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Journal Abstract Search

173 related items for PubMed ID: 3821846

  • 1. Branched-chain alpha-keto acids for the diagnosis of maple-syrup-urine disease.
    Parsons H, Fung E, Snyder FF.
    N Engl J Med; 1987 Apr 09; 316(15):951. PubMed ID: 3821846
    [No Abstract] [Full Text] [Related]

  • 2. The relationship between the branched chain amino acids and their alpha-ketoacids in maple syrup urine disease.
    Snyderman SE, Goldstein F, Sansaricq C, Norton PM.
    Pediatr Res; 1984 Sep 09; 18(9):851-3. PubMed ID: 6483508
    [Abstract] [Full Text] [Related]

  • 3. Prospective study of maple-syrup-urine disease for the first four days of life.
    DiGeorge AM, Rezvani I, Garibaldi LR, Schwartz M.
    N Engl J Med; 1982 Dec 09; 307(24):1492-5. PubMed ID: 7144815
    [No Abstract] [Full Text] [Related]

  • 4. Detection of maple syrup urine disease on resin coated chromatosheets.
    Kovács J.
    Acta Biochim Biophys Acad Sci Hung; 1979 Dec 09; 14(3):119-21. PubMed ID: 547666
    [No Abstract] [Full Text] [Related]

  • 5. Quantification of branched-chain amino acids in blood spots and plasma by liquid chromatography tandem mass spectrometry for the diagnosis of maple syrup urine disease.
    Sowell J, Pollard L, Wood T.
    J Sep Sci; 2011 Mar 09; 34(6):631-9. PubMed ID: 21328532
    [Abstract] [Full Text] [Related]

  • 6. Diagnosis of MSUD by newborn screening allows early intervention without extraneous detoxification.
    Heldt K, Schwahn B, Marquardt I, Grotzke M, Wendel U.
    Mol Genet Metab; 2005 Apr 09; 84(4):313-6. PubMed ID: 15781191
    [Abstract] [Full Text] [Related]

  • 7. Maple-syrup-urine disease.
    Wendel U, Lombeck I, Bremer HJ.
    N Engl J Med; 1983 May 05; 308(18):1100-1. PubMed ID: 6835327
    [No Abstract] [Full Text] [Related]

  • 8. [3 patients with maple syrup urine disease].
    Merinero B, del Valle JA, García MJ, García Miguel MJ, Barrio MI, García Hortelano J, Morales E, González F, García Aparicio J, Sáez Pérez E.
    An Esp Pediatr; 1983 Nov 05; 19(5):393-400. PubMed ID: 6660657
    [Abstract] [Full Text] [Related]

  • 9. Nasogastric drip feeding as the only treatment of neonatal maple syrup urine disease.
    Parini R, Sereni LP, Bagozzi DC, Corbetta C, Rabier D, Narcy C, Hubert P, Saudubray JM.
    Pediatrics; 1993 Aug 05; 92(2):280-3. PubMed ID: 8337030
    [No Abstract] [Full Text] [Related]

  • 10. Maple syrup urine disease in Thai infants.
    Pangkanon S, Charoensiriwatana W, Sangtawesin V.
    J Med Assoc Thai; 2008 Oct 05; 91 Suppl 3():S41-4. PubMed ID: 19255991
    [Abstract] [Full Text] [Related]

  • 11. Branched-chain amino acid-free parenteral nutrition in the treatment of acute metabolic decompensation in patients with maple syrup urine disease.
    Berry GT, Heidenreich R, Kaplan P, Levine F, Mazur A, Palmieri MJ, Yudkoff M, Segal S.
    N Engl J Med; 1991 Jan 17; 324(3):175-9. PubMed ID: 1898534
    [No Abstract] [Full Text] [Related]

  • 12. Total branched-chain amino acids requirement in patients with maple syrup urine disease by use of indicator amino acid oxidation with L-[1-13C]phenylalanine.
    Riazi R, Rafii M, Clarke JT, Wykes LJ, Ball RO, Pencharz PB.
    Am J Physiol Endocrinol Metab; 2004 Jul 17; 287(1):E142-9. PubMed ID: 14970005
    [Abstract] [Full Text] [Related]

  • 13. [Clinical characteristics and analysis of mass spectrometric data in 33 patients with maple syrup urine disease].
    Yang N, Han LS, Ye J, Qiu WJ, Zhang HW, Gao XL, Wang Y, Li XY, Xu H, Gu XF.
    Zhonghua Yi Xue Za Zhi; 2012 Oct 30; 92(40):2839-42. PubMed ID: 23290213
    [Abstract] [Full Text] [Related]

  • 14. Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine disease.
    Langenbeck U, Wendel U, Mench-Hoinowski A, Kuschel D, Becker K, Przyrembel H, Bremer HJ.
    Clin Chim Acta; 1978 Sep 01; 88(2):283-91. PubMed ID: 699323
    [Abstract] [Full Text] [Related]

  • 15. Plasma amino acid analyses in two cases of maple syrup urine disease.
    Surarit R, Srisomsap C, Wasant P, Svasti J, Suthatvoravut U, Chokchaichamnankit D, Liammongkolkul S.
    Southeast Asian J Trop Med Public Health; 1999 Sep 01; 30 Suppl 2():138-9. PubMed ID: 11400750
    [Abstract] [Full Text] [Related]

  • 16. Definition of the mutation responsible for maple syrup urine disease in Poll Shorthorns and genotyping Poll Shorthorns and Poll Herefords for maple syrup urine disease alleles.
    Dennis JA, Healy PJ.
    Res Vet Sci; 1999 Aug 01; 67(1):1-6. PubMed ID: 10425233
    [Abstract] [Full Text] [Related]

  • 17. Implications of Maple Syrup Urine Disease in Newborns.
    Harris-Haman P, Brown L, Massey S, Ramamoorthy S.
    Nurs Womens Health; 2017 Aug 01; 21(3):196-206. PubMed ID: 28599741
    [Abstract] [Full Text] [Related]

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