206 related articles for article (PubMed ID: 11148550)
1. Long-term management of patients with urea cycle disorders.
Berry GT; Steiner RD
J Pediatr; 2001 Jan; 138(1 Suppl):S56-60; discussion S60-1. PubMed ID: 11148550
[TBL] [Abstract][Full Text] [Related]
2. Proceedings of a satellite meeting on advances in inherited urea cycle disorders. Vienna, 20-21 May 1997.
J Inherit Metab Dis; 1998; 21 Suppl 1():1-159. PubMed ID: 9686340
[No Abstract] [Full Text] [Related]
3. Management of heritable disorders of the urea cycle and of Refsum's and Fabry's diseases.
Moser HW; Batshaw ML; Murray C; Braine H; Brusilow SW
Prog Clin Biol Res; 1979; 34():183-200. PubMed ID: 93755
[No Abstract] [Full Text] [Related]
4. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.
Brusilow SW
J Clin Invest; 1984 Dec; 74(6):2144-8. PubMed ID: 6511918
[TBL] [Abstract][Full Text] [Related]
5. Disorders of the urea cycle.
Brusilow SW
Hosp Pract (Off Ed); 1985 Oct; 20(10):65-72. PubMed ID: 3930543
[No Abstract] [Full Text] [Related]
6. Congenital hyperammonemic syndromes.
Shih VE
Clin Perinatol; 1976 Mar; 3(1):3-14. PubMed ID: 954343
[TBL] [Abstract][Full Text] [Related]
7. Alternative pathway therapy for urea cycle disorders.
Feillet F; Leonard JV
J Inherit Metab Dis; 1998; 21 Suppl 1():101-11. PubMed ID: 9686348
[TBL] [Abstract][Full Text] [Related]
8. Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis.
Brusilow SW; Danney M; Waber LJ; Batshaw M; Burton B; Levitsky L; Roth K; McKeethren C; Ward J
N Engl J Med; 1984 Jun; 310(25):1630-4. PubMed ID: 6427608
[TBL] [Abstract][Full Text] [Related]
9. [Urea cycle disorders].
Tazawa Y
Ryoikibetsu Shokogun Shirizu; 1995; (8):367-9. PubMed ID: 8581654
[No Abstract] [Full Text] [Related]
10. 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. PubMed ID: 3306877
[No Abstract] [Full Text] [Related]
11. Attempted dietary treatment of a boy with hyperammonemia due to ornithine transferase deficiency.
van der Heiden C; Bakker HD; Desplanque J; Brink M; de Bree PK; Wadman SK
Eur J Pediatr; 1978 Jul; 128(4):261-72. PubMed ID: 668733
[TBL] [Abstract][Full Text] [Related]
12. Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion.
Batshaw ML; Brusilow S; Waber L; Blom W; Brubakk AM; Burton BK; Cann HM; Kerr D; Mamunes P; Matalon R; Myerberg D; Schafer IA
N Engl J Med; 1982 Jun; 306(23):1387-92. PubMed ID: 7078580
[TBL] [Abstract][Full Text] [Related]
13. Use of citrulline as a diagnostic marker in the prospective treatment of urea cycle disorders.
Batshaw ML; Berry GT
J Pediatr; 1991 Jun; 118(6):914-7. PubMed ID: 2040929
[No Abstract] [Full Text] [Related]
14. Urea cycle disorders: clinical presentation outside the newborn period.
Smith W; Kishnani PS; Lee B; Singh RH; Rhead WJ; Sniderman King L; Smith M; Summar M
Crit Care Clin; 2005 Oct; 21(4 Suppl):S9-17. PubMed ID: 16227115
[TBL] [Abstract][Full Text] [Related]
15. Alternative pathway therapy for urea cycle disorders: twenty years later.
Batshaw ML; MacArthur RB; Tuchman M
J Pediatr; 2001 Jan; 138(1 Suppl):S46-54; discussion S54-5. PubMed ID: 11148549
[TBL] [Abstract][Full Text] [Related]
16. Prospective treatment of urea cycle disorders.
Maestri NE; Hauser ER; Bartholomew D; Brusilow SW
J Pediatr; 1991 Dec; 119(6):923-8. PubMed ID: 1720458
[TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 16227112
[TBL] [Abstract][Full Text] [Related]
18. Detection of urea cycle enzymopathies in childhood.
Trauner DA; Self TW
Arch Neurol; 1984 Jul; 41(7):758-60. PubMed ID: 6743067
[TBL] [Abstract][Full Text] [Related]
19. Effect of alternative pathway therapy on branched chain amino acid metabolism in urea cycle disorder patients.
Scaglia F; Carter S; O'Brien WE; Lee B
Mol Genet Metab; 2004 Apr; 81 Suppl 1():S79-85. PubMed ID: 15050979
[TBL] [Abstract][Full Text] [Related]
20. Liver transplantation for the treatment of urea cycle disorders.
Whitington PF; Alonso EM; Boyle JT; Molleston JP; Rosenthal P; Emond JC; Millis JM
J Inherit Metab Dis; 1998; 21 Suppl 1():112-8. PubMed ID: 9686349
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]