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3. [Progressive muscle dystrophy. II. Enzyme activity chages in serum in progressive muscle dystrophy]. Lujf A; Sluga E; Moser K Wien Klin Wochenschr; 1971 Feb; 83(7):109-13. PubMed ID: 5547427 [No Abstract] [Full Text] [Related]
4. [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. The effect of exercise on serum enzymes. Fowler WM; Gardner GW; Kazerunian HH; Lauvstad WA Arch Phys Med Rehabil; 1968 Oct; 49(10):554-65. PubMed ID: 5685050 [No Abstract] [Full Text] [Related]
7. [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]
8. Studies on enzymatic activity in serum obtained from muscular dystrophic patients. Yamaji K; Imai H; Esaki K; Tokoro T; Hotta K Nagoya Med J; 1968 Apr; 14(1):55-64. PubMed ID: 5696330 [No Abstract] [Full Text] [Related]
9. An investigation of physical factors influencing the behaviour in vitro of serum creatine phosphokinase and other enzymes. Thomson WH Clin Chim Acta; 1969 Jan; 23(1):105-20. PubMed ID: 5762120 [No Abstract] [Full Text] [Related]
10. [Histological, serum enzyme and electromyographic studies in thyreomyopathies in children (research on hypothroid patients)]. Iafusco F; Canani MB; Granata E Pediatria (Napoli); 1967 Dec; 75(6):893-913. PubMed ID: 5617794 [No Abstract] [Full Text] [Related]
11. A serum isozyme study in muscular dystrophy. Particular reference to creatine kinase, aspartate aminotransferase, and lactic acid dehydrogenase isozymes. Somer H; Donner M; Murros J; Konttinen A Arch Neurol; 1973 Nov; 29(5):343-5. PubMed ID: 4743886 [No Abstract] [Full Text] [Related]
12. 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]
14. [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]
15. Diagnosis of occult muscular dystrophy: importance of the "chance" finding of elevated serum aminotransferase activities. Morse RP; Rosman NP J Pediatr; 1993 Feb; 122(2):254-6. PubMed ID: 8429443 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. Serum muscle-specific enolase in progressive muscular dystrophy and other neuromuscular diseases. Mokuno K; Riku S; Matsuoka Y; Sobue I; Kato K J Neurol Sci; 1984 Mar; 63(3):345-52. PubMed ID: 6726277 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Contribution on the study of pseudohypertrophic muscular dystrophies. II. Pseudohypertrophic muscular dystrophies in females]. Radu H; Stenzel K Dtsch Z Nervenheilkd; 1969; 196(2):116-35. PubMed ID: 5800953 [No Abstract] [Full Text] [Related] [Next] [New Search]