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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

57 related articles for article (PubMed ID: 4805065)

  • 1. [Arginino-succinate aciduria].
    Dogan K; Schmutzer L; Dogan S; Lipovac K; Rudar D
    Neuropsihijatrija; 1973; 21(3-4):237-46. PubMed ID: 4805065
    [No Abstract]   [Full Text] [Related]  

  • 2. Argininosuccinic aciduria: antenatal investigations in an affected family.
    Burgess EA; Oberholzer VG; Palmer T; Wagstaff TI
    Am J Obstet Gynecol; 1974 Oct; 120(4):560-2. PubMed ID: 4412079
    [No Abstract]   [Full Text] [Related]  

  • 3. [Letter: Survival to the age of 3 months of an infant with neonatal arginino-succinyluria].
    Farriaux JP; Mesmacque-Caby D; Delattre P; Louis J; Fontaine G
    Nouv Presse Med; 1974 Apr; 3(17):1102. PubMed ID: 4843066
    [No Abstract]   [Full Text] [Related]  

  • 4. Arginnosuccinic aciduria.
    Nutr Rev; 1967 Aug; 25(8):235-7. PubMed ID: 4864208
    [No Abstract]   [Full Text] [Related]  

  • 5. Letter: Survival of infant with argininosuccinic aciduria to 3 months of age.
    Farriaux JP; Pieraert C; Fontaine G
    J Pediatr; 1975 Apr; 86(4):639. PubMed ID: 1127512
    [No Abstract]   [Full Text] [Related]  

  • 6. Neonatal arginosuccinic aciduria.
    Kuttan R; Devarajan LV; Jadhav M; Radhakrishnan AN
    Indian Pediatr; 1981 Jun; 18(6):405-10. PubMed ID: 7287170
    [No Abstract]   [Full Text] [Related]  

  • 7. [Argininosuccinic acid, technics of biochemical study (apropos of a case of argininosuccinyluria)].
    Cartigny B; Dhondt JL; Farriaux JP
    Lille Med; 1975 Mar; 20(3):169-79. PubMed ID: 1160489
    [No Abstract]   [Full Text] [Related]  

  • 8. [Congenital disorders in the urea cycle].
    Jagenburg R; Meberg A; Steen G
    Lakartidningen; 1972 Oct; 69(42):4797-802. PubMed ID: 4634535
    [No Abstract]   [Full Text] [Related]  

  • 9. [Lysinuric protein intolerance: a severe hyperammonemia secondary to l-arginine deficiency (author's transl)]].
    Coude FX; Ogier H; Charpentier C; Cathelineau L; Grimber G; Parvy P; Saudubray JM; Frezal J
    Arch Fr Pediatr; 1981 Dec; 38 Suppl 1():829-35. PubMed ID: 6800334
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Ammonia metabolism in a family affected by hyperargininemia.
    Qureshi IA; Letarte J; Ouellet R; Lelièvre M; Laberge C
    Diabete Metab; 1981 Mar; 7(1):5-11. PubMed ID: 7238975
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies].
    Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP
    Z Kinderheilkd; 1970; 107(4):313-23. PubMed ID: 5438972
    [No Abstract]   [Full Text] [Related]  

  • 12. [Cystinuria in children in the light of our observations].
    Hanicka M; Bernasowska-Knapczykowa K; Kos S
    Przegl Lek; 1966; 22(11):700-2. PubMed ID: 5959614
    [No Abstract]   [Full Text] [Related]  

  • 13. [Special course of arginine succinic acid disease].
    Porath U; Liebler G; Schreier K
    Arch Kinderheilkd; 1969 Sep; 179(3):283-8. PubMed ID: 5356533
    [No Abstract]   [Full Text] [Related]  

  • 14. [Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies].
    Terheggen HG; Schwenk A; Lowenthal A; van Sande M; Colombo JP
    Z Kinderheilkd; 1970; 107(4):298-312. PubMed ID: 5438971
    [No Abstract]   [Full Text] [Related]  

  • 15. D-2-hydroxyglutaric aciduria in three patients with proven SSADH deficiency: genetic coincidence or a related biochemical epiphenomenon?
    Struys EA; Verhoeven NM; Salomons GS; Berthelot J; Vianay-Saban C; Chabrier S; Thomas JA; Tsai AC; Gibson KM; Jakobs C
    Mol Genet Metab; 2006 May; 88(1):53-7. PubMed ID: 16442322
    [TBL] [Abstract][Full Text] [Related]  

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

  • 17. [Monilethrix: value of the determination of urinary amino acids].
    Chapuis JL; Gavanou J; Lambert D; Oudot C; Turk C
    Lyon Med; 1971 Apr; 225(7):642-3. PubMed ID: 5558870
    [No Abstract]   [Full Text] [Related]  

  • 18. Glutaryl-CoA dehydrogenase deficiency presenting as 3-hydroxyglutaric aciduria.
    Nyhan WL; Zschocke J; Hoffmann G; Stein DE; Bao L; Goodman S
    Mol Genet Metab; 1999 Mar; 66(3):199-204. PubMed ID: 10066389
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Glutaric aciduria type I with a low-excretion biochemical phenotype associated to a new mutation].
    Madruga-Garrido M; Garcia-Villoria J; Ruiz-Del Portal L; Delgado-Pecellin C; Garcia-Valdecasas MS; Blanco-Martinez B; Perez-Perez M; Ribes A; Campistol J; Rufo-Campos M
    Rev Neurol; 2007 Jul 16-31; 45(2):127-8. PubMed ID: 17642054
    [No Abstract]   [Full Text] [Related]  

  • 20. Inborn metabolic errors of urea cycle.
    Wu WK
    Va Med Mon (1918); 1967 Nov; 94(11):723-5. PubMed ID: 6063458
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.