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Neurology|April 1, 1992
Mapping of the gene for X-linked dominant Charcot-Marie-Tooth neuropathyV V Ionasescu, J Trofatter, J L Haines, et al.Neurology|August 1, 1996
Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathyV V Ionasescu, C Searby, R Ionasescu, et al.American Journal of Human Genetics|January 1, 1988
Evidence for linkage of Charcot-Marie-Tooth neuropathy (CMT1) to apolipoprotein A2 (Apo-A2)V Ionasescu, R Anderson, T L Burns, et al.Human Molecular Genetics|September 1, 1996
Autosomal dominant Charcot-Marie-Tooth axonal neuropathy mapped on chromosome 7p (CMT2D)V Ionasescu, C Searby, V C Sheffield, et al.Muscle & Nerve|October 27, 1997
Severe Charcot-Marie-Tooth neuropathy type 1A with 1-base pair deletion and frameshift mutation in the peripheral myelin protein 22 geneV V Ionasescu, C C Searby, R Ionasescu, et al.Muscle & Nerve|January 1, 1997
Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 geneV V Ionasescu, C C Searby, R Ionasescu, et al.Journal of the Neurological Sciences|May 1, 1981
Alterations in lipid incorporation in Duchenne muscular dystrophy. Studies of fresh and cultured muscleV Ionasescu, L Monaco, A Sandra, et al.Muscle & Nerve|March 1, 1992
X-linked recessive Charcot-Marie-Tooth neuropathy: clinical and genetic studyV V Ionasescu, J Trofatter, J L Haines, et al.American Journal of Human Genetics|June 1, 1991
Heterogeneity in X-linked recessive Charcot-Marie-Tooth neuropathyV V Ionasescu, J Trofatter, J L Haines, et al.Annals of Neurology|April 1, 1981
Alterations in creatine kinase in fresh muscle and cell cultures in Duchenne dystrophyV Ionasescu, R Ionasescu, R Feld, et al.Pageof 4