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 *

87 related articles for article (PubMed ID: 480035)

  • 1. Asymptomatic propionyl CoA carboxylase deficiency in a 13-year-old girl.
    Wolf B; Paulsen EP; Hsia YE
    J Pediatr; 1979 Oct; 95(4):563-5. PubMed ID: 480035
    [No Abstract]   [Full Text] [Related]  

  • 2. Biotin-dependent carboxylase deficiencies (propionyl-CoA and pyruvate carboxylases).
    Gravel RA; Robinson BH
    Ann N Y Acad Sci; 1985; 447():225-34. PubMed ID: 3925855
    [No Abstract]   [Full Text] [Related]  

  • 3. Propionyl coenzyme A carboxylase deficiency presenting as non-ketotic hyperglycinaemia.
    Harris DJ; Thompson RM; Wolf B; Yang BI
    J Med Genet; 1981 Apr; 18(2):156-7. PubMed ID: 7241536
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Propionyl-CoA carboxylase deficiency in a patient with biotin-responsive 3-methylcrotonylglycinuria.
    Sweetman L; Bates SP; Hull D; Nyhan WL
    Pediatr Res; 1977 Nov; 11(11):1144-7. PubMed ID: 917614
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Coexistence of defective activity in glycine-cleavage reaction and propionyl-CoA carboxylase in the liver of a hyperglycinemic child.
    Nishimura Y; Tada K; Arakawa T
    Tohoku J Exp Med; 1974 Jul; 113(3):267-71. PubMed ID: 4454060
    [No Abstract]   [Full Text] [Related]  

  • 6. Molecular basis for genetic complementation in propionyl CoA carboxylase deficiency.
    Wolf B
    Exp Cell Res; 1980 Feb; 125(2):502-7. PubMed ID: 7353607
    [No Abstract]   [Full Text] [Related]  

  • 7. Cell genetic studies on propionyl-CoA carboxylase deficient cell lines.
    Van Leeuwen GH; De Vrieze G; Gimpel JA; Huisjes HJ; Hommes FA
    J Inherit Metab Dis; 1982; 5(2):115-20. PubMed ID: 6820421
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Propionic acidemia: a neuropathology case report and review of prior cases.
    Feliz B; Witt DR; Harris BT
    Arch Pathol Lab Med; 2003 Aug; 127(8):e325-8. PubMed ID: 12873194
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Urinary acid profiles of asymptomatic propionyl CoA carboxylase deficiency.
    Kuhara T; Inoue Y; Matsumoto I
    J Pediatr; 1988 Oct; 113(4):787. PubMed ID: 3171805
    [No Abstract]   [Full Text] [Related]  

  • 10. Abnormal metabolites of isoleucine in a patient with propionyl-CoA carboxylase deficiency.
    Sweetman L; Weyler W; Nyhan WL; de Céspedes C; Loria AR; Estrada Y
    Biomed Mass Spectrom; 1978 Mar; 5(3):198-207. PubMed ID: 630060
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Propionyl-CoA carboxylase deficiency with overflow of metabolites of isoleucine catabolism at all levels.
    Przyrembel H; Bremer HJ; Duran M; Bruinvis L; Ketting D; Wadman SK; Baumgartner R; Irle U; Bachmann C
    Eur J Pediatr; 1979 Jan; 130(1):1-14. PubMed ID: 759179
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation analysis of the propionyl-CoA carboxylase alpha-subunit gene in four Japanese patients with propionic acidaemia.
    Ohura T; Narisawa K; Iinuma K
    J Inherit Metab Dis; 1999 Oct; 22(7):851-2. PubMed ID: 10518292
    [No Abstract]   [Full Text] [Related]  

  • 13. Heterozygote expression in propionyl coenzyme A carboxylase deficiency. Differences between major complementation groups.
    Wolf B; Rosenberg LE
    J Clin Invest; 1978 Nov; 62(5):931-6. PubMed ID: 711858
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Interallelic complementation of beta-subunit defects in fibroblasts of patients with propionyl-CoA carboxylase deficiency microinjected with mutant cDNA constructs.
    Loyer M; Leclerc D; Gravel RA
    Hum Mol Genet; 1995 Jun; 4(6):1035-9. PubMed ID: 7655456
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Transfection screening for defects in the PCCA and PCCB genes encoding propionyl-CoA carboxylase subunits.
    Rodriguez-Pombo P; Pérez-Cerdá C; Desviat LR; Pérez B; Ugarte M; Rodríguez-Pombo P
    Mol Genet Metab; 2002 Mar; 75(3):276-9. PubMed ID: 11914040
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Fatty-acid-responsive alopecia in multiple carboxylase deficiency.
    Munnich A; Saudubray JM; Coude FX; Charpentier C; Saurat JH; Frezal J
    Lancet; 1980 May; 1(8177):1080-1. PubMed ID: 6103410
    [No Abstract]   [Full Text] [Related]  

  • 17. [A case of malonyl-CoA decarboxylase deficiency: clinical and genetic study].
    Peng J; Wu LQ; Zhou MX; Zhong L; Yin F
    Zhongguo Dang Dai Er Ke Za Zhi; 2012 Nov; 14(11):879-80. PubMed ID: 23146740
    [No Abstract]   [Full Text] [Related]  

  • 18. L-carnitine enhances excretion of propionyl coenzyme A as propionylcarnitine in propionic acidemia.
    Roe CR; Millington DS; Maltby DA; Bohan TP; Hoppel CL
    J Clin Invest; 1984 Jun; 73(6):1785-8. PubMed ID: 6725560
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of 3-hydroxy-3-ethylglutaric acid in urine of patients with propionic acidaemia.
    Kuhara T; Inoue Y; Shinka T; Matsumoto I; Matsuo M
    Biomed Mass Spectrom; 1983 Dec; 10(12):629-32. PubMed ID: 6200156
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dipropylacetate and propionyl CoA carboxylase.
    Wolf B
    Lancet; 1978 Aug; 2(8085):369. PubMed ID: 79729
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.