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3. Serum pyruvate-kinase (PK) activity during pregnancy in potential carriers for Duchenne muscular dystrophy. Zatz M; Passos MR; Bortolini ER Am J Med Genet; 1983 May; 15(1):149-51. PubMed ID: 6859115 [No Abstract] [Full Text] [Related]
4. Serum creatine phosphokinase and pyruvate kinase in neuromuscular disorders and Duchenne dystrophy carriers. Seay AR; Ziter FA; Wu LH; Wu JT Neurology; 1978 Oct; 28(10):1047-50. PubMed ID: 570660 [TBL] [Abstract][Full Text] [Related]
6. [A study on the serum biochemistry in carrier detection of Duchenne muscular dystrophy]. Xie B Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1991 Jun; 24(3):165-8, 189. PubMed ID: 1889329 [TBL] [Abstract][Full Text] [Related]
7. Evaluation of carrier detection rates for Duchenne and Becker muscular dystrophies using serum creatine-kinase (CK) and pyruvate-kinase (PK) through discriminant analysis. Zatz M; Otto PA Am J Med Genet; 1986 Oct; 25(2):219-30. PubMed ID: 3777019 [TBL] [Abstract][Full Text] [Related]
8. Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophy. Hyser CL; Griggs RC; Mendell JR; Polakowska R; Quirk S; Brooke MH; Fenichel GM; Doherty RA Neurology; 1987 Jan; 37(1):4-10. PubMed ID: 2879259 [TBL] [Abstract][Full Text] [Related]
9. Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase, hemopexin, pyruvate kinase, and lactate dehydrogenase in combination. Percy ME; Andrews DF; Thompson MW Am J Med Genet; 1982 Sep; 13(1):27-38. PubMed ID: 7137219 [TBL] [Abstract][Full Text] [Related]
10. Detection of carriers of X-linked gene for Duchenne muscular dystrophy by levels of creatine kinase and pyruvate kinase. Falcão-Conceição DN; Gonçalves-Pimentel MM; Baptista ML; Ubatuba S J Neurol Sci; 1983 Dec; 62(1-3):171-80. PubMed ID: 6668472 [TBL] [Abstract][Full Text] [Related]
11. Creatine-kinase and pyruvate-kinase activities in normal children: implications in Duchenne muscular dystrophy carrier detection. Passos MR; Gonzalez CH; Zatz M Am J Med Genet; 1985 Oct; 22(2):255-62. PubMed ID: 4050856 [TBL] [Abstract][Full Text] [Related]
12. Duchenne muscular dystrophy: comparison among different racial groups. Bortolini ER; Zatz M Am J Med Genet; 1987 Dec; 28(4):925-9. PubMed ID: 3688030 [TBL] [Abstract][Full Text] [Related]
13. Estimate of the intrafamilial correlation for serum creatine kinase and pyruvate kinase in females at risk for Duchenne and Becker muscular dystrophies. Rabbi-Bortolini E; Dal Colletto GM; Passos-Bueno MR; Vainzof M; Rapaport D; Zatz M Hum Hered; 1991; 41(6):370-8. PubMed ID: 1797630 [TBL] [Abstract][Full Text] [Related]
14. Duchenne muscular dystrophy in a girl with a 45,X/46,XX/47,XXX chromosome constitution. Bortolini ER; da Silva DM; Chequer RS; Vianna-Morgante AM; Zatz M Am J Med Genet; 1986 Oct; 25(2):239-43. PubMed ID: 3777022 [TBL] [Abstract][Full Text] [Related]
15. The importance of serum pyruvate kinase in neuromuscular diseases and carrier states. Sage J; Inati Y; Samaha F Muscle Nerve; 1979; 2(5):390-3. PubMed ID: 492215 [TBL] [Abstract][Full Text] [Related]
16. Serum pyruvate kinase in different neuromuscular diseases and in carriers of muscular dystrophy. Savonitto C; Bonadonna G; Bongiovanni LG; Duso E; De Grandis D Ital J Neurol Sci; 1983 Dec; 4(4):417-22. PubMed ID: 6674240 [TBL] [Abstract][Full Text] [Related]
17. Pyruvate kinase: diagnostic value in neuromuscular disease. Weinstock IM; Behrendt J; Wittshire HE; Keleman J; Louis S Clin Chim Acta; 1977 Nov; 80(3):415-22. PubMed ID: 912912 [TBL] [Abstract][Full Text] [Related]
18. Serum pyruvate-kinase (PK) and creatine-phosphokinase (CPK) in female relatives and patients with X-linked muscular dystrophies (Duchenne and Becker). Zatz M; Shapiro LJ; Campion DS; Kaback MM; Otto PA J Neurol Sci; 1980 Jun; 46(3):267-79. PubMed ID: 7381516 [TBL] [Abstract][Full Text] [Related]
19. Genetic and environmental components of serum creatine kinase (CK) and pyruvate kinase (PK) in normal twins: implication for genetic risks estimates in Duchenne muscular dystrophy carriers. Rapaport D; Colletto GM; Zatz M Am J Med Genet; 1988 Oct; 31(2):291-8. PubMed ID: 3232697 [TBL] [Abstract][Full Text] [Related]
20. Results of blind testing a method to detect carriers of the Duchenne muscular dystrophy gene. Monckton G; Zatz M; Mion CS; Marusyk H Am J Hum Genet; 1984 Jul; 36(4):926-30. PubMed ID: 6475962 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]