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PUBMED FOR HANDHELDS

Journal Abstract Search


214 related items for PubMed ID: 5431208

  • 1. Congenital lysinuria: a new inherited transport disorder of dibasic amino acids.
    Oyanagi K, Miura R, Yamanouchi T.
    J Pediatr; 1970 Aug; 77(2):259-66. PubMed ID: 5431208
    [No Abstract] [Full Text] [Related]

  • 2. Hyperdibasicaminoaciduria in a mentally retarded homozygote with a peculiar response to phenothiazines.
    Kihara H, Valente M, Porter MT, Fluharty AL.
    Pediatrics; 1973 Feb; 51(2):223-9. PubMed ID: 4144453
    [No Abstract] [Full Text] [Related]

  • 3. [Certain aspects of the biochemistry of urine in families with handicapped children].
    Petrescu L, Mogoş-Tănase I, Meilă P, Ciortoloman H.
    Physiologie; 1982 Feb; 19(2):133-41. PubMed ID: 6810393
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  • 8. Inherited disorders of transport: aminoacidurias.
    Segal S.
    Monogr Hum Genet; 1978 Feb; 9():147-51. PubMed ID: 732832
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  • 11. Cerebellar ataxia with glutamic aciduria.
    Sawada H, Seriu N, Udaka F, Kameyama M, Sugiyama H.
    Acta Neurol Scand; 1991 Jul; 84(1):70-2. PubMed ID: 1681667
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  • 13. Urinary excretion of total cystine and the dibasic amino acids arginine, lysine and ornithine in relation to genetic findings in patients with cystinuria treated with sulfhydryl compounds.
    Fjellstedt E, Harnevik L, Jeppsson JO, Tiselius HG, Söderkvist P, Denneberg T.
    Urol Res; 2003 Dec; 31(6):417-25. PubMed ID: 14586528
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  • 14. Lysinuric protein intolerance.
    Simell O, Perheentupa J, Rapola J, Visakorpi JK, Eskelin LE.
    Am J Med; 1975 Aug; 59(2):229-40. PubMed ID: 1155480
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  • 15. [Cystinuria in children in the light of our observations].
    Hanicka M, Bernasowska-Knapczykowa K, Kos S.
    Przegl Lek; 1966 Aug; 22(11):700-2. PubMed ID: 5959614
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  • 16. Aminoaciduria resulting from cycloleucine administration in man.
    Brown RR.
    Science; 1967 Jul 28; 157(3787):432-4. PubMed ID: 6028026
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  • 17. Argininosuccinic aciduria: antenatal investigations in an affected family.
    Burgess EA, Oberholzer VG, Palmer T, Wagstaff TI.
    Am J Obstet Gynecol; 1974 Oct 15; 120(4):560-2. PubMed ID: 4412079
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  • 18. Biochemical and genetic studies in cystinuria: observations on double heterozygotes of genotype I-II.
    Morin CL, Thompson MW, Jackson SH, Sass-Kortsak A.
    J Clin Invest; 1971 Sep 15; 50(9):1961-76. PubMed ID: 5564399
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  • 19. Hyperdibasicaminoaciduria and hyperammonemia in familial protein intolerance.
    Kato T, Tanaka E, Horisawa S.
    Am J Dis Child; 1976 Dec 15; 130(12):1340-4. PubMed ID: 998577
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