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Journal Abstract Search

264 related items for PubMed ID: 7267239

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  • 6. [Inborn metabolic errors due to disorders in the urea synthesis cycle].
    Kardosová A, Hruskovic I, Strnová J.
    Cesk Pediatr; 1986 Jan; 41(1):31-3. PubMed ID: 3948272
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  • 7. Introduction to urea cycle symposium.
    Koch R.
    Pediatrics; 1981 Aug; 68(2):271-2. PubMed ID: 7267237
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  • 11. [Inherited hyperammonemia].
    Bik-Multanowski M.
    Przegl Lek; 1998 Aug; 55(6):337-41. PubMed ID: 9857711
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  • 12. Biochemical aspects of urea cycle disorders.
    Snodgrass PJ.
    Pediatrics; 1981 Aug; 68(2):273-83, 295-7. PubMed ID: 7267238
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  • 13. [Urgent needs in genetics: clinical diagnosis of acute amino acid disorders of delayed onset].
    Saudubray JM, Lyonnet S, Lombes A, Hervé F, Bonnefont JP, Munnich A, Ogier H.
    J Genet Hum; 1989 Dec; 37(4-5):299-310. PubMed ID: 2635710
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  • 15. Congenital disorders of the urea cycle and ammonia detoxication.
    Colombo JP.
    Monogr Paediatr; 1971 Dec; 1():1-150. PubMed ID: 4946766
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  • 16. [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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  • 17. Inborn errors of urea synthesis.
    Batshaw ML.
    Ann Neurol; 1994 Feb; 35(2):133-41. PubMed ID: 7906500
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  • 18. Detection of urea cycle enzymopathies in childhood.
    Trauner DA, Self TW.
    Arch Neurol; 1984 Jul; 41(7):758-60. PubMed ID: 6743067
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  • 19. [Differential diagnosis of genetically-induced hyperammonemias].
    Ullrich T, Grimm U, Seidlitz G, Lubs H.
    Kinderarztl Prax; 1988 Jun; 56(6):271-6. PubMed ID: 3063872
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