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Items: 8

1.

Mitochondrial abnormalities of liver in primary ornithine transcarbamylase deficiency.

Shapiro JM, Schaffner F, Tallan HH, Gaull GE.

Pediatr Res. 1980 May;14(5):735-9.

PMID:
7383749
2.

Primary ornithine transcarbamylase deficiency. A case report and electron microscopic study.

Aida S, Ogata T, Kamota T, Nakamura N.

Acta Pathol Jpn. 1989 Jul;39(7):451-6. Review.

PMID:
2678891
3.

Ornithine transcarbamylase in liver mitochondria.

Mori M, Miura S, Morita T, Takiguchi M, Tatibana M.

Mol Cell Biochem. 1982 Nov 26;49(2):97-111. Review.

PMID:
6759918
4.

[Reye's syndrome].

Tomaszewski L.

Pediatr Pol. 1982 Nov;57(11):981-8. Review. Polish. No abstract available.

PMID:
6763187
5.

Metabolic mechanisms in Reye syndrome. End of a Mystery?

Thaler MM.

Am J Dis Child. 1976 Mar;130(3):241-3. Review. No abstract available.

PMID:
769533
6.

[Congenital deficiency of ornithine transcarbamylase. Description of 2 clinical cases].

D'Eufemia P, Corrado G, Sabetta G, Castro M, Martino F, Cantani A, Ruberto U.

Minerva Pediatr. 1983 Mar 15;35(5):219-24. Review. Italian. No abstract available.

PMID:
6343831
7.

Ornithine transcarbamylase deficiency: a urea cycle defect.

Gordon N.

Eur J Paediatr Neurol. 2003;7(3):115-21. Review.

PMID:
12788037
8.

[Etiological mechanism of Reye's syndrome--from the viewpoint of metabolic disorders].

Yoshida I, Yamashita F.

Nihon Rinsho. 1984 Dec;42(12):2824-36. Review. Japanese. No abstract available.

PMID:
6397640

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