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Items: 10

1.

A variant form of citrullinemia.

Matsuda I, Anakura M, Arashima S, Saito Y, Oka Y.

J Pediatr. 1976 May;88(5):824-6. No abstract available.

PMID:
1271146
2.

[Enzymatic analysis of citrullinemia in Japan].

Saheki T.

Seikagaku. 1982;54(7):435-43. Review. Japanese. No abstract available.

PMID:
6754830
3.

The human argininosuccinate synthetase locus and citrullinemia.

Beaudet AL, O'Brien WE, Bock HG, Freytag SO, Su TS.

Adv Hum Genet. 1986;15:161-96, 291-2. Review. No abstract available.

PMID:
3513483
4.

Hereditary disorders of the urea cycle in man: biochemical and molecular approaches.

Saheki T, Kobayashi K, Inoue I.

Rev Physiol Biochem Pharmacol. 1987;108:21-68. Review. No abstract available.

PMID:
3306877
5.

[Adverse effects of branched chain amino acid transfusion on type-II citrullinemia--report of an adult case].

Shindo K, Tsunoda S, Shiozawa Z.

Rinsho Shinkeigaku. 1991 Apr;31(4):407-11. Review. Japanese.

PMID:
1914326
6.

[Adult-onset type II citrullinemia in a patient undergoing continuous ambulatory peritoneal dialysis].

Ogawa K, Takashima S, Hirade S, Futamura A, Ueno H, Inoue H.

Rinsho Shinkeigaku. 1998 Sep;38(9):826-30. Review. Japanese.

PMID:
10078035
7.

[Argininosuccinate synthetase deficiency].

Kobayashi K, Saheki T.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):175-8. Review. Japanese. No abstract available.

PMID:
9590020
8.

[Citrullinemia: management and clinical course. Apropos of a familial case].

Gay C, Tronchon H, Divry P, Teyssier G, Freycon MT, Freycon F.

Pediatrie. 1993;48(12):894-7. Review. French.

PMID:
8047401
9.

[Citrullinemia].

Matsuura T.

Ryoikibetsu Shokogun Shirizu. 2001;(33):452-4. Review. Japanese. No abstract available.

PMID:
11462512
10.

Hereditary metabolic disorders of the urea cycle.

Levin B.

Adv Clin Chem. 1971;14:65-143. Review. No abstract available.

PMID:
4944564
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