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Journal Abstract Search

233 related items for PubMed ID: 5621096

  • 21. [Personal experience in the clinical use of free amino acids in the blood and urine].
    Borota J, Velisavljev M, Jojić M.
    Med Pregl; 1984; 37(9-10):387-91. PubMed ID: 6530984
    [No Abstract] [Full Text] [Related]

  • 22. [Free blood and urine amino acids in children with rheumatism].
    Kliukina SS, Gavriushova LP.
    Vopr Okhr Materin Det; 1971 Jun; 16(6):28-31. PubMed ID: 5112028
    [No Abstract] [Full Text] [Related]

  • 23. [Methylmalonic aciduria - diagnosis and therapy using as example 2 cases of this genetic metabolic disorder].
    Lubs H, Seidlitz G, Pfau E.
    Padiatr Grenzgeb; 1982 Jun; 21(4):319-26. PubMed ID: 7177670
    [No Abstract] [Full Text] [Related]

  • 24. [Paper chromatography in the detection of aminoacidopathies].
    Sietti C.
    Minerva Pediatr; 1971 Dec 22; 23(51):2123-4. PubMed ID: 5136311
    [No Abstract] [Full Text] [Related]

  • 25. [Diagnostic methods for the detection of amino acid metabolism disorders].
    Lutz P.
    Monatsschr Kinderheilkd (1902); 1973 May 22; 121(5):184-9. PubMed ID: 4197345
    [No Abstract] [Full Text] [Related]

  • 26. Rapid screening methods for the detection of inherited and acquired aminoacidopathies.
    Saifer A.
    Adv Clin Chem; 1971 May 22; 14():145-218. PubMed ID: 4109903
    [No Abstract] [Full Text] [Related]

  • 27. [The contribution of the laboratory in the diagnosis of hereditary intermediate metabolism disorders].
    Khiari D, Tebib N, Kaabachi N, Ben Dridi MF, Mebazaa A.
    Tunis Med; 1995 May 22; 73(5):159-67. PubMed ID: 9507277
    [No Abstract] [Full Text] [Related]

  • 28. [Personal experience with chromatographic methods of demonstrating aminated substances (amino acids and amines)].
    Berio A.
    Minerva Pediatr; 1968 Mar 10; 20(10):536-45. PubMed ID: 5739013
    [No Abstract] [Full Text] [Related]

  • 29. The assessment of serum amino acids.
    Swallow WH, Carrell RW.
    N Z Med J; 1970 Feb 10; 71(453):85-8. PubMed ID: 5267129
    [No Abstract] [Full Text] [Related]

  • 30. [1H-NMR urinalysis: simultaneous screening of inborn errors of metabolism of amino acid and organic acid disorders].
    Yamamoto H, Yamaguchi S.
    Rinsho Byori; 1988 Feb 10; 36(2):182-90. PubMed ID: 3379790
    [No Abstract] [Full Text] [Related]

  • 31. A new genetic defect of branched chain amino acid metabolism?
    Buneta D, Raić F, Lipovac K, Velikonja N.
    Monogr Hum Genet; 1972 Feb 10; 6():130-40. PubMed ID: 4663885
    [No Abstract] [Full Text] [Related]

  • 32. [Chromatographic analysis in the diagnosis of metabolic aminoacidopathies].
    Sietti C.
    Minerva Pediatr; 1971 Dec 22; 23(51):2125-8. PubMed ID: 5136312
    [No Abstract] [Full Text] [Related]

  • 33. [Long-term personal experience in the diagnosis of amino acidopathies by chromatography of serum according to the method of Scriver et al].
    Berio A.
    Minerva Pediatr; 1985 Dec 31; 37(23-24):947-54. PubMed ID: 3834309
    [No Abstract] [Full Text] [Related]

  • 34. Hypervalinemia. Its metabolic lesion and therapeutic approach.
    Tada K, Wada Y, Arakawa T.
    Am J Dis Child; 1967 Jan 31; 113(1):64-7. PubMed ID: 6066688
    [No Abstract] [Full Text] [Related]

  • 35. [Hereditary tyrosinemia. II. Presentation of a system of detection].
    Bélanger M, Saint-Hilaire B.
    Pediatrie; 1973 Jan 31; 28(1):19-22. PubMed ID: 4715464
    [No Abstract] [Full Text] [Related]

  • 36. [Screening for amino acid diseases: column chromatography of amino acids from a paper sampling].
    Castets JC, Jérome H.
    Arch Fr Pediatr; 1972 Jan 31; 29(6):675-6. PubMed ID: 5078374
    [No Abstract] [Full Text] [Related]

  • 37. A study of aminoacidemia and aminoaciduria in epileptic children.
    Tudor I, Tănase-Mogoş I, Tănăsie E, Bădescu E, Răşcanu M.
    Neurol Psychiatr (Bucur); 1976 Jan 31; 14(4):277-82. PubMed ID: 1024264
    [No Abstract] [Full Text] [Related]

  • 38. [Free amino acids in plasma. Normal values in pediatrics].
    Cohen AL, Monesiglio JC.
    Arch Argent Pediatr; 1971 Sep 31; 69(7):281-7. PubMed ID: 5113471
    [No Abstract] [Full Text] [Related]

  • 39. Ion-pairing reversed-phase liquid chromatography/electrospray ionization mass spectrometric analysis of 76 underivatized amino acids of biological interest: a new tool for the diagnosis of inherited disorders of amino acid metabolism.
    Piraud M, Vianey-Saban C, Petritis K, Elfakir C, Steghens JP, Bouchu D.
    Rapid Commun Mass Spectrom; 2005 Sep 31; 19(12):1587-602. PubMed ID: 15915446
    [Abstract] [Full Text] [Related]

  • 40. [Further results of studies on metabolic disorders in a population of severely retarded children (2)].
    Opałka S, Galewicz A, Pisarska E, Wegrzynowicz Z.
    Psychiatr Neurol Med Psychol Beih; 1968 Sep 31; 8-9():126-9. PubMed ID: 5006367
    [Abstract] [Full Text] [Related]

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