antonietta; Furling Denis; Mouly Vincent; Butler-Browne Gillian S; Bottinelli Roberto; Cossu Giulio; Bresolin Nereo
Human circulating AC133(+) stem cells restore dystrophin expression and ameliorate function in dystrophic skeletal muscle.
The Journal of clinical investigation 2004;114(2):182-95.
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2004: Borgatti R; Zucca C; Cavallini A; Ferrario M; Panzeri C; Castaldo P; Soldovieri M V; Baschirotto C; Bresolin N; Dalla Bernardina B; Taglialatela M; Bassi M T
A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation.
Neurology 2004;63(1):57-65.
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2004: Conti Giancarlo; Rostami Abdolmohammed; Scarpini Elio; Baron PierLuigi; Galimberti Daniela; Bresolin Nereo; Contri Miranda; Palumbo Carla; De Pol Anto
Inducible nitric oxide synthase (iNOS) in immune-mediated demyelination and Wallerian degeneration of the rat peripheral nervous system.
Experimental neurology 2004;187(2):350-8.
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2004: Cagliani Rachele; Sironi Manuela; Ciafaloni Emma; Bardoni Alessandra; Fortunato Francesco; Prelle Alessandro; Serafini Massimo; Bresolin Nereo; Comi Giacomo P
An intragenic deletion/inversion event in the DMD gene determines a novel exon creation and results in a BMD phenotype.
Human genetics 2004;115(1):13-8.
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2004: Galimberti Daniela; Bresolin Nereo; Scarpini Elio
Chemokine network in multiple sclerosis: role in pathogenesis and targeting for future treatments.
Expert review of neurotherapeutics 2004;4(3):439-53.
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2004: Crimi Marco; Papadimitriou Alexandros; Galbiati Sara; Palamidou Phani; Fortunato Francesco; Bordoni Andreina; Papandreou Urania; Papadimitriou Dimitra; Hadjigeorgiou George M; Drogari Eurydiki; Bresolin Nereo; Comi Giacomo Pietro
A new mitochondrial DNA mutation in ND3 gene causing severe Leigh syndrome with early lethality.
Pediatric research 2004;55(5):842-6.
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2004: Crimi Marco; Galbiati Sara; Sciacco Monica; Bordoni Andreina; Natali Maria Grazia; Raimondi Monica; Bresolin Nereo; Comi Giacomo Pietro
Mitochondrial-DNA nucleotides G4298A and T10010C as pathogenic mutations: the confirmation in two new cases.
Mitochondrion 2004;3(5):279-83.
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2004: Gironi M; Lamperti C; Nemni R; Moggio M; Comi G; Guerini F R; Ferrante P; Canal N; Naini A; Bresolin N; DiMauro S
Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency.
Neurology 2004;62(5):818-20.
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2004: Gorio A; Torrente Y; Madaschi L; Di Stefano A B; Pisati F; Marchesi C; Belicchi M; Di Giulio A M; Bresolin N
Fate of autologous dermal stem cells transplanted into the spinal cord after traumatic injury (TSCI).
Neuroscience 2004;125(1):179-89.
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2004: Sironi Manuela; Menozzi Giorgia; Riva Laura; Cagliani Rachele; Comi Giacomo P; Bresolin Nereo; Giorda Roberto; Pozzoli Uberto
Silencer elements as possible inhibitors of pseudoexon splicing.
Nucleic acids research 2004;32(5):1783-91.
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2004: Fabbro F; Tavano A; Corti S; Bresolin N; De Fabritiis P; Borgatti R
Long-term neuropsychological deficits after cerebellar infarctions in two young adult twins.
Neuropsychologia 2004;42(4):536-45.
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2003: Cagliani R; Fortunato F; Giorda R; Rodolico C; Bonaglia M C; Sironi M; D'Angelo M G; Prelle A; Locatelli F; Toscano A; Bresolin N; Comi G P
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population.
Neuromuscular disorders : NMD 2003;13(10):788-95.
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2003: Sciacco Monica; Prelle Alessandro; D'Adda Elisabetta; Lamperti Costanza; Bordoni Andreina; Rango Mario; Crimi Marco; Comi Giacomo P; Bresolin Nereo; Moggio Maurizio
Familial mtDNA T8993C transition causing both the NARP and the MILS phenotype in the same generation. A morphological, genetic and spectroscopic study.
Journal of neurology 2003;250(12):1498-500.
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2003: Cagliani R; Bresolin N; Prelle A; Gallanti A; Fortunato F; Sironi M; Ciscato P; Fagiolari G; Bonato S; Galbiati S; Corti S; Lamperti C; Moggio M; Comi G P
A CAV3 microdeletion differentially affects skeletal muscle and myocardium.
Neurology 2003;61(11):1513-9.
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2003: Di Fonzo Alessio; Bordoni Andreina; Crimi Marco; Sara Galbiati; Del Bo Roberto; Bresolin Nereo; Comi Giacomo P
POLG mutations in sporadic mitochondrial disorders with multiple mtDNA deletions.
Human mutation 2003;22(6):498-9.
-
2003: Crimi Marco; Del Bo Roberto; Galbiati Sara; Sciacco Monica; Bordoni Andreina; Bresolin Nereo; Comi Giacomo Pietro
Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion.
European journal of human genetics : EJHG 2003;11(11):896-8.
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2003: Del Bo R; Bordoni A; Sciacco M; Di Fonzo A; Galbiati S; Crimi M; Bresolin N; Comi G P
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domain.
Neurology 2003;61(7):903-8.
-
2003: Lucchiari S; Donati M A; Melis D; Filocamo M; Parini R; Bresolin N; Comi G P
Mutational analysis of the AGL gene: five novel mutations in GSD III patients.
Human mutation 2003;22(4):337.
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2003: Del Bo Roberto; Crimi Marco; Sciacco Monica; Malferrari Giulia; Bordoni Andreina; Napoli Laura; Prelle Alessandro; Biunno Ida; Moggio Maurizio; Bresolin Nereo; Scarlato Guglielmo; Pietro Comi Giacomo
High mutational burden in the mtDNA control region from aged muscles: a single-fiber study.
Neurobiology of aging 2003;24(6):829-38.
-
2003: Greco Marilena; Villani Gaetano; Mazzucchelli Franca; Bresolin Nereo; Papa Sergio; Attardi Giuseppe
Marked aging-related decline in efficiency of oxidative phosphorylation in human skin fibroblasts.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2003;17(12):1706-8.
-
2003: Torrente Yvan; Camirand Geoffrey; Pisati Federica; Belicchi Marzia; Rossi Barbara; Colombo Fabio; El Fahime Mosthapha; Caron Nicolas J; Issekutz Andrew C; Constantin Gabriela; Tremblay Jacques P; Bresolin Nereo
Identification of a putative pathway for the muscle homing of stem cells in a muscular dystrophy model.
The Journal of cell biology 2003;162(3):511-20.
-
2003: Sampaolesi Maurilio; Torrente Yvan; Innocenzi Anna; Tonlorenzi Rossana; D'Antona Giuseppe; Pellegrino M Antonietta; Barresi Rita; Bresolin Nereo; De Angelis M Gabriella Cusella; Campbell Kevin P; Bottinelli Roberto; Cossu Giulio
Cell therapy of alpha-sarcoglycan null dystrophic mice through intra-arterial delivery of mesoangioblasts.
Science (New York, N.Y.) 2003;301(5632):487-92.
-
2003: Del Bo Roberto; Baron Pierluigi; Prelle Alessandro; Serafini Massimo; Moggio Maurizio; Fonzo Alessio Di; Castagni Marina; Bresolin Nereo; Comi Giacomo Pietro
Novel missense mutation and large deletion of GNE gene in autosomal-recessive inclusion-body myopathy.
Muscle & nerve 2003;28(1):113-7.
-
2003: Del Bo Roberto; Comi Giacomo Pietro; Giorda Roberto; Crimi Marco; Locatelli Federica; Martinelli-Boneschi Filippo; Pozzoli Uberto; Castelli Enrico; Bresolin Nereo; Scarlato Guglielmo
The 129 codon polymorphism of the prion protein gene influences earlier cognitive performance in Down syndrome subjects.
Journal of neurology 2003;250(6):688-92.
-
2003: Begni Barbara; Brighina Laura; Fumagalli Lorenzo; Andreoni Simona; Castelli Enrico; Francesconi Claudia; Del Bo Roberto; Bresolin Nereo; Ferrarese Carlo
Altered glutamate uptake in peripheral tissues from Down syndrome patients.
Neuroscience letters 2003;343(2):73-6.
-
2003: Prelle A; Sciacco M; Tancredi L; Fagiolari G; Comi G P; Ciscato P; Serafini M; Fortunato F; Zecca C; Gallanti A; Chiveri L; Bresolin N; Scarlato G; Moggio M
Clinical, morphological and immunological evaluation of six patients with dysferlin deficiency.
Acta neuropathologica 2003;105(6):537-42.
-
2003: Pozzoli Uberto; Elgar Greg; Cagliani Rachele; Riva Laura; Comi Giacomo P; Bresolin Nereo; Bardoni Alessandra; Sironi Manuela
Comparative analysis of vertebrate dystrophin loci indicate intron gigantism as a common feature.
Genome research 2003;13(5):764-72.
-
2003: Crimi M; Galbiati S; Perini M P; Bordoni A; Malferrari G; Sciacco M; Biunno I; Strazzer S; Moggio M; Bresolin N; Comi G P
A mitochondrial tRNA(His) gene mutation causing pigmentary retinopathy and neurosensorial deafness.
Neurology 2003;60(7):1200-3.
-
2003: Sironi Manuela; Pozzoli Uberto; Cagliani Rachele; Giorda Roberto; Comi Giacomo P; Bardoni Alessandra; Menozzi Giorgia; Bresolin Nereo
Relevance of sequence and structure elements for deletion events in the dystrophin gene major hot-spot.
Human genetics 2003;112(3):272-88.
-
2003: Sironi M; Cagliani R; Comi G P; Pozzoli U; Bardoni A; Giorda R; Bresolin N
Trans-acting factors may cause dystrophin splicing misregulation in BMD skeletal muscles.
FEBS letters 2003;537(1-3):30-4.
-
2003: Cagliani R; Bardoni A; Sironi M; Fortunato F; Prelle A; Felisari G; Bonaglia M C; D'Angelo M G; Moggio M; Bresolin N; Comi G P
Two dystrophin proteins and transcripts in a mild dystrophinopathic patient.
Neuromuscular disorders : NMD 2003;13(1):13-6.
-
2003: Torrente Y; El Fahime E; Caron N J; Del Bo R; Belicchi M; Pisati F; Tremblay J P; Bresolin N
Tumor necrosis factor-alpha (TNF-alpha) stimulates chemotactic response in mouse myogenic cells.
Cell transplantation 2003;12(1):91-100.
-
2002: Corti S; Locatelli F; Donadoni C; Strazzer S; Salani S; Del Bo R; Caccialanza M; Bresolin N; Scarlato G; Comi G P
Neuroectodermal and microglial differentiation of bone marrow cells in the mouse spinal cord and sensory ganglia.
Journal of neuroscience research 2002;70(6):721-33.
-
2002: Lucchiari S; Donati M A; Parini R; Melis D; Gatti R; Bresolin N; Scarlato G; Comi G P
Molecular characterisation of GSD III subjects and identification of six novel mutations in AGL.
Human mutation 2002;20(6):480.
-
2002: Crimi Marco; Sciacco Monica; Galbiati Sara; Bordoni Andreina; Malferrari Giulia; Del Bo Roberto; Biunno Ida; Bresolin Nereo; Comi Giacomo P
A collection of 33 novel human mtDNA homoplasmic variants.
Human mutation 2002;20(5):409.
-
2002: Corti S; Locatelli F; Strazzer S; Salani S; Del Bo R; Soligo D; Bossolasco P; Bresolin N; Scarlato G; Comi G P
Modulated generation of neuronal cells from bone marrow by expansion and mobilization of circulating stem cells with in vivo cytokine treatment.
Experimental neurology 2002;177(2):443-52.
-
2002: Del Bo Roberto; Bordoni Andreina; Martinelli Boneschi Filippo; Crimi Marco; Sciacco Monica; Bresolin Nereo; Scarlato Guglielmo; Comi Giacomo Pietri
Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients.
Journal of the neurological sciences 2002;202(1-2):85-91.
-
2002: Corti S; Strazzer S; Del Bo R; Salani S; Bossolasco P; Fortunato F; Locatelli F; Soligo D; Moggio M; Ciscato P; Prelle A; Borsotti C; Bresolin N; Scarlato G; Comi G P
A subpopulation of murine bone marrow cells fully differentiates along the myogenic pathway and participates in muscle repair in the mdx dystrophic mouse.
Experimental cell research 2002;277(1):74-85.
-
2002: Lucchiari S; Fogh I; Prelle A; Parini R; Bresolin N; Melis D; Fiori L; Scarlato G; Comi G P
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean area.
American journal of medical genetics 2002;109(3):183-90.
-
2002: Sironi M; Cagliani R; Pozzoli U; Bardoni A; Comi G P; Giorda R; Bresolin N
The dystrophin gene is alternatively spliced throughout its coding sequence.
FEBS letters 2002;517(1-3):163-6.
-
2002: Prelle Alessandro; Tancredi Lucia; Sciacco Monica; Chiveri Luca; Comi Giacomo P; Battistel Alessandro; Bazzi Paola; Martinelli Boneschi Filippo; Bagnardi Vincenzo; Ciscato Patrizia; Bordoni Andreina; Fortunato Franco; Strazzer Sandra; Bresolin Nereo; Scarlato Guglielmo; Moggio Maurizio
Retrospective study of a large population of patients with asymptomatic or minimally symptomatic raised serum creatine kinase levels.
Journal of neurology 2002;249(3):305-11.
-
2002: Pozzoli Uberto; Sironi Manuela; Cagliani Rachele; Comi Giacomo P; Bardoni Alessandra; Bresolin Nereo
Comparative analysis of the human dystrophin and utrophin gene structures.
Genetics 2002;160(2):793-8.
-
2002: Comi Giacomo P; Strazzer Sandra; Galbiati Sara; Bresolin Nereo
Cytochrome c oxidase deficiency.
International review of neurobiology 2002;53():205-40.
-
2002: Torrente Yvan; Belicchi Marzia; Pisati Federica; Pagano Stefano F; Fortunato Francesco; Sironi Manuela; D'Angelo Maria Grazia; Parati Eugenio A; Scarlato Guglielmo; Bresolin Nereo
Alternative sources of neurons and glia from somatic stem cells.
Cell transplantation 2002;11(1):25-34.
-
2001: Colombo F R; Torrente Y; Casati R; Benti R; Corti S; Salani S; D'Angelo M G; DeLiso A; Scarlato G; Bresolin N; Gerundini P
Biodistribution studies of 99mTc-labeled myoblasts in a murine model of muscular dystrophy.
Nuclear medicine and biology 2001;28(8):935-40.
-
2001: Sciacco M; Prelle A; Comi G P; Napoli L; Battistel A; Bresolin N; Tancredi L; Lamperti C; Bordoni A; Fagiolari G; Ciscato P; Chiveri L; Perini M P; Fortunato F; Adobbati L; Messina S; Toscano A; Martinelli-Boneschi F; Papadimitriou A; Scarlato G; Moggio M
Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation.
Journal of neurology 2001;248(9):778-88.
-
2001: Comi G P; Fortunato F; Lucchiari S; Bordoni A; Prelle A; Jann S; Keller A; Ciscato P; Galbiati S; Chiveri L; Torrente Y; Scarlato G; Bresolin N
Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis.
Annals of neurology 2001;50(2):202-7.
-
2001: Corti S; Salani S; Del Bo R; Sironi M; Strazzer S; D'Angelo M G; Comi G P; Bresolin N; Scarlato G
Chemotactic factors enhance myogenic cell migration across an endothelial monolayer.
Experimental cell research 2001;268(1):36-44.
-
2001: Sironi M; Pozzoli U; Cagliani R; Comi G P; Bardoni A; Bresolin N
Analysis of splicing parameters in the dystrophin gene: relevance for physiological and pathogenetic splicing mechanisms.
Human genetics 2001;109(1):73-84.
-
2001: Sironi M; Bardoni A; Felisari G; Cagliani R; Robotti M; Comi G P; Moggio M; Bresolin N
Transcriptional activation of the non-muscle, full-length dystrophin isoforms in Duchenne muscular dystrophy skeletal muscle.
Journal of the neurological sciences 2001;186(1-2):51-7.
-
2001: Cagliani R; Comi G P; Tancredi L; Sironi M; Fortunato F; Giorda R; Bardoni A; Moggio M; Prelle A; Bresolin N; Scarlato G
Primary beta-sarcoglycanopathy manifesting as recurrent exercise-induced myoglobinuria.
Neuromuscular disorders : NMD 2001;11(4):389-94.
-
2001: Sciacco M; Fagiolari G; Lamperti C; Messina S; Bazzi P; Napoli L; Chiveri L; Prelle A; Comi G P; Bresolin N; Scarlato G; Moggio M
Lack of apoptosis in mitochondrial encephalomyopathies.
Neurology 2001;56(8):1070-4.
-
2001: Del Bo R; Torrente Y; Corti S; D'Angelo M G; Comi G P; Fagiolari G; Salani S; Cova A; Pisati F; Moggio M; Ausenda C; Scarlato G; Bresolin N
In vitro and in vivo tetracycline-controlled myogenic conversion of NIH-3T3 cells: evidence of programmed cell death after muscle cell transplantation.
Cell transplantation 2001;10(2):209-21.
-
2001: Torrente Y; Tremblay J P; Pisati F; Belicchi M; Rossi B; Sironi M; Fortunato F; El Fahime M; D'Angelo M G; Caron N J; Constantin G; Paulin D; Scarlato G; Bresolin N
Intraarterial injection of muscle-derived CD34(+)Sca-1(+) stem cells restores dystrophin in mdx mice.
The Journal of cell biology 2001;152(2):335-48.
-
2001: Corti S; Salani S; Del Bo R; Torrente Y; Strazzer S; Belicchi M; Paganoni S; Li Z; Comi G P; Bresolin N; Paulin D; Scarlato G
T-antigen regulated expression reduces apoptosis of tag-transformed human myoblasts.
Cellular and molecular life sciences : CMLS 2001;58(1):135-40.
-
2001: Del Bo R; Comi G P; Perini M P; Strazzer S; Bresolin N; Scarlato G
Down's syndrome fibroblasts anticipate the accumulation of specific ageing-related mtDNA mutations.
Annals of neurology 2001;49(1):137-8.
-
2001: Rango M; Bozzali M; Prelle A; Scarlato G; Bresolin N
Brain activation in normal subjects and in patients affected by mitochondrial disease without clinical central nervous system involvement: a phosphorus magnetic resonance spectroscopy study.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2001;21(1):85-91.
-
2000: Felisari G; Martinelli Boneschi F; Bardoni A; Sironi M; Comi G P; Robotti M; Turconi A C; Lai M; Corrao G; Bresolin N
Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy.
Neurology 2000;55(4):559-64.
-
2000: Torrente Y; El Fahime E; Caron N J; Bresolin N; Tremblay J P
Intramuscular migration of myoblasts transplanted after muscle pretreatment with metalloproteinases.
Cell transplantation 2000;9(4):539-49.
-
2000: Torrente Y; D'Angelo M G; Li Z; Del Bo R; Corti S; Mericskay M; DeLiso A; Fassati A; Paulin D; Comi G P; Scarlato G; Bresolin N
Transplacental injection of somite-derived cells in mdx mouse embryos for the correction of dystrophin deficiency.
Human molecular genetics 2000;9(12):1843-52.
-
2000: Bardoni A; Felisari G; Sironi M; Comi G; Lai M; Robotti M; Bresolin N
Loss of Dp140 regulatory sequences is associated with cognitive impairment in dystrophinopathies.
Neuromuscular disorders : NMD 2000;10(3):194-9.
-
1999: Turconi A C; Benti R; Castelli E; Pochintesta S; Felisari G; Comi G; Gagliardi C; Del Piccolo L; Bresolin N
Focal cognitive impairment in mitochondrial encephalomyopathies: a neuropsychological and neuroimaging study.
Journal of the neurological sciences 1999;170(1):57-63.
-
1999: Michikawa Y; Mazzucchelli F; Bresolin N; Scarlato G; Attardi G
Aging-dependent large accumulation of point mutations in the human mtDNA control region for replication.
Science (New York, N.Y.) 1999;286(5440):774-9.
-
1999: Hadjigeorgiou G M; Comi G P; Bordoni A; Shen J; Chen Y T; Salani S; Toscano A; Fortunato F; Lucchiari S; Bresolin N; Rodolico C; Piscaglia M G; Franceschina L; Papadimitriou A; Scarlato G
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa.
Journal of inherited metabolic disease 1999;22(6):762-3.
-
1999: Torrente Y; D'Angelo M G; Del Bo R; DeLiso A; Casati R; Benti R; Corti S; Comi G P; Gerundini P; Anichini A; Scarlato G; Bresolin N
Extracorporeal circulation as a new experimental pathway for myoblast implantation in mdx mice.
Cell transplantation 1999;8(3):247-58.
-
1999: Bardoni A; Sironi M; Felisari G; Comi G P; Bresolin N
Absence of brain Dp140 isoform and cognitive impairment in Becker muscular dystrophy.
Lancet 1999;353(9156):897-8.
-
1998: Franceschina L; Salani S; Bordoni A; Sciacco M; Napoli L; Comi G P; Prelle A; Fortunato F; Hadjigeorgiou G M; Farina E; Bresolin N; D'Angelo M G; Scarlato G
A novel mitochondrial tRNA(Ile) point mutation in chronic progressive external ophthalmoplegia.
Journal of neurology 1998;245(11):755-8.
-
1998: Papadimitriou A; Comi G P; Hadjigeorgiou G M; Bordoni A; Sciacco M; Napoli L; Prelle A; Moggio M; Fagiolari G; Bresolin N; Salani S; Anastasopoulos I; Giassakis G; Divari R; Scarlato G
Partial depletion and multiple deletions of muscle mtDNA in familial MNGIE syndrome.
Neurology 1998;51(4):1086-92.
-
1998: Comi G P; Bordoni A; Salani S; Franceschina L; Sciacco M; Prelle A; Fortunato F; Zeviani M; Napoli L; Bresolin N; Moggio M; Ausenda C D; Taanman J W; Scarlato G
Cytochrome c oxidase subunit I microdeletion in a patient with motor neuron disease.
Annals of neurology 1998;43(1):110-6.
-
1997: Prelle A; Comi G P; Rigoletto C; Turconi A; Felisari G; Ciscato P; Fortunato F; Messina S; Bresolin N; Mora M; Moggio M; Scarlato G
An atypical case of partial merosin deficiency congenital muscular dystrophy.
Journal of neurology 1997;244(6):391-5.
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1997: Bresolin N; Ausenda C D; Casati R; Torrente Y; DeLiso A; D'Angelo M G; Benti R; Moggio M; Baldessari S; Comi G P; Colombo F; Gerundini P; Scarlato G
Intra-aortic injection of myoblasts in mdx mice: genetic and technetium-99m cell labeling and biodistribution.
Muscle & nerve 1997;20(6):757-9.
-
1997: Del Bo R; Comi G P; Bresolin N; Castelli E; Conti E; Degiuli A; Ausenda C D; Scarlato G
The apolipoprotein E epsilon4 allele causes a faster decline of cognitive performances in Down's syndrome subjects.
Journal of the neurological sciences 1997;145(1):87-91.
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1996: Ausenda C D; Bresolin N; De Liso A; D'Angelo M G; Moggio M; Del Bo R; Gallanti A; Comi G P; Torrente Y; Bordoni A; Scarlato G
In vivo biolistic technique in control and mdx dystrophic mice.
Muscle & nerve 1996;19(7):912-4.
-
1996: Laderman K A; Penny J R; Mazzucchelli F; Bresolin N; Scarlato G; Attardi G
Aging-dependent functional alterations of mitochondrial DNA (mtDNA) from human fibroblasts transferred into mtDNA-less cells.
The Journal of biological chemistry 1996;271(27):15891-7.
-
1996: Papadimitriou A; Hadjigeorgiou G M; Divari R; Papagalanis N; Comi G; Bresolin N
The influence of Coenzyme Q10 on total serum calcium concentration in two patients with Kearns-Sayre Syndrome and hypoparathyroidism.
Neuromuscular disorders : NMD 1996;6(1):49-53.
-
1995: Ninfali P; Baronciani L; Bardoni A; Bresolin N
Muscle expression of glucose-6-phosphate dehydrogenase deficiency in different variants.
Clinical genetics 1995;48(5):232-7.
-
1995: Comi G P; Ciafaloni E; de Silva H A; Prelle A; Bardoni A; Rigoletto C; Robotti M; Bresolin N; Moggio M; Fortunato F
A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient.
Human molecular genetics 1995;4(11):2171-4.
-
1995: Toscano A; Fazio M C; Vita G; Cannavó S; Bresolin N; Bet L; Prelle A; Barbiroli B; Iotti S; Zaniol P
Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C.
Journal of neurology 1995;242(4):203-9.
-
1995: Moroni I; Gonano E F; Comi G P; Tegazzin V; Prelle A; Bordoni A; Bresolin N; Scarlato G
Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility.
Journal of neurology 1995;242(3):127-33.
-
1994: Meola G; Sansone V; Rotondo G; Radice S; Sterlicchio M; Mauri M; Bresolin N; Moggio M
Neural regulation of acid maltase in an unusual adult onset deficiency.
Clinical neuropathology 1994;13(5):286-91.
-
1994: Bresolin N; Castelli E; Comi G P; Felisari G; Bardoni A; Perani D; Grassi F; Turconi A; Mazzucchelli F; Gallotti D
Cognitive impairment in Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1994;4(4):359-69.
-
1994: Bet L; Moggio M; Comi G P; Mariani C; Prelle A; Checcarelli N; Bordoni A; Bresolin N; Scarpini E; Scarlato G
Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseases.
Journal of neurology 1994;241(8):511-6.
-
1994: Fassati A; Tedeschi S; Bordoni A; Amboni P; Curcio C; Bresolin N; Scarlato G
Rapid direct diagnosis of deletions carriers of Duchenne and Becker muscular dystrophies.
Lancet 1994;344(8918):302-3.
-
1994: Chomyn A; Lai S T; Shakeley R; Bresolin N; Scarlato G; Attardi G
Platelet-mediated transformation of mtDNA-less human cells: analysis of phenotypic variability among clones from normal individuals--and complementation behavior of the tRNALys mutation causing myoclonic epilepsy and ragged red fibers.
American journal of human genetics 1994;54(6):966-74.
-
1994: Vita G; Migliorato A; Toscano A; Bordoni A; Bresolin N; Fiumara A; Messina C
Immunocytochemistry of muscle cytoskeletal proteins in acid maltase deficiency.
Muscle & nerve 1994;17(6):655-61.
-
1994: Checcarelli N; Prelle A; Moggio M; Comi G; Bresolin N; Papadimitriou A; Fagiolari G; Bordoni A; Scarlato G
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy.
Journal of the neurological sciences 1994;123(1-2):74-9.
-
1994: Fassati A; Bordoni A; Amboni P; Fortunato F; Fagiolari G; Bresolin N; Prelle A; Comi G; Scarlato G
Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.
Journal of the neurological sciences 1994;123(1-2):140-6.
-
1994: Vita G; Toscano A; Bresolin N; Meola G; Fortunato F; Baradello A; Barbiroli B; Frassineti C; Zaniol P; Messina C
Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopy.
Journal of neurology 1994;241(5):289-94.
-
1994: Comi G P; Prelle A; Bresolin N; Moggio M; Bardoni A; Gallanti A; Vita G; Toscano A; Ferro M T; Bordoni A
Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.
Brain : a journal of neurology 1994;117 ( Pt 1)():1-14.
-
1993: Prelle A; Moggio M; Checcarelli N; Comi G; Bresolin N; Battistel A; Bordoni A; Scarlato G
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis.
Journal of the neurological sciences 1993;117(1-2):24-7.
-
1993: Meola G; Tremblay J P; Sansone V; Rotondo G; Radice S; Bresolin N; Huard J; Scarlato G
Muscle glucose-6-phosphate dehydrogenase deficiency: restoration of enzymatic activity in hybrid myotubes.
Muscle & nerve 1993;16(6):594-600.
-
1993: Bresolin N; Comi G P; Fortunato F; Meola G; Gallanti A; Tajana A; Velicogna M; Gonano E F; Ninfali P; Pifferi S
Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiency.
Journal of neurology 1993;240(5):272-7.
-
1993: Vita G; Toscano A; Mileto G; Pitrone F; Ferrò M T; Gagliardi E; Bresolin N; Fortunato F; Messina C
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism.
European neurology 1993;33(2):168-72.
-
1993: Vita G; Toscano A; Prelle A; Bordoni A; Checcarelli N; Bresolin N; Baradello A; Messina C
Muscle mitochondria investigation in myotonic dystrophy.
European neurology 1993;33(6):423-7.
-
1992: Mongini T; Doriguzzi C; Palmucci L; De Francesco A; Bet L; Manfredi L; Ponzetto C; Bresolin N
Lipid storage myopathy in multiple acyl-CoA dehydrogenase deficiency: an adult case.
European neurology 1992;32(3):170-6.
-
1992: Prelle A; Moggio M; Comi G P; Gallanti A; Checcarelli N; Bresolin N; Ciscato P; Fortunato F; Scarlato G
Congenital myopathy associated with abnormal accumulation of desmin and dystrophin.
Neuromuscular disorders : NMD 1992;2(3):169-75.
-
1991: Cortelli P; Montagna P; Avoni P; Sangiorgi S; Bresolin N; Moggio M; Zaniol P; Mantovani V; Barboni P; Barbiroli B
Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian family.
Neurology 1991;41(8):1211-5.
-
1991: Bresolin N; Martinelli P; Barbiroli B; Zaniol P; Ausenda C; Montagna P; Gallanti A; Comi G P; Scarlato G; Lugaresi E
Muscle mitochondrial DNA deletion and 31P-NMR spectroscopy alterations in a migraine patient.
Journal of the neurological sciences 1991;104(2):182-9.
-
1991: Mariani C; Bresolin N; Farina E; Moggio M; Ferrante C; Ciafaloni E; Sertorelli S; Ciccone A; Scarlato G
Muscle biopsy in Alzheimer's disease: morphological and biochemical findings.
Clinical neuropathology 1991;10(4):171-6.
-
1991: Meola G; Rotondo G; Velicogna M; Toppi R; Sansone V; Bresolin N; Comi G; Bordoni A; Amati P; Ausenda C
[Expression of a defect in the respiratory chain in cultured human cells]
Rivista di neurologia 1991;61(4):122-34.
-
1991: Chomyn A; Meola G; Bresolin N; Lai S T; Scarlato G; Attardi G
In vitro genetic transfer of protein synthesis and respiration defects to mitochondrial DNA-less cells with myopathy-patient mitochondria.
Molecular and cellular biology 1991;11(4):2236-44.
-
1991: Zeviani M; Amati P; Bresolin N; Antozzi C; Piccolo G; Toscano A; DiDonato S
Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF).
American journal of human genetics 1991;48(2):203-11.
-
1991: Scarlato G; Bresolin N; Moroni I; Doriguzzi C; Castelli E; Comi G; Angelini C; Carenzi A
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies.
Revue neurologique 1991;147(6-7):542-8.
-
1991: Ninfali P; Bresolin N; Baronciani L; Fortunato F; Comi G; Magnani M; Scarlato G
Glucose-6-phosphate dehydrogenase Lodi844C: a study on its expression in blood cells and muscle.
Enzyme 1991;45(4):180-7.
-
1990: Bresolin N; Doriguzzi C; Ponzetto C; Angelini C; Moroni I; Castelli E; Cossutta E; Binda A; Gallanti A; Gabellini S
Ubidecarenone in the treatment of mitochondrial myopathies: a multi-center double-blind trial.
Journal of the neurological sciences 1990;100(1-2):70-8.
-
1990: Zeviani M; Bresolin N; Gellera C; Bordoni A; Pannacci M; Amati P; Moggio M; Servidei S; Scarlato G; DiDonato S
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant disease.
American journal of human genetics 1990;47(6):904-14.
-
1990: Bet L; Bresolin N; Moggio M; Meola G; Prelle A; Schapira A H; Binzoni T; Chomyn A; Fortunato F; Cerretelli P
A case of mitochondrial myopathy, lactic acidosis and complex I deficiency.
Journal of neurology 1990;237(7):399-404.
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1990: Papadimitriou A; Manta P; Divari R; Karabetsos A; Papadimitriou E; Bresolin N
McArdle's disease: two clinical expressions in the same pedigree.
Journal of neurology 1990;237(4):267-70.
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1990: Ponzetto C; Bresolin N; Bordoni A; Moggio M; Meola G; Bet L; Prelle A; Scarlato G
Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues.
Journal of the neurological sciences 1990;96(2-3):207-10.
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1989: Scarlato G; Bresolin N; Moggio M; Bet L; Meola G
[Mitochondrial encephalomyopathy]
Recenti progressi in medicina 1989;80(12):665-72.
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1989: Scarlato G; Moggio M; Bet L; Gallanti A; Bresolin N
Mitochondrial encephalomyopathies.
Acta neurologica 1989;11(5):322-9.
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1989: Bresolin N; Bet L; Moggio M; Meola G; Fortunato F; Comi G; Adobbati L; Geremia L; Pittalis S; Scarlato G
Muscle glucose-6-phosphate dehydrogenase deficiency.
Journal of neurology 1989;236(4):193-8.
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1989: Sacquegna T; Montagna P; Moggio M; De Carolis P; Agati R; Bresolin N
Normal muscle mitochondrial function in Ramsay-Hunt syndrome.
Italian journal of neurological sciences 1989;10(1):73-5.
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1989: Doriguzzi C; Palmucci L; Mongini T; Bresolin N; Bet L; Comi G; Lala R
Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency.
Journal of neurology, neurosurgery, and psychiatry 1989;52(1):122-5.
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1989: Mongini T; Doriguzzi C; Palmucci L; Pollo B; Arnaudo E; Bresolin N
Sporadic distal myopathy with early adult onset: study of muscle biopsies and muscle cell cultures.
European neurology 1989;29(5):287-90.
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1989: Moggio M; Bresolin N; Scarpini E; Adobbati L; Prelle A; Gallanti A; Bet L; Fortunato F; Pellegrini G; Scarlato G
Cytochrome c oxidase during human fetal development.
International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 1989;7(1):5-14.
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1988: Bresolin N; Bet L; Binda A; Moggio M; Comi G; Nador F; Ferrante C; Carenzi A; Scarlato G
Clinical and biochemical correlations in mitochondrial myopathies treated with coenzyme Q10.
Neurology 1988;38(6):892-9.
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1988: Doriguzzi C; Palmucci L; Mongini T; Arnaudo E; Bet L; Bresolin N
Body building and myoglobinuria: report of three cases.
British medical journal (Clinical research ed.) 1988;296(6625):826-7.
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1988: Bresolin N; Bet L; Ferrante C; Binda A; Carenzi A; Moggio M; Comi G; Scarlato G
Immunological and biochemical studies and pilot therapeutic trial with ubidecarenone in Kearns-Sayre patients.
Advances in neurology 1988;48():239-56.
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1988: Bresolin N; Monza G; Scarpini E; Scarlato G; Straneo G; Martinazzoli A; Benincà G; Cattoni C; De Candia R; Belloni G
Treatment of anxiety with ketazolam in elderly patients.
Clinical therapeutics 1988;10(5):536-42.
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1988: Scarpini E; Baron P G; Bet L; Bottini G; Bresolin N; Meola G; Pezzoli G; Vallar G; Monza G C; Scarlato G
Low doses of ketazolam in anxiety: a double-blind, placebo-controlled study.
Neuropsychobiology 1988;20(2):74-7.
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1987: Meola G; Bresolin N; Rimoldi M; Velicogna M; Fortunato F; Scarlato G
Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and platelets.
Journal of neurology 1987;235(2):74-9.
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1987: Biral D; Damiani E; Scarpini E; Bet L; Bresolin N; Moggio M; Pellegrini G; Barbieri S; Scarlato G
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic features.
Neurology 1987;37(10):1658-62.
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1987: Bresolin N; Bet L; Moggio M; Meola G; Comi G; Gilardi A; Scarlato G
Muscle G6PD deficiency.
Lancet 1987;2(8552):212-3.
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1987: Bresolin N; Moggio M; Bet L; Gallanti A; Prelle A; Nobile-Orazio E; Adobbati L; Ferrante C; Pellegrini G; Scarlato G
Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues.
Annals of neurology 1987;21(6):564-72.
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1986: Angelini C; Bresolin N; Pegolo G; Bet L; Rinaldo P; Trevisan C; Vergani L
Childhood encephalomyopathy with cytochrome c oxidase deficiency, ataxia, muscle wasting, and mental impairment.
Neurology 1986;36(8):1048-52.
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1984: Bresolin N; Freddo L; Tegazzin V; Bet L; Armani M; Angelini C
Carnitine and acyltransferase in experimental neurogenic atrophies: changes with treatment.
Journal of neurology 1984;231(4):170-5.
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1982: Bresolin N; Freddo L; Vergani L; Angelini C
Carnitine, carnitine acyltransferases, and rat brain function.
Experimental neurology 1982;78(2):285-92.
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1981: Angelini C; Freddo L; Battistella P; Bresolin N; Pierobon-Bormioli S; Armani M; Vergani L
Carnitine palmityl transferase deficiency: clinical variability, carrier detection, and autosomal-recessive inheritance.
Neurology 1981;31(7):883-6.
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