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Items: 18

1.

Ornithine transcarbamylase deficiency in a boy with normal development.

Yudkoff M, Yang W, Snodgrass PJ, Segal S.

J Pediatr. 1980 Mar;96(3 Pt 1):441-3. No abstract available.

PMID:
7188954
2.

The role of orthotopic liver transplantation in the treatment of ornithine transcarbamylase deficiency.

Busuttil AA, Goss JA, Seu P, Dulkanchainun TS, Yanni GS, McDiarmid SV, Busuttil RW.

Liver Transpl Surg. 1998 Sep;4(5):350-4. Review.

3.

[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
4.

[Ornithine transcarbamylase deficiency (OTCD)].

Matsuura T, Matsuda I.

Ryoikibetsu Shokogun Shirizu. 1998;(18 Pt 1):170-4. Review. Japanese. No abstract available.

PMID:
9590019
5.

[Hyperammonemias of childhood. I. Enzymopathies of the urea cycle].

Kopieczna-Grzebieniak E, Toborek M, Tarnawski R, Jakubowska D.

Pediatr Pol. 1987 Oct;62(10):727-32. Review. Polish. No abstract available.

PMID:
3328149
6.

Urea cycle disorders: diagnosis, pathophysiology, and therapy.

Brusilow SW, Maestri NE.

Adv Pediatr. 1996;43:127-70. Review. No abstract available.

PMID:
8794176
7.

Treating genetic diseases: lessons from three children.

Rosenberg LE.

Pediatr Res. 1990 Jun;27(6 Suppl):S10-6. Review. No abstract available.

PMID:
2192347
8.

Enzyme induction (first of three parts).

Gelehrter TD.

N Engl J Med. 1976 Mar 4;294(10):522-6. Review. No abstract available.

PMID:
2868
9.

[Disorders of the urea cycle].

Matsumura R.

Ryoikibetsu Shokogun Shirizu. 2000;(29 Pt 4):390-2. Review. Japanese. No abstract available.

PMID:
11031978
10.

Treatment of urea cycle disorders.

Thoene JG.

J Pediatr. 1999 Mar;134(3):255-6. Review. No abstract available.

PMID:
10064655
11.

Inborn errors of urea synthesis.

Batshaw ML.

Ann Neurol. 1994 Feb;35(2):133-41. Review.

PMID:
7906500
12.

[Diseases of altered amino acid metabolism].

Bulgarelli R, Berio A.

Minerva Nipiol. 1970 Jan-Feb;20(1):1-33. Review. Italian. No abstract available.

PMID:
4936594
13.

Some regulatory aspects of urea synthesis.

Colombo JP.

Enzyme. 1981;26(5):225-32. Review. No abstract available.

PMID:
7028476
14.

[Ammonia nitrogen and amino nitrogen--how to read its figures].

Takahashi T, Fujisawa K, Tanaka T, Kurihara N, Nishikawa H.

Nihon Rinsho. 1971 Jan;29:Suppl:231-8. Review. Japanese. No abstract available.

PMID:
4930450
15.

Ornithine transcarbamylase deficiency: a model for gene therapy.

Morsy MA, Caskey CT.

Adv Exp Med Biol. 1994;368:145-54. Review. No abstract available.

PMID:
7741006
16.

Garrod's legacy to the nations of mice and men.

Scriver CR.

Prog Clin Biol Res. 1981;45:169-92. Review. No abstract available.

PMID:
7017751
17.

Advantages of supplementary alanine in infants with genetic defects of amino acid metabolism.

[No authors listed]

Nutr Rev. 1986 May;44(5):164-6. Review. No abstract available.

PMID:
3523316
18.

[Therapeutic trials in amino acid disorders].

Saudubray JM, Boisse J.

Ann Biol Clin (Paris). 1974;32(5):461-71. Review. French. No abstract available.

PMID:
4142368

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