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4. Plasma alpha-ketoglutarate in urea cycle enzymopathies and its role as a harbinger of hyperammonemic coma. Batshaw ML, Walser M, Brusilow SW. Pediatr Res; 1980 Dec; 14(12):1316-9. PubMed ID: 7208146 [Abstract] [Full Text] [Related]
10. Risk of hyperammonemic coma in the puerperium: two cases of women with diagnosed and undiagnosed deficiency of urea cycle enzymes. Tihtonen K, Uotila J, Lähde J, Salo M, Keskinen P. Acta Obstet Gynecol Scand; 2010 Mar; 89(3):404-6. PubMed ID: 20102292 [Abstract] [Full Text] [Related]
12. Hyperammonemic coma due to parenteral nutrition in a woman with heterozygous ornithine transcarbamylase deficiency. Felig DM, Brusilow SW, Boyer JL. Gastroenterology; 1995 Jul; 109(1):282-4. PubMed ID: 7797025 [Abstract] [Full Text] [Related]
13. [Prenatal diagnosis of ornithine transcarbamylase deficiency using a DNA marker analysis]. Schwartz M, Skovby F, Christensen E, Christensen NC. Ugeskr Laeger; 1988 Oct 31; 150(44):2641-3. PubMed ID: 3201597 [No Abstract] [Full Text] [Related]
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19. [Living related liver transplantation for patients with ornithine transcarbamylase deficiency]. Tazuke M, Murakawa M, Nakao S, Mukaida K, Toda H, Mori K. Masui; 1997 Jun 24; 46(6):783-7. PubMed ID: 9223881 [Abstract] [Full Text] [Related]