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

137 related items for PubMed ID: 5713621

  • 21. [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]

  • 22. Familial pancreatitis associated with hyperglycinuria.
    Bergström K, Hellström K, Kallner M, Lundh G.
    Scand J Gastroenterol; 1973 Sep 29; 8(3):217-23. PubMed ID: 4724921
    [No Abstract] [Full Text] [Related]

  • 23. Iminoglycinuria: a benign type of inherited aminoaciduria.
    Coşkun T, Ozalp I, Tokatli A.
    Turk J Pediatr; 1993 Sep 29; 35(2):121-5. PubMed ID: 7504361
    [Abstract] [Full Text] [Related]

  • 24. Renal imino acid and glycine transport system ontogeny and involvement in developmental iminoglycinuria.
    Vanslambrouck JM, Bröer A, Thavyogarajah T, Holst J, Bailey CG, Bröer S, Rasko JE.
    Biochem J; 2010 May 27; 428(3):397-407. PubMed ID: 20377526
    [Abstract] [Full Text] [Related]

  • 25. Atypical gyrate atrophy of the choroid and retina associated with iminoglycinuria.
    Hayasaka S, Mizuno K, Yabata K, Saito T, Tada K.
    Arch Ophthalmol; 1982 Mar 27; 100(3):423-5. PubMed ID: 7065959
    [Abstract] [Full Text] [Related]

  • 26. Glycylproline peptiduria in familial hyperostosis of obscure nature.
    Alderman MH, Frimpter GW, Isaacs M, Scheiner E.
    Metabolism; 1969 Aug 27; 18(8):692-9. PubMed ID: 4895065
    [No Abstract] [Full Text] [Related]

  • 27. Hydroxyproline metabolism in type II hyperprolinaemia.
    Similä S.
    Ann Clin Biochem; 1979 Jul 27; 16(4):177-81. PubMed ID: 533224
    [Abstract] [Full Text] [Related]

  • 28. Hyperprolinaemia.
    Piesowicz AT.
    Arch Dis Child; 1968 Dec 27; 43(232):748. PubMed ID: 5702251
    [No Abstract] [Full Text] [Related]

  • 29. Excretion of hydroxyproline and other amino acids in scorbutic guinea-pigs.
    Barnes MJ, Constable BJ, Kodicek E.
    Biochim Biophys Acta; 1969 Jul 30; 184(2):358-65. PubMed ID: 5809720
    [No Abstract] [Full Text] [Related]

  • 30. Amino acid excretion in infancy and early childhood. A survey of 200,000 infants.
    Turner B, Brown DA.
    Med J Aust; 1972 Jan 08; 1(2):62-5. PubMed ID: 5025157
    [No Abstract] [Full Text] [Related]

  • 31. Further studies on a patient with iminodipeptiduria: a probable case of prolidase deficiency.
    Buist NR, Strandholm JJ, Bellinger JF, Kennaway NG.
    Metabolism; 1972 Dec 08; 21(12):1113-23. PubMed ID: 4674498
    [No Abstract] [Full Text] [Related]

  • 32. Ontogeny of amino acid reabsorption in human kidney. Evidence from the homozygous infant with familial renal iminoglycinuria for multiple proline and glycine systems.
    Lasley L, Scriver CR.
    Pediatr Res; 1979 Jan 08; 13(1):65-70. PubMed ID: 432003
    [Abstract] [Full Text] [Related]

  • 33. Sarcosinaemia in a retarded, amaurotic child.
    Sewell AC, Krille M, Wilhelm I.
    Eur J Pediatr; 1986 Feb 08; 144(5):508-10. PubMed ID: 2420598
    [Abstract] [Full Text] [Related]

  • 34. [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]

  • 35. Iminoglycinuria. A defect of renal tubular transport.
    Bank H, Crispin M, Ehrlich D, Szeinberg A.
    Isr J Med Sci; 1972 May 24; 81(5):606-12. PubMed ID: 5042951
    [No Abstract] [Full Text] [Related]

  • 36. Cystathioninuria, renal iminoglycinuria and...alpha 1-antitrypsin...deficiency in the same family: relevance in medical practice.
    Halal F, Scriver CR, Cox DW, Jaber L, Varsano I.
    Can Med Assoc J; 1979 Jul 07; 121(1):64-8. PubMed ID: 313837
    [No Abstract] [Full Text] [Related]

  • 37. Combined iminoglycinuria and cystine- and dibasic aminoaciduria in patients with propionic acidaemia and 3-methylcrotonylglycinuria.
    Purkiss P, Chalmers RA, Borud O.
    J Inherit Metab Dis; 1980 Jul 07; 3(3):85-6. PubMed ID: 6775144
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. [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 07; 15(11):64-8. PubMed ID: 4928437
    [No Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 7.