BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

137 related articles for article (PubMed ID: 4842795)

  • 1. Citrullinemia: investigation and treatment over a four-year period.
    Buist NR; Kennaway NG; Hepburn CA; Strandholm JJ; Ramberg DA
    J Pediatr; 1974 Aug; 85(2):208-14. PubMed ID: 4842795
    [No Abstract]   [Full Text] [Related]  

  • 2. Diagnostic value of orotic acid excretion in heritable disorders of the urea cycle and in hyperammonemia due to organic acidurias.
    Bachmann C; Colombo JP
    Eur J Pediatr; 1980 Aug; 134(2):109-13. PubMed ID: 7439194
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hyperammonemia due to a defect in hepatic ornithine transcarbamylase.
    Sunshine P; Lindenbaum JE; Levy HL; Freeman JM
    Pediatrics; 1972 Jul; 50(1):100-11. PubMed ID: 5038084
    [No Abstract]   [Full Text] [Related]  

  • 4. Citrullinemia: a new case, with implications concerning adaptation to defective urea synthesis.
    Scott-Emuakpor A; Higgins JV; Kohrman AF
    Pediatr Res; 1972 Jul; 6(7):626-33. PubMed ID: 5057291
    [No Abstract]   [Full Text] [Related]  

  • 5. Prospective management of a child with neonatal citrullinemia.
    Melnyk AR; Matalon R; Henry BW; Zeller WP; Lange C
    J Pediatr; 1993 Jan; 122(1):96-8. PubMed ID: 8419623
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial protein intolerance with deficient transport of basic amino acids. An analysis of 10 patients.
    Kekomäki M; Visakorpi JK; Perheentupa J; Saxén L
    Acta Paediatr Scand; 1967 Nov; 56(6):617-30. PubMed ID: 6076999
    [No Abstract]   [Full Text] [Related]  

  • 7. Carrier detection of urea cycle disorders.
    Ng WG; Oizumi J; Koch R; Shaw KN; McLaren J; Donnel GN; Carter M
    Pediatrics; 1981 Sep; 68(3):448-52. PubMed ID: 7279481
    [No Abstract]   [Full Text] [Related]  

  • 8. Inborn errors of metabolism in acutely sick children.
    Dhareshwar SS; Ambani LM; Suchak RH; Danthi V
    Indian J Med Res; 1982 Nov; 76():716-22. PubMed ID: 7166367
    [No Abstract]   [Full Text] [Related]  

  • 9. [Protein intolerance with lysinuria. Value of orotic aciduria in adjusting treatment with citrulline].
    de Parscau L; Vianey-Liaud C; Hermier M; Divry P; Guibaud P
    Arch Fr Pediatr; 1988 Dec; 45(10):809-12. PubMed ID: 3149174
    [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. Severe neonatal citrullinaemia.
    Danks DM; Tippett P; Zentner G
    Arch Dis Child; 1974 Jul; 49(7):579-81. PubMed ID: 4854268
    [No Abstract]   [Full Text] [Related]  

  • 12. A case of transient neonatal citrullinemia.
    Ohtake A; Takayanagi M; Ogura N; Nakajima H
    Eur J Pediatr; 1983 Oct; 141(1):60-1. PubMed ID: 6641770
    [TBL] [Abstract][Full Text] [Related]  

  • 13. From the NIH: Therapy developed for group of fatal genetic diseases.
    JAMA; 1981 Mar; 245(9):917. PubMed ID: 6894005
    [No Abstract]   [Full Text] [Related]  

  • 14. Argininemia: report of a new case and mechanisms of orotic aciduria and hyperammonemia.
    Yoshino M; Kubota K; Yoshida I; Murakami T; Yamashita F
    Adv Exp Med Biol; 1982; 153():121-5. PubMed ID: 7164892
    [No Abstract]   [Full Text] [Related]  

  • 15. Lysinuric protein intolerance. Urinary amino acid excretion at 2 and 9 days of age.
    Candito M; Vianey-Saban C; Ferraci JP; Bébin B; Chazalette JP; Sebag F; Mathieu M; Chambon P
    J Inherit Metab Dis; 1994; 17(2):252-3. PubMed ID: 7967486
    [No Abstract]   [Full Text] [Related]  

  • 16. [Chronic hyperammonemia with orotic aciduria: evidence of pyrimidine pathway stimulation (author's transl)].
    Beaudry MA; Letarte J; Collu R; Leboeuf G; Ducharme JR; Melancon SB; Dallairf L
    Diabete Metab; 1975 Mar; 1():29-37. PubMed ID: 1234064
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Citrullinemia: early diagnosis & successful management of an otherwise lethal disorder.
    Balsekar MV; Ambani LM; Bhatia RS; Shah SB; Apte BN
    Indian Pediatr; 1989 Jun; 26(6):589-92. PubMed ID: 2583813
    [No Abstract]   [Full Text] [Related]  

  • 18. Studies on amino acid metabolism in citrullinuria.
    Mohyuddin F; Rathbun JC; McMurray WC
    Am J Dis Child; 1967 Jan; 113(1):152-6. PubMed ID: 6015893
    [No Abstract]   [Full Text] [Related]  

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

  • 20. Comparison between amino acids and orotic acid analysis in the detection of urea cycle disorders in the Quebec Urinary Screening Program.
    Lemieux B; Auray-Blais C; Giguère R
    Adv Exp Med Biol; 1982; 153():321-9. PubMed ID: 7164907
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.