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Journal Abstract Search

169 related items for PubMed ID: 4811018

  • 1. Lethal neonatal deficiency of carbamyl phosphate synthetase.
    Gelehrter TD, Snodgrass PJ.
    N Engl J Med; 1974 Feb 21; 290(8):430-3. PubMed ID: 4811018
    [No Abstract] [Full Text] [Related]

  • 2. [Congenital hyperammoniemia caused by ornithine carbamoyl-transferase and carbamyl phosphate synthetase deficiency].
    Salle B, Levin B, Longin B, Richard P, Andre M, Gauthier J.
    Arch Fr Pediatr; 1972 May 21; 29(5):493-504. PubMed ID: 4655647
    [No Abstract] [Full Text] [Related]

  • 3. [Hyperammonemia--congenital abnormality of the urea cycle].
    Arashima I.
    Saishin Igaku; 1972 Apr 21; 27(4):730-42. PubMed ID: 5026635
    [No Abstract] [Full Text] [Related]

  • 4.
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    [No Abstract] [Full Text] [Related]

  • 5. A case of carbamyl phosphate synthetase deficiency.
    Arashima S, Matsuda I.
    Tohoku J Exp Med; 1972 Jun 21; 107(2):143-7. PubMed ID: 4641111
    [No Abstract] [Full Text] [Related]

  • 6. [Constitutional hyperammonemia with carbamoylphosphate synthetase deficiency. Course treatment during dietetic].
    Odievre M, Charpentier C, Cathelineau L, Vedrenne J, Delacoux des Roseaux F, Mercie C.
    Arch Fr Pediatr; 1973 Jan 21; 30(1):5-13. PubMed ID: 4721588
    [No Abstract] [Full Text] [Related]

  • 7. [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 Jan 21; 29(7):713-36. PubMed ID: 4644461
    [No Abstract] [Full Text] [Related]

  • 8. Ornithine transcarbamylase deficiency: a cause of lethal neonatal hyperammonemia in males.
    Campbell AG, Rosenberg LE, Snodgrass PJ, Nuzum CT.
    N Engl J Med; 1973 Jan 04; 288(1):1-6. PubMed ID: 4681895
    [No Abstract] [Full Text] [Related]

  • 9. Carbamyl-phosphate-synthetase deficiency with neonatal onset of symptoms.
    Farriaux JP, Ponte C, Pollitt RJ, Lequien P, Formstecher P, Dhondt JL.
    Acta Paediatr Scand; 1977 Jul 04; 66(4):529-34. PubMed ID: 197778
    [Abstract] [Full Text] [Related]

  • 10. Neonatal hyperammonaemia with complete absence of liver carbamyl phosphate synthetase activity.
    Mantagos S, Tsagaraki S, Burgess EA, Oberholzer V, Palmer T, Sacks J, Baibas S, Valaes T.
    Arch Dis Child; 1978 Mar 04; 53(3):230-4. PubMed ID: 206210
    [Abstract] [Full Text] [Related]

  • 11. Inborn errors of urea synthesis.
    Batshaw ML.
    Ann Neurol; 1994 Feb 04; 35(2):133-41. PubMed ID: 7906500
    [Abstract] [Full Text] [Related]

  • 12. Ornithine transcarbamylase deficiency: case report and review.
    Bueno JD, Lutz R, Cho S.
    Kans Med; 1995 Feb 04; 96(3):135-8. PubMed ID: 8583741
    [No Abstract] [Full Text] [Related]

  • 13. Blood levels of ammonia and nitrogen scavenging amino acids in patients with inherited hyperammonemia.
    Tuchman M, Yudkoff M.
    Mol Genet Metab; 1999 Jan 04; 66(1):10-5. PubMed ID: 9973542
    [Abstract] [Full Text] [Related]

  • 14. Carbamyl phosphate synthetase in the chick.
    Maresh CG, Kwan TH, Kalman SM.
    Can J Biochem; 1969 Jan 04; 47(1):61-3. PubMed ID: 5763651
    [No Abstract] [Full Text] [Related]

  • 15. Methylmalonyl coenzyme A racemase defect: another cause of methylmalonic aciduria.
    Kang ES, Snodgrass PJ, Gerald PS.
    Pediatr Res; 1972 Dec 04; 6(12):875-9. PubMed ID: 4643536
    [No Abstract] [Full Text] [Related]

  • 16. [Lethal neonatal deficiency of carbamyl phosphate synthetase (author's transl)].
    Plöchl E, Bachmann C, Stöllinger O, Colombo JP, Rassem T, Czihak G.
    Padiatr Padol; 1982 Dec 04; 17(2):371-82. PubMed ID: 7099689
    [Abstract] [Full Text] [Related]

  • 17. In vitro "responsive" methylmalonic acidemia: a new variant.
    Kaye CI, Morrow G, Nadler HL.
    J Pediatr; 1974 Jul 04; 85(1):55-9. PubMed ID: 4852378
    [No Abstract] [Full Text] [Related]

  • 18. Treatment of carbamyl phosphate synthetase deficiency with keto analogues of essential amino acids.
    Batshaw M, Brusilow S, Walser M.
    N Engl J Med; 1975 May 22; 292(21):1085-90. PubMed ID: 165404
    [Abstract] [Full Text] [Related]

  • 19. Ornithine transcarbamylase deficiency in the newborn infant.
    Kang ES, Snodgrass PJ, Gerald PS.
    J Pediatr; 1973 Apr 22; 82(4):642-9. PubMed ID: 4698340
    [No Abstract] [Full Text] [Related]

  • 20. Partial ornithine carbamyl transferase deficiency: an inborn error of the urea cycle presenting as orotic aciduria in a male infant.
    MacLeod P, Mackenzie S, Scriver CR.
    Can Med Assoc J; 1972 Sep 09; 107(5):405-8. PubMed ID: 5074751
    [Abstract] [Full Text] [Related]

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