TREVISAN, CARLO PIETRO

TREVISAN, CARLO PIETRO  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy. 2000 PEGORARO, ELENAFANIN, MARINATREVISAN, CARLO PIETROANGELINI, CORRADO + NEUROLOGY - -
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 - -
Adverse reaction after tetrathiomolybdate treatment for Wilson's disease: A case report 2006 TREVISAN, CARLO PIETROMARTINES, DIEGOSTURNIOLO, GIACOMO + MOVEMENT DISORDERS - -
Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2 2010 PEGORARO, ELENASORARU', GIANNIPALMIERI, ARIANNATREVISAN, CARLO PIETROERMANI, MARIOMANARA RANGELINI, CORRADO + JOURNAL OF NEUROLOGY - -
Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency 2003 BOSCARO, MARCOFANIN, MARINATREVISAN, CARLO PIETROANGELINI, CORRADOPEGORARO, ELENA + HUMAN MUTATION - -
Clinical varieties of carnitine and carnitine palmitoyltransferase deficiency 1987 Angelini C.Trevisan C.Vergani L. + CLINICAL BIOCHEMISTRY - -
Comparative transcriptional and biochemical studies in muscle of myotonic dystrophies (DM1 and DM2) 2009 SALVATORI, SERGIOFANIN, MARINAPICARD, ANNE ALEIDAPASTORELLO, EBEROMEO, VINCENZOTREVISAN, CARLO PIETROANGELINI, CORRADO + NEUROLOGICAL SCIENCES - -
Congenital muscular dystrophies with defective glycosylation of dystroglycan: apopulation study 2009 PEGORARO, ELENALAVERDA, ANNA MARIAPEZZANI, RAFFAELETREVISAN, CARLO PIETRO + NEUROLOGY - -
Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1 2005 SALVATORI, SERGIOFANIN, MARINATREVISAN, CARLO PIETROANGELINI, CORRADO + NEUROLOGICAL SCIENCES - -
Diagnosis and management of Wilson's disease - Results of a single center experience 2006 TREVISAN, CARLO PIETROMARTINES, DIEGOIRATO, PAOLASTURNIOLO, GIACOMO + JOURNAL OF CLINICAL GASTROENTEROLOGY - -
Dominant muscular dystrophy with a novel SYNE1 gene mutation 2015 Nascimbeni A. C.Trevisan C. P.Angelini C. + MUSCLE & NERVE - -
Eight novel mutations in SPG4 in a large sample of patients with hereditary spastic paraplegia 2006 MARTINUZZI, ANDREAVAZZA, GIOVANNIMOSTACCIUOLO, MARIA LUISAORSO GTREVISAN, CARLO PIETRO + ARCHIVES OF NEUROLOGY - -
Exploring mental status in Friedreich's ataxia: a combined neuropsychological, behavioral and neuroimaging study. 2006 MACCHI, CARLOTREVISAN, CARLO PIETROANGELINI, CORRADO + EUROPEAN JOURNAL OF NEUROLOGY - -
Facioscapulohumeral muscular dystrophy and occurrence of heart arrhythmia 2006 TREVISAN, CARLO PIETROANGELINI, CORRADO + EUROPEAN NEUROLOGY - -
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample 2009 MOSTACCIUOLO, MARIA LUISAVAZZA, GIOVANNIANGELINI, CORRADOTREVISAN, CARLO PIETRO + CLINICAL GENETICS - -
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions 2008 TREVISAN, CARLO PIETROPASTORELLO, EBE + EUROPEAN JOURNAL OF NEUROLOGY - -
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 2002 VETTORI, ANDREATREVISAN, CARLO PIETROVAZZA, GIOVANNIARMANI, MARIOMOSTACCIUOLO, MARIA LUISA + JOURNAL OF MEDICAL GENETICS - -
Integrin alpha 7 beta 1 in muscular dystrophy/myopathy of unknown etiology 2002 PEGORARO, ELENAFANIN, MARINATREVISAN, CARLO PIETROANGELINI, CORRADO + THE AMERICAN JOURNAL OF PATHOLOGY - -
Integrin α7β1 in muscular dystrophy/myopathy of unknown etiology 2002 Pegoraro E.Cepollaro F.Prandini P.Trevisan C. P.Angelini C. + THE AMERICAN JOURNAL OF PATHOLOGY - -
Laminin alpha 2 muscular dystrophy: genotype/phenotype study in 22 patients 1998 PEGORARO, ELENAFANIN, MARINATREVISAN, CARLO PIETROANGELINI, CORRADO + NEUROLOGY - -