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4. [Clinico-biochemical and genetic studies of myopathy]. Davidenkova EF, Droznina TA, Markelov IM. Zh Nevropatol Psikhiatr Im S S Korsakova; 1966; 66(11):1623-8. PubMed ID: 6001049 [No Abstract] [Full Text] [Related]
6. [Contribution on the study of pseudohypertrophic muscular dystrophies. I. Benign pseudohypertrophic muscular dystrophy]. Radu H, Stenzel K. Dtsch Z Nervenheilkd; 1969; 196(2):92-115. PubMed ID: 5800957 [No Abstract] [Full Text] [Related]
8. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia]. Ben Hamida M, Attia N, Chabouni H, Fardeau M. Rev Neurol (Paris); 1983; 139(4):289-97. PubMed ID: 6612142 [Abstract] [Full Text] [Related]
10. [Changes in the activity of blood serum enzymes in relatives of children with myopathy]. Grinio LP. Vopr Med Khim; 1966; 12(6):600-3. PubMed ID: 6000902 [No Abstract] [Full Text] [Related]
11. [Evaluation of serum pyruvate kinase in patients with Duchenne's muscular dystrophy and carriers. Comparison with other enzyme determinations]. Calandi C, Adami Lami C, Guidotti T, Nistri R, Papuzza S, Tozzi P, Poggi G. Minerva Pediatr; 1981 May 31; 33(10):453-64. PubMed ID: 7254147 [No Abstract] [Full Text] [Related]
19. [Membrane effects of insulin in x-chromosome recessive hereditary progressive muscular dystrophy (Duchenne form)]. Blietz R, Kruchten J, Riedl K, Wagner J. Hoppe Seylers Z Physiol Chem; 1967 Dec 31; 348(12):1609-15. PubMed ID: 5586908 [No Abstract] [Full Text] [Related]
20. Echinogenic action of L-alpha-lysophosphatidylcholine in Duchenne muscular dystrophy: a study on carrier detection. Tangorra A, Curatola G, Milani-Comparetti M, Ferretti G. Am J Med Genet; 1989 Apr 31; 32(4):540-4. PubMed ID: 2774000 [Abstract] [Full Text] [Related] Page: [Next] [New Search]