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Journal Abstract Search

423 related items for PubMed ID: 7499756

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  • 2. Unusual biochemical and clinical features in a girl with ornithine transcarbamylase deficiency.
    Lacey DJ, Duffner PK, Cohen ME, Mosovich L.
    Pediatr Neurol; 1986; 2(1):51-3. PubMed ID: 3508674
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  • 3.
    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Lichter-Konecki U, Caldovic L, Morizono H, Simpson K, Ah Mew N, MacLeod E.
    ; 1993. PubMed ID: 24006547
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  • 4. Carnitine deficiency associated with ornithine transcarbamylase deficiency.
    Mayatepek E, Kurczynski TW, Hoppel CL, Gunning WT.
    Pediatr Neurol; 1991; 7(3):196-9. PubMed ID: 1908679
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  • 5. Natural history of symptomatic partial ornithine transcarbamylase deficiency.
    Rowe PC, Newman SL, Brusilow SW.
    N Engl J Med; 1986 Feb 27; 314(9):541-7. PubMed ID: 3945292
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  • 7. Partial ornithine transcarbamylase deficiency in females: diagnosis by an immunohistochemical method.
    Hayasaka K, Metoki K, Ishiguro S, Kato S, Chiba T, Hirooka M, Kikuchi M, Kurobane I, Narisawa K, Tada K.
    Eur J Pediatr; 1987 Jul 27; 146(4):370-2. PubMed ID: 3308467
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  • 8. 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 27; 46(1):28-34. PubMed ID: 6842197
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  • 9. Long-term treatment of girls with ornithine transcarbamylase deficiency.
    Maestri NE, Brusilow SW, Clissold DB, Bassett SS.
    N Engl J Med; 1996 Sep 19; 335(12):855-9. PubMed ID: 8778603
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  • 13. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency.
    Batshaw ML, Msall M, Beaudet AL, Trojak J.
    J Pediatr; 1986 Feb 19; 108(2):236-41. PubMed ID: 3944708
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  • 14. Acute hemiparesis as the presenting sign in a heterozygote for ornithine transcarbamylase deficiency.
    de Grauw TJ, Smit LM, Brockstedt M, Meijer Y, vd Klei-von Moorsel J, Jakobs C.
    Neuropediatrics; 1990 Aug 19; 21(3):133-5. PubMed ID: 2234317
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  • 15. Hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency due to a novel combined heterozygous mutations.
    Gao J, Gao F, Hong F, Yu H, Jiang P.
    Am J Emerg Med; 2015 Mar 19; 33(3):474.e1-3. PubMed ID: 25227973
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  • 16. Intermittent hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency.
    Gulati S, Menon S, Kabra M, Kalra V.
    Indian J Pediatr; 2004 Jul 19; 71(7):645-7. PubMed ID: 15280615
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  • 17. Prenatal counseling in heterozygotes for ornithine transcarbamylase deficiency.
    Fries MH, Kuller JA, Jurecki E, Packman S.
    Clin Pediatr (Phila); 1994 Sep 19; 33(9):525-9. PubMed ID: 8001320
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