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Journal Abstract Search

131 related items for PubMed ID: 4663888

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

  • 22. High urinary excretion of N-(pyrrole-2-carboxyl) glycine in type II hyperprolinemia.
    Wajner M, Wannmacher CM, Purkiss P.
    Clin Genet; 1990 Jun; 37(6):485-9. PubMed ID: 2383933
    [Abstract] [Full Text] [Related]

  • 23. Asymptomatic type II hyperprolinaemia associated with hyperglycinaemia in three sibs.
    Pavone L, Mollica F, Levy HL.
    Arch Dis Child; 1975 Aug; 50(8):637-41. PubMed ID: 1200680
    [Abstract] [Full Text] [Related]

  • 24. Dietary proline in familial aminoaciduria.
    Nutr Rev; 1969 Sep; 27(9):263-5. PubMed ID: 4900948
    [No Abstract] [Full Text] [Related]

  • 25. Hyperprolinaemia type 2.
    Emery FA, Goldie L, Stern J.
    J Ment Defic Res; 1968 Sep; 12(3):187-95. PubMed ID: 4972625
    [No Abstract] [Full Text] [Related]

  • 26. Familial iminoglycinuria with normal intestinal absorption of glycine and imino acids in association with profound mental retardation, a possible "cerebral phenotype".
    Statter M, Ben-Zvi A, Shina A, Schein R, Russell A.
    Helv Paediatr Acta; 1976 Aug; 31(2):173-82. PubMed ID: 955941
    [Abstract] [Full Text] [Related]

  • 27. Non-chromatographic screening test for hyperprolinemia.
    Yamaguchi Y.
    Clin Chem; 1978 Dec; 24(12):2178-9. PubMed ID: 719867
    [Abstract] [Full Text] [Related]

  • 28. Clinical, biochemical and enzymatic studies in type I hyperprolinemia associated with chromosomal abnormality.
    Oyanagi K, Tsuchiyama A, Itakura Y, Tamura Y, Nakao T, Fujita S, Shiono H.
    Tohoku J Exp Med; 1987 Apr; 151(4):465-75. PubMed ID: 3617056
    [Abstract] [Full Text] [Related]

  • 29. Biochemical and clinical features of hereditary hyperprolinemia.
    Mitsubuchi H, Nakamura K, Matsumoto S, Endo F.
    Pediatr Int; 2014 Aug; 56(4):492-6. PubMed ID: 24931297
    [Abstract] [Full Text] [Related]

  • 30. Low proline diet in type I hyperprolinaemia.
    Harries JT, Piesowicz AT, Seakins JW, Francis DE, Wolff OH.
    Arch Dis Child; 1971 Feb; 46(245):72-81. PubMed ID: 5555491
    [Abstract] [Full Text] [Related]

  • 31. [A case of type I hyperprolinemia associated with photogenic epilepsy].
    Ishikawa Y, Kameda K, Okabe M, Imai T, Nagaoka M, Minami R.
    No To Hattatsu; 1991 Jan; 23(1):81-6. PubMed ID: 1994998
    [Abstract] [Full Text] [Related]

  • 32. Hyperprolinemia and prolinuria in a new inbred strain of mice, PRO-Re.
    Blake RL, Russell ES.
    Science; 1972 May 19; 176(4036):809-11. PubMed ID: 5031477
    [Abstract] [Full Text] [Related]

  • 33. [Results of a period of research (1967-1974) in the field of disorders of transport amino acid and metabolism using chromatographic, electrophoretic and dosimetric methods].
    Berio A, Allegranza A, Scapaticci E, Cadoni M, Camozzi C, Cavallo V, Di Stefano A, Santos JG.
    Minerva Pediatr; 1975 Sep 29; 27(30):1609-23. PubMed ID: 1177852
    [No Abstract] [Full Text] [Related]

  • 34. [A family with pyroglutamic aciduria (author's transl)].
    Porath U, Schreier K.
    Dtsch Med Wochenschr; 1978 Jun 02; 103(22):939-42. PubMed ID: 657978
    [No Abstract] [Full Text] [Related]

  • 35. Metabolic epilepsy in hyperprolinemia type II due to a novel nonsense ALDH4A1 gene variant.
    Kaur R, Paria P, Saini AG, Suthar R, Bhatia V, Attri SV.
    Metab Brain Dis; 2021 Aug 02; 36(6):1413-1417. PubMed ID: 34037900
    [Abstract] [Full Text] [Related]

  • 36. Familial iminoglycinuria. An inborn error of renal tubular transport.
    Rosenberg LE, Durant JL, Elsas LJ.
    N Engl J Med; 1968 Jun 27; 278(26):1407-13. PubMed ID: 5652624
    [No Abstract] [Full Text] [Related]

  • 37. Biochemical, morphological and hybrid studies in hyperprolinemic mice.
    Kanwar YS, Krakower CA, Manaligod JR, Justice P, Wong PW.
    Biomedicine; 1975 May 27; 22(3):209-16. PubMed ID: 240452
    [Abstract] [Full Text] [Related]

  • 38. [Primary and secondary hyperaminoaciduria in children (review of the literature)].
    Lebedev VP, Iur'eva EA, Mukhina IuG, Buravina TA, Koroleva IA.
    Vopr Okhr Materin Det; 1970 Nov 27; 15(11):64-8. PubMed ID: 4928437
    [No Abstract] [Full Text] [Related]

  • 39. Type I hyperprolinemia in a family suffering from aniridia and severe dystrophia of ocular tissues.
    Fusco G, Carlomagno S, Romano A, Rinaldi E, Cedrola G, Cianciaruso L, Curto A, Rosolia S, Auricchio G.
    Ophthalmologica; 1976 Nov 27; 173(1):1-10. PubMed ID: 958671
    [No Abstract] [Full Text] [Related]

  • 40. Hyperprolinaemia in two successive generations of a North American Indian family.
    Perry TL, Hardwick DF, Lowry RB, Hansen S.
    Ann Hum Genet; 1968 May 27; 31(4):401-7. PubMed ID: 4299764
    [No Abstract] [Full Text] [Related]

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