FANIN, MARINA

FANIN, MARINA  

Dipartimento di Neuroscienze - DNS  

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Risultati 1 - 20 di 104 (tempo di esecuzione: 0.028 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
La rigenerazione muscolare nelle distrofie 1987 FANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO + RIVISTA DI NEUROBIOLOGIA - -
Muscle fiber regeneration in Dystrophies and Neurogenic Atrophies. 1987 FANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO + NEUROLOGY - neurology
Regeneration in muscular dystrophies: a review and immunohistochemical study. 1988 ANGELINI, CORRADOPEGORARO, ELENAFANIN, MARINA + - - Sarcomeric and Non-Sarcomeric Muscles: Basic and Applied Research Prospects for the 90's
Fetal Myosin Heavy Chain (FMHC) and Vimentin (VM) as markers of muscle regeneration in neurogenic disorders. 1988 FANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO + - - Sarcomeric and Non-Sarcomeric Muscles: Basic and Applied Research Prospects for the 90's
Enormous dystrophin in a patient with becker muscular dystrophy 1990 Angelini C.Fanin M. + NEUROLOGY - -
Diagnosis and treatment of cardiac involvement in Becker muscular dystrophy 1991 MELACINI, PAOLAFANIN, MARINAVITIELLO, LIBEROPEGORARO, ELENAANGELINI, CORRADO + ACTA CARDIOMIOLOGICA - -
Prevalence of dystrophin-positive fibers in 85 duchenne muscular dystrophy patients 1992 FANIN, MARINADANIELI, GIAN ANTONIOVITIELLO, LIBEROANGELINI, CORRADO + NEUROMUSCULAR DISORDERS - -
Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect. 1993 ANGELINI, CORRADOMELACINI, PAOLAVALENTE, MARIALUISAFANIN, MARINAVERGANI, LODOVICABOFFA, GIOVANNIFASOLI, GIUSEPPE + JAPANESE HEART JOURNAL - -
Cardiac involvement in Becker muscular dystrophy 1993 MELACINI, PAOLAFANIN, MARINADANIELI, GIAN ANTONIOFASOLI, GIUSEPPEANGELINI, CORRADOVITIELLO, LIBEROBUJA, GIANFRANCOMOSTACCIUOLO, MARIA LUISAPEGORARO, ELENADALLA VOLTA, SERGIO + JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY - -
Clinical-molecular correlation in 104 mild X-linked muscular dystrophy patients: characterization of sub-clinical phenotypes. 1994 ANGELINI, CORRADOFANIN, MARINAPEGORARO, ELENA + NEUROMUSCULAR DISORDERS - -
Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients. 1994 FANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO JOURNAL OF THE NEUROLOGICAL SCIENCES - -
Dystrophin-positive fibers in duchenne dystrophy: Origin and correlation to clinical course 1995 FANIN, MARINADANIELI, GIAN ANTONIOVITIELLO, LIBEROANGELINI, CORRADO + MUSCLE & NERVE - -
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size? 1996 FANIN, MARINAVITIELLO, LIBERODANIELI, GIAN ANTONIOPEGORARO, ELENAANGELINI, CORRADO + MUSCLE & NERVE - -
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. 1996 FANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO + JOURNAL OF THE NEUROLOGICAL SCIENCES - -
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size? 1996 FANIN, MARINAVITIELLO, LIBEROPEGORARO, ELENAANGELINI, CORRADO + MUSCLE & NERVE - -
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophy. 1996 MELACINI, PAOLAVIANELLO, ANDREAFANIN, MARINAMIORIN, MARTAANGELINI, CORRADODALLA VOLTA, SERGIO + NEUROMUSCULAR DISORDERS - -
Diagnosis and therapy of myophosphorylase deficiency: experience with a group of italian patients 1996 VERGANI, LODOVICAFANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO + BASIC AND APPLIED MYOLOGY - -
A severe case of Duchenne-like muscular dystrophy due to a mutation in the alpha-sarcoglycan (adhalin) gene 1996 FANIN, MARINAPEGORARO, ELENASORARU', GIANNIMOSTACCIUOLO, MARIA LUISATREVISAN, CARLO PIETROANGELINI, CORRADO + BASIC AND APPLIED MYOLOGY - -
Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy. 1996 FANIN, MARINAPEGORARO, ELENAANGELINI, CORRADO + HUMAN MOLECULAR GENETICS - -
Myocardial involvement is very frequent among patients affected with subclinical muscular dystrophy 1996 MELACINI, PAOLAFANIN, MARINADANIELI, GIAN ANTONIOMOSTACCIUOLO, MARIA LUISAFASOLI, GIUSEPPEANGELINI, CORRADODALLA VOLTA, SERGIO + CIRCULATION - -