145 related articles for article (PubMed ID: 11148526)
1. Ornithine transcarbamylase deficiency and pancreatitis.
Anadiotis G; Ierardi-Curto L; Kaplan PB; Berry GT
J Pediatr; 2001 Jan; 138(1):123-4. PubMed ID: 11148526
[TBL] [Abstract][Full Text] [Related]
2. Coagulopathy unmasking hepatic failure in a child with ornithine transcarbamylase deficiency.
Samuel N; Politansky AK; Hoffman R; Itzkovich S; Mandel H
Isr Med Assoc J; 2013 Dec; 15(12):777-9. PubMed ID: 24449986
[No Abstract] [Full Text] [Related]
3. Ornithine transcarbamylase deficiency presenting as recurrent abdominal pain in childhood.
Mhanni AA; Prasad C; Rockman-Greenberg C
Pediatr Emerg Care; 2011 Sep; 27(9):850-3. PubMed ID: 21926883
[TBL] [Abstract][Full Text] [Related]
4. A case of acrodermatitis enteropathica-like dermatosis caused by ornithine transcarbamylase deficiency.
Lee JY; Chang SE; Suh CW; Choi JH; Sung KJ; Moon KC; Koh JK
J Am Acad Dermatol; 2002 Jun; 46(6):965-7. PubMed ID: 12063505
[No Abstract] [Full Text] [Related]
5. Stupor in an adolescent following Yom Kippur fast, due to late-onset ornithine transcarbamylase deficiency.
Marcus N; Scheuerman O; Hoffer V; Zilbershot-Fink E; Reiter J; Garty BZ
Isr Med Assoc J; 2008 May; 10(5):395-6. PubMed ID: 18605371
[No Abstract] [Full Text] [Related]
6. Hyperammonemic coma in an ornithine transcarbamylase mutation carrier following antepartum corticosteroids.
Lipskind S; Loanzon S; Simi E; Ouyang DW
J Perinatol; 2011 Oct; 31(10):682-4. PubMed ID: 21956151
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial DNA 8993T>G mutation in a child with ornithine transcarbamylase deficiency and leigh syndrome: an unexpected association.
Henriques M; Diogo L; Garcia P; Pratas J; Simões M; Grazina M
J Child Neurol; 2012 Aug; 27(8):1059-61. PubMed ID: 22241703
[TBL] [Abstract][Full Text] [Related]
8. Diagnosis of ornithine transcarbamylase deficiency secondary to p.Leu301Phe mutation in an adult patient.
Morel N; Corne C; Aquaviva C; Besson G
Rev Neurol (Paris); 2012 Mar; 168(3):296-7. PubMed ID: 22340867
[No Abstract] [Full Text] [Related]
9. Peripartum management of two parturients with ornithine transcarbamylase deficiency.
Ituk U; Constantinescu OC; Allen TK; Small MJ; Habib AS
Int J Obstet Anesth; 2012 Jan; 21(1):90-3. PubMed ID: 22138526
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 11793468
[TBL] [Abstract][Full Text] [Related]
11. Fatal cerebral edema from late-onset ornithine transcarbamylase deficiency in a juvenile male patient receiving valproic acid.
Thakur V; Rupar CA; Ramsay DA; Singh R; Fraser DD
Pediatr Crit Care Med; 2006 May; 7(3):273-6. PubMed ID: 16575347
[TBL] [Abstract][Full Text] [Related]
12. Low citrulline may not be diagnostic of ornithine transcarbamylase deficiency: a case report.
Chiong MA; Carpenter K; Christodoulou J
J Inherit Metab Dis; 2007 Jun; 30(3):405. PubMed ID: 17407001
[TBL] [Abstract][Full Text] [Related]
13. [Hyperammonemia type II as an example of urea cycle disorder].
Hawrot-Kawecka AM; Kawecki GP; Duława J
Wiad Lek; 2006; 59(7-8):512-5. PubMed ID: 17209350
[TBL] [Abstract][Full Text] [Related]
14. [Ornithine transcarbamylase deficiency].
Matsuda I
Nihon Rinsho; 2002 Apr; 60 Suppl 4():775-8. PubMed ID: 12013997
[No Abstract] [Full Text] [Related]
15. Recurrent pancreatitis in ornithine transcarbamylase deficiency.
Prada CE; Kaul A; Hopkin RJ; Page KI; Nathan JD; Bartholomew DW; Cohen MB; Heubi JE; Leslie ND; Burrow TA
Mol Genet Metab; 2012 Aug; 106(4):482-4. PubMed ID: 22728053
[TBL] [Abstract][Full Text] [Related]
16. Hyperammonemia-induced encephalopathy due to ornithine transcarbamylase deficiency in an adult woman: identification of novel missense mutations.
Tanaka A; Wada T; Maruyama M; Tanaka A; Takikawa H; Komatsu Y
J Gastroenterol; 2005 Jan; 40(1):106-7. PubMed ID: 15692798
[No Abstract] [Full Text] [Related]
17. Acrodermatitis enteropathica-like dermatosis associated with ornithine transcarbamylase deficiency.
Pascual JC; Matarredona J; Mut J
Pediatr Dermatol; 2007; 24(4):394-6. PubMed ID: 17845164
[TBL] [Abstract][Full Text] [Related]
18. Ornithine transcarbamylase deficiency presenting as hepatitis.
Aronson PL; Mistry RD
Pediatr Emerg Care; 2011 Jun; 27(6):527-9. PubMed ID: 21642786
[TBL] [Abstract][Full Text] [Related]
19. Hypocitrullinemia in expanded newborn screening by LC-MS/MS is not a reliable marker for ornithine transcarbamylase deficiency.
Cavicchi C; Malvagia S; la Marca G; Gasperini S; Donati MA; Zammarchi E; Guerrini R; Morrone A; Pasquini E
J Pharm Biomed Anal; 2009 Jul; 49(5):1292-5. PubMed ID: 19359120
[TBL] [Abstract][Full Text] [Related]
20. Interaction between murine spf-ash mutation and genetic background yields different metabolic phenotypes.
Marini JC; Erez A; Castillo L; Lee B
Am J Physiol Endocrinol Metab; 2007 Dec; 293(6):E1764-71. PubMed ID: 17925451
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
