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Corrado Angelini

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)

Disorders

Anatomy

Physiology

Chemicals & Drugs

Procedures

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Italy

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Infant

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Publications

TOP 3
Cima V; Logroscino G; D'Ascenzo C; Palmieri A; Volpe M; Briani C; Pegoraro E; Angelini C; Soraru G
Epidemiology of ALS in Padova district, Italy, from 1992 to 2005.
Angelini C; Bello L; Spinazzi M; Ferrati C
Mitochondrial disorders of the nuclear genome.
Salvatori Sergio; Furlan Sandra; Fanin Marina; Picard Anne; Pastorello Ebe; Romeo Vincenzo; Trevisan Carlo Pietro; Angelini Corrado
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2).

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All Publications

2009: Cima V; Logroscino G; D'Ascenzo C; Palmieri A; Volpe M; Briani C; Pegoraro E; Angelini C; Soraru G
Epidemiology of ALS in Padova district, Italy, from 1992 to 2005.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2009;16(8):920-4.
2009: Angelini C; Bello L; Spinazzi M; Ferrati C
Mitochondrial disorders of the nuclear genome.
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 2009;28(1):16-23.
2009: Salvatori Sergio; Furlan Sandra; Fanin Marina; Picard Anne; Pastorello Ebe; Romeo Vincenzo; Trevisan Carlo Pietro; Angelini Corrado
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2).
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2009;30(3):185-92.
2009: Mostacciuolo M L; Pastorello E; Vazza G; Miorin M; Angelini C; Tomelleri G; Galluzzi G; Trevisan C P
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample.
Clinical genetics 2009;75(6):550-5.
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: Fanin Marina; Nascimbeni Anna Chiara; Tasca Elisabetta; Angelini Corrado
How to tackle the diagnosis of limb-girdle muscular dystrophy 2A.
European journal of human genetics : EJHG 2009;17(5):598-603.
2009: Fanin M; Nascimbeni A C; Aurino S; Tasca E; Pegoraro E; Nigro V; Angelini C
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes.
Neurology 2009;72(16):1432-5.
2009: Fanin Marina; Tasca Elisabetta; Nascimbeni Anna Chiara; Angelini Corrado
Sarcolemmal neuronal nitric oxide synthase defect in limb-girdle muscular dystrophy: an adverse modulating factor in the disease course?
Journal of neuropathology and experimental neurology 2009;68(4):383-90.
2009: Palmieri A; Abrahams S; Sorarù G; Mattiuzzi L; D'Ascenzo C; Pegoraro E; Angelini C
Emotional Lability in MND: Relationship to cognition and psychopathology and impact on caregivers.
Journal of the neurological sciences 2009;278(1-2):16-20.
2009: Martignago S; Fanin M; Albertini E; Pegoraro E; Angelini C
Muscle histopathology in myasthenia gravis with antibodies against MuSK and AChR.
Neuropathology and applied neurobiology 2009;35(1):103-10.
2009: Gualandi F; Neri M; Bovolenta M; Martoni E; Rimessi P; Fini S; Spitali P; Fabris M; Pane M; Angelini C; Mora M; Morandi L; Mongini T; Bertini E; Ricci E; Vattemi G; Mercuri E; Merlini L; Ferlini A
Transcriptional behavior of DMD gene duplications in DMD/BMD males.
Human mutation 2009;30(2):E310-9.
2009: Millino Caterina; Fanin Marina; Vettori Andrea; Laveder Paolo; Mostacciuolo Maria Luisa; Angelini Corrado; Lanfranchi Gerolamo
Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy.
BMC medicine 2009;7():14.
2008: Spinazzi Marco; Cazzola Silvia; Bortolozzi Mario; Baracca Alessandra; Loro Emanuele; Casarin Alberto; Solaini Giancarlo; Sgarbi Gianluca; Casalena Gabriella; Cenacchi Giovanna; Malena Adriana; Frezza Christian; Carrara Franco; Angelini Corrado; Scorrano Luca; Salviati Leonardo; Vergani Lodovica
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function.
Human molecular genetics 2008;17(21):3291-302.
2008: Pegoraro E; Borsato C; Dal Bello F; Stramare R; Fanin M; Palu G; Angelini C
Sphingomonas paucimobilis associated with localised calf myositis.
Journal of neurology, neurosurgery, and psychiatry 2008;79(10):1194-5.
2008: Botta A; Rinaldi F; Catalli C; Vergani L; Bonifazi E; Romeo V; Loro E; Viola A; Angelini C; Novelli G
The CTG repeat expansion size correlates with the splicing defects observed in muscles from myotonic dystrophy type 1 patients.
Journal of medical genetics 2008;45(10):639-46.
2008: Sorarù Gianni; D'Ascenzo Carla; Nicolao Piero; Volpe Marco; Martignago Sara; Palmieri Arianna; Romeo Vincenzo; Koutsikos Konstantinos; Piccione Francesco; Cima Valentina; Pegoraro Elena; Angelini Corrado
Muscle histopathology in upper motor neuron-dominant amyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2008;9(5):287-93.
2008: Gastaldello Stefano; D'Angelo Simona; Franzoso Susanna; Fanin Marina; Angelini Corrado; Betto Romeo; Sandonà Dorianna
Inhibition of proteasome activity promotes the correct localization of disease-causing alpha-sarcoglycan mutants in HEK-293 cells constitutively expressing beta-, gamma-, and delta-sarcoglycan.
The American journal of pathology 2008;173(1):170-81.
2008: Nascimbeni Anna Chiara; Fanin Marina; Tasca Elisabetta; Angelini Corrado
Molecular pathology and enzyme processing in various phenotypes of acid maltase deficiency.
Neurology 2008;70(8):617-26.
2008: Sorarù Gianni; D'Ascenzo Carla; Polo Alberto; Palmieri Arianna; Baggio Linda; Vergani Lodovica; Gellera Cinzia; Moretto Giuseppe; Pegoraro Elena; Angelini Corrado
Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females.
Journal of the neurological sciences 2008;264(1-2):100-5.
2008: Trevisan Carlo P; Pastorello Ebe; Ermani Mario; Angelini Corrado; Tomelleri Giuliano; Tonin Paola; Mongini Tiziana; Palmucci Laura; Galluzzi Giuliana; Tupler Rossella G; Marioni Gino; Rimini Alessandro
Facioscapulohumeral muscular dystrophy: a multicenter study on hearing function.
Audiology & neuro-otology 2008;13(1):1-6.
2007: Boito Chiara A; Fanin Marina; Gavassini Bruno F; Cenacchi Giovanna; Angelini Corrado; Pegoraro Elena
Biochemical and ultrastructural evidence of endoplasmic reticulum stress in LGMD2I.
Virchows Archiv : an international journal of pathology 2007;451(6):1047-55.
2007: Angelini Corrado
The role of corticosteroids in muscular dystrophy: a critical appraisal.
Muscle & nerve 2007;36(4):424-35.
2007: Fanin M; Nardetto L; Nascimbeni A C; Tasca E; Spinazzi M; Padoan R; Angelini C
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A.
Journal of medical genetics 2007;44(10):609-14.
2007: Spinazzi Marco; De Lazzari Franca; Tavolato Bruno; Angelini Corrado; Manara Renzo; Armani Mario
Myelo-optico-neuropathy in copper deficiency occurring after partial gastrectomy. Do small bowel bacterial overgrowth syndrome and occult zinc ingestion tip the balance?
Journal of neurology 2007;254(8):1012-7.
2007: Sorarù G; Vergani L; Fedrizzi L; D'Ascenzo C; Polo A; Bernazzi B; Angelini C
Activities of mitochondrial complexes correlate with nNOS amount in muscle from ALS patients.
Neuropathology and applied neurobiology 2007;33(2):204-11.
2007: Pegoraro Elena; Gavassini Bruno F; Borsato Carlo; Melacini Paola; Vianello Andrea; Stramare Roberto; Cenacchi Giovanna; Angelini Corrado
MYH7 gene mutation in myosin storage myopathy and scapulo-peroneal myopathy.
Neuromuscular disorders : NMD 2007;17(4):321-9.
2007: Fanin M; Nascimbeni A C; Angelini C
Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations.
Journal of medical genetics 2007;44(1):38-43.
2007: Botta Annalisa; Vallo Laura; Rinaldi Fabrizio; Bonifazi Emanuela; Amati Francesca; Biancolella Michela; Gambardella Stefano; Mancinelli Enzo; Angelini Corrado; Meola Giovanni; Novelli Giuseppe
Gene expression analysis in myotonic dystrophy: indications for a common molecular pathogenic pathway in DM1 and DM2.
Gene expression 2007;13(6):339-51.
2007: Salehi Leila Baghernajad; Bonifazi Emanuela; Stasio Enrico Di; Gennarelli Massimo; Botta Annalisa; Vallo Laura; Iraci Raniero; Massa Roberto; Antonini Giovanni; Angelini Corrado; Novelli Giuseppe
Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients.
Genetic testing 2007;11(1):84-90.
2006: Sorarù Gianni; Pegoraro Elena; Spinella Paolo; Turra Silvia; D'Ascenzo Carla; Baggio Linda; Mantovan Maria Cristina; Vergani Lodovica; Angelini Corrado
A pilot trial with clenbuterol in amyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2006;7(4):246-8.
2006: Morandi L; Angelini C; Prelle A; Pini A; Grassi B; Bernardi G; Politano L; Bruno C; De Grandis D; Cudia P; Citterio A
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithm.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2006;27(5):303-11.
2006: Fanin Marina; Nascimbeni Anna Chiara; Angelini Corrado
Muscle protein analysis in the detection of heterozygotes for recessive limb girdle muscular dystrophy type 2B and 2E.
Neuromuscular disorders : NMD 2006;16(11):792-9.
2006: Bonifati D M; Witchel S F; Ermani M; Hoffman E P; Angelini C; Pegoraro E
The glucocorticoid receptor N363S polymorphism and steroid response in Duchenne dystrophy.
Journal of neurology, neurosurgery, and psychiatry 2006;77(10):1177-9.
2006: Angelini C; Federico A; Reichmann H; Lombes A; Chinnery P; Turnbull D
Task force guidelines handbook: EFNS guidelines on diagnosis and management of fatty acid mitochondrial disorders.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2006;13(9):923-9.
2006: Mantovan M C; Martinuzzi A; Squarzanti F; Bolla A; Silvestri I; Liessi G; Macchi C; Ruzza G; Trevisan C P; Angelini C
Exploring mental status in Friedreich's ataxia: a combined neuropsychological, behavioral and neuroimaging study.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2006;13(8):827-35.
2006: Fanin Marina; Nascimbeni Anna C; Fulizio Luigi; Spinazzi Marco; Melacini Paola; Angelini Corrado
Generalized lysosome-associated membrane protein-2 defect explains multisystem clinical involvement and allows leukocyte diagnostic screening in Danon disease.
The American journal of pathology 2006;168(4):1309-20.
2006: Bakay Marina; Wang Zuyi; Melcon Gisela; Schiltz Louis; Xuan Jianhua; Zhao Po; Sartorelli Vittorio; Seo Jinwook; Pegoraro Elena; Angelini Corrado; Shneiderman Ben; Escolar Diana; Chen Yi-Wen; Winokur Sara T; Pachman Lauren M; Fan Chenguang; Mandler Raul; Nevo Yoram; Gordon Erynn; Zhu Yitan; Dong Yibin; Wang Yue; Hoffman Eric P
Nuclear envelope dystrophies show a transcriptional fingerprint suggesting disruption of Rb-MyoD pathways in muscle regeneration.
Brain : a journal of neurology 2006;129(Pt 4):996-1013.
2006: Léger Bertrand; Vergani Lodovica; Sorarù Gianni; Hespel Peter; Derave Wim; Gobelet Charles; D'Ascenzio Carla; Angelini Corrado; Russell Aaron P
Human skeletal muscle atrophy in amyotrophic lateral sclerosis reveals a reduction in Akt and an increase in atrogin-1.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2006;20(3):583-5.
2006: Gianazza Elisabetta; Vergani Lodovica; Wait Robin; Brizio Carmen; Brambilla Daniela; Begum Shajna; Giancaspero Teresa A; Conserva Francesca; Eberini Ivano; Bufano Daniela; Angelini Corrado; Pegoraro Elena; Tramontano Anna; Barile Maria
Coordinated and reversible reduction of enzymes involved in terminal oxidative metabolism in skeletal muscle mitochondria from a riboflavin-responsive, multiple acyl-CoA dehydrogenase deficiency patient.
Electrophoresis 2006;27(5-6):1182-98.
2006: Gualandi F; Rimessi P; Trabanelli C; Spitali P; Neri M; Patarnello T; Angelini C; Yau S C; Abbs S; Muntoni F; Calzolari E; Ferlini A
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5' mutation hot spot of the dystrophin gene.
Gene 2006;370():26-33.
2006: Trevisan Carlo Pietro; Pastorello Ebe; Armani Mario; Angelini Corrado; Nante Giovanni; Tomelleri Giuliano; Tonin Paola; Mongini Tiziana; Palmucci Laura; Galluzzi Giuliana; Tupler Rossella G; Barchitta Agata
Facioscapulohumeral muscular dystrophy and occurrence of heart arrhythmia.
European neurology 2006;56(1):1-5.
2005: Boito Chiara A; Melacini Paola; Vianello Andrea; Prandini Paola; Gavassini Bruno F; Bagattin Alessia; Siciliano Gabriele; Angelini Corrado; Pegoraro Elena
Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I.
Archives of neurology 2005;62(12):1894-9.
2005: Pegoraro Elena; Gavassini Bruno F; Benedetti Sara; Menditto Immacolata; Zara Gabriella; Padoan Roberta; Mostacciuolo Maria Luisa; Ferrari Maurizio; Angelini Corrado
Co-segregation of LMNA and PMP22 gene mutations in the same family.
Neuromuscular disorders : NMD 2005;15(12):858-62.
2005: Salvatori S; Fanin M; Trevisan C P; Furlan S; Reddy S; Nagy J I; Angelini C
Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2005;26(4):235-42.
2005: Piluso G; Politano L; Aurino S; Fanin M; Ricci E; Ventriglia V M; Belsito A; Totaro A; Saccone V; Topaloglu H; Nascimbeni A C; Fulizio L; Broccolini A; Canki-Klain N; Comi L I; Nigro G; Angelini C; Nigro V
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes.
Journal of medical genetics 2005;42(9):686-93.
2005: Salviati L; Sacconi S; Murer L; Zacchello G; Franceschini L; Laverda A M; Basso G; Quinzii C; Angelini C; Hirano M; Naini A B; Navas P; DiMauro S; Montini G
Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition.
Neurology 2005;65(4):606-8.
2005: Benedetti S; Bertini E; Iannaccone S; Angelini C; Trisciani M; Toniolo D; Sferrazza B; Carrera P; Comi G; Ferrari M; Quattrini A; Previtali S C
Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy.
Journal of neurology, neurosurgery, and psychiatry 2005;76(7):1019-21.
2005: Fanin Marina; Nascimbeni Anna Chiara; Fulizio Luigi; Angelini Corrado
The frequency of limb girdle muscular dystrophy 2A in northeastern Italy.
Neuromuscular disorders : NMD 2005;15(3):218-24.
2005: Mercuri Eugenio; Bushby Kate; Ricci Enzo; Birchall Daniel; Pane Marika; Kinali Maria; Allsop Joanna; Nigro Vincenzo; Sáenz Amets; Nascimbeni Annachiara; Fulizio Luigi; Angelini Corrado; Muntoni Francesco
Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures.
Neuromuscular disorders : NMD 2005;15(2):164-71.
2005: Andrigo Cinzia; Boito Chiara; Prandini Paola; Mostacciuolo Maria Luisa; Siciliano Gabriele; Angelini Corrado; Pegoraro Elena
A novel out-of-frame mutation in the neurofilament light chain gene (NEFL) does not result in Charcot-Marie-Tooth disease type 2E.
Neurogenetics 2005;6(1):49-50.
2005: Fulizio Luigi; Nascimbeni Anna Chiara; Fanin Marina; Piluso Giulio; Politano Luisa; Nigro Vincenzo; Angelini Corrado
Molecular and muscle pathology in a series of caveolinopathy patients.
Human mutation 2005;25(1):82-9.
2004: Angelini C
Limb-girdle muscular dystrophies: heterogeneity of clinical phenotypes and pathogenetic mechanisms.
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 2004;23(3):130-6.
2004: Zaninotto Giovanni; Marchese Ragona Rosario; Briani Chiara; Costantini Mario; Rizzetto Christian; Portale Giuseppe; Zanetti Lia; Masiero Stefano; Costantino Michela; Nicoletti Loredana; Polidoro Alessandro; Feltrin GianPiero; Angelini Corrado; Ancona Ermanno; Guidolin Diego; Parenti Anna R
The role of botulinum toxin injection and upper esophageal sphincter myotomy in treating oropharyngeal dysphagia.
Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract 2004;8(8):997-1006.
2004: Prandini P; Berardinelli A; Fanin M; Morello F; Zardini E; Pichiecchio A; Uggetti C; Lanzi G; Angelini C; Pegoraro E
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy.
Neurology 2004;63(6):1118-21.
2004: Fanin M; Fulizio L; Nascimbeni A C; Spinazzi M; Piluso G; Ventriglia V M; Ruzza G; Siciliano G; Trevisan C P; Politano L; Nigro V; Angelini C
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?
Human mutation 2004;24(1):52-62.
2004: Molon A; Di Giovanni S; Chen Y W; Clarkson P M; Angelini C; Pegoraro E; Hoffman E P
Large-scale disruption of microtubule pathways in morphologically normal human spastin muscle.
Neurology 2004;62(7):1097-104.
2003: Angelini C; Cenacchi G; Nascimbeni A C; Fulizio L
Morphological changes in late onset acid Maltase deficient patients with splicing gene mutation.
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 2003;22(3):90-6.
2003: Russell Aaron P; Schrauwen Patrick; Somm Emmanuel; Gastaldi Giacomo; Hesselink Matthijs K C; Schaart Gert; Kornips Esther; Lo Sing Kai; Bufano Daniela; Giacobino Jean-Paul; Muzzin Patrick; Ceccon Mara; Angelini Corrado; Vergani Lodovica
Decreased fatty acid beta-oxidation in riboflavin-responsive, multiple acylcoenzyme A dehydrogenase-deficient patients is associated with an increase in uncoupling protein-3.
The Journal of clinical endocrinology and metabolism 2003;88(12):5921-6.
2003: Fanin Marina; Nascimbeni Anna Chiara; Fulizio Luigi; Trevisan Carlo Pietro; Meznaric-Petrusa Marija; Angelini Corrado
Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression.
The American journal of pathology 2003;163(5):1929-36.
2003: Molon Annamaria; Montagna Pasquale; Angelini Corrado; Pegoraro Elena
Novel spastin mutations and their expression analysis in two Italian families.
European journal of human genetics : EJHG 2003;11(9):710-3.
2003: Fanin M; Melacini P; Boito C; Pegoraro E; Angelini C
LGMD2E patients risk developing dilated cardiomyopathy.
Neuromuscular disorders : NMD 2003;13(4):303-9.
2003: Mantovan M C; Baggio L; Dalla Barba G; Smith P; Pegoraro E; Soraru' G; Bonometto P; Angelini C
Memory deficits and retrieval processes in ALS.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2003;10(3):221-7.
2003: Boito C; Fanin M; Siciliano G; Angelini C; Pegoraro E
Novel sarcoglycan gene mutations in a large cohort of Italian patients.
Journal of medical genetics 2003;40(5):e67.
2003: Martinuzzi Andrea; Sartori Elena; Fanin Marina; Nascimbeni Annachiara; Valente Lucia; Angelini Corrado; Siciliano Gabriele; Mongini Tiziana; Tonin Paola; Tomelleri Giuliano; Toscano Antonio; Merlini Luciano; Bindoff Laurence A; Bertelli Stefano
Phenotype modulators in myophosphorylase deficiency.
Annals of neurology 2003;53(4):497-502.
2003: Tezak Zivana; Prandini Paola; Boscaro Marco; Marin Alessandra; Devaney Joseph; Marino Michael; Fanin Marina; Trevisan Carlo P; Park Julie; Tyson Weslie; Finkel R; Garcia Carlos; Angelini Corrado; Hoffman Eric P; Pegoraro Elena
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency.
Human mutation 2003;21(2):103-11.
2002: Fanin M; Angelini C
Muscle pathology in dysferlin deficiency.
Neuropathology and applied neurobiology 2002;28(6):461-70.
2002: Toffolatti Luisa; Cardazzo Barbara; Nobile Carlo; Danieli Gian Antonio; Gualandi Francesca; Muntoni Francesco; Abbs Steve; Zanetti Patrizia; Angelini Corrado; Ferlini Alessandra; Fanin Marina; Patarnello Tomaso
Investigating the mechanism of chromosomal deletion: characterization of 39 deletion breakpoints in introns 47 and 48 of the human dystrophin gene.
Genomics 2002;80(5):523-30.
2002: Fanin M; Angelini C
Defective assembly of sarcoglycan complex in patients with beta-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubes.
Neuropathology and applied neurobiology 2002;28(3):190-9.
2002: Pegoraro Elena; Cepollaro Fulvio; Prandini Paola; Marin Alessandra; Fanin Marina; Trevisan Carlo P; El-Messlemani Abdul Hassib; Tarone Guido; Engvall Eva; Hoffman Eric P; Angelini Corrado
Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology.
The American journal of pathology 2002;160(6):2135-43.
2001: Siciliano G; Manca M; Gennarelli M; Angelini C; Rocchi A; Iudice A; Miorin M; Mostacciuolo M
Epidemiology of myotonic dystrophy in Italy: re-apprisal after genetic diagnosis.
Clinical genetics 2001;59(5):344-9.
2001: Wu F F; Takahashi M P; Pegoraro E; Angelini C; Colleselli P; Cannon S C; Hoffman E P
A new mutation in a family with cold-aggravated myotonia disrupts Na(+) channel inactivation.
Neurology 2001;56(7):878-84.
2001: Fanin M; Pegoraro E; Matsuda-Asada C; Brown R H; Angelini C
Calpain-3 and dysferlin protein screening in patients with limb-girdle dystrophy and myopathy.
Neurology 2001;56(5):660-5.
2001: Sandri M; El Meslemani A H; Sandri C; Schjerling P; Vissing K; Andersen J L; Rossini K; Carraro U; Angelini C
Caspase 3 expression correlates with skeletal muscle apoptosis in Duchenne and facioscapulo human muscular dystrophy. A potential target for pharmacological treatment?
Journal of neuropathology and experimental neurology 2001;60(3):302-12.
2001: Melacini P; Gambino A; Caforio A; Barchitta A; Valente M L; Angelini A; Fanin M; Thiene G; Angelini C; Casarotto D; Danieli G A; Dalla-Volta S
Heart transplantation in patients with inherited myopathies associated with end-stage cardiomyopathy: molecular and biochemical defects on cardiac and skeletal muscle.
Transplantation proceedings 2001;33(1-2):1596-9.
2000: Soraru' G; Negrin P; Angelini C
Unilateral calf hypertrophy due to S1-radiculopathy.
Neuromuscular disorders : NMD 2000;10(7):514.
2000: Pegoraro E; Fanin M; Trevisan C P; Angelini C; Hoffman E P
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy.
Neurology 2000;55(8):1128-34.
2000: Mostacciuolo M L; Rampoldi L; Righetti E; Vazza G; Schiavon F; Angelini C
Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entity.
Neuromuscular disorders : NMD 2000;10(7):497-502.
2000: Bonifati M D; Ruzza G; Bonometto P; Berardinelli A; Gorni K; Orcesi S; Lanzi G; Angelini C
A multicenter, double-blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophy.
Muscle & nerve 2000;23(9):1344-7.
2000: Salviati L; Laverda A M; Zancan L; Fanin M; Angelini C; Meznaric-Petrusa M
Acute quadriplegic myopathy in a 17-month-old boy.
Journal of child neurology 2000;15(1):63-6.
2000: Vlak M; van der Kooi E; Angelini C
Correlation of clinical function and muscle CT scan images in limb-girdle muscular dystrophy.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2000;21(5 Suppl):S975-7.
2000: Angelini C; Bonifati D M
New therapies in muscular dystrophies.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2000;21(5 Suppl):S919-24.
2000: Bonifati D M; Ori C; Rossi C R; Caira S; Fanin M; Angelini C
Neuromuscular damage after hyperthermic isolated limb perfusion in patients with melanoma or sarcoma treated with chemotherapeutic agents.
Cancer chemotherapy and pharmacology 2000;46(6):517-22.
2000: Fanin M; Hoffman E P; Angelini C; Pegoraro E
Private beta- and gamma-sarcoglycan gene mutations: evidence of a founder effect in Northern Italy.
Human mutation 2000;16(1):13-7.
1999: Vergani L; Barile M; Angelini C; Burlina A B; Nijtmans L; Freda M P; Brizio C; Zerbetto E; Dabbeni-Sala F
Riboflavin therapy. Biochemical heterogeneity in two adult lipid storage myopathies.
Brain : a journal of neurology 1999;122 ( Pt 12)():2401-11.
1999: Perini G I; Menegazzo E; Ermani M; Zara M; Gemma A; Ferruzza E; Gennarelli M; Angelini C
Cognitive impairment and (CTG)n expansion in myotonic dystrophy patients.
Biological psychiatry 1999;46(3):425-31.
1999: Fanin M; Melacini P; Angelini C; Danieli G A
Could utrophin rescue the myocardium of patients with dystrophin gene mutations?
Journal of molecular and cellular cardiology 1999;31(8):1501-8.
1999: Pegoraro E; Fanin M; Angelini C; Hoffman E P
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy.
Neuromuscular disorders : NMD 1999;9(5):323-5.
1999: Vergani L; Angelini C
Infantile lipid storage myopathy with nocturnal hypoventilation shows abnormal low-affinity muscle carnitine uptake in vitro.
Neuromuscular disorders : NMD 1999;9(5):320-2.
1999: Fanin M; Angelini C
Regeneration in sarcoglycanopathies: expression studies of sarcoglycans and other muscle proteins.
Journal of the neurological sciences 1999;165(2):170-7.
1999: Gennarelli M; Pavoni M; Amicucci P; Angelini C; Menegazzo E; Zelano G; Novelli G; Dallapiccola B
Reduction of the DM-associated homeo domain protein (DMAHP) mRNA in different brain areas of myotonic dystrophy patients.
Neuromuscular disorders : NMD 1999;9(4):215-9.
1999: Korade-Mirnics Z; Tarleton J; Servidei S; Casey R R; Gennarelli M; Pegoraro E; Angelini C; Hoffman E P
Myotonic dystrophy: tissue-specific effect of somatic CTG expansions on allele-specific DMAHP/SIX5 expression.
Human molecular genetics 1999;8(6):1017-23.
1999: Melacini P; Fanin M; Duggan D J; Freda M P; Berardinelli A; Danieli G A; Barchitta A; Hoffman E P; Dalla Volta S; Angelini C
Heart involvement in muscular dystrophies due to sarcoglycan gene mutations.
Muscle & nerve 1999;22(4):473-9.
1999: Martinello F; Piazza A; Pastorello E; Angelini C; Trevisan C P
Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophy.
Journal of neurology 1999;246(3):186-92.
1999: Chou F L; Angelini C; Daentl D; Garcia C; Greco C; Hausmanowa-Petrusewicz I; Fidzianska A; Wessel H; Hoffman E P
Calpain III mutation analysis of a heterogeneous limb-girdle muscular dystrophy population.
Neurology 1999;52(5):1015-20.
1999: Angelini C; Fanin M; Freda M P; Duggan D J; Siciliano G; Hoffman E P
The clinical spectrum of sarcoglycanopathies.
Neurology 1999;52(1):176-9.
1998: Melacini P; Fanin M; Angelini A; Pegoraro E; Livi U; Danieli G A; Hoffman E P; Thiene G; Dalla Volta S; Angelini C
Cardiac transplantation in a Duchenne muscular dystrophy carrier.
Neuromuscular disorders : NMD 1998;8(8):585-90.
1998: Dubrovsky A L; Angelini C; Bonifati D M; Pegoraro E; Mesa L
Steroids in muscular dystrophy: where do we stand?
Neuromuscular disorders : NMD 1998;8(6):380-4.
1998: Martinello F; Angelini C; Trevisan C P
Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsy.
European neurology 1998;40(1):37-45.
1998: Pegoraro E; Marks H; Garcia C A; Crawford T; Mancias P; Connolly A M; Fanin M; Martinello F; Trevisan C P; Angelini C; Stella A; Scavina M; Munk R L; Servidei S; Bönnemann C C; Bertorini T; Acsadi G; Thompson C E; Gagnon D; Hoganson G; Carver V; Zimmerman R A; Hoffman E P
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.
Neurology 1998;51(1):101-10.
1998: Angelini C; Fanin M; Menegazzo E; Freda M P; Duggan D J; Hoffman E P
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient.
Muscle & nerve 1998;21(6):769-75.
1998: Marcon M; Briani C; Ermani M; Menegazzo E; Iurilli V; Feltrin G P; Novelli G; Gennarelli M; Angelini C
Positive correlation of CTG expansion and pharyngoesophageal alterations in myotonic dystrophy patients.
Italian journal of neurological sciences 1998;19(2):75-80.
1998: Briani C; Marcon M; Ermani M; Costantini M; Bottin R; Iurilli V; Zaninotto G; Primon D; Feltrin G; Angelini C
Radiological evidence of subclinical dysphagia in motor neuron disease.
Journal of neurology 1998;245(4):211-6.
1998: Schiavon F; Rampazzo A; Merlini L; Angelini C; Mostacciuolo M L
Mutations of the same sequence of the myelin P0 gene causing two different phenotypes.
Human mutation 1998;Suppl 1():S217-9.
1997: Fanin M; Duggan D J; Mostacciuolo M L; Martinello F; Freda M P; Sorarù G; Trevisan C P; Hoffman E P; Angelini C
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations.
Journal of medical genetics 1997;34(12):973-7.
1997: Bonifati D M; Angelini C
Long-term cyclosporine treatment in a group of severe myasthenia gravis patients.
Journal of neurology 1997;244(9):542-7.
1997: Morrone A; Pegoraro E; Angelini C; Zammarchi E; Marconi G; Hoffman E P
RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.
The Journal of clinical investigation 1997;99(7):1691-8.
1997: Duggan D J; Gorospe J R; Fanin M; Hoffman E P; Angelini C
Mutations in the sarcoglycan genes in patients with myopathy.
The New England journal of medicine 1997;336(9):618-24.
1997: Saad F A; Mostacciuolo M L; Trevisan C P; Tomelleri G; Angelini C; Abdel Salam E; Danieli G A
Novel mutations and polymorphisms in the human dystrophin gene detected by double-strand conformation analysis.
Human mutation 1997;9(2):188-90.
1996: Melacini P; Fanin M; Danieli G A; Villanova C; Martinello F; Miorin M; Freda M P; Miorelli M; Mostacciuolo M L; Fasoli G; Angelini C; Dalla Volta S
Myocardial involvement is very frequent among patients affected with subclinical Becker's muscular dystrophy.
Circulation 1996;94(12):3168-75.
1996: Gennarelli M; Novelli G; Andreasi Bassi F; Martorell L; Cornet M; Menegazzo E; Mostacciuolo M L; Martinez J M; Angelini C; Pizzuti A; Baiget M; Dallapiccola B
Prediction of myotonic dystrophy clinical severity based on the number of intragenic [CTG]n trinucleotide repeats.
American journal of medical genetics 1996;65(4):342-7.
1996: McNally E M; Duggan D; Gorospe J R; Bönnemann C G; Fanin M; Pegoraro E; Lidov H G; Noguchi S; Ozawa E; Finkel R S; Cruse R P; Angelini C; Kunkel L M; Hoffman E P
Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy.
Human molecular genetics 1996;5(11):1841-7.
1996: Melacini P; Vianello A; Villanova C; Fanin M; Miorin M; Angelini C; Dalla Volta S
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophy.
Neuromuscular disorders : NMD 1996;6(5):367-76.
1996: Angelini C; Fanin M; Freda M P; Martinello F; Miorin M; Melacini P; Siciliano G; Pegoraro E; Rosa M; Danieli G A
Prognostic factors in mild dystrophinopathies.
Journal of the neurological sciences 1996;142(1-2):70-8.
1996: Costantini M; Zaninotto G; Anselmino M; Marcon M; Iurilli V; Boccù C; Feltrin G P; Angelini C; Ancona E
Esophageal motor function in patients with myotonic dystrophy.
Digestive diseases and sciences 1996;41(10):2032-8.
1996: Koty P P; Pegoraro E; Hobson G; Marks H G; Turel A; Flagler D; Cadaldini M; Angelini C; Hoffman E P
Myotonia and the muscle chloride channel: dominant mutations show variable penetrance and founder effect.
Neurology 1996;47(4):963-8.
1996: Duggan D J; Fanin M; Pegoraro E; Angelini C; Hoffman E P
alpha-Sarcoglycan (adhalin) deficiency: complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations.
Journal of the neurological sciences 1996;140(1-2):30-9.
1996: Fanin M; Freda M P; Vitiello L; Danieli G A; Pegoraro E; Angelini C
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?
Muscle & nerve 1996;19(9):1154-60.
1996: Capon F; Levato C; Merlini L; Angelini C; Mostacciuolo M L; Politano L; Novelli G; Dallapiccola B
Discordant clinical outcome in type III spinal muscular atrophy sibships showing the same deletion pattern.
Neuromuscular disorders : NMD 1996;6(4):261-4.
1996: Martinuzzi A; Tsujino S; Vergani L; Schievano G; Cadaldini M; Bartoloni L; Fanin M; Siciliano G; Shanske S; DiMauro S; Angelini C
Molecular characterization of myophosphorylase deficiency in a group of patients from northern Italy.
Journal of the neurological sciences 1996;137(1):14-9.
1996: Mostacciuolo M L; Miorin M; Martinello F; Angelini C; Perini P; Trevisan C P
Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy.
Human genetics 1996;97(3):277-9.
1996: Siciliano G; Rossi B; Manca L; Angelini C; Tessa A; Vergani L; Martinuzzi A; Muratorio A
Residual muscle cytochrome c oxidase activity accounts for submaximal exercise lactate threshold in chronic progressive external ophthalmoplegia.
Muscle & nerve 1996;19(3):342-9.
1996: Pegoraro E; Carelli V; Zeviani M; Cortelli P; Montagna P; Barboni P; Angelini C; Hoffman E P
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinant.
American journal of medical genetics 1996;61(4):356-62.
1996: Mastrogiacomo I; Bonanni G; Menegazzo E; Santarossa C; Pagani E; Gennarelli M; Angelini C
Clinical and hormonal aspects of male hypogonadism in myotonic dystrophy.
Italian journal of neurological sciences 1996;17(1):59-65.
1996: Damiani E; Angelini C; Pelosi M; Sacchetto R; Bortoloso E; Margreth A
Skeletal muscle sarcoplasmic reticulum phenotype in myotonic dystrophy.
Neuromuscular disorders : NMD 1996;6(1):33-47.
1996: Briani C; Marcon M; Dam M; Beghi E; Pegoraro E; Angelini C
Motor neuron disease in the Padua district of Italy: an epidemiological study.
Neuroepidemiology 1996;15(4):173-9.
1995: Bönnemann C G; Modi R; Noguchi S; Mizuno Y; Yoshida M; Gussoni E; McNally E M; Duggan D J; Angelini C; Hoffman E P
Beta-sarcoglycan (A3b) mutations cause autosomal recessive muscular dystrophy with loss of the sarcoglycan complex.
Nature genetics 1995;11(3):266-73.
1995: Tregnaghi A; De Candia A; Calderone M; Talenti E; Sartori V; Bonifatti D M; Angelini C; Fiore D; Muzzio P C
[Imaging of the thymus gland in myasthenia gravis (computerized tomography and magnetic resonance)]
La Radiologia medica 1995;90(4):404-9.
1995: Fanin M; Danieli G A; Cadaldini M; Miorin M; Vitiello L; Angelini C
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course.
Muscle & nerve 1995;18(10):1115-20.
1995: Gennarelli M; Lucarelli M; Capon F; Pizzuti A; Merlini L; Angelini C; Novelli G; Dallapiccola B
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients.
Biochemical and biophysical research communications 1995;213(1):342-8.
1995: Massari A; Gennarelli M; Menegazzo E; Pizzuti A; Silani V; Mastrogiacomo I; Pagani E; Angelini C; Scarlato G; Novelli G
Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in sperm.
Journal of neurology 1995;242(6):379-83.
1995: Vergani L; Martinuzzi A; Carelli V; Cortelli P; Montagna P; Schievano G; Carrozzo R; Angelini C; Lugaresi E
MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.
Biochemical and biophysical research communications 1995;210(3):880-8.
1995: Pegoraro E; Schimke R N; Garcia C; Stern H; Cadaldini M; Angelini C; Barbosa E; Carroll J; Marks W A; Neville H E; Marks H; Appleton S; Toriello H; Wessel H B; Donnelly J; Bernes S M; Taber J W; Weiss L; Hoffman E P
Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy: evidence for failure of dystrophin production in dystrophin-competent myonuclei.
Neurology 1995;45(4):677-90.
1995: Wang J; Pegoraro E; Menegazzo E; Gennarelli M; Hoop R C; Angelini C; Hoffman E P
Myotonic dystrophy: evidence for a possible dominant-negative RNA mutation.
Human molecular genetics 1995;4(4):599-606.
1995: Novelli G; Gennarelli M; Menegazzo E; Angelini C; Dallapiccola B
Discordant clinical outcome in myotonic dystrophy relatives showing (CTG)n > 700 repeats.
Neuromuscular disorders : NMD 1995;5(2):157-9.
1995: Melacini P; Villanova C; Menegazzo E; Novelli G; Danieli G; Rizzoli G; Fasoli G; Angelini C; Buja G; Miorelli M
Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy.
Journal of the American College of Cardiology 1995;25(1):239-45.
1995: Siciliano G; Rossi B; Martini A; Angelini C; Martinuzzi A; Lodi R; Zaniol P; Barbiroli B; Muratorio A
Myophosphorylase deficiency affects muscle mitochondrial respiration as shown by 31P-MR spectroscopy in a case with associated multifocal encephalopathy.
Journal of the neurological sciences 1995;128(1):84-91.
1995: Mostacciuolo M L; Schiavon F; Angelini C; Miccoli B; Piccolo F; Danieli G A
Frequency of duplication at 17p11.2 in families of northeast Italy with Charcot-Marie-Tooth disease type 1.
Neuroepidemiology 1995;14(2):49-53.
1995: Trevisan C P; Martinello F; Ferruzza E; Angelini C
Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up.
European neurology 1995;35(4):230-5.
1995: Zanette G; Manani G; Pittoni G; Angelini C; Trevisan C P; Turra S
Prevalence of unsuspected myopathy in infants presenting for clubfoot surgery.
Paediatric anaesthesia 1995;5(3):165-70.
1994: Schiavon F; Mostacciuolo M L; Saad F; Merlini L; Siciliano G; Angelini C; Danieli G A
Non-radioactive detection of 17p11.2 duplication in CMT1A: a study of 78 patients.
Journal of medical genetics 1994;31(11):880-3.
1994: Galvagni F; Saad F A; Danieli G A; Miorin M; Vitiello L; Mostacciuolo M L; Angelini C
A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intron.
Human genetics 1994;94(1):83-7.
1994: Siciliano G; Fanin M; Angelini C; Pollina L E; Miorin M; Saad F A; Freda M P; Muratorio A
Prevalent cardiac involvement in dystrophin Becker type mutation.
Neuromuscular disorders : NMD 1994;4(4):381-6.
1994: Angelini C; Fanin M; Pegoraro E; Freda M P; Cadaldini M; Martinello F
Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypes.
Neuromuscular disorders : NMD 1994;4(4):349-58.
1994: Mastrogiacomo I; Pagani E; Novelli G; Angelini C; Gennarelli M; Menegazzo E; Bonanni G; Dallapiccola B
Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutation.
Journal of endocrinological investigation 1994;17(5):381-3.
1994: Fanin M; Pegoraro E; Angelini C
Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients.
Journal of the neurological sciences 1994;123(1-2):88-94.
1994: Angelini C; Pegoraro E; Turella E; Intino M T; Pini A; Costa C
Deflazacort in Duchenne dystrophy: study of long-term effect.
Muscle & nerve 1994;17(4):386-91.
1994: Mostacciuolo M L; Miorin M; Vitiello L; Rampazzo A; Fanin M; Angelini C; Danieli G A
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy.
American journal of medical genetics 1994;50(1):84-6.
1993: Melacini P; Fanin M; Danieli G A; Fasoli G; Villanova C; Angelini C; Vitiello L; Miorelli M; Buja G F; Mostacciuolo M L
Cardiac involvement in Becker muscular dystrophy.
Journal of the American College of Cardiology 1993;22(7):1927-34.
1993: Martinuzzi A; Vergani L; Carrozzo R; Fanin M; Bartoloni L; Angelini C; Askanas V; Engel W K
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency.
The Journal of clinical investigation 1993;92(4):1774-80.
1993: Fanin M; Hoffman E P; Saad F A; Martinuzzi A; Danieli G A; Angelini C
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients.
Neuromuscular disorders : NMD 1993;3(2):119-27.
1993: Angelini C; Melacini P; Valente M L; Reichmann H; Carrozzo R; Fanin M; Vergani L; Boffa G M; Martinuzzi A; Fasoli G
Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect.
Japanese heart journal 1993;34(1):63-77.
1993: Angelini C; Menegazzo E; Fanin M
Multifactorial study of inflammatory myopathies. Report of 29 cases.
Italian journal of neurological sciences 1993;14(1):69-76.
1993: Mostacciuolo M L; Miorin M; Pegoraro E; Fanin M; Schiavon F; Vitiello L; Saad F A; Angelini C; Danieli G A
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis.
Neuroepidemiology 1993;12(6):326-30.
1992: Martinuzzi A; Bartolomei L; Carrozzo R; Mostacciuolo M; Carbonin C; Toso V; Ciafaloni E; Shanske S; DiMauro S; Angelini C
Correlation between clinical and molecular features in two MELAS families.
Journal of the neurological sciences 1992;113(2):222-9.
1992: Müller E; Mostacciuolo M L; Micaglio G; Angelini C; Danieli G A
Further evidence of a duplication in 17p11.2 in families with recurrence of HMSN Ia (Charcot-Marie-Tooth neuropathy type Ia).
Human genetics 1992;90(3):231-4.
1992: Vitiello L; Mostacciuolo M L; Oliviero S; Schiavon F; Nicoletti L; Angelini C; Danieli G A
Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients.
Journal of medical genetics 1992;29(2):127-30.
1992: Colombo G; Perini G I; Miotti M V; Armani M; Angelini C
Cognitive and psychiatric evaluation of 40 patients with myotonic dystrophy.
Italian journal of neurological sciences 1992;13(1):53-8.
1992: Mostacciuolo M L; Danieli G A; Trevisan C; Müller E; Angelini C
Epidemiology of spinal muscular atrophies in a sample of the Italian population.
Neuroepidemiology 1992;11(1):34-8.
1992: Fanin M; Danieli G A; Vitiello L; Senter L; Angelini C
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients.
Neuromuscular disorders : NMD 1992;2(1):41-5.
1992: Angelini C; Vergani L; Martinuzzi A
Clinical and biochemical aspects of carnitine deficiency and insufficiency: transport defects and inborn errors of beta-oxidation.
Critical reviews in clinical laboratory sciences 1992;29(3-4):217-42.
1992: Siciliano G; Rossi B; Angelini C; Martinuzzi A; Carrozzo R; Bevilacqua G; Viacava P; Federico A; Fabrizi G M; Muratorio A
Variability of the expression of muscle mitochondrial damage in ocular mitochondrial myopathy.
Neuromuscular disorders : NMD 1992;2(5-6):397-404.
1991: Martinuzzi A; Vergani L; Rosa M; Angelini C
L-carnitine uptake in differentiating human cultured muscle.
Biochimica et biophysica acta 1991;1095(3):217-22.
1991: Brevetti G; Angelini C; Rosa M; Carrozzo R; Perna S; Corsi M; Matarazzo A; Marcialis A
Muscle carnitine deficiency in patients with severe peripheral vascular disease.
Circulation 1991;84(4):1490-5.
1991: Hoffman E P; Garcia C A; Chamberlain J S; Angelini C; Lupski J R; Fenwick R
Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of Duchenne muscular dystrophy.
Annals of neurology 1991;30(4):605-10.
1991: Beggs A H; Hoffman E P; Snyder J R; Arahata K; Specht L; Shapiro F; Angelini C; Sugita H; Kunkel L M
Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.
American journal of human genetics 1991;49(1):54-67.
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.
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: Vergani L; Fanin M; Martinuzzi A; Galassi A; Appi A; Carrozzo R; Rosa M; Angelini C
Liver fatty acid-binding protein in two cases of human lipid storage.
Molecular and cellular biochemistry 1990;98(1-2):225-30.
1990: Angelini C; Beggs A H; Hoffman E P; Fanin M; Kunkel L M
Enormous dystrophin in a patient with Becker muscular dystrophy.
Neurology 1990;40(5):808-12.
1990: Melacini P; Angelini C; Buja G; Micaglio G; Valente M L
Evolution of cardiac involvement in progressive ophthalmoplegia with deleted mitochondrial DNA.
Japanese heart journal 1990;31(1):115-20.
1990: Baldo-Enzi G; Bernardo M; Vitale E; Baiocchi M R; Trevisan C; Micaglio G F; Angelini C; Fellin R; Crepaldi G
Serum lipids, lipoprotein analysis and apoprotein A-I, A-II and B levels in Friedreich's ataxia.
European neurology 1990;30(3):132-7.
1989: Perini G I; Colombo G; Armani M; Pellegrini A; Ermani M; Miotti M; Angelini C
Intellectual impairment and cognitive evoked potentials in myotonic dystrophy.
The Journal of nervous and mental disease 1989;177(12):750-4.
1989: Caforio A L; Rossi B; Risaliti R; Siciliano G; Marchetti A; Angelini C; Crea F; Mariani M; Muratorio A
Type 1 fiber abnormalities in skeletal muscle of patients with hypertrophic and dilated cardiomyopathy: evidence of subclinical myogenic myopathy.
Journal of the American College of Cardiology 1989;14(6):1464-73.
1989: Hoffman E P; Kunkel L M; Angelini C; Clarke A; Johnson M; Harris J B
Improved diagnosis of Becker muscular dystrophy by dystrophin testing.
Neurology 1989;39(8):1011-7.
1989: Facco E; Micaglio G; Liviero M C; Ceccato M B; Toffoletto F; Martinuzzi A; Angelini C
Sensory-motor conduction time in amyotrophic lateral sclerosis.
Rivista di neurologia 1989;59(3):108-12.
1989: Magni G; Micaglio G; Ceccato M B; Lalli R; Bejato L; Angelini C
The role of life events in the myasthenia gravis outcome: a one-year longitudinal study.
Acta neurologica Scandinavica 1989;79(4):288-91.
1989: Biral D; Scarpini E; Angelini C; Salviati G; Margreth A
Myosin heavy chain composition of muscle fibers in spinal muscular atrophy.
Muscle & nerve 1989;12(1):43-51.
1988: Magni G; Micaglio G F; Lalli R; Bejato L; Candeago M R; Merskey H; Angelini C
Psychiatric disturbances associated with myasthenia gravis.
Acta psychiatrica Scandinavica 1988;77(4):443-5.
1988: Melacini P; Buja G; Fasoli G; Angelini C; Armani M; Scognamiglio R; Dalla Volta S
The natural history of cardiac involvement in myotonic dystrophy: an eight-year follow-up in 17 patients.
Clinical cardiology 1988;11(4):231-8.
1988: Brevetti G; Chiariello M; Ferulano G; Policicchio A; Nevola E; Rossini A; Attisano T; Ambrosio G; Siliprandi N; Angelini C
Increases in walking distance in patients with peripheral vascular disease treated with L-carnitine: a double-blind, cross-over study.
Circulation 1988;77(4):767-73.
1988: Angelini C; Martinuzzi A; Micaglio G; Vergani L
[Myopathies caused by defects of lipid and carbohydrate metabolism]
Rivista di neurologia 1988;58(1):15-25.
1988: Micaglio G; Fardin P; Battilana M; Lombardi A; Mostacciuolo M L; Danieli G A; Angelini C
Heterogeneity of Charcot-Marie-Tooth disease suggested by a linkage study.
Advances in neurology 1988;48():209-19.
1987: Micaglio G; Ceccato M B; Trevisan C; Angelini C
Quantitative histopathology in congenital myopathies.
Rivista di neurologia 1987;57(4):261-8.
1987: Mostacciuolo M L; Barbujani G; Armani M; Danieli G A; Angelini C
Genetic epidemiology of myotonic dystrophy.
Genetic epidemiology 1987;4(4):289-98.
1987: Angelini C; Candeago R M; Armani M
Epidemiology of motor neuron disease in north-east Veneto region: Venice, Padua, and Belluno Provinces (1972-1981).
Advances in experimental medicine and biology 1987;209():333-7.
1987: Armani M; Pierobon-Bormioli S; Mostacciuolo M L; Cacciavillani M; Cassol M A; Candeago R M; Angelini C
Familial ALS: clinical, genetic and morphological features.
Advances in experimental medicine and biology 1987;209():109-10.
1986: Bejato L; Trevisan C; Angelini C
[Psychological aspects of neuromuscular diseases]
Minerva pediatrica 1986;38(15-16):683-4.
1986: Angelini C; Micaglio G F; Trevisan C; Baron C; Bejato L; Intino M T; Comi L; Nigro G; Santucci M; Rossi B
[Natural history of muscular dystrophy inferred from a multicenter trial and the results of a dietetic trial]
Minerva pediatrica 1986;38(15-16):645-9.
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.
1985: Salviati G; Pierobon-Bormioli S; Betto R; Damiani E; Angelini C; Ringel S P; Salvatori S; Margreth A
Tubular aggregates: sarcoplasmic reticulum origin, calcium storage ability, and functional implications.
Muscle & nerve 1985;8(4):299-306.
1985: Pierobon-Bormioli S; Armani M; Ringel S P; Angelini C; Vergani L; Betto R; Salviati G
Familial neuromuscular disease with tubular aggregates.
Muscle & nerve 1985;8(4):291-8.
1984: Gobbi G; Armani M; Pierobon Bormioli S; Giovanardi Rossi P; Angelini C
A childhood case of hypokalemic periodic paralysis.
Acta neurologica 1984;6(2):147-51.
1984: Fardin P; Micaglio G F; Angelini C; Negrin P; Siciliano G
[Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results]
Rivista di neurobiologia : organo ufficiale della Società dei neurologi, neuroradiologi e neurochirurghi ospedalieri 1984;30(2-3):222-8.
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.
1982: Bresolin N; Freddo L; Vergani L; Angelini C
Carnitine, carnitine acyltransferases, and rat brain function.
Experimental neurology 1982;78(2):285-92.
1981: Bertoli M; Battistella P A; Vergani L; Naso A; Gasparotto M L; Romagnoli G F; Angelini C
Carnitine deficiency induced during hemodialysis and hyperlipidemia: effect of replacement therapy.
The American journal of clinical nutrition 1981;34(8):1496-500.
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.
1981: Melacini P; Egloff C; Armani M; Miraglia G; Angelini C; Marinato P G; Buja G F
Atrio-ventricular conduction system in myotonic dystrophy: value of electrophysiological investigation.
Acta neurologica 1981;3(2):396-400.
1981: Angelini C; Battistella P A; Laverda A; Pierobon-Bormioli S; Salviati G; Vergani L
Fatal lipid storage with abnormal mitochondria in an infant.
Acta neuropathologica. Supplementum 1981;7():221-5.
1981: Pierobon-Bormioli S; Angelini C; Armani M; Testa G F
Myopathological findings in progressive myoclonus epilepsy.
Acta neuropathologica. Supplementum 1981;7():334-7.
1981: Angelini C; Micaglio G F; Armani M; Pierobon-Bormioli S; Giordano R; Testa G F
Peroneal muscular atrophy with ataxia and partial myoclonic epilepsy.
Journal of neurology 1981;226(1):1-13.
1980: Battistella P A; Vergani L; Donzelli F; Rubaltelli F F; Angelini C
Plasma and urine carnitine levels during development.
Pediatric research 1980;14(12):1379.
1980: Angelini C; Micaglio G F; Trevisan C
Guanidine hydrochloride in infantile and juvenile spinal muscular atrophy. A double blind controlled study.
Acta neurologica 1980;2(6):460-5.
1980: Ferrari M; Armani M; Melacini P; Egloff C; Scattolin G; Fasoli G; Cardin G; Miraglia G; Angelini C; Dalla Volta S
[The heart in myotonic dystrophy. Clinical and instrumental study in 17 patients (author's transl)]
Giornale italiano di cardiologia 1980;10(10):1288-98.

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