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

Journal Abstract Search


215 related items for PubMed ID: 11134453

  • 21. Megalencephaly in the neonatal period as the initial manifestation of glutaric aciduria type I.
    Iafolla AK, Kahler SG.
    J Pediatr; 1989 Jun; 114(6):1004-6. PubMed ID: 2627209
    [No Abstract] [Full Text] [Related]

  • 22. Vigabatrin in the treatment of glutaric aciduria type I.
    Francois B, Jaeken J, Gillis P.
    J Inherit Metab Dis; 1990 Jun; 13(3):352-4. PubMed ID: 2122100
    [No Abstract] [Full Text] [Related]

  • 23. Glutaric aciduria type 1 in a Kuwaiti infant.
    Elsori HA, Naguib KK, Hammoud MS.
    East Mediterr Health J; 2004 Jun; 10(4-5):680-4. PubMed ID: 16335663
    [No Abstract] [Full Text] [Related]

  • 24. Glutaric aciduria type I: value of diffusion-weighted magnetic resonance imaging for diagnosing acute striatal necrosis.
    Elster AW.
    J Comput Assist Tomogr; 2004 Jun; 28(1):98-100. PubMed ID: 14716240
    [Abstract] [Full Text] [Related]

  • 25. Glutaric aciduria type 1 in adulthood.
    Prevett MC, Howard RS, Dalton RN, Olpin SE.
    J Neurol Neurosurg Psychiatry; 1996 Mar; 60(3):352-3. PubMed ID: 8609526
    [No Abstract] [Full Text] [Related]

  • 26. [Macrocephaly as the initial manifestation of glutaryl-CoA-dehydrogenase deficiency (glutaric aciduria type I)].
    Trefz FK, Hoffmann GF, Mayatepek E, Lichter-Konecki U, Weisser J, Otten A, Wendel U, Rating D, Bremer HJ.
    Monatsschr Kinderheilkd; 1991 Nov; 139(11):754-8. PubMed ID: 1775140
    [Abstract] [Full Text] [Related]

  • 27. Glutaric aciduria type I: enzymatic and neuroradiologic investigations of two kindreds.
    Amir N, Elpeleg ON, Shalev RS, Christensen E.
    J Pediatr; 1989 Jun; 114(6):983-9. PubMed ID: 2723913
    [Abstract] [Full Text] [Related]

  • 28. [Glutaric aciduria type I: an organic acidemia without acidosis with severe movement disorders].
    Prats Viñas J.
    Neurologia; 2001 Oct; 16(8):337-41. PubMed ID: 11738010
    [No Abstract] [Full Text] [Related]

  • 29. [Macrocephaly and dystonic cerebral palsy in a child with type I glutaric aciduria].
    Plöchl E, Christensen E, Colombo JP, Weiss-Wichert P, Wenger E.
    Padiatr Padol; 1991 Oct; 26(2):97-101. PubMed ID: 1945471
    [Abstract] [Full Text] [Related]

  • 30. Biochemistry of glutaric aciduria type I: activities of in vitro expressed wild-type and mutant cDNA encoding human glutaryl-CoA dehydrogenase.
    Liesert M, Zschocke J, Hoffmann GF, Mühlhäuser N, Buckel W.
    J Inherit Metab Dis; 1999 May; 22(3):256-8. PubMed ID: 10384381
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Glutaric aciduria type 1: proton magnetic resonance spectroscopy findings.
    Kurul S, Cakmakçi H, Dirik E.
    Pediatr Neurol; 2004 Sep; 31(3):228-31. PubMed ID: 15351027
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 36. Glutaric aciduria: improved MR appearance after aggressive therapy.
    Cho CH, Mamourian AC, Filiano J, Nordgren RE.
    Pediatr Radiol; 1995 Sep; 25(6):484-5. PubMed ID: 7491211
    [Abstract] [Full Text] [Related]

  • 37. Glutaryl-CoA dehydrogenase deficiency presenting as 3-hydroxyglutaric aciduria.
    Nyhan WL, Zschocke J, Hoffmann G, Stein DE, Bao L, Goodman S.
    Mol Genet Metab; 1999 Mar; 66(3):199-204. PubMed ID: 10066389
    [Abstract] [Full Text] [Related]

  • 38. Occurrence of subdural hematomas in Dutch glutaric aciduria type 1 patients.
    Vester ME, Visser G, Wijburg FA, van Spronsen FJ, Williams M, van Rijn RR.
    Eur J Pediatr; 2016 Jul; 175(7):1001-6. PubMed ID: 27246831
    [Abstract] [Full Text] [Related]

  • 39. Glutaric aciduria type I: prenatal exclusion using GC-MS analysis of amniotic fluid and enzymology with oxidation of [6-14C]lysine.
    Chalmers RA, Cheng KN, English NR, Jones MA, Savage W.
    J Inherit Metab Dis; 1989 Jul; 12(3):335-6. PubMed ID: 2515380
    [No Abstract] [Full Text] [Related]

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


    Page: [Previous] [Next] [New Search]
    of 11.