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2. [Contribution to the study of the enzymology of primary myopathies of childhood]. Vitetta M Biol Lat; 1965; 18(4):359-66. PubMed ID: 5871253 [No Abstract] [Full Text] [Related]
3. [Enzymatic activity of the serum in the family of a progressive muscular dystrophy patient]. Esaki K; Tokoro T; Yamamoto K; Kato T; Asano B Iryo; 1969 Oct; 23(10):1306-11. PubMed ID: 5364982 [No Abstract] [Full Text] [Related]
5. Blood enzymes in Duchene's progressive muscular dystrophy and their correlation with the clinical and histological pictures. Niebrój-Dobosz I; Jedrzejowska H; Hetnarska L Acta Med Pol; 1970; 11(4):387-93. PubMed ID: 5493781 [No Abstract] [Full Text] [Related]
6. Improved detection of Duchenne muscular dystrophy heterozygotes using discriminant analysis of creatine kinase levels. Muir WA; Knoke J; Martin A; Vignos P; McErlean A Am J Med Genet; 1983 Jan; 14(1):125-34. PubMed ID: 6829600 [TBL] [Abstract][Full Text] [Related]
8. [Effect of drug administration on the child with progressive muscular dystrophy]. Nakahara T; Annaka S; Baba T; Kanno M Iryo; 1969 Oct; 23(10):1319-27. PubMed ID: 5364983 [No Abstract] [Full Text] [Related]
9. [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]
10. [Experimental hypocalcemia in cattle: effect on various blood parameters]. Berger U; Gerber H Schweiz Arch Tierheilkd; 1977 Jan; 119(1):9-21. PubMed ID: 403603 [No Abstract] [Full Text] [Related]
11. Slowly progressive X-linked recessive muscular dystrophy (type 3b). Report of cases and review of the literature. Zellweger H; Hanson JW Arch Intern Med; 1967 Nov; 120(5):525-35. PubMed ID: 6054585 [No Abstract] [Full Text] [Related]
12. Carrier detection in X-linked Duchenne type muscular dystrophy. A pluridimensional investigation. Radu H; Migea S; Török Z; Bordeianu L; Radu A J Neurol Sci; 1968; 6(2):289-300. PubMed ID: 4179111 [No Abstract] [Full Text] [Related]
13. The biochemical identification of the carrier state in X-linked recessive (Duchenne) muscular dystrophy. Thomson WH Clin Chim Acta; 1969 Nov; 26(2):207-21. PubMed ID: 5352692 [No Abstract] [Full Text] [Related]
15. Evidence against the existence of a subclinical form of X-linked Duchenne muscular dystrophy. Emery AE; Spikesman A J Neurol Sci; 1970 Jun; 10(6):523-33. PubMed ID: 5422556 [No Abstract] [Full Text] [Related]
16. [Serum aldolase and creatine phosphokinase in progressive muscular dystrophy]. Ceccarelli A; Leone P Clin Pediatr (Bologna); 1967 May; 49(5):237-45. PubMed ID: 6080497 [No Abstract] [Full Text] [Related]