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	61.	Linkage between the loci for Duffy (FY) and serum amyloid P component (APCS) on human chromosome 1. [electronic resource] by Ionasescu, V Burns, T Searby, C Ionasescu, R Producer: 19880212 In: Cytogenetics and cell genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	62.	Respiratory control and oxidative phosphorylation in the denervated muscle of patients with amyotrophic lateral sclerosis. Biochemical comparison with diabetes mellitus. [electronic resource] by Ionăşescu, V Luca, N Vuia, O Popa, V Producer: 19681221 In: Acta neurologica Scandinavica vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	63.	Collagen synthesis by Duchenne myogenic clones: pathogenic implications for the disease. [electronic resource] by Ionasescu, V Ionasescu, R Massimini, G Sandra, A Producer: 19820708 In: American journal of medical genetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	64.	New point mutations and deletions of the connexin 32 gene in X-linked Charcot-Marie-Tooth neuropathy. [electronic resource] by Ionasescu, V Searby, C Ionasescu, R Meschino, W Producer: 19951127 In: Neuromuscular disorders : NMD vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	65.	Recombinant DNA study of Duchenne muscular dystrophy occurring in a myotonic dystrophy family. [electronic resource] by Ionasescu, V Searby, C Ionasescu, R Burns, T Producer: 19881013 In: Acta neurologica Scandinavica vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	66.	[Clinical and pathologico-anatomical manifestations of acute intermittent porphyria]. [electronic resource] by KREINDLER, A POILICI, I IONASESCU, V APPEL, E Producer: 19981101 In: Deutsche Zeitschrift fur Nervenheilkunde vol. 185 Availability: No items available. Save to lists Add to cart (remove)
	67.	Spinal muscular atrophy with autosomal dominant inheritance. Report of a new kindred. [electronic resource] by Zellweger, H Simpson, J McCormick, W F Ionasescu, V Producer: 19730105 In: Neurology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	68.	Identification of carriers of Duchenne muscular dystrophy by muscle protein synthesis. [electronic resource] by Ionasescu, V Zellweger, H Shirk, P Conway, T W Producer: 19730621 In: Neurology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	69.	Is the duplication present in all family members affected with Charcot-Marie-Tooth neuropathy type 1 A? [electronic resource] by Ionăşescu, V Ionăşescu, G Searby, C Barker, D F Producer: 19940722 In: Romanian journal of neurology and psychiatry = Revue roumaine de neurologie et psychiatrie vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	70.	Stimulatory effects of drugs for protein synthesis on muscle cell cultures in Duchenne dystrophy. [electronic resource] by Ionasescu, V Stern, L Z Ionasescu, R Rubenstein, P Producer: 19790523 In: Annals of neurology vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	71.	Serial position memory of boys with Duchenne muscular dystrophy. [electronic resource] by Anderson, S W Routh, D K Ionasescu, V V Producer: 19880914 In: Developmental medicine and child neurology vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	72.	Abnormal protein synthesis in facioscapulohumeral muscular dystrophy. [electronic resource] by Ionasescu, V Zellweger, H Shirk, P Conway, T W Producer: 19730405 In: Neurology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	73.	Dejerine-Sottas disease with de novo dominant point mutation of the PMP22 gene. [electronic resource] by Ionasescu, V V Ionasescu, R Searby, C Neahring, R Producer: 19951017 In: Neurology vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	74.	Letter: Screening of the newborn for duchenne muscular dystrophy. [electronic resource] by Zellweger, H Ionasescu, V Simpson, J Waziri, M Antinik, A Producer: 19751218 In: British medical journal vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	75.	Increased collagen synthesis in arthrogryposis multiplex congenita. [electronic resource] by Ionasescu, V Zellweger, H Filer, L J Conway, T W Producer: 19700908 In: Archives of neurology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	76.	Comparison of ribosomal protein synthesis in Becker and Duchenne muscular dystrophies. [electronic resource] by Ionasescu, V Zellweger, H McCormick, W F Conway, T W Producer: 19730606 In: Neurology vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	77.	Clinical and morphologic features of a myopathy associated with a point mutation in the mitochondrial tRNA(Pro) gene. [electronic resource] by Ionasescu, V V Hart, M DiMauro, S Moraes, C T Producer: 19940620 In: Neurology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	78.	X-linked dominant Charcot-Marie-Tooth neuropathy with 15 cases in a family genetic linkage study. [electronic resource] by Ionasescu, V V Burns, T L Searby, C Ionasescu, R Producer: 19890328 In: Muscle & nerve vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	79.	Multiple congenital anomalies syndrome with myopathy in chromosome 16 abnormality. [electronic resource] by Ionasescu, V Patil, S Hart, M Rhead, W Smith, W Producer: 19870304 In: American journal of medical genetics vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	80.	Linkage between the loci for autosomal dominant Charcot-Marie-Tooth neuropathy type 1 and human glucocerebrosidase. [electronic resource] by Ionasescu, V Burns, T Ionasescu, R Searby, C Ginns, E Producer: 19880727 In: Cytogenetics and cell genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 138 results.