BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

118 related articles for article (PubMed ID: 6438399)

  • 1. Biochemical evidence of carnitine effect on propionate elimination.
    Sugiyama N; Morishita H; Nagaya S; Nakajima T; Kawase A; Ohya A; Sugiyama S; Kamiya K; Watanabe I; Togari H
    J Inherit Metab Dis; 1984; 7(3):137-8. PubMed ID: 6438399
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. L-carnitine therapy in propionicacidaemia.
    Roe CR; Bohan TP
    Lancet; 1982 Jun; 1(8286):1411-2. PubMed ID: 6123699
    [No Abstract]   [Full Text] [Related]  

  • 4. Identification of undescribed medium-chain acylcarnitines present in urine of patients with propionic and methylmalonic acidemias.
    Libert R; Van Hoof F; Thillaye M; Vincent MF; Nassogne MC; de Hoffmann E; Schanck A
    Clin Chim Acta; 2000 May; 295(1-2):87-96. PubMed ID: 10767396
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pyroglutamic aciduria in propionyl CoA carboxylase deficiency.
    Morishita H; Nagaya S; Nakajima T; Kawase A; Ohya A; Sugiyama S; Kamiya K; Watanabe I; Togari H; Suzuki Y
    J Inherit Metab Dis; 1984; 7(3):139-40. PubMed ID: 6438400
    [No Abstract]   [Full Text] [Related]  

  • 6. Propionic acidemia--biochemical studies.
    Barash V; Elpeleg O; Amit R; Gottfried S; Yatziv S; Gutman A
    Isr J Med Sci; 1989 Feb; 25(2):103-6. PubMed ID: 2495260
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Dietary treatment and biochemical studies on a neonatal case of propionyl-CoA carboxylase deficiency.
    DelValle JA; Merinero B; Jiménez A; García MJ; Ugarte M; Omeñaca F; Neustadt G; Quero J
    J Inherit Metab Dis; 1982; 5(2):121-4. PubMed ID: 6820422
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Studies on cultured fibroblasts from patients with defects of biotin-dependent carboxylation.
    Bartlett K; Ng H; Dale G; Green A; Leonard JV
    J Inherit Metab Dis; 1981; 4(4):183-9. PubMed ID: 6118468
    [No Abstract]   [Full Text] [Related]  

  • 10. The biotin requirement of human fibroblasts in culture.
    Chalifour LE; Dakshinamurti K
    Biochem Biophys Res Commun; 1982 Feb; 104(3):1047-53. PubMed ID: 7073724
    [No Abstract]   [Full Text] [Related]  

  • 11. Propionic acidaemia: sequence analysis of mutant mRNAs from Japanese beta subunit-deficient patients.
    Ohura T; Narisawa K; Tada K
    J Inherit Metab Dis; 1993; 16(5):863-7. PubMed ID: 8295402
    [No Abstract]   [Full Text] [Related]  

  • 12. Gas chromatographic-mass spectrometric newborn screening for propionic acidaemia by targeting methylcitrate in dried filter-paper urine samples.
    Kuhara T; Ohse M; Inoue Y; Yorifuji T; Sakura N; Mitsubuchi H; Endo F; Ishimatu J
    J Inherit Metab Dis; 2002 May; 25(2):98-106. PubMed ID: 12118533
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A study of the ultrastructure of the organs and of cultured fibroblasts incubated with isoleucine from a patient with propionic acidemia.
    Kott-Blumenkranz R; Pappas CT; Bensch KG
    Hum Pathol; 1981 Dec; 12(12):1141-8. PubMed ID: 7333577
    [No Abstract]   [Full Text] [Related]  

  • 14. Stimulation of propionyl CoA and beta-methylcrotonyl CoA carboxylase activities in human leukocytes and cultured fibroblasts by biotin.
    Wolf B; Rosenberg LE
    Pediatr Res; 1979 Nov; 13(11):1275-9. PubMed ID: 514693
    [No Abstract]   [Full Text] [Related]  

  • 15. [Propionic acidemia].
    Ohura T
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):276-9. PubMed ID: 9590046
    [No Abstract]   [Full Text] [Related]  

  • 16. Propionic acidaemia presenting with pancytopaenia in infancy.
    Sweetman L; Nyhan WL; Cravens J; Zomer Y; Plunket DC
    J Inherit Metab Dis; 1980; 2(3):65-9. PubMed ID: 6796762
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Blood propionic acid with hyperammonemic coma].
    Stöckler S; Kastner U; Pokits B; Müller W; Roscher A
    Klin Padiatr; 1987; 199(5):348-50. PubMed ID: 3682709
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Liver transplantation for propionic acidaemia in a 14-month-old male.
    Kim TW; Hall SR
    Paediatr Anaesth; 2003 Jul; 13(6):554-6. PubMed ID: 12846721
    [No Abstract]   [Full Text] [Related]  

  • 19. An 84 bp insertion found in a propionic acidaemia patient is not a disease-causing mutation but a product of cryptic mRNA.
    Ohura T; Narisawa K; Tada K; Iinuma K
    J Inherit Metab Dis; 1999 Jun; 22(5):676-7. PubMed ID: 10399105
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.