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 *

154 related articles for article (PubMed ID: 3930543)

  • 1. Disorders of the urea cycle.
    Brusilow SW
    Hosp Pract (Off Ed); 1985 Oct; 20(10):65-72. PubMed ID: 3930543
    [No Abstract]   [Full Text] [Related]  

  • 2. [Urea cycle disorders].
    Tazawa Y
    Ryoikibetsu Shokogun Shirizu; 1995; (8):367-9. PubMed ID: 8581654
    [No Abstract]   [Full Text] [Related]  

  • 3. Congenital hyperammonemic syndromes.
    Shih VE
    Clin Perinatol; 1976 Mar; 3(1):3-14. PubMed ID: 954343
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Double deficiencies of urea cycle enzymes in human liver.
    Raijman L
    Biochem Med; 1979 Apr; 21(2):226-33. PubMed ID: 465019
    [No Abstract]   [Full Text] [Related]  

  • 5. Hereditary disorders of the urea cycle in man: biochemical and molecular approaches.
    Saheki T; Kobayashi K; Inoue I
    Rev Physiol Biochem Pharmacol; 1987; 108():21-68. PubMed ID: 3306877
    [No Abstract]   [Full Text] [Related]  

  • 6. [Molecular basis of urea cycle disorders].
    Matsuda I; Matsuura T; Hoshide R; Uchino T; Matsubasa T
    Nihon Rinsho; 1993 Feb; 51(2):520-4. PubMed ID: 8464164
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Urea cycle enzymopathies.
    Walser M
    Semin Liver Dis; 1982 Nov; 2(4):329-39. PubMed ID: 6763345
    [No Abstract]   [Full Text] [Related]  

  • 8. [Molecular genetics of urea cycle diseases].
    Ohtake A; Mori M
    Seikagaku; 1990 Sep; 62(9):1170-7. PubMed ID: 2258657
    [No Abstract]   [Full Text] [Related]  

  • 9. Urea biosynthesis II. Normal and abnormal regulation.
    Shambaugh GE
    Am J Clin Nutr; 1978 Jan; 31(1):126-33. PubMed ID: 339704
    [No Abstract]   [Full Text] [Related]  

  • 10. [Prenatal diagnosis of enzymopathies of the urea cycle].
    Chadefaux B; Rabier D; Kamoun P
    Ann Biol Clin (Paris); 1988; 46(7):471-6. PubMed ID: 3056128
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Diagnosis of urea cycle disorders.
    Palmer T; Oberholzer VG
    Ann Clin Biochem; 1977 May; 14(3):136-8. PubMed ID: 17345
    [No Abstract]   [Full Text] [Related]  

  • 13. Prospective treatment of urea cycle disorders.
    Maestri NE; Hauser ER; Bartholomew D; Brusilow SW
    J Pediatr; 1991 Dec; 119(6):923-8. PubMed ID: 1720458
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Hereditary diseases related to a disorder of the enzymatic activity of the urea formation cycle].
    Kazanskaia NS; Alekseenko LP
    Vopr Med Khim; 1976; 22(4):435-43. PubMed ID: 800301
    [No Abstract]   [Full Text] [Related]  

  • 15. Editorial: Ammonia disposal in Reye's syndrome.
    Smith AL
    N Engl J Med; 1976 Apr; 294(16):897-8. PubMed ID: 1250317
    [No Abstract]   [Full Text] [Related]  

  • 16. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Proceedings of a satellite meeting on advances in inherited urea cycle disorders. Vienna, 20-21 May 1997.
    J Inherit Metab Dis; 1998; 21 Suppl 1():1-159. PubMed ID: 9686340
    [No Abstract]   [Full Text] [Related]  

  • 18. Definitive cure of hyperammonemia by liver transplantation in urea cycle defects: report of three cases.
    Jan D; Poggi F; Jouvet P; Rabier D; Laurent J; Beringer A; Hubert P; Saudubray JM; Revillon Y
    Transplant Proc; 1994 Feb; 26(1):188. PubMed ID: 8108934
    [No Abstract]   [Full Text] [Related]  

  • 19. 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; 306(23):1387-92. PubMed ID: 7078580
    [TBL] [Abstract][Full Text] [Related]  

  • 20. False positive alanine tolerance test results in heterozygote detection of urea cycle disorders.
    Batshaw ML; Naylor EW; Thomas GH
    J Pediatr; 1989 Oct; 115(4):595-8. PubMed ID: 2795354
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.