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Items: 11

1.

Ornithine transcarbamylase deficiency and pancreatitis.

Anadiotis G, Ierardi-Curto L, Kaplan PB, Berry GT.

J Pediatr. 2001 Jan;138(1):123-4.

PMID:
11148526
2.

Ornithine transcarbamylase deficiency: a urea cycle defect.

Gordon N.

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

PMID:
12788037
3.

Mutations and polymorphisms in the human ornithine transcarbamylase gene.

Tuchman M, Jaleel N, Morizono H, Sheehy L, Lynch MG.

Hum Mutat. 2002 Feb;19(2):93-107. Review.

PMID:
11793468
4.

[Hyperammonemia type II as an example of urea cycle disorder].

Hawrot-Kawecka AM, Kawecki GP, DuĊ‚awa J.

Wiad Lek. 2006;59(7-8):512-5. Review. Polish.

PMID:
17209350
5.

[Ornithine transcarbamylase deficiency].

Matsuda I.

Nihon Rinsho. 2002 Apr;60 Suppl 4:775-8. Review. Japanese. No abstract available.

PMID:
12013997
6.

[Hyperammonaemia type II as one of the congenital urea cycle defects].

Ciara E.

Med Wieku Rozwoj. 1999 Jan-Mar;3(1):83-95. Review. Polish.

PMID:
10910641
7.

Ornithine carbamoyltransferase deficiency.

Wraith JE.

Arch Dis Child. 2001 Jan;84(1):84-88. Review. No abstract available.

8.

Considerations in the difficult-to-manage urea cycle disorder patient.

Lee B, Singh RH, Rhead WJ, Sniderman King L, Smith W, Summar ML.

Crit Care Clin. 2005 Oct;21(4 Suppl):S19-25. Review.

PMID:
16227112
9.

[Lipase/amylase ratio and liver function tests for the etiological assessment of acute pancreatitis: facts and fiction].

Pezzilli R, Fantini L.

Recenti Prog Med. 2006 Sep;97(9):477-80. Review. Italian.

PMID:
17017300
10.

Prenatal diagnosis of ornithine transcarbamylase deficiency.

Bale AE.

Prenat Diagn. 1999 Nov;19(11):1052-4. Review. No abstract available.

PMID:
10589058
11.

Problems in the management of urea cycle disorders.

Wilcken B.

Mol Genet Metab. 2004 Apr;81 Suppl 1:S86-91. Review.

PMID:
15050980

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