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.


PUBMED FOR HANDHELDS

Journal Abstract Search


178 related items for PubMed ID: 691351

  • 1. [Hyperammonemia].
    Arashima S.
    Nihon Rinsho; 1978 May; Suppl():1352-3. PubMed ID: 691351
    [No Abstract] [Full Text] [Related]

  • 2. [Neonatal hyperammonemia].
    Jaeken J, Devlieger H, Evens M, Casaer P, Eggermont E.
    Tijdschr Kindergeneeskd; 1983 Jun; 51(3):101-4. PubMed ID: 6636106
    [Abstract] [Full Text] [Related]

  • 3. [Hyperammonemias of childhood. I. Enzymopathies of the urea cycle].
    Kopieczna-Grzebieniak E, Toborek M, Tarnawski R, Jakubowska D.
    Pediatr Pol; 1987 Oct; 62(10):727-32. PubMed ID: 3328149
    [No Abstract] [Full Text] [Related]

  • 4. [Urea cycle disorders].
    Tazawa Y.
    Ryoikibetsu Shokogun Shirizu; 1995 Oct; (8):367-9. PubMed ID: 8581654
    [No Abstract] [Full Text] [Related]

  • 5. Congenital hyperammonemic syndromes.
    Shih VE.
    Clin Perinatol; 1976 Mar; 3(1):3-14. PubMed ID: 954343
    [Abstract] [Full Text] [Related]

  • 6. [Comments on the contribution, Therapy of hyperammonemia in carbamylphosphate synthetase deficiency with peritoneal dialysis and venovenous hemofiltration, by B. Lettgen et al].
    Brockstedt M.
    Monatsschr Kinderheilkd; 1992 Jul; 140(7):431. PubMed ID: 1308100
    [No Abstract] [Full Text] [Related]

  • 7. Plasma alpha-ketoglutarate in urea cycle enzymopathies and its role as a harbinger of hyperammonemic coma.
    Batshaw ML, Walser M, Brusilow SW.
    Pediatr Res; 1980 Dec; 14(12):1316-9. PubMed ID: 7208146
    [Abstract] [Full Text] [Related]

  • 8. [Therapy of hyperammonemia in carbamyl phosphate synthase deficiency with peritoneal dialysis and venovenous hemofiltration].
    Lettgen B, Bonzel KE, Colombo JP, Fuchs B, Kordass U, Wendel K, Rascher W.
    Monatsschr Kinderheilkd; 1991 Sep; 139(9):612-7. PubMed ID: 1745252
    [Abstract] [Full Text] [Related]

  • 9. Severe neonatal deficiency of carbamylphosphate synthetase.
    Lambotte C, Adam A, Van Der Hofstadt J, Dodinval-Versie J, Gielen J.
    Acta Paediatr Belg; 1977 Sep; 30(3):151-5. PubMed ID: 204150
    [No Abstract] [Full Text] [Related]

  • 10. Urea cycle enzymopathies.
    Walser M.
    Semin Liver Dis; 1982 Nov; 2(4):329-39. PubMed ID: 6763345
    [No Abstract] [Full Text] [Related]

  • 11. Quantitative analysis of urinary pyroglutamic acid in patients with hyperammonemia.
    Nakanishi T, Shimizu A, Saiki K, Fujiwara F, Funahashi S, Hayashi A.
    Clin Chim Acta; 1991 Mar 29; 197(3):249-55. PubMed ID: 2049866
    [No Abstract] [Full Text] [Related]

  • 12. Sodium benzoate and arginine: alternative pathway therapy in inborn errors of urea synthesis.
    Batshaw ML.
    Prog Clin Biol Res; 1983 Mar 29; 127():69-83. PubMed ID: 6889404
    [No Abstract] [Full Text] [Related]

  • 13. [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 Mar 29; 17(2):371-82. PubMed ID: 7099689
    [Abstract] [Full Text] [Related]

  • 14. Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.
    Brusilow SW.
    J Clin Invest; 1984 Dec 29; 74(6):2144-8. PubMed ID: 6511918
    [Abstract] [Full Text] [Related]

  • 15. Disorders of the urea cycle.
    Brusilow SW.
    Hosp Pract (Off Ed); 1985 Oct 15; 20(10):65-72. PubMed ID: 3930543
    [No Abstract] [Full Text] [Related]

  • 16. Carbamylphosphate synthetase-I deficiency in a newborn: survival after early diagnosis and therapy.
    Raghavan K, Chabra S, Mondkar J, Aiyar R, Ambani LM, Fernandez A.
    Indian Pediatr; 1991 May 15; 28(5):551-4. PubMed ID: 1752685
    [No Abstract] [Full Text] [Related]

  • 17. [Pulmonary hemorrhages in newborn infants with inborn errors of the 1st 2 phases of the urea cycle].
    Plöchl E, Bachmann C.
    Monatsschr Kinderheilkd; 1983 Oct 15; 131(10):714-5. PubMed ID: 6646142
    [Abstract] [Full Text] [Related]

  • 18. Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis.
    Brusilow SW, Danney M, Waber LJ, Batshaw M, Burton B, Levitsky L, Roth K, McKeethren C, Ward J.
    N Engl J Med; 1984 Jun 21; 310(25):1630-4. PubMed ID: 6427608
    [Abstract] [Full Text] [Related]

  • 19. Hyperammonemia (ornithinemia) presenting as a unilateral cerebral mass lesion.
    Amacher AL, Bolton RJ, Gatfield PD.
    Surg Neurol; 1976 Sep 21; (3):159-62. PubMed ID: 959986
    [No Abstract] [Full Text] [Related]

  • 20. Detection of urea cycle enzymopathies in childhood.
    Trauner DA, Self TW.
    Arch Neurol; 1984 Jul 21; 41(7):758-60. PubMed ID: 6743067
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 9.