These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

90 related articles for article (PubMed ID: 4117228)

  • 1. X-linked transmission of ornithine-transcarbamylase deficiency.
    Scott CR; Teng CC; Goodman SI; Greensher A; Mace JW
    Lancet; 1972 Nov; 2(7787):1148. PubMed ID: 4117228
    [No Abstract]   [Full Text] [Related]  

  • 2. X-linked transmission of structural gene mutations responsible for ornithine-transcarbamylase deficiencies.
    Cathelineau L; Navarro J; Polonovski C; Saudubray JM
    Lancet; 1973 Feb; 1(7797):261-2. PubMed ID: 4119401
    [No Abstract]   [Full Text] [Related]  

  • 3. Metabolic and genetic studies of a family with ornithine transcarbamylase deficiency.
    Goldstein AS; Hoogenraad NJ; Johnson JD; Fukanaga K; Swierczewski E; Cann HM; Sunshine P
    Pediatr Res; 1974 Jan; 8(1):5-12. PubMed ID: 4809308
    [No Abstract]   [Full Text] [Related]  

  • 4. Identification of 'private' mutations in patients with ornithine transcarbamylase deficiency.
    Tuchman M; Morizono H; Rajagopal BS; Plante RJ; Allewell NM
    J Inherit Metab Dis; 1997 Aug; 20(4):525-7. PubMed ID: 9266388
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Fatal clinical course of ornithine transcarbamylase deficiency in an adult heterozygous female patient.
    Heringlake S; Böker K; Manns M
    Digestion; 1997; 58(1):83-6. PubMed ID: 9018015
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary ornithine transcarbamylase deficiency. Report of two male cases with residual enzymatic activity.
    Saudubray JM; Cathelineau L; Laugier JM; Charpentier C; Lejeune JA; Mozziconacci P
    Acta Paediatr Scand; 1975 May; 64(3):464-72. PubMed ID: 168725
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hyperammonaemia: a deficiency of liver ornithine transcarbamylase. Occurrence in mother and child.
    Levin B; Abraham JM; Oberholzer VG; Burgess EA
    Arch Dis Child; 1969 Apr; 44(234):152-61. PubMed ID: 5779426
    [No Abstract]   [Full Text] [Related]  

  • 8. Ornithine transcarbamylase deficiency in the newborn infant.
    Kang ES; Snodgrass PJ; Gerald PS
    J Pediatr; 1973 Apr; 82(4):642-9. PubMed ID: 4698340
    [No Abstract]   [Full Text] [Related]  

  • 9. Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.
    Levin B; Dobbs RH; Burgess EA; Palmer T
    Arch Dis Child; 1969 Apr; 44(234):162-9. PubMed ID: 5779427
    [No Abstract]   [Full Text] [Related]  

  • 10. [Hyperammonemia due to an inborn error of metabolism. Ornithine-transcarbamylase deficiency].
    Chevrel B
    Presse Med (1893); 1969 Sep; 77(40):1370. PubMed ID: 5821578
    [No Abstract]   [Full Text] [Related]  

  • 11. Partial duplication [dup. TCAC (178)] and novel point mutations (T125M, G188R, A209V, and H302L) of the ornithine transcarbamylase gene in congenital hyperammonemia.
    Gilbert-Dussardier B; Segues B; Rozet JM; Rabier D; Calvas P; de Lumley L; Bonnefond JP; Munnich A
    Hum Mutat; 1996; 8(1):74-6. PubMed ID: 8807340
    [No Abstract]   [Full Text] [Related]  

  • 12. Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity.
    Staudt M; Wermuth B; Freisinger P; Hässler A; Pontz BF
    J Inherit Metab Dis; 1998 Feb; 21(1):71-2. PubMed ID: 9501271
    [No Abstract]   [Full Text] [Related]  

  • 13. Ornithine transcarbamylase deficiency: a model for gene therapy.
    Morsy MA; Caskey CT
    Adv Exp Med Biol; 1994; 368():145-54. PubMed ID: 7741006
    [No Abstract]   [Full Text] [Related]  

  • 14. [Hereditary hyperammonemia due to qualitative abnormality of hepatic and intestinal ornithine carbamoyl-transferase].
    Cathelineau L; Navarro J; Aymard P; Baudon JJ; Mondet Y; Polonovski C; Laplane R
    Arch Fr Pediatr; 1972; 29(7):713-36. PubMed ID: 4644461
    [No Abstract]   [Full Text] [Related]  

  • 15. Evidence for x-linked dominant inheritance of ornithine transcarbamylase deficiency.
    Short EM; Conn HO; Snodgrass PJ; Campbell AG; Rosenberg LE
    N Engl J Med; 1973 Jan; 288(1):7-12. PubMed ID: 4681915
    [No Abstract]   [Full Text] [Related]  

  • 16. Reye's syndrome due to a novel protein-tolerant variant of ornithine-transcarbamylase deficiency.
    Thaler MM; Hoogenraad NJ; Boswell M
    Lancet; 1974 Aug; 2(7878):438-40. PubMed ID: 4137171
    [No Abstract]   [Full Text] [Related]  

  • 17. Lethal neonatal hyperammonaemia due to complete ornithine-transcarbamylase deficiency.
    Campbell AG; Rosenberg LE; Snodgrass PJ; Nuzum CT
    Lancet; 1971 Jul; 2(7717):217-8. PubMed ID: 4104881
    [No Abstract]   [Full Text] [Related]  

  • 18. [Ornithine-transcarbamylase deficiency: prognostic difficulties].
    Sanjurjo Crespo P; Sasieta Altuna M; Rubio Zamora V; Prats Viñas JM; Vallo Boado A
    An Esp Pediatr; 1991 Dec; 35(6):407-8. PubMed ID: 1793191
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hyperammonemia: a deficiency of liver ornithine transcarbamylase.
    Nagayama E; Kitayama T; Oguchi H; Ogata K; Tamura E
    Paediatr Univ Tokyo; 1970 Dec; 18():167-73. PubMed ID: 5514641
    [No Abstract]   [Full Text] [Related]  

  • 20. [Chromosome X transmission of the ornithine-carbamyl-transferase structural gene. A study of 3 families].
    Cathelineau L; Saudubray JM; Navarro J; Polonovski C
    Ann Genet; 1973 Sep; 16(3):173-82. PubMed ID: 4543206
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.