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Journal Abstract Search

265 related items for PubMed ID: 7180871

  • 1. Pyruvate-kinase (PK) and creatine-kinase (CK) in normal pregnancy and its implication in genetic counseling of Duchenne muscular dystrophy (DMD).
    Zatz M, Karp LE, Rogatko A.
    Am J Med Genet; 1982 Nov; 13(3):257-62. PubMed ID: 7180871
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  • 2. Serum creatine kinase and pyruvate kinase in Duchenne muscular dystrophy carrier detection.
    Percy ME, Chang LS, Murphy EG, Oss I, Verellen-Dumoulin C, Thompson MW.
    Muscle Nerve; 1979 Nov; 2(5):329-39. PubMed ID: 492209
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  • 3. 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
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  • 4. 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
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  • 5. Pyruvate kinase in fetal plasma and amniotic fluid unsuccessful for the prenatal diagnosis of Duchenne muscular dystrophy.
    Edwards RJ, Rodeck CH, Watts DC.
    Am J Med Genet; 1984 Jun; 18(2):231-5. PubMed ID: 6465199
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  • 6. Creatine-kinase (CK) and pyruvate-kinase (PK) activities in cord blood of normal newborn infants: application to Duchenne muscular dystrophy screening programs.
    Passos MR, Zatz M.
    Am J Med Genet; 1983 Nov; 16(3):367-72. PubMed ID: 6650572
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  • 7. 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
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  • 8. Clinical investigation in Duchenne dystrophy: V. Use of creatine kinase and pyruvate kinase in carrier detection.
    Griggs RC, Mendell JR, Brooke MH, Fenichel GM, Miller JP, Province M, Moxley RT, Huntzinger D, Vaughn A, Cohen M.
    Muscle Nerve; 1985 Jan; 8(1):60-7. PubMed ID: 4058458
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  • 12. [Systematic neonatal screening for Duchenne muscular dystrophy].
    Dellamonica C, Robert JM, Cotte J, Plauchu H, Dorche C.
    Nouv Presse Med; 1979 Apr 21; 8(18):1491-3. PubMed ID: 471723
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  • 13. Carrier detection and genetic counselling in Duchenne muscular dystrophy: a follow-up study.
    Hutton EM, Thompson MW.
    Can Med Assoc J; 1976 Oct 23; 115(8):749-52. PubMed ID: 974964
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  • 16. Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase and hemopexin in combination.
    Percy ME, Andrews DF, Thompson MW.
    Am J Med Genet; 1981 Oct 23; 8(4):397-409. PubMed ID: 7246612
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  • 20. Plasma creatine kinase and myoglobin levels, before and after abortion, in human fetuses at risk for Duchenne muscular dystrophy.
    Edwards RJ, Rodeck CH, Watts DC.
    Am J Med Genet; 1983 Jul 23; 15(3):475-82. PubMed ID: 6881213
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