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Journal Abstract Search

105 related items for PubMed ID: 19376100

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

  • 22. Hyperprolinemia type II: identification of the glycine conjugate of pyrrole-2-carboxylic acid in urine.
    Applegarth DA, Goodman SI, Irvine DG, Jellum E.
    Clin Biochem; 1977 Feb; 10(1):20-3. PubMed ID: 837521
    [Abstract] [Full Text] [Related]

  • 23. Iminoglycinuria in a child in Czechoslovakia.
    Blehová B, Păzoutová N, Hyánek J, Jirásek J.
    Humangenetik; 1973 Jul 20; 19(2):207-10. PubMed ID: 4744406
    [No Abstract] [Full Text] [Related]

  • 24. Identification of Δ-1-pyrroline-5-carboxylate derived biomarkers for hyperprolinemia type II.
    Merx J, van Outersterp RE, Engelke UFH, Hendriks V, Wevers RA, Huigen MCDG, Waterval HWAH, Körver-Keularts IMLW, Mecinović J, Rutjes FPJT, Oomens J, Coene KLM, Martens J, Boltje TJ.
    Commun Biol; 2022 Sep 21; 5(1):997. PubMed ID: 36131087
    [Abstract] [Full Text] [Related]

  • 25. Hyperprolinemia. I. Study of a large family.
    Potter JL, Waickman FJ.
    J Pediatr; 1973 Oct 21; 83(4):635-8. PubMed ID: 4729989
    [No Abstract] [Full Text] [Related]

  • 26. [Renal clearance of amino acid in a hyperprolinemic child].
    Dodinval P, Willems C, Heusden AM, Hainaut H, Gottschalk C.
    J Genet Hum; 1969 Oct 21; 17(3):297-315. PubMed ID: 5387412
    [No Abstract] [Full Text] [Related]

  • 27. Analysis of organic acids and acylglycines for the diagnosis of related inborn errors of metabolism by GC- and HPLC-MS.
    la Marca G, Rizzo C.
    Methods Mol Biol; 2011 Oct 21; 708():73-98. PubMed ID: 21207284
    [Abstract] [Full Text] [Related]

  • 28. Synthesis and characterisation of acyl glycines. Their measurement in single blood spots by gas chromatography-mass spectrometry to diagnose inborn errors of metabolism.
    Bonham Carter SM, Watson DG, Midgley JM, Logan RW.
    J Chromatogr B Biomed Appl; 1996 Feb 23; 677(1):29-35. PubMed ID: 8925099
    [Abstract] [Full Text] [Related]

  • 29. Crystal structure of Thermus thermophilus Delta1-pyrroline-5-carboxylate dehydrogenase.
    Inagaki E, Ohshima N, Takahashi H, Kuroishi C, Yokoyama S, Tahirov TH.
    J Mol Biol; 2006 Sep 22; 362(3):490-501. PubMed ID: 16934832
    [Abstract] [Full Text] [Related]

  • 30. Hyperprolinemia: clinical and biochemical family study.
    Woody NC, Snyder CH, Harris JA.
    Pediatrics; 1969 Oct 22; 44(4):554-63. PubMed ID: 5346634
    [No Abstract] [Full Text] [Related]

  • 31. Renal iminoglycinuria without intestinal malabsorption of glycine and imino acids.
    Tancredi F, Guazzi G, Auricchio S.
    J Pediatr; 1970 Mar 22; 76(3):386-92. PubMed ID: 5308714
    [No Abstract] [Full Text] [Related]

  • 32. 3-Hydroxy-3-methylglutaric aciduria: a possible pitfall in diagnosis.
    Mills GA, Hill MA, Buchanan R, Corina DL, Walker V.
    Clin Chim Acta; 1991 Dec 31; 204(1-3):131-6. PubMed ID: 1726424
    [No Abstract] [Full Text] [Related]

  • 33. Quantitative liquid chromatography coupled with tandem mass spectrometry analysis of urinary acylglycines: application to the diagnosis of inborn errors of metabolism.
    Ombrone D, Salvatore F, Ruoppolo M.
    Anal Biochem; 2011 Oct 01; 417(1):122-8. PubMed ID: 21704015
    [Abstract] [Full Text] [Related]

  • 34. Iminoacidopathy in renal failure.
    Simon NM, Bell NH, Del Greco F.
    Arch Intern Med; 1970 Feb 01; 125(2):299-301. PubMed ID: 5412018
    [No Abstract] [Full Text] [Related]

  • 35. Hyperprolinaemia.
    Piesowicz AT.
    Arch Dis Child; 1968 Dec 01; 43(232):748. PubMed ID: 5702251
    [No Abstract] [Full Text] [Related]

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