BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 6731721)

  • 1. A female case of ornithine transcarbamylase deficiency with marked computed tomographic abnormalities of the brain.
    Takayanagi M; Ohtake A; Ogura N; Nakajima H; Hoshino M
    Brain Dev; 1984; 6(1):58-60. PubMed ID: 6731721
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Unusual biochemical and clinical features in a girl with ornithine transcarbamylase deficiency.
    Lacey DJ; Duffner PK; Cohen ME; Mosovich L
    Pediatr Neurol; 1986; 2(1):51-3. PubMed ID: 3508674
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.
    Pridmore CL; Clarke JT; Blaser S
    J Child Neurol; 1995 Sep; 10(5):369-74. PubMed ID: 7499756
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Neurological features and computed tomography of the brain in children with ornithine carbamoyl transferase deficiency.
    Kendall BE; Kingsley DP; Leonard JV; Lingam S; Oberholzer VG
    J Neurol Neurosurg Psychiatry; 1983 Jan; 46(1):28-34. PubMed ID: 6842197
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Ornithine transcarbamylase deficiency: a case report.
    Martland T; Mbamali AC; Rittey C; Tanner S; Bonham JR; Griffiths PD
    Neuropediatrics; 1998 Dec; 29(6):331-2. PubMed ID: 10029357
    [No Abstract]   [Full Text] [Related]  

  • 6. CT and MRI in a girl with late-onset ornithine transcarbamylase deficiency: case report.
    Bajaj SK; Kurlemann G; Schuierer G; Peters PE
    Neuroradiology; 1996 Nov; 38(8):796-9. PubMed ID: 8957809
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Ornithine transcarbamylase deficiency: enzyme studies on a further case and a method of diagnosis using plasma enzyme ratios.
    Gray RG; Black JA; Lyons VH; Pollitt RJ
    Pediatr Res; 1976 Nov; 10(11):918-23. PubMed ID: 980551
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Urea cycle defect: a case with MR and CT findings resembling infarct.
    Mamourian AC; du Plessis A
    Pediatr Radiol; 1991; 21(8):594-5. PubMed ID: 1815186
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. Electroencephalographic findings in ornithine transcarbamylase deficiency.
    Brunquell P; Tezcan K; DiMario FJ
    J Child Neurol; 1999 Aug; 14(8):533-6. PubMed ID: 10456765
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Continuous venovenous haemofiltration in hyperammonaemic coma of an adult with non-diagnosed partial ornithine transcarbamylase deficiency.
    Chang MY; Fang JT; Chen YC; Huang CC
    Nephrol Dial Transplant; 1999 May; 14(5):1282-4. PubMed ID: 10344381
    [No Abstract]   [Full Text] [Related]  

  • 13. [Hyperammonemia due to ornithine transcarbamylase deficiency--a cause of lethal metabolic crisis during the newborn period and infancy (author's transl)].
    Schuchmann L; Colombo JP; Fischer H
    Klin Padiatr; 1980 May; 192(3):281-5. PubMed ID: 7191930
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Carbamyl phosphate synthetase and ornithine transcarbamylase activities in enzyme-deficient human liver measured by radiochromatography and correlated with outcome.
    Tuchman M; Tsai MY; Holzknecht RA; Brusilow SW
    Pediatr Res; 1989 Jul; 26(1):77-82. PubMed ID: 2771513
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [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]  

  • 16. Amino acid and DNA analyses in a family with ornithine transcarbamylase deficiency.
    Hou JW; Wang TR
    J Formos Med Assoc; 1996 Feb; 95(2):144-7. PubMed ID: 9064003
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Neonatal hyperammonemia due to ornithine transcarbamylase deficiency (author's transl)].
    del Valle JA; Urbón A; García MJ; Cuadrado P; Ugarte M
    An Esp Pediatr; 1982 May; 16(5):416-20. PubMed ID: 7114619
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The role of orthotopic liver transplantation in the treatment of ornithine transcarbamylase deficiency.
    Busuttil AA; Goss JA; Seu P; Dulkanchainun TS; Yanni GS; McDiarmid SV; Busuttil RW
    Liver Transpl Surg; 1998 Sep; 4(5):350-4. PubMed ID: 9724471
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ornithine transcarbamylase (OTC) deficiency in a female patient with a de nova deletion of the paternal X chromosome.
    Slomski R; Braulke I; Behrend C; Schröder E; Colombo JP; Reiss J
    Hum Genet; 1992 Aug; 89(6):632-4. PubMed ID: 1511981
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentration.
    Wendel U; Wieland J; Bremer HJ; Bachmann C
    Eur J Pediatr; 1989 Jan; 148(4):349-52. PubMed ID: 2707281
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.