148 related articles for article (PubMed ID: 93755)
1. 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]
2. Sodium benzoate and arginine: alternative pathway therapy in inborn errors of urea synthesis.
Batshaw ML
Prog Clin Biol Res; 1983; 127():69-83. PubMed ID: 6889404
[No Abstract] [Full Text] [Related]
3. Congenital hyperammonemic syndromes.
Shih VE
Clin Perinatol; 1976 Mar; 3(1):3-14. PubMed ID: 954343
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. [Urea cycle disorders].
Tazawa Y
Ryoikibetsu Shokogun Shirizu; 1995; (8):367-9. PubMed ID: 8581654
[No Abstract] [Full Text] [Related]
7. Urea cycle enzymopathies.
Walser M
Semin Liver Dis; 1982 Nov; 2(4):329-39. PubMed ID: 6763345
[No Abstract] [Full Text] [Related]
8. Therapeutic trial of plasmapheresis in Refsum disease and in Fabry disease.
Moser HW; Braine H; Pyeritz RE; Ullman D; Murray C; Asbury AK
Birth Defects Orig Artic Ser; 1980; 16(1):491-7. PubMed ID: 6160883
[No Abstract] [Full Text] [Related]
9. [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. PubMed ID: 3328149
[No Abstract] [Full Text] [Related]
10. 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]
11. 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]
12. Amino acid acylation: a mechanism of nitrogen excretion in inborn errors of urea synthesis.
Brusilow S; Tinker J; Batshaw ML
Science; 1980 Feb; 207(4431):659-61. PubMed ID: 6243418
[TBL] [Abstract][Full Text] [Related]
13. Refsum's disease: management by diet and plasmapheresis.
Hungerbühler JP; Meier C; Rousselle L; Quadri P; Bogousslavsky J
Eur Neurol; 1985; 24(3):153-9. PubMed ID: 2581787
[TBL] [Abstract][Full Text] [Related]
14. Heredopathia atactica polyneuritiformis (refsum's disease) treated by diet and plasma-exchange.
Gibberd FB; Billimoria JD; Page NG; Retsas S
Lancet; 1979 Mar; 1(8116):575-8. PubMed ID: 85164
[TBL] [Abstract][Full Text] [Related]
15. [Neonatal hyperammonemia].
Jaeken J; Devlieger H; Evens M; Casaer P; Eggermont E
Tijdschr Kindergeneeskd; 1983 Jun; 51(3):101-4. PubMed ID: 6636106
[TBL] [Abstract][Full Text] [Related]
16. Cascade filtration in Refsum's disease.
Siegmund JB; Meier H; Hoppmann I; Gutsche HU
Nephrol Dial Transplant; 1995; 10(1):117-9. PubMed ID: 7536903
[No Abstract] [Full Text] [Related]
17. 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]
18. 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]
19. [Disorders of the urea cycle].
Matsumura R
Ryoikibetsu Shokogun Shirizu; 2000; (29 Pt 4):390-2. PubMed ID: 11031978
[No Abstract] [Full Text] [Related]
20. Urea cycle disorders: diagnosis, pathophysiology, and therapy.
Brusilow SW; Maestri NE
Adv Pediatr; 1996; 43():127-70. PubMed ID: 8794176
[No Abstract] [Full Text] [Related]
[Next] [New Search]
