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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

263 related items for PubMed ID: 7267240

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  • 4. Urea cycle disorders: diagnosis, pathophysiology, and therapy.
    Brusilow SW, Maestri NE.
    Adv Pediatr; 1996; 43():127-70. PubMed ID: 8794176
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  • 5. Treatment of inborn errors of urea synthesis: activation of alternative pathways of waste nitrogen synthesis and excretion.
    Batshaw ML, Brusilow S, Waber L, Blom W, Brubakk AM, Burton BK, Cann HM, Kerr D, Mamunes P, Matalon R, Myerberg D, Schafer IA.
    N Engl J Med; 1982 Jun 10; 306(23):1387-92. PubMed ID: 7078580
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  • 9. Inborn errors of urea synthesis.
    Batshaw ML.
    Ann Neurol; 1994 Feb 10; 35(2):133-41. PubMed ID: 7906500
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  • 12. [Inborn metabolic errors due to disorders in the urea synthesis cycle].
    Kardosová A, Hruskovic I, Strnová J.
    Cesk Pediatr; 1986 Jan 10; 41(1):31-3. PubMed ID: 3948272
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  • 13. [Argininosuccinate lyase deficiency].
    Matsubasa T.
    Ryoikibetsu Shokogun Shirizu; 1998 Jan 10; (18 Pt 1):179-81. PubMed ID: 9590021
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  • 14. Carrier detection of urea cycle disorders.
    Ng WG, Oizumi J, Koch R, Shaw KN, McLaren J, Donnel GN, Carter M.
    Pediatrics; 1981 Sep 10; 68(3):448-52. PubMed ID: 7279481
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  • 17. Urea cycle disorders: clinical presentation outside the newborn period.
    Smith W, Kishnani PS, Lee B, Singh RH, Rhead WJ, Sniderman King L, Smith M, Summar M.
    Crit Care Clin; 2005 Oct 10; 21(4 Suppl):S9-17. PubMed ID: 16227115
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  • 18. [Congenital metabolic disorders of the urea cycle].
    Hooft C, Carton D, De Schrijver F.
    Verh K Vlaam Acad Geneeskd Belg; 1969 Oct 10; 31(1):27-52. PubMed ID: 5800843
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  • 20. [Attempt at antenatal diagnosis of argininosuccinic aciduria].
    Dhondt JL, Farriaux JP, Pollitt RJ, Vamos E, Richard P, Blanckaert D, Delecour M, Monnier JC, Fontaine G.
    Ann Genet; 1976 Mar 10; 19(1):23-7. PubMed ID: 1084118
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