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Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|November 24, 2006
High plasma creatine kinase: review of the literature and proposal for a diagnostic algorithmL Morandi, C Angelini, A Prelle, et al.Journal of Medical Genetics|February 9, 2000
Disruption of heart sarcoglycan complex and severe cardiomyopathy caused by beta sarcoglycan mutationsR Barresi, C Di Blasi, T Negri, et al.Journal of Viral Hepatitis|March 6, 2002
In situ polymerase chain reaction detection of transfusion-transmitted virus in liver biopsyM Comar, F Ansaldi, L Morandi, et al.The Journal of Clinical Investigation|January 1, 1994
Immunohistochemical analysis of dystrophin-associated proteins in Becker/Duchenne muscular dystrophy with huge in-frame deletions in the NH2-terminal and rod domains of dystrophinK Matsumura, A H Burghes, M Mora, et al.Neuromuscular Disorders : NMD|February 17, 2015
Non-coding VMA21 deletions cause X-linked myopathy with excessive autophagyA Ruggieri, N Ramachandran, P Wang, et al.Neuromuscular Disorders : NMD|October 29, 2000
Unusual expression of emerin in a patient with X-linked Emery-Dreifuss muscular dystrophyC Di Blasi, L Morandi, M Raffaele di Barletta, et al.Human Molecular Genetics|October 1, 1995
Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the diseaseS Bione, K Small, V M Aksmanovic, et al.Neuromuscular Disorders : NMD|May 23, 2001
Superoxide dismutase gene mutations in Italian patients with familial and sporadic amyotrophic lateral sclerosis: identification of three novel missense mutationsC Gellera, B Castellotti, M C Riggio, et al.Neurology|December 17, 2008
Management and treatment of glycogenosis type IIB Bembi, E Cerini, C Danesino, et al.Pathologica|November 24, 2015
Pathological spectrum in recurrences of glioblastoma multiformeG Marucci, P V Fabbri, L Morandi, et al.Pageof 11