These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

190 related items for PubMed ID: 5560617

  • 1. 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; 48(2):225-31. PubMed ID: 5560617
    [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. Hyperprolinemia: clinical and biochemical family study.
    Woody NC, Snyder CH, Harris JA.
    Pediatrics; 1969 Oct 24; 44(4):554-63. PubMed ID: 5346634
    [No Abstract] [Full Text] [Related]

  • 4. 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]

  • 5. [Renal clearance of amino acid in a hyperprolinemic child].
    Dodinval P, Willems C, Heusden AM, Hainaut H, Gottschalk C.
    J Genet Hum; 1969 Oct 27; 17(3):297-315. PubMed ID: 5387412
    [No Abstract] [Full Text] [Related]

  • 6. [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]

  • 7. Intravenous proline tolerance in a patient with hyperprolinaemia type II and his relatives.
    Similä S.
    Helv Paediatr Acta; 1970 Jul 31; 25(3):287-92. PubMed ID: 5518053
    [No Abstract] [Full Text] [Related]

  • 8. [Familial hyperprolinemia].
    Dogan K, Dogan S, Lipovac K.
    Neuropsihijatrija; 1968 Jul 31; 16(1):15-23. PubMed ID: 5191809
    [No Abstract] [Full Text] [Related]

  • 9. Pyroglutamic aciduria (5-oxoprolinuria), an inborn error in glutathione metabolism.
    Larsson A, Zetterström R, Hagenfeldt L, Andersson R, Dreborg S, Hörnell H.
    Pediatr Res; 1974 Oct 31; 8(10):852-6. PubMed ID: 4415411
    [No Abstract] [Full Text] [Related]

  • 10. Cystathioninuria and renal iminoglycinuria in a pedigree.
    Whelan DT, Scriver CR.
    N Engl J Med; 1968 Apr 25; 278(17):924-7. PubMed ID: 5644557
    [No Abstract] [Full Text] [Related]

  • 11. [Familial hyperprolinemia--a case in a family].
    Oknińska A, Grygalewicz J, Kowalewska-Kantecka B, Iwańska J.
    Pol Arch Med Wewn; 1974 Feb 25; 51(2):189-97. PubMed ID: 4816363
    [No Abstract] [Full Text] [Related]

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

  • 13. Type II hyperprolinemia. Delta1-pyrroline-5-carboxylic acid dehydrogenase deficiency in cultured skin fibroblasts and circulating lymphocytes.
    Valle D, Goodman SI, Applegarth DA, Shih VE, Phang JM.
    J Clin Invest; 1976 Sep 25; 58(3):598-603. PubMed ID: 956388
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.