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Journal Abstract Search

227 related items for PubMed ID: 6646142

  • 1. [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; 131(10):714-5. PubMed ID: 6646142
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  • 2. [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 Oct; 17(2):371-82. PubMed ID: 7099689
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  • 3. Congenital hyperammonemic syndromes.
    Shih VE.
    Clin Perinatol; 1976 Mar; 3(1):3-14. PubMed ID: 954343
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  • 4. [Neonatal hyperammonemia].
    Jaeken J, Devlieger H, Evens M, Casaer P, Eggermont E.
    Tijdschr Kindergeneeskd; 1983 Jun; 51(3):101-4. PubMed ID: 6636106
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  • 6. [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
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  • 7. [Urea cycle disorders].
    Tazawa Y.
    Ryoikibetsu Shokogun Shirizu; 1995 Sep; (8):367-9. PubMed ID: 8581654
    [No Abstract] [Full Text] [Related]

  • 8. Valproate-induced hyperammonemia.
    Batshaw ML, Brusilow SW.
    Ann Neurol; 1982 Mar; 11(3):319-21. PubMed ID: 6807193
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  • 9. [Hyperammonemia].
    Arashima S.
    Nihon Rinsho; 1978 May; Suppl():1352-3. PubMed ID: 691351
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  • 12. Severe neonatal deficiency of carbamylphosphate synthetase.
    Lambotte C, Adam A, Van Der Hofstadt J, Dodinval-Versie J, Gielen J.
    Acta Paediatr Belg; 1977 May; 30(3):151-5. PubMed ID: 204150
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  • 13. 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
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  • 14. [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
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  • 19. [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]

  • 20. Management of heritable disorders of the urea cycle and of Refsum's and Fabry's diseases.
    Moser HW, Batshaw ML, Murray C, Braine H, Brusilow SW.
    Prog Clin Biol Res; 1979 Jul; 34():183-200. PubMed ID: 93755
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