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Journal Abstract Search

164 related items for PubMed ID: 6434837

  • 1. The management and long term outcome of organic acidaemias.
    Leonard JV, Daish P, Naughten ER, Bartlett K.
    J Inherit Metab Dis; 1984; 7 Suppl 1():13-7. PubMed ID: 6434837
    [Abstract] [Full Text] [Related]

  • 2. Long term outcome of organic acidurias: survey of 105 French cases (1967-1983).
    Rousson R, Guibaud P.
    J Inherit Metab Dis; 1984; 7 Suppl 1():10-2. PubMed ID: 6434836
    [Abstract] [Full Text] [Related]

  • 3.
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  • 4. Breastfeeding experience in inborn errors of metabolism other than phenylketonuria.
    Huner G, Baykal T, Demir F, Demirkol M.
    J Inherit Metab Dis; 2005; 28(4):457-65. PubMed ID: 15902548
    [Abstract] [Full Text] [Related]

  • 5. Methylmalonic and propionic acidaemias: management and outcome.
    de Baulny HO, Benoist JF, Rigal O, Touati G, Rabier D, Saudubray JM.
    J Inherit Metab Dis; 2005; 28(3):415-23. PubMed ID: 15868474
    [Abstract] [Full Text] [Related]

  • 6. Erythematous skin lesions and partial deficiency of 3-methylcrotonyl-CoA carboxylase in peripheral lymphocytes in a patient with propionic acidaemia.
    Yoshino M, Aramaki S, Yamashita F, Sato K, Inoue Y, Kuhara T, Matsumoto I.
    J Inherit Metab Dis; 1991; 14(5):839-40. PubMed ID: 1779636
    [No Abstract] [Full Text] [Related]

  • 7. The identification of (E)-2-methylglutaconic acid, a new isoleucine metabolite, in the urine of patients with beta-ketothiolase deficiency, propionic acidaemia and methylmalonic acidaemia.
    Duran M, Bruinvis L, Ketting D, Kamerling JP, Wadman SK, Schutgens RB.
    Biomed Mass Spectrom; 1982 Jan; 9(1):1-5. PubMed ID: 7059658
    [Abstract] [Full Text] [Related]

  • 8. Selective screening for inborn errors of metabolism on clinical patients using tandem mass spectrometry in China: a four-year report.
    Han LS, Ye J, Qiu WJ, Gao XL, Wang Y, Gu XF.
    J Inherit Metab Dis; 2007 Aug; 30(4):507-14. PubMed ID: 17347912
    [Abstract] [Full Text] [Related]

  • 9. [Human fibroblast bank for studying amino acid disorders and organic acidemias].
    del Valle JA, Merinero B, Pérez-Cerdá C, Ugarte M.
    Rev Esp Fisiol; 1982 Aug; 38 Suppl():207-10. PubMed ID: 7146578
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  • 10.
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  • 11. The impact of screening for propionic and methylmalonic acidaemia.
    Leonard JV, Vijayaraghavan S, Walter JH.
    Eur J Pediatr; 2003 Dec; 162 Suppl 1():S21-4. PubMed ID: 14586648
    [Abstract] [Full Text] [Related]

  • 12. Nutrition therapy of organic acidaemias with amino acid-based formulas: emphasis on methylmalonic and propionic acidaemia.
    Yannicelli S.
    J Inherit Metab Dis; 2006 Dec; 29(2-3):281-7. PubMed ID: 16763889
    [Abstract] [Full Text] [Related]

  • 13. L-carnitine in inborn errors of metabolism: what is the evidence?
    Walter JH.
    J Inherit Metab Dis; 2003 Dec; 26(2-3):181-8. PubMed ID: 12889659
    [Abstract] [Full Text] [Related]

  • 14. Anaesthesia for liver transplantation in two infants with an organic acidaemia.
    Manzoni D, Spotti A, Carrara B, Gritti P, Sonzogni V.
    Pediatr Transplant; 2006 Aug; 10(5):623-8. PubMed ID: 16857001
    [Abstract] [Full Text] [Related]

  • 15. On the differences between urinary metabolite excretion and odd-numbered fatty acid production in propionic and methylmalonic acidaemias.
    Wendel U, Eissler A, Sperl W, Schadewaldt P.
    J Inherit Metab Dis; 1995 Aug; 18(5):584-91. PubMed ID: 8598639
    [Abstract] [Full Text] [Related]

  • 16. An asymptomatic infant with isolated 3-methylcrotonyl-coenzyme: a carboxylase deficiency detected by newborn screening for maple syrup urine disease.
    Ihara K, Kuromaru R, Inoue Y, Kuhara T, Matsumoto I, Yoshino M, Fukushige J.
    Eur J Pediatr; 1997 Sep; 156(9):713-5. PubMed ID: 9296536
    [Abstract] [Full Text] [Related]

  • 17. The use of metronidazole in management of methylmalonic and propionic acidaemias.
    Thompson GN, Chalmers RA, Walter JH, Bresson JL, Lyonnet SL, Reed PJ, Saudubray JM, Leonard JV, Halliday D.
    Eur J Pediatr; 1990 Aug; 149(11):792-6. PubMed ID: 2226555
    [Abstract] [Full Text] [Related]

  • 18. Multiple carboxylase deficiency.
    Nyhan WL.
    Int J Biochem; 1988 Aug; 20(4):363-70. PubMed ID: 3284772
    [Abstract] [Full Text] [Related]

  • 19. [Methylcrotonyl-CoA carboxylase deficiency].
    Narisawa K.
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):592-4. PubMed ID: 3270869
    [No Abstract] [Full Text] [Related]

  • 20. Peritoneal dialysis in the treatment of metabolic crises caused by inherited disorders of organic and amino acid metabolism.
    Gortner L, Leupold D, Pohlandt F, Bartmann P.
    Acta Paediatr Scand; 1989 Sep; 78(5):706-11. PubMed ID: 2596277
    [Abstract] [Full Text] [Related]

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