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Journal of the Neurological Sciences|April 1, 1982
Increased collagen synthesis by Duchenne myogenic clonesV Ionasescu, R IonasescuIn Vitro Cellular & Developmental Biology : Journal of the Tissue Culture Association|July 1, 1985
Human smooth muscle cell cultures of the stomach. Morphologic and biochemical studiesR Ionasescu, V IonasescuHuman Molecular Genetics|February 1, 1994
Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathyV Ionasescu, C Searby, R IonasescuAmerican Journal of Medical Genetics|June 14, 1996
Correlation between connexin 32 gene mutations and clinical phenotype in X-linked dominant Charcot-Marie-Tooth neuropathyV Ionasescu, R Ionasescu, C SearbyMuscle & Nerve|November 1, 1993
Screening of dominantly inherited Charcot-Marie-Tooth neuropathiesV V Ionasescu, R Ionasescu, C SearbyActa Neurologica Scandinavica|May 1, 1988
Recombinant DNA study of Duchenne muscular dystrophy occurring in a myotonic dystrophy familyV Ionasescu, C Searby, R Ionasescu, et al.Acta Neurologica Scandinavica|June 1, 1989
Manifesting carrier of Becker muscular dystrophy (BMD): clinical and recombinant DNA studiesV V Ionasescu, C C Searby, R IonasescuAmerican Journal of Medical Genetics|March 1, 1982
Collagen synthesis by Duchenne myogenic clones: pathogenic implications for the diseaseV Ionasescu, R Ionasescu, G Massimini, et al.Muscle & Nerve|April 1, 1988
Becker muscular dystrophy recombinant DNA studies in identical twinsV Ionasescu, R Ionasescu, C Searby, et al.Neuromuscular Disorders : NMD|July 1, 1995
New point mutations and deletions of the connexin 32 gene in X-linked Charcot-Marie-Tooth neuropathyV Ionasescu, C Searby, R Ionasescu, et al.Pageof 4