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Neurology|September 1, 1995
Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 geneV V Ionasescu, R Ionasescu, C Searby, et al.Annals of Neurology|February 1, 1979
Stimulatory effects of drugs for protein synthesis on muscle cell cultures in Duchenne dystrophyV Ionasescu, L Z Stern, R Ionasescu, et al.European Neurology|January 1, 1977
Protein synthesis in muscle cultures from patients with myotonic dystrophy. Influence of A23187 ionophore and calcium: preliminary investigationV Ionasescu, R Ionasescu, P Cancilla, et al.American Journal of Medical Genetics|June 1, 1984
Inherited metabolic myopathy with storage of glycoproteins and glycosaminoglycansV Ionasescu, V Pedrini, C Aschenbrener, et al.Human Molecular Genetics|April 1, 1993
Charcot-Marie-Tooth neuropathy type 1A with both duplication and non-duplicationV V Ionasescu, R Ionasescu, C Searby, et al.Muscle & Nerve|November 1, 1988
X-linked dominant Charcot-Marie-Tooth neuropathy with 15 cases in a family genetic linkage studyV V Ionasescu, T L Burns, C Searby, et al.American Journal of Medical Genetics|May 1, 1989
Duchenne muscular dystrophy in monozygotic twins: deletion of 5' fragments of the geneV V Ionasescu, C C Searby, R Ionasescu, et al.Acta Neurologica Scandinavica|May 1, 1977
Fibroblast cultures in Duchenne muscular dystrophy. Alterations in synthesis and secretion of collagen and noncollagen proteinsV Ionasescu, C Lara-Braud, H Zellweger, et al.Acta Neurologica Scandinavica|September 1, 1976
Protein synthesis in muscle cultures from patients with Duchenne muscular dystrophy. Calcium and A23187 ionophore dependent changesV Ionasescu, H Zellweger, R Ionasescu, et al.American Journal of Medical Genetics|March 1, 1992
Charcot-Marie-Tooth neuropathy related to chromosome 1V V Ionasescu, J Trofatter, J L Haines, et al.Pageof 4