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Journal Abstract Search

173 related items for PubMed ID: 6842197

  • 1. Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.
    Kendall BE, Kingsley DP, Leonard JV, Lingam S, Oberholzer VG.
    J Neurol Neurosurg Psychiatry; 1983 Jan; 46(1):28-34. PubMed ID: 6842197
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  • 2. Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.
    Pridmore CL, Clarke JT, Blaser S.
    J Child Neurol; 1995 Sep; 10(5):369-74. PubMed ID: 7499756
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  • 3. Unusual biochemical and clinical features in a girl with ornithine transcarbamylase deficiency.
    Lacey DJ, Duffner PK, Cohen ME, Mosovich L.
    Pediatr Neurol; 1986 Sep; 2(1):51-3. PubMed ID: 3508674
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  • 6. Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency.
    Oechsner M, Steen C, Stürenburg HJ, Kohlschütter A.
    J Neurol Neurosurg Psychiatry; 1998 May; 64(5):680-2. PubMed ID: 9598692
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  • 12. Ornithine carbamoyl transferase deficiency: a neuropathological study.
    Harding BN, Leonard JV, Erdohazi M.
    Eur J Pediatr; 1984 Feb; 141(4):215-20. PubMed ID: 6734670
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  • 13. The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation.
    Kölker S, Garcia-Cazorla A, Valayannopoulos V, Lund AM, Burlina AB, Sykut-Cegielska J, Wijburg FA, Teles EL, Zeman J, Dionisi-Vici C, Barić I, Karall D, Augoustides-Savvopoulou P, Aksglaede L, Arnoux JB, Avram P, Baumgartner MR, Blasco-Alonso J, Chabrol B, Chakrapani A, Chapman K, I Saladelafont EC, Couce ML, de Meirleir L, Dobbelaere D, Dvorakova V, Furlan F, Gleich F, Gradowska W, Grünewald S, Jalan A, Häberle J, Haege G, Lachmann R, Laemmle A, Langereis E, de Lonlay P, Martinelli D, Matsumoto S, Mühlhausen C, de Baulny HO, Ortez C, Peña-Quintana L, Ramadža DP, Rodrigues E, Scholl-Bürgi S, Sokal E, Staufner C, Summar ML, Thompson N, Vara R, Pinera IV, Walter JH, Williams M, Burgard P.
    J Inherit Metab Dis; 2015 Nov; 38(6):1041-57. PubMed ID: 25875215
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  • 16. 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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  • 17. Clinical course, early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency.
    Hoffmann GF, Athanassopoulos S, Burlina AB, Duran M, de Klerk JB, Lehnert W, Leonard JV, Monavari AA, Müller E, Muntau AC, Naughten ER, Plecko-Starting B, Superti-Furga A, Zschocke J, Christensen E.
    Neuropediatrics; 1996 Jun; 27(3):115-23. PubMed ID: 8837070
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  • 18. Central pontine myelinolysis as a complication of partial ornithine carbamoyl transferase deficiency.
    Mattson LR, Lindor NM, Goldman DH, Goodwin JT, Groover RV, Vockley J.
    Am J Med Genet; 1995 Jun 19; 60(3):210-3. PubMed ID: 7573173
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