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Archives of Neurology|February 20, 1999
Clinical correlations in 16 patients with total or partial laminin alpha2 deficiency characterized using antibodies against 2 fragments of the proteinL Morandi, C Di Blasi, L Farina, et al.Neurology|June 15, 2011
Type I interferon and Toll-like receptor expression characterizes inflammatory myopathiesC Cappelletti, F Baggi, F Zolezzi, et al.Histology and Histopathology|December 6, 2005
Molecular alterations of monophasic synovial sarcoma: loss of chromosome 3p does not alter RASSF1 and MLH1 transcriptional activityL Pazzaglia, M S Benassi, P Ragazzini, et al.Arquivos Brasileiros De Cardiologia|February 7, 2001
Fatal pulmonary embolism in hospitalized patients. Clinical diagnosis versus pathological confirmationC T Mesquita, J L Morandi Júnior, F T Perrone, et al.Acta Neuropathologica|July 1, 1997
Concomitant deficiency of beta- and gamma-sarcoglycans in 20 alpha-sarcoglycan (adhalin)-deficient patients: immunohistochemical analysis and clinical aspectsR Barresi, V Confalonieri, M Lanfossi, et al.Neuromuscular Disorders : NMD|January 2, 2014
Adult polyglucosan body disease in a patient originally diagnosed with Fabry's diseaseA Sagnelli, M Savoiardo, C Marchesi, et al.Journal of the Neurological Sciences|May 5, 2012
Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain diseaseS Saredi, A Ardissone, A Ruggieri, et al.Annals of Neurology|August 1, 1997
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sampleM Mora, L Cartegni, C Di Blasi, et al.Neuromuscular Disorders : NMD|October 29, 2000
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndromeM Villanova, E Mercuri, E Bertini, et al.Pageof 11