BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

334 related articles for article (PubMed ID: 34035022)

  • 1. Valproate-induced fatal acute hyperammonaemia-related encephalopathy in late-onset ornithine transcarbamylase deficiency.
    Kazmierski D; Sharma N; O'Leary K; Ochieng P
    BMJ Case Rep; 2021 May; 14(5):. PubMed ID: 34035022
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Corticosteroid-induced hyperammonaemic encephalopathy in a woman with late-onset ornithine transcarbamylase deficiency.
    McCormick BJ; Ritchie LV; Porter IE
    BMJ Case Rep; 2024 May; 17(5):. PubMed ID: 38697679
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fatal hyperammonaemia due to late-onset ornithine transcarbamylase deficiency.
    Bijvoet GP; van der Sijs-Bos CJ; Wielders JP; Groot OA
    Neth J Med; 2016 Jan; 74(1):36-9. PubMed ID: 26819360
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Valproate-induced hyperammonemia - uncovering an underlying inherited metabolic disorder: a case report.
    Mehta S; Tayabali S; Lachmann R
    J Med Case Rep; 2018 May; 12(1):134. PubMed ID: 29769109
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 8. Status epilepticus secondary to hyperammonaemia: a late presentation of an undiagnosed urea cycle defect.
    Beddoes P; Nerone G; Tai C
    BMJ Case Rep; 2021 May; 14(5):. PubMed ID: 34059532
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Late-onset ornithine transcarbamylase deficiency mimicking a focal opercular syndrome.
    Donlon E; McGettigan J; Gaffney C; Ahmad MW; Boers P; Treacy E; Chaila E
    Pract Neurol; 2022 Jun; 22(3):224-227. PubMed ID: 35046116
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [Hyperammonaemic coma after valproate therapy as adult onset of ornithine transcarbamylase deficiency].
    Padilla Mde L; Miguélez M; Riverola A; Bueno J
    Med Clin (Barc); 2002 Feb; 118(5):199. PubMed ID: 11852003
    [No Abstract]   [Full Text] [Related]  

  • 12. 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]  

  • 13. Heterozygote ornithine transcarbamylase deficiency presenting as symptomatic hyperammonemia during initiation of valproate therapy.
    Honeycutt D; Callahan K; Rutledge L; Evans B
    Neurology; 1992 Mar; 42(3 Pt 1):666-8. PubMed ID: 1549234
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hyperammonaemic encephalopathy after initiation of valproate therapy in unrecognised ornithine transcarbamylase deficiency.
    Oechsner M; Steen C; Stürenburg HJ; Kohlschütter A
    J Neurol Neurosurg Psychiatry; 1998 May; 64(5):680-2. PubMed ID: 9598692
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Complete recovery from acute encephalopathy of late-onset ornithine transcarbamylase deficiency in a 3-year-old boy.
    Mak CM; Siu TS; Lam CW; Chan GC; Poon GW; Wong KY; Low LC; Tang NL; Li SK; Lau KY; Kwong NS; Tam S
    J Inherit Metab Dis; 2007 Nov; 30(6):981. PubMed ID: 17922216
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Psychiatric Symptoms as the First or Solitary Manifestation of Somatic Illnesses: Hyperammonaemia Type II.
    Niwinski P; Remberk B; Rybakowski F; Rokicki D
    Neuropsychobiology; 2021; 80(3):271-275. PubMed ID: 32688360
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Ornithine transcarbamylase deficiency diagnosed in pregnancy.
    Celik O; Buyuktas D; Aydin A; Acbay O
    Gynecol Endocrinol; 2011 Dec; 27(12):1052-4. PubMed ID: 21736537
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 17.