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3. Change of serum creatine phosphokinase activity after exercise in Duchenne type of progressive muscular dystrophy. Nakane K Nagoya Med J; 1972 Feb; 17(3):203-16. PubMed ID: 5050757 [No Abstract] [Full Text] [Related]
4. Quantitative measurements in female siblings and mothers of boys with Duchenne dystrophy. Fowler WM; Gardner GW; Taylor RG; Scavarda A; Busheikin JB Arch Phys Med Rehabil; 1969 Jun; 50(6):301-10. PubMed ID: 5788486 [No Abstract] [Full Text] [Related]
5. The value of determination of serum creatine phosphokinase activity in detection of carriers of progressive muscular dystrophy. Hetnarska L Pol Med J; 1968; 7(1):224-7. PubMed ID: 5650194 [No Abstract] [Full Text] [Related]
8. [Lipid peroxidation in children with Duchenne's hereditary myopathy]. Grinio LP; Orlov ON; Prilipko LL; Kagan VE Biull Eksp Biol Med; 1984 Oct; 98(10):423-5. PubMed ID: 6498321 [TBL] [Abstract][Full Text] [Related]
9. [Tests of serum creatine phosphokinase activity in patients with progressive muscular dystrophy and their relatives for the detection of genetic carriers]. László A; Salgó L Orv Hetil; 1981 Jun; 122(24):1453-6. PubMed ID: 7290660 [No Abstract] [Full Text] [Related]
10. [Correlation of aminoaciduria and the clinical state of patients with progressive muscular dystrophy]. Górecka A; Teczyńska T Neurol Neurochir Pol; 1969; 3(6):699-704. PubMed ID: 5365626 [No Abstract] [Full Text] [Related]
11. The carrier problem in progressive muscular dystrophy. Knight JO; Kakulas BA Proc Aust Assoc Neurol; 1970; 7():85-8. PubMed ID: 5514828 [No Abstract] [Full Text] [Related]
12. [Progressive muscle dystrophy. 8. Occurrence, clinical aspects and genetics of types I and II]. Moser H; Wiesmann U; Richterich R; Rossi E Schweiz Med Wochenschr; 1966 Feb; 96(6):169-74 contd. PubMed ID: 4861055 [No Abstract] [Full Text] [Related]
13. A report on two African children with pseudohypertrophic muscular dystrophy. Wasunna AE East Afr Med J; 1969 Jul; 46(7):437-42. PubMed ID: 5354900 [No Abstract] [Full Text] [Related]
14. [Significances of the elevated activity of serum creatine phosphokinase and transaminase in progressive muscular dystrophy]. Kondo F; Ikeda M; Abe E; Mue S Iryo; 1966 Jul; 20(7):683-93. PubMed ID: 5981769 [No Abstract] [Full Text] [Related]
15. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy]. Guízar Vázquez J; Navarrete Cadena C; Rico R; Mora G; Zavala C Bol Med Hosp Infant Mex; 1981; 38(1):23-33. PubMed ID: 7284070 [TBL] [Abstract][Full Text] [Related]
16. [Serum enzyme activities in the families of patients with progressive muscular dystrophy]. Tani J; Yano I; Masaki H; Fukuyama K; Saeki B Iryo; 1967 Jul; 21(7):848-53. PubMed ID: 5582480 [No Abstract] [Full Text] [Related]
17. [Current theories on the pathogenesis of muscular dystrophy]. Davidenkova EF; Shvarts EI; Rozenberg OA Zh Nevropatol Psikhiatr Im S S Korsakova; 1971; 71(10):1446-52. PubMed ID: 5139404 [No Abstract] [Full Text] [Related]