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M Fanin

Showing results (51-60 of 68) with videos related to

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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.
Japanese Heart Journal|January 1, 1993
Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defectC Angelini, P Melacini, M L Valente, et al.
Journal of the Neurological Sciences|October 1, 1996
Prognostic factors in mild dystrophinopathiesC Angelini, M Fanin, M P Freda, et al.
Journal of the Neurological Sciences|April 1, 1996
Molecular characterization of myophosphorylase deficiency in a group of patients from northern ItalyA Martinuzzi, S Tsujino, L Vergani, 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|March 27, 1999
Cardiac transplantation in a Duchenne muscular dystrophy carrierP Melacini, M Fanin, A Angelini, 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.
Muscle & Nerve|April 16, 1999
Heart involvement in muscular dystrophies due to sarcoglycan gene mutationsP Melacini, M Fanin, D J Duggan, et al.
Jac-Antimicrobial Resistance|June 30, 2025
<i>Escherichia coli</i> producing AmpC DHA-1 bacteraemia in neutropenic leukemic patient: continuous infusion ceftazidime/avibactam as a carbapenem sparing regimenS Giuliano, A Piccirilli, J Angelini, et al.
Clinical Genetics|September 15, 2011
Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT-II deficiencyM Fanin, A Anichini, D Cassandrini, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
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.
Japanese Heart Journal|January 1, 1993
Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defectC Angelini, P Melacini, M L Valente, et al.
Journal of the Neurological Sciences|October 1, 1996
Prognostic factors in mild dystrophinopathiesC Angelini, M Fanin, M P Freda, et al.
Journal of the Neurological Sciences|April 1, 1996
Molecular characterization of myophosphorylase deficiency in a group of patients from northern ItalyA Martinuzzi, S Tsujino, L Vergani, 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|March 27, 1999
Cardiac transplantation in a Duchenne muscular dystrophy carrierP Melacini, M Fanin, A Angelini, 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.
Muscle & Nerve|April 16, 1999
Heart involvement in muscular dystrophies due to sarcoglycan gene mutationsP Melacini, M Fanin, D J Duggan, et al.
Jac-Antimicrobial Resistance|June 30, 2025
<i>Escherichia coli</i> producing AmpC DHA-1 bacteraemia in neutropenic leukemic patient: continuous infusion ceftazidime/avibactam as a carbapenem sparing regimenS Giuliano, A Piccirilli, J Angelini, et al.
Clinical Genetics|September 15, 2011
Allelic and phenotypic heterogeneity in 49 Italian patients with the muscle form of CPT-II deficiencyM Fanin, A Anichini, D Cassandrini, et al.
Pageof 7