BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

243 related articles for article (PubMed ID: 24616362)

  • 1. Late-onset ornithine transcarbamylase deficiency: treatment and outcome of hyperammonemic crisis.
    Bergmann KR; McCabe J; Smith TR; Guillaume DJ; Sarafoglou K; Gupta S
    Pediatrics; 2014 Apr; 133(4):e1072-6. PubMed ID: 24616362
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Successful early management of a female patient with a metabolic stroke due to ornithine transcarbamylase deficiency.
    Tummolo A; Favia V; Bellantuono R; Bellino V; Ranieri A; Morrone A; De Palo T; Papadia F
    Pediatr Emerg Care; 2013 May; 29(5):656-8. PubMed ID: 23640148
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Late-onset ornithine transcarbamylase deficiency associated with hyperammonemia.
    Daijo K; Kawaoka T; Nakahara T; Nagaoki Y; Tsuge M; Hiramatsu A; Imamura M; Kawakami Y; Aikata H; Hara K; Tajima G; Kobayashi M; Chayama K
    Clin J Gastroenterol; 2017 Aug; 10(4):383-387. PubMed ID: 28597413
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hyperammonemia in a Woman with Late-onset Ornithine Transcarbamylase Deficiency.
    Koya Y; Shibata M; Senju M; Honma Y; Hiura M; Ishii M; Matsumoto S; Harada M
    Intern Med; 2019 Apr; 58(7):937-942. PubMed ID: 30449781
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hyperammonemic coma in a patient with late-onset OTC deficiency.
    D'Onofrio V; Poma F; Enea A; Santarelli F; Lovera C; Spada M
    Pediatr Med Chir; 2014 Jun; 36(3):9. PubMed ID: 25573644
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Urea cycle disorders in Thai infants: a report of 5 cases.
    Wasant P; Srisomsap C; Liammongkolkul S; Svasti J
    J Med Assoc Thai; 2002 Aug; 85 Suppl 2():S720-31. PubMed ID: 12403252
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Vomiting, ataxia, and altered mental status in an adolescent: late-onset ornithine transcarbamylase deficiency.
    Myers JH; Shook JE
    Am J Emerg Med; 1996 Oct; 14(6):553-7. PubMed ID: 8857803
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hyperammonemia in a patient with late-onset ornithine carbamoyltransferase deficiency.
    Choi DE; Lee KW; Shin YT; Na KR
    J Korean Med Sci; 2012 May; 27(5):556-9. PubMed ID: 22563224
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hyperammonemia type II as an example of urea cycle disorder].
    Hawrot-Kawecka AM; Kawecki GP; DuĊ‚awa J
    Wiad Lek; 2006; 59(7-8):512-5. PubMed ID: 17209350
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Late-onset of ornithine transcarbamylase deficiency: A rare medical examiner case.
    Gitto L; Fuller CE; Calleo VJ; Tawil M; Thach R; Revercomb C
    J Forensic Sci; 2022 Mar; 67(2):813-819. PubMed ID: 34726276
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia.
    Mohamed S; Hamad MH; Kondkar AA; Abu-Amero KK
    Saudi Med J; 2015 Oct; 36(10):1229-32. PubMed ID: 26446336
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hyperammonemic encephalopathy in a child with ornithine transcarbamylase deficiency due to a novel combined heterozygous mutations.
    Gao J; Gao F; Hong F; Yu H; Jiang P
    Am J Emerg Med; 2015 Mar; 33(3):474.e1-3. PubMed ID: 25227973
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Ammonia toxicity and its prevention in inherited defects of the urea cycle.
    Walker V
    Diabetes Obes Metab; 2009 Sep; 11(9):823-35. PubMed ID: 19531057
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Parieto-occipital encephalomalacia in neonatal hyperammonemia with ornithine transcarbamylase deficiency: A case report.
    Okanishi T; Ito T; Nakajima Y; Ito K; Kakita H; Yamada Y; Kobayashi S; Ando N; Togari H
    Brain Dev; 2010 Aug; 32(7):567-70. PubMed ID: 19640662
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Ammonia and coma - a case report of late onset hemizygous ornithine carbamyltransferase deficiency in 68-year-old female.
    Marquetand J; Freisinger P; Lindig T; Euler S; Gasser M; Overkamp D
    BMC Neurol; 2020 Apr; 20(1):118. PubMed ID: 32252669
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Adult-onset ornithine transcarbamylase (OTC) deficiency unmasked by the Atkins' diet.
    Ben-Ari Z; Dalal A; Morry A; Pitlik S; Zinger P; Cohen J; Fattal I; Galili-Mosberg R; Tessler D; Baruch RG; Nuoffer JM; Largiader CR; Mandel H
    J Hepatol; 2010 Feb; 52(2):292-5. PubMed ID: 20031247
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Abrupt onset and rapid deterioration in the course of congenital ornithine transcarbamylase deficiency: a case report].
    Fukuizumi H; Kudo J; Shimamura R; Fujimoto K; Ishibashi H; Niho Y; Taniyama T; Kumashiro T
    Fukuoka Igaku Zasshi; 1990 Jul; 81(7):247-53. PubMed ID: 2210591
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fatal coma in a young adult due to late-onset urea cycle deficiency presenting with a prolonged seizure: a case report.
    Alameri M; Shakra M; Alsaadi T
    J Med Case Rep; 2015 Nov; 9():267. PubMed ID: 26593089
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.