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PUBMED FOR HANDHELDS

Journal Abstract Search


168 related items for PubMed ID: 5486371

  • 1. [Familial hyperprolinemia with nephropathy].
    Ortuño Mirete J, Guardiola Vicente JM, Botella García J.
    Rev Clin Esp; 1970 Jul 31; 118(2):141-50. PubMed ID: 5486371
    [No Abstract] [Full Text] [Related]

  • 2. [Familial essential hyperprolinemia].
    Hainaut H, Hariga J, Willems C, Heusden A, Chapelle P.
    Presse Med (1893); 1971 Apr 24; 79(21):945-8. PubMed ID: 5580522
    [No Abstract] [Full Text] [Related]

  • 3. Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family.
    Mollica F, Pavone L, Antener I.
    Pediatrics; 1971 Aug 24; 48(2):225-31. PubMed ID: 5560617
    [No Abstract] [Full Text] [Related]

  • 4. [Familial hyperprolinemia--a case in a family].
    Oknińska A, Grygalewicz J, Kowalewska-Kantecka B, Iwańska J.
    Pol Arch Med Wewn; 1974 Feb 24; 51(2):189-97. PubMed ID: 4816363
    [No Abstract] [Full Text] [Related]

  • 5. [Familial hyperprolinemia].
    Dogan K, Dogan S, Lipovac K.
    Neuropsihijatrija; 1968 Feb 24; 16(1):15-23. PubMed ID: 5191809
    [No Abstract] [Full Text] [Related]

  • 6. [Renal clearance of amino acid in a hyperprolinemic child].
    Dodinval P, Willems C, Heusden AM, Hainaut H, Gottschalk C.
    J Genet Hum; 1969 Oct 24; 17(3):297-315. PubMed ID: 5387412
    [No Abstract] [Full Text] [Related]

  • 7. [Hyperprolinemia and hydroxyprolinemia].
    Berger R, Broyer M.
    Presse Med (1893); 1969 May 28; 77(26):957-8. PubMed ID: 5795142
    [No Abstract] [Full Text] [Related]

  • 8. [Type I hyperprolinemia. Study of a familial case].
    Fontaine G, Farriaux JP, Dautrevaux M.
    Helv Paediatr Acta; 1970 Apr 28; 25(2):165-75. PubMed ID: 5419477
    [No Abstract] [Full Text] [Related]

  • 9. Familial hyperprolinemia without mental retardation and hereditary nephropathy.
    Mollica F, Pavone L, Antener I.
    Monogr Hum Genet; 1972 Apr 28; 6():144-5. PubMed ID: 4663888
    [No Abstract] [Full Text] [Related]

  • 10. [Hyperprolinemia type I].
    Thomsen B, Vetner M, Rosleff F, Reske-Nielsen E.
    Ugeskr Laeger; 1974 Oct 28; 136(44):2460-1. PubMed ID: 4420280
    [No Abstract] [Full Text] [Related]

  • 11. Hydroxyprolinemia: an apparently harmless familial metabolic disorder.
    Pelkonen R, Kivirikko KI.
    N Engl J Med; 1970 Aug 27; 283(9):451-6. PubMed ID: 4393577
    [No Abstract] [Full Text] [Related]

  • 12. [Hyperleucinisoleucinemia due to partial transamination defect associated with type 2 hyperprolinemia. Familial case of double aminoacidopathy].
    Jeune M, Collombel C, Michel M, David M, Guibaud P, Guerrier G, Albert J.
    Ann Pediatr (Paris); 1970 Feb 02; 17(2):349-63. PubMed ID: 5513158
    [No Abstract] [Full Text] [Related]

  • 13. [Hyperprolinemia type II].
    Thomsen B, Vetner M, Rosleff F, Reske-Nielsen E.
    Ugeskr Laeger; 1974 Nov 04; 136(45):2530. PubMed ID: 4420281
    [No Abstract] [Full Text] [Related]

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  • 16. Ocular manifestations of familial hyperlysinemia.
    Smith TH, Holland MG, Woody NC.
    Trans Am Acad Ophthalmol Otolaryngol; 1971 Nov 04; 75(2):355-60. PubMed ID: 5557172
    [No Abstract] [Full Text] [Related]

  • 17. Familial nephropathy and deafness: first observation of a family and close relatives in Switzerland.
    Dubach UC, Minder FC, Antener I.
    Helv Med Acta; 1966 Apr 04; 33(1):36-43. PubMed ID: 5927986
    [No Abstract] [Full Text] [Related]

  • 18. Hyperprolinemia: clinical and biochemical family study.
    Woody NC, Snyder CH, Harris JA.
    Pediatrics; 1969 Oct 04; 44(4):554-63. PubMed ID: 5346634
    [No Abstract] [Full Text] [Related]

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