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Journal Abstract Search

176 related items for PubMed ID: 3308467

  • 41. Heritable urea cycle enzyme deficiency-liver disease in 16 patients.
    LaBrecque DR, Latham PS, Riely CA, Hsia YE, Klatskin G.
    J Pediatr; 1979 Apr; 94(4):580-7. PubMed ID: 219172
    [No Abstract] [Full Text] [Related]

  • 42. Proceedings: Hepatic ultrastructure in a child with carbamyl phosphate synthetase deficiency, hyperornithinaemia, hyperammonaemia, and homocitrullinuria.
    Haust MD, Gatfield PD.
    Arch Dis Child; 1975 Aug; 50(8):663. PubMed ID: 173245
    [No Abstract] [Full Text] [Related]

  • 43. [Hyperammonemias of childhood. I. Enzymopathies of the urea cycle].
    Kopieczna-Grzebieniak E, Toborek M, Tarnawski R, Jakubowska D.
    Pediatr Pol; 1987 Oct; 62(10):727-32. PubMed ID: 3328149
    [No Abstract] [Full Text] [Related]

  • 44. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.
    Brusilow SW.
    J Clin Invest; 1984 Dec; 74(6):2144-8. PubMed ID: 6511918
    [Abstract] [Full Text] [Related]

  • 45. Detection of urea cycle enzymopathies in childhood.
    Trauner DA, Self TW.
    Arch Neurol; 1984 Jul; 41(7):758-60. PubMed ID: 6743067
    [Abstract] [Full Text] [Related]

  • 46. [DNA diagnosis of ornithine transcarbamylase deficiency by PCR method].
    Matsuura T, Matsuda I.
    Tanpakushitsu Kakusan Koso; 1990 Dec; 35(17):3113-9. PubMed ID: 2287729
    [No Abstract] [Full Text] [Related]

  • 47. Prenatal diagnosis of ornithine transcarbamylase deficiency utilizing fetal liver biopsy.
    Holzgreve W, Golbus MS.
    Am J Hum Genet; 1984 Mar; 36(2):320-8. PubMed ID: 6711559
    [Abstract] [Full Text] [Related]

  • 48. Liver peroxisome damage during acute hepatic failure in partial ornithine transcarbamylase deficiency.
    Landrieu P, François B, Lyon G, Van Hoof F.
    Pediatr Res; 1982 Dec; 16(12):977-81. PubMed ID: 7155674
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  • 50. Vomiting, ataxia, and altered mental status in an adolescent: late-onset ornithine transcarbamylase deficiency.
    Myers JH, Shook JE.
    Am J Emerg Med; 1996 Oct; 14(6):553-7. PubMed ID: 8857803
    [Abstract] [Full Text] [Related]

  • 51. Congenital hyperammonemia: symptomatic carrier girl patient and her asymptomatic heterozygous mother for ornithine transcarbamylase (OTC) deficiency: specific enzyme diagnostic and kinetic investigations for the detection of heterozygous genostatus.
    László A, Karsai T, Várkonyi A.
    Acta Paediatr Hung; 1991 Oct; 31(3):291-7. PubMed ID: 1742044
    [Abstract] [Full Text] [Related]

  • 52. Efficient mitochondrial import of newly synthesized ornithine transcarbamylase (OTC) and correction of secondary metabolic alterations in spf(ash) mice following gene therapy of OTC deficiency.
    Zimmer KP, Bendiks M, Mori M, Kominami E, Robinson MB, Ye X, Wilson JM.
    Mol Med; 1999 Apr; 5(4):244-53. PubMed ID: 10448647
    [Abstract] [Full Text] [Related]

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  • 56. Late onset ornithine carbamoyl transferase deficiency in males.
    Drogari E, Leonard JV.
    Arch Dis Child; 1988 Nov; 63(11):1363-7. PubMed ID: 3202644
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  • 58. Intracranial haemorrhage in siblings and ornithine transcarbamylase deficiency.
    Amir J, Alpert G, Statter M, Gutman A, Reisner SH.
    Acta Paediatr Scand; 1982 Jul; 71(4):671-3. PubMed ID: 7136688
    [No Abstract] [Full Text] [Related]

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  • 60. A case of ornithine transcarbamylase deficiency with Rett syndrome manifestations.
    Hyman SL, Batshaw ML.
    Am J Med Genet Suppl; 1986 Jul; 1():339-43. PubMed ID: 3087194
    [Abstract] [Full Text] [Related]

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