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 *

179 related articles for article (PubMed ID: 6743067)

  • 21. 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]  

  • 22. [Hyperammonemia].
    Arashima S
    Nihon Rinsho; 1978 May; Suppl():1352-3. PubMed ID: 691351
    [No Abstract]   [Full Text] [Related]  

  • 23. [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]  

  • 24. Transient hyperammonemias in infants with and without organic acidemia.
    Nyhan WL; Rubio V; Jordá A; Grisolia S; Gutierez F; Canosa C
    Adv Exp Med Biol; 1982; 153():331-8. PubMed ID: 7164908
    [No Abstract]   [Full Text] [Related]  

  • 25. The activity of carbamoyl-phosphate synthetase I and ornithine carbamoyltransferase (OCT) in the intestine and screening for OCT deficiency in the rectal mucosa.
    Matsushima A; Orii T
    J Inherit Metab Dis; 1981; 4(2):83-4. PubMed ID: 6790859
    [No Abstract]   [Full Text] [Related]  

  • 26. Inborn defects of the mitochondrial portion of the urea cycle.
    Colombo JP; Bachmann C; Schrämmli A
    Ann N Y Acad Sci; 1986; 488():109-17. PubMed ID: 3555250
    [No Abstract]   [Full Text] [Related]  

  • 27. Liver ultrastructure in mitochondrial urea cycle enzyme deficiencies and comparison with Reye's syndrome.
    Latham PS; LaBrecque DR; McReynolds JW; Klatskin G
    Hepatology; 1984; 4(3):404-7. PubMed ID: 6724509
    [TBL] [Abstract][Full Text] [Related]  

  • 28. [Prenatal diagnosis of carbamyl phosphate synthetase deficiency by fetal liver biopsy].
    Murotsuki J; Uehara S; Okamura K; Yajima A; Kikuchi M; Oura T; Miyabayashi S
    Nihon Sanka Fujinka Gakkai Zasshi; 1991 Dec; 43(12):1613-6. PubMed ID: 1744457
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Treatment of urea cycle disorders.
    Thoene JG
    J Pediatr; 1999 Mar; 134(3):255-6. PubMed ID: 10064655
    [No Abstract]   [Full Text] [Related]  

  • 30. Hyperammonemia.
    Batshaw ML
    Curr Probl Pediatr; 1984 Nov; 14(11):1-69. PubMed ID: 6510017
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Urea cycle defect: a case with MR and CT findings resembling infarct.
    Mamourian AC; du Plessis A
    Pediatr Radiol; 1991; 21(8):594-5. PubMed ID: 1815186
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies.
    Msall M; Batshaw ML; Suss R; Brusilow SW; Mellits ED
    N Engl J Med; 1984 Jun; 310(23):1500-5. PubMed ID: 6717540
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Focal glycogenosis of the liver in disorders of ureagenesis: its occurrence and diagnostic significance.
    Badizadegan K; Perez-Atayde AR
    Hepatology; 1997 Aug; 26(2):365-73. PubMed ID: 9252147
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Postpartum coma and death due to carbamoyl-phosphate synthetase I deficiency.
    Wong LJ; Craigen WJ; O'Brien WE
    Ann Intern Med; 1994 Feb; 120(3):216-7. PubMed ID: 8273985
    [No Abstract]   [Full Text] [Related]  

  • 36. 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]  

  • 37. Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis.
    Brusilow SW; Danney M; Waber LJ; Batshaw M; Burton B; Levitsky L; Roth K; McKeethren C; Ward J
    N Engl J Med; 1984 Jun; 310(25):1630-4. PubMed ID: 6427608
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Liver transplantation for the treatment of urea cycle disorders.
    Whitington PF; Alonso EM; Boyle JT; Molleston JP; Rosenthal P; Emond JC; Millis JM
    J Inherit Metab Dis; 1998; 21 Suppl 1():112-8. PubMed ID: 9686349
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. A defect of the urea cycle--a case report.
    Naughten ER; Flavin MP; O'Brien NG
    Ir J Med Sci; 1984 Dec; 153(12):439-40. PubMed ID: 6519931
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.