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Journal Abstract Search

143 related items for PubMed ID: 5019834

  • 1. The diagnostic significance of serum enzymes and electrocardiogram in various muscular dystrophies.
    Zellweger H, Durnin R, Simpson J.
    Acta Neurol Scand; 1972; 48(1):87-101. PubMed ID: 5019834
    [No Abstract] [Full Text] [Related]

  • 2. [Muscular dystrophies].
    Zellweger H, Ionasescu V, Conway TW.
    Schweiz Med Wochenschr; 1972 Jun 03; 102(22):753-9. PubMed ID: 5035931
    [No Abstract] [Full Text] [Related]

  • 3. 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 03; 14(1):55-64. PubMed ID: 5696330
    [No Abstract] [Full Text] [Related]

  • 4. 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 03; 29(5):343-5. PubMed ID: 4743886
    [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 03; 49(10):554-65. PubMed ID: 5685050
    [No Abstract] [Full Text] [Related]

  • 6. [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 03; 23(10):1306-11. PubMed ID: 5364982
    [No Abstract] [Full Text] [Related]

  • 7. Serum enzyme alterations in neuromuscular disorders.
    Munsat TL, Baloh R, Pearson CM, Fowler W.
    JAMA; 1973 Dec 24; 226(13):1536-43. PubMed ID: 4800933
    [No Abstract] [Full Text] [Related]

  • 8. An investigation of physical factors influencing the behaviour in vitro of serum creatine phosphokinase and other enzymes.
    Thomson WH.
    Clin Chim Acta; 1969 Jan 24; 23(1):105-20. PubMed ID: 5762120
    [No Abstract] [Full Text] [Related]

  • 9. Benign congenital muscular dystrophy: a special form of congenital hypotonia.
    Zellweger H, Afifi A, McCormick WF, Mergner W.
    Clin Pediatr (Phila); 1967 Nov 24; 6(11):655-63. PubMed ID: 6058423
    [No Abstract] [Full Text] [Related]

  • 10. Serum enzyme studies in inherited disease of skeletal muscle.
    Thomson WH.
    Clin Chim Acta; 1971 Nov 24; 35(1):183-91. PubMed ID: 5126991
    [No Abstract] [Full Text] [Related]

  • 11. [Progressive muscle dystrophy. II. Enzyme activity chages in serum in progressive muscle dystrophy].
    Lujf A, Sluga E, Moser K.
    Wien Klin Wochenschr; 1971 Feb 19; 83(7):109-13. PubMed ID: 5547427
    [No Abstract] [Full Text] [Related]

  • 12. Biochemical aspects of genetically determined progressive muscular dystrophies.
    Luca N, Haţegan D.
    Rev Roum Neurol; 1973 Feb 19; 10(6):531-7. PubMed ID: 4771091
    [No Abstract] [Full Text] [Related]

  • 13. Evidence against the existence of a subclinical form of X-linked Duchenne muscular dystrophy.
    Emery AE, Spikesman A.
    J Neurol Sci; 1970 Jun 19; 10(6):523-33. PubMed ID: 5422556
    [No Abstract] [Full Text] [Related]

  • 14. [Progressive muscular dystrophy: CPK, LDH, ALD (aldolase)--EMG, ECG in patients and their families].
    Diotallevi P, Bargilli E, Danni M, Dellantonio R, Tocchini M, Milani-Comparetti M.
    Boll Soc Ital Biol Sper; 1988 Jun 19; 64(6):523-30. PubMed ID: 3190905
    [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 19; 122(2):254-6. PubMed ID: 8429443
    [Abstract] [Full Text] [Related]

  • 16. 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 Feb 19; 11(4):387-93. PubMed ID: 5493781
    [No Abstract] [Full Text] [Related]

  • 17. [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 19; 21(7):848-53. PubMed ID: 5582480
    [No Abstract] [Full Text] [Related]

  • 18. Marked cardiac involvement in limb-girdle muscular dystrophy.
    Kawashima S, Ueno M, Kondo T, Yamamoto J, Iwasaki T.
    Am J Med Sci; 1990 Jun 19; 299(6):411-4. PubMed ID: 2356853
    [Abstract] [Full Text] [Related]

  • 19. [Contribution to the study of the enzymology of primary myopathies of childhood].
    Vitetta M.
    Biol Lat; 1965 Jun 19; 18(4):359-66. PubMed ID: 5871253
    [No Abstract] [Full Text] [Related]

  • 20. [Enzyme diagnosis in progressive muscular dystrophies, especially in the Duchenne type].
    Pernice W, Beckmann R, Renner S, Wais U.
    Klin Padiatr; 1989 Jun 19; 201(3):167-76. PubMed ID: 2739342
    [Abstract] [Full Text] [Related]

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