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M L Mostacciuolo

Showing results (41-50 of 58) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
PMP22 related congenital hypomyelination neuropathyG M Fabrizi, A Simonati, F Taioli, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1993
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patientsG Novelli, M Gennarelli, E Menegazzo, et al.
Neuroepidemiology|January 1, 1993
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosisM L Mostacciuolo, M Miorin, E Pegoraro, et al.
Journal of Medical Genetics|March 1, 1994
X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphismsS Cochrane, J Bergoffen, N D Fairweather, et al.
Molecular Psychiatry|September 14, 2006
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26G Vazza, C Bertolin, E Scudellaro, et al.
Journal of Medical Genetics|January 16, 1998
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutationsM Fanin, D J Duggan, M L Mostacciuolo, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy geneW Kress, E Müller, K Kausch, et al.
Journal of the American College of Cardiology|December 1, 1993
Cardiac involvement in Becker muscular dystrophyP Melacini, M Fanin, G A Danieli, et al.
European Journal of Neurology|June 27, 2013
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathyE Gregianin, G Vazza, E Scaramel, et al.
Clinical Endocrinology|February 21, 2004
Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytomaG Opocher, F Schiavi, A Vettori, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Journal of Neurology, Neurosurgery, and Psychiatry|December 16, 2000
PMP22 related congenital hypomyelination neuropathyG M Fabrizi, A Simonati, F Taioli, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1993
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patientsG Novelli, M Gennarelli, E Menegazzo, et al.
Neuroepidemiology|January 1, 1993
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosisM L Mostacciuolo, M Miorin, E Pegoraro, et al.
Journal of Medical Genetics|March 1, 1994
X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphismsS Cochrane, J Bergoffen, N D Fairweather, et al.
Molecular Psychiatry|September 14, 2006
Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26G Vazza, C Bertolin, E Scudellaro, et al.
Journal of Medical Genetics|January 16, 1998
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutationsM Fanin, D J Duggan, M L Mostacciuolo, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Multipoint linkage mapping of the Emery-Dreifuss muscular dystrophy geneW Kress, E Müller, K Kausch, et al.
Journal of the American College of Cardiology|December 1, 1993
Cardiac involvement in Becker muscular dystrophyP Melacini, M Fanin, G A Danieli, et al.
European Journal of Neurology|June 27, 2013
A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathyE Gregianin, G Vazza, E Scaramel, et al.
Clinical Endocrinology|February 21, 2004
Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytomaG Opocher, F Schiavi, A Vettori, et al.
Pageof 6