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Journal Abstract Search

107 related items for PubMed ID: 13143362

  • 1.
    ; . PubMed ID:
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  • 2. On the relationship of urinary copper excretion to the aminoaciduria in Wilson's disease (hepatolenticular degeneration).
    UZMAN LL.
    Am J Med Sci; 1953 Dec; 226(6):645-52. PubMed ID: 13104417
    [No Abstract] [Full Text] [Related]

  • 3. [Studies on the free amino acid content of urine from healthy and sick children].
    Stuber A.
    Orv Hetil; 1966 Dec 11; 107(50):2358-61. PubMed ID: 5981950
    [No Abstract] [Full Text] [Related]

  • 4.
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  • 5. The metabolic disorder in hepato-lenticular degeneration.
    MATTHEWS WB, MILNE MD, BELL M.
    Q J Med; 1952 Oct 11; 21(84):425-46. PubMed ID: 13004260
    [No Abstract] [Full Text] [Related]

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  • 8. Amino acids of plasma and urine in muscular dystrophies.
    Bank WJ, Rowland LP, Ipsen J.
    Trans Am Neurol Assoc; 1968 Oct 11; 93():185-7. PubMed ID: 5711014
    [No Abstract] [Full Text] [Related]

  • 9. Paper chromatographic studies of progressive muscular dystrophy as well as of other myopathies.
    SCHONENBERG H.
    Klin Wochenschr; 1955 Jun 01; 33(21-22):513-5. PubMed ID: 14392866
    [No Abstract] [Full Text] [Related]

  • 10.
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  • 11. [Amino-aciduria with reference to metabolic disorders in hepatolenticular diseases; morbus Wilson and pseudosclerosis].
    BLAHA H, GASTAGER H, TSCHABITSCHER H, WEWALKA F.
    Wien Klin Wochenschr; 1954 Dec 03; 66(48):915-8. PubMed ID: 14359877
    [No Abstract] [Full Text] [Related]

  • 12. Urinary excretion of peptides and of hydroxyproline in Wilson's disease.
    Asatoor AM, Miline MD, Walshe JM.
    Clin Sci Mol Med; 1976 Oct 03; 51(4):369-78. PubMed ID: 971577
    [Abstract] [Full Text] [Related]

  • 13. Aminoaciduria in representative neuromuscular disorders.
    CARVER MJ, DUTCH SJ, WITTSON CL.
    Metabolism; 1961 Jul 03; 10():582-4. PubMed ID: 13691206
    [No Abstract] [Full Text] [Related]

  • 14. [Aminoaciduria in patients with progressive muscular dystrophy].
    Yoshino Y, Mozai T.
    Rinsho Shinkeigaku; 1972 Apr 03; 12(4):197-204. PubMed ID: 4674560
    [No Abstract] [Full Text] [Related]

  • 15. [Urinary excretion of methylamino acids in myogenic and neurogenic muscular atrophy (author's transl)].
    Inoue R.
    Rinsho Shinkeigaku; 1980 Jul 03; 20(7):510-5. PubMed ID: 7460420
    [No Abstract] [Full Text] [Related]

  • 16. [Amino acids and peptides in the urine of healthy children and in children with disorder of the function of liver parenchyma].
    Kahanec D, Adam J, Grega B, Adamová M.
    Cesk Pediatr; 1975 Aug 03; 30(7-8):339-43. PubMed ID: 1204102
    [No Abstract] [Full Text] [Related]

  • 17. [Clinico-biochemical aspects of studies in progressive muscular dystrophy].
    Badalan L.
    Neurol Neurochir Pol; 1969 Aug 03; 3(3):291-6. PubMed ID: 5803004
    [No Abstract] [Full Text] [Related]

  • 18. [Paper chromatography of the amino acids and polypeptides of some biological fluids. III. Urinary amino acids and peptides].
    BOULANGER P, BISERTE G, COURTOT F.
    Bull Soc Chim Biol (Paris); 1952 Aug 03; 34(3-4):366-79. PubMed ID: 12978708
    [No Abstract] [Full Text] [Related]

  • 19. Abnormal copper metabolism and hepatolenticular degeneration.
    DENNY-BROWN D.
    Res Publ Assoc Res Nerv Ment Dis; 1953 Aug 03; 32():190-7. PubMed ID: 13134643
    [No Abstract] [Full Text] [Related]

  • 20. [Hepatolenticular degeneration in brother and sister; liver puncture biopsy, amino aciduria].
    NAYRAC P, HOUCKE E, BISERTE G, RABACHE R.
    Rev Neurol (Paris); 1951 Aug 03; 85(5):388-92. PubMed ID: 14930556
    [No Abstract] [Full Text] [Related]

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