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C Cianchetti

Showing results (71-80 of 81) with videos related to

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The Journal of Clinical Investigation|August 1, 1995
A mutation in the dystrophin gene selectively affecting dystrophin expression in the heartF Muntoni, L Wilson, G Marrosu, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Familial cardiomyopathy, mental retardation and myopathy associated with desmin-type intermediate filamentsF Muntoni, G Catani, A Mateddu, et al.
European Neurology|January 1, 1978
Surface markers on lymphocytes from human cerebrospinal fluid. Predominance of T lymphocytes bearing receptors for the Fc segment of IgGP E Manconi, D Zaccheo, O Bugiani, et al.
Archives of Neurology|March 1, 1993
Role of predisposing and protective HLA-DQA and HLA-DQB alleles in Sardinian multiple sclerosisM G Marrosu, F Muntoni, M R Murru, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyF Muntoni, A Mateddu, C Cianchetti, et al.
Neurology|April 1, 1992
HLA-DQB1 genotype in Sardinian multiple sclerosis: evidence for a key role of DQB1 *0201 and *0302 allelesM G Marrosu, F Muntoni, M R Murru, et al.
Epilepsia|July 1, 1995
Efficacy and tolerability of vigabatrin in children with refractory partial seizures: a single-blind dose-increasing studyB Dalla Bernardina, E Fontana, F Vigevano, et al.
The New England Journal of Medicine|September 23, 1993
Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathyF Muntoni, M Cau, A Ganau, et al.
American Journal of Medical Genetics|April 1, 1992
Brief screening questionnaire for determining affected state in fragile X syndrome: a consensus recommendationA L Reiss, C Cianchetti, I L Cohen, et al.
American Journal of Medical Genetics|August 1, 1991
Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X familiesC Cianchetti, G Sannio-Fancello, A L Fratta, et al.
Pageof 9

Showing results (71-80 of 81) with videos related to

Sort By:
Pageof 9
The Journal of Clinical Investigation|August 1, 1995
A mutation in the dystrophin gene selectively affecting dystrophin expression in the heartF Muntoni, L Wilson, G Marrosu, et al.
Neuromuscular Disorders : NMD|May 1, 1994
Familial cardiomyopathy, mental retardation and myopathy associated with desmin-type intermediate filamentsF Muntoni, G Catani, A Mateddu, et al.
European Neurology|January 1, 1978
Surface markers on lymphocytes from human cerebrospinal fluid. Predominance of T lymphocytes bearing receptors for the Fc segment of IgGP E Manconi, D Zaccheo, O Bugiani, et al.
Archives of Neurology|March 1, 1993
Role of predisposing and protective HLA-DQA and HLA-DQB alleles in Sardinian multiple sclerosisM G Marrosu, F Muntoni, M R Murru, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1993
Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophyF Muntoni, A Mateddu, C Cianchetti, et al.
Neurology|April 1, 1992
HLA-DQB1 genotype in Sardinian multiple sclerosis: evidence for a key role of DQB1 *0201 and *0302 allelesM G Marrosu, F Muntoni, M R Murru, et al.
Epilepsia|July 1, 1995
Efficacy and tolerability of vigabatrin in children with refractory partial seizures: a single-blind dose-increasing studyB Dalla Bernardina, E Fontana, F Vigevano, et al.
The New England Journal of Medicine|September 23, 1993
Brief report: deletion of the dystrophin muscle-promoter region associated with X-linked dilated cardiomyopathyF Muntoni, M Cau, A Ganau, et al.
American Journal of Medical Genetics|April 1, 1992
Brief screening questionnaire for determining affected state in fragile X syndrome: a consensus recommendationA L Reiss, C Cianchetti, I L Cohen, et al.
American Journal of Medical Genetics|August 1, 1991
Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X familiesC Cianchetti, G Sannio-Fancello, A L Fratta, et al.
Pageof 9