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Giacomo Comi

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Anatomy

Physiology

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Chemicals & Drugs

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Italy

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Mice

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Publications

TOP 3
Flanigan Kevin M; Dunn Diane M; von Niederhausern Andrew; Howard Michael T; Mendell Jerry; Connolly Anne; Saunders Carol; Modrcin Ann; Dasouki Majed; Comi Giacomo P; Del Bo Roberto; Pickart Angela; Jacobson Richard; Finkel Richard; Medne Livija; Weiss Robert B
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy.
Demir Ercan; Gucuyener Kivilcim; Akturk Aysima; Talim Beril; Konus Oznur; Del Bo Roberto; Ghezzi Serena; Comi Giacomo P
An unusual presentation of muscle-eye-brain disease: severe eye abnormalities with mild muscle and brain involvement.
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).

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All Publications

2009: Flanigan Kevin M; Dunn Diane M; von Niederhausern Andrew; Howard Michael T; Mendell Jerry; Connolly Anne; Saunders Carol; Modrcin Ann; Dasouki Majed; Comi Giacomo P; Del Bo Roberto; Pickart Angela; Jacobson Richard; Finkel Richard; Medne Livija; Weiss Robert B
DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy.
Neuromuscular disorders : NMD 2009;19(11):743-8.
2009: Demir Ercan; Gucuyener Kivilcim; Akturk Aysima; Talim Beril; Konus Oznur; Del Bo Roberto; Ghezzi Serena; Comi Giacomo P
An unusual presentation of muscle-eye-brain disease: severe eye abnormalities with mild muscle and brain involvement.
Neuromuscular disorders : NMD 2009;19(10):692-5.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
2008: Seibel Peter; Di Nunno Chiara; Kukat Christian; Schäfer Ingo; Del Bo Roberto; Bordoni Andreina; Comi Giacomo P; Schön Astrid; Capuano Ferdinando; Latorre Dominga; Villani Gaetano
Cosegregation of novel mitochondrial 16S rRNA gene mutations with the age-associated T414G variant in human cybrids.
Nucleic acids research 2008;36(18):5872-81.
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.
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.
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.
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.
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.
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.
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.
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.
2007: Musumeci Olimpia; Aguennouz Mohammed; Comi Giacomo Pietro; Rodolico Carmelo; Autunno Massimo; Bordoni Andreina; Baratta Silvia; Taroni Franco; Vita Giuseppe; Toscano Antonio
Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency.
Neuromuscular disorders : NMD 2007;17(11-12):960-3.
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.
2007: Lucchiari S; Santoro D; Pagliarani S; Comi G P
Clinical, biochemical and genetic features of glycogen debranching enzyme deficiency.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2007;26(1):72-4.
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.
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.
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.
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.
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.
2007: Milic Astrid; Daniele Nathalie; Lochmüller Hanns; Mora Marina; Comi Giacomo P; Moggio Maurizio; Noulet Fanny; Walter Maggie C; Morandi Lucia; Poupiot Jérôme; Roudaut Carinne; Bittner Reginald E; Bartoli Marc; Richard Isabelle
A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay.
Neuromuscular disorders : NMD 2007;17(2):148-56.
2007: Valente Lucia; Tiranti Valeria; Marsano Rene Massimiliano; Malfatti Edoardo; Fernandez-Vizarra Erika; Donnini Claudia; Mereghetti Paolo; De Gioia Luca; Burlina Alberto; Castellan Claudio; Comi Giacomo P; Savasta Salvatore; Ferrero Iliana; Zeviani Massimo
Infantile encephalopathy and defective mitochondrial DNA translation in patients with mutations of mitochondrial elongation factors EFG1 and EFTu.
American journal of human genetics 2007;80(1):44-58.
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.
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.
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.
2006: Bruno Claudio; Cassandrini Denise; Martinuzzi Andrea; Toscano Antonio; Moggio Maurizio; Morandi Lucia; Servidei Serena; Mongini Tiziana; Angelini Corrado; Musumeci Olimpia; Comi Giacomo P; Lamperti Costanza; Filosto Massimiliano; Zara Federico; Minetti Carlo
McArdle disease: the mutation spectrum of PYGM in a large Italian cohort.
Human mutation 2006;27(7):718.
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.
2006: Capasso Margherita; De Angelis Maria Vittoria; Di Muzio Antonio; Scarciolla Oronzo; Pace Marta; Stuppia Liborio; Comi Giacomo Pietro; Uncini Antonino
Familial idiopathic hyper-CK-emia: an underrecognized condition.
Muscle & nerve 2006;33(6):760-5.
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.
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.
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.
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.
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.
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: 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.
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.
2005: Crimi Marco; O'Hearn Sean F; Wallace Douglas C; Comi Giacomo P
Molecular research technologies in mitochondrial diseases: the microarray approach.
IUBMB life 2005;57(12):811-8.
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.
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.
2005: Guglieri Michela; Magri Francesca; Comi Giacomo P
Molecular etiopathogenesis of limb girdle muscular and congenital muscular dystrophies: boundaries and contiguities.
Clinica chimica acta; international journal of clinical chemistry 2005;361(1-2):54-79.
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.
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.
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.
2005: Scarlato Marina; Previtali Stefano Carlo; Carpo Marinella; Pareyson Davide; Briani Chiara; Del Bo Roberto; Nobile-Orazio Eduardo; Quattrini Angelo; Comi Giacomo Pietro
Polyneuropathy in POEMS syndrome: role of angiogenic factors in the pathogenesis.
Brain : a journal of neurology 2005;128(Pt 8):1911-20.
2005: Corti S; Locatelli F; Papadimitriou D; Strazzer S; Bonato S; Comi G P
Nuclear reprogramming and adult stem cell potential.
Histology and histopathology 2005;20(3):977-86.
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.
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.
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.
2004: Corti Stefania; Locatelli Federica; Donadoni Chiara; Guglieri Michela; Papadimitriou Dimitra; Strazzer Sandra; Del Bo Roberto; Comi Giacomo P
Wild-type bone marrow cells ameliorate the phenotype of SOD1-G93A ALS mice and contribute to CNS, heart and skeletal muscle tissues.
Brain : a journal of neurology 2004;127(Pt 11):2518-32.
2004: Donadoni Chiara; Corti Stefania; Locatelli Federica; Papadimitriou Dimitra; Guglieri Michela; Strazzer Sandra; Bossolasco Patrizia; Salani Sabrina; Comi Giacomo P
Improvement of combined FISH and immunofluorescence to trace the fate of somatic stem cells after transplantation.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2004;52(10):1333-9.
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.
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.
2004: Corti Stefania; Locatelli Federica; Papadimitriou Dimitra; Strazzer Sandra; Comi G P
Somatic stem cell research for neural repair: current evidence and emerging perspectives.
Journal of cellular and molecular medicine 2004;8(3):329-37.
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.
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.
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.
2004: Musumeci Olimpia; Aguennouz Mohammed; Cagliani Rachele; Comi Giacomo Pietro; Ciranni Anna; Rodolico Carmelo; Messina Corrado; Vita Giuseppe; Toscano Antonio
Calpain 3 deficiency in Quail Eater's disease.
Annals of neurology 2004;55(1):146-7.
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.
2003: Locatelli F; Corti S; Donadoni C; Guglieri M; Capra F; Strazzer S; Salani S; Del Bo R; Fortunato F; Bordoni A; Comi G P
Neuronal differentiation of murine bone marrow Thy-1- and Sca-1-positive cells.
Journal of hematotherapy & stem cell research 2003;12(6):727-34.
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.
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.
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.
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.
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.
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: Crimi Marco; Galbiati Sara; Moroni Isabella; Bordoni Andreina; Perini Maria Paola; Lamantea Eleonora; Sciacco Monica; Zeviani Massimo; Biunno Ida; Moggio Maurizio; Scarlato Guglielmo; Comi Giacomo Pietro
A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome.
Neurology 2003;60(11):1857-61.
2003: Corti S; Locatelli F; Strazzer S; Guglieri M; Comi G P
Neuronal generation from somatic stem cells: current knowledge and perspectives on the treatment of acquired and degenerative central nervous system disorders.
Current gene therapy 2003;3(3):247-72.
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.
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: Scarlato Guglielmo; Comi Giacomo P
Metabolic and drug-induced muscle disorders.
Current opinion in neurology 2002;15(5):533-8.
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: Lamantea Eleonora; Tiranti Valeria; Bordoni Andreina; Toscano Antonio; Bono Francesco; Servidei Serena; Papadimitriou Alex; Spelbrink Hans; Silvestri Laura; Casari Giorgio; Comi Giacomo P; Zeviani Massimo
Mutations of mitochondrial DNA polymerase gammaA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia.
Annals of neurology 2002;52(2):211-9.
2002: Fagiolari Gigliola; Sciacco Monica; Chiveri Luca; Lamperti Costanza; Comi Giacomo Pietro; Scarlato Guglielmo; Moggio Maurizio; Prelle Alessandro
Lack of apoptosis in patients with progressive external ophthalmoplegia and mutated adenine nucleotide translocator-1 gene.
Muscle & nerve 2002;26(2):265-9.
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.
2001: Napoli L; Bordoni A; Zeviani M; Hadjigeorgiou G M; Sciacco M; Tiranti V; Terentiou A; Moggio M; Papadimitriou A; Scarlato G; Comi G P
A novel missense adenine nucleotide translocator-1 gene mutation in a Greek adPEO family.
Neurology 2001;57(12):2295-8.
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: Savasta S; Comi G P; Perini M P; Lupi A; Strazzer S; Rognoni F; Rossoni R
Leigh disease: clinical, neuroradiologic, and biochemical study of three new cases with cytochrome c oxidase deficiency.
Journal of child neurology 2001;16(8):608-13.
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: Sironi M; Corti S; Locatelli F; Cagliani R; Comi G P
A novel splice site mutation (3157+1G>T) in the dystrophin gene causing total exon skipping and DMD phenotype.
Human mutation 2001;17(3):239.
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.
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: Prelle A; Sciacco M; Comi G P; Messina S; Carpo M; Ciscato P; Nobile Orazio E; Fortunato F; Mora G; Bignotti V; Fagiolari G; Moggio M; Scarlato G
A sporadic, atypical case of desminopathy: morphological and immunological characterization.
Clinical neuropathology 2000;19(4):208-12.
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.
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: Prelle A; Comi G P; Tancredi L; Rigoletto C; Ciscato P; Fortunato F; Nesti S; Sciacco M; Robotti M; Bazzi P; Felisari G; Moggio M; Scarlato G
Sarcoglycan deficiency in a large Italian population of myopathic patients.
Acta neuropathologica 1998;96(5):509-14.
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.
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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