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

130 related items for PubMed ID: 9164788

  • 21. Rhabdomyolysis in the military: recognizing late-onset very long-chain acyl Co-A dehydrogenase deficiency.
    Hoffman JD, Steiner RD, Paradise L, Harding CO, Ding L, Strauss AW, Kaplan P.
    Mil Med; 2006 Jul; 171(7):657-8. PubMed ID: 16895136
    [Abstract] [Full Text] [Related]

  • 22. Muscular carnitine palmitoyltransferase II deficiency in infancy.
    Hurvitz H, Klar A, Korn-Lubetzki I, Wanders RJ, Elpeleg ON.
    Pediatr Neurol; 2000 Feb; 22(2):148-50. PubMed ID: 10738923
    [Abstract] [Full Text] [Related]

  • 23. Post-mortem recognition of inherited metabolic disorders from specific acylcarnitines in tissue in cases of sudden infant death.
    Roe CR, Millington DS, Maltby DA, Wellman RB.
    Lancet; 1987 Feb 28; 1(8531):512. PubMed ID: 2881073
    [No Abstract] [Full Text] [Related]

  • 24. Neonatal screening for very long-chain acyl-coA dehydrogenase deficiency: enzymatic and molecular evaluation of neonates with elevated C14:1-carnitine levels.
    Liebig M, Schymik I, Mueller M, Wendel U, Mayatepek E, Ruiter J, Strauss AW, Wanders RJ, Spiekerkoetter U.
    Pediatrics; 2006 Sep 28; 118(3):1065-9. PubMed ID: 16950999
    [Abstract] [Full Text] [Related]

  • 25. Lipoamide dehydrogenase deficiency: a new cause for recurrent myoglobinuria.
    Elpeleg ON, Saada AB, Shaag A, Glustein JZ, Ruitenbeek W, Tein I, Halevy J.
    Muscle Nerve; 1997 Feb 28; 20(2):238-40. PubMed ID: 9040667
    [No Abstract] [Full Text] [Related]

  • 26. A genetic defect in carnitine transport causing primary carnitine deficiency.
    Stanley CA, Treem WR, Hale DE, Coates PM.
    Prog Clin Biol Res; 1990 Feb 28; 321():457-64. PubMed ID: 2326306
    [No Abstract] [Full Text] [Related]

  • 27. Very long chain acyl coenzyme A dehydrogenase deficiency in a 5-month-old Korean boy: identification of a novel mutation.
    Hahn SH, Lee EH, Jung JW, Hong CH, Yoon HR, Rinaldo P, Sims H, Gibson B, Strauss AW.
    J Pediatr; 1999 Aug 28; 135(2 Pt 1):250-3. PubMed ID: 10431122
    [Abstract] [Full Text] [Related]

  • 28. Medium chain acyl-coenzyme A dehydrogenase deficiency.
    Bennett MJ, Hale DE.
    N J Med; 1992 Sep 28; 89(9):675-8. PubMed ID: 1436730
    [Abstract] [Full Text] [Related]

  • 29. Neonatal screening for inborn errors of metabolism.
    Morris AA.
    Indian Pediatr; 2000 Dec 28; 37(12):1303-6. PubMed ID: 11119331
    [No Abstract] [Full Text] [Related]

  • 30. Frequency of G-985 mutation in medium chain acyl-coenzyme A dehydrogenase (MCAD) deficiency in sudden infant death syndrome (SIDS).
    Miller M, Brooks J, Forbes N, Insel R.
    Prog Clin Biol Res; 1992 Dec 28; 375():495-8. PubMed ID: 1438393
    [No Abstract] [Full Text] [Related]

  • 31. Screening for inherited metabolic disease in newborn infants using tandem mass spectrometry.
    Leonard JV, Dezateux C.
    BMJ; 2002 Jan 05; 324(7328):4-5. PubMed ID: 11777783
    [No Abstract] [Full Text] [Related]

  • 32. Diagnostic assessment and long-term follow-up of 13 patients with Very Long-Chain Acyl-Coenzyme A dehydrogenase (VLCAD) deficiency.
    Laforêt P, Acquaviva-Bourdain C, Rigal O, Brivet M, Penisson-Besnier I, Chabrol B, Chaigne D, Boespflug-Tanguy O, Laroche C, Bedat-Millet AL, Behin A, Delevaux I, Lombès A, Andresen BS, Eymard B, Vianey-Saban C.
    Neuromuscul Disord; 2009 May 05; 19(5):324-9. PubMed ID: 19327992
    [Abstract] [Full Text] [Related]

  • 33. An unusual presentation of medium-chain acyl coenzyme A dehydrogenase deficiency.
    Marsden D, Sege-Petersen K, Nyhan WL, Roschinger W, Sweetman L.
    Am J Dis Child; 1992 Dec 05; 146(12):1459-62. PubMed ID: 1456259
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 39. Investigation of inborn errors of metabolism in unexpected infant deaths.
    Emery JL, Howat AJ, Variend S, Vawter GF.
    Lancet; 1988 Jul 02; 2(8601):29-31. PubMed ID: 2898629
    [No Abstract] [Full Text] [Related]

  • 40.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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