BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

184 related articles for article (PubMed ID: 1438388)

  • 1. Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden death.
    Kelly DP; Whelan AJ; Hale DE; Rinaldo P; Rutledge SL; Zhang Z; Strauss AW
    Prog Clin Biol Res; 1992; 375():463-72. PubMed ID: 1438388
    [No Abstract]   [Full Text] [Related]  

  • 2. The molecular basis of medium chain acyl-CoA dehydrogenase deficiency: survey and evolution of 985A----G transition, and identification of five rare types of mutation within the medium chain acyl-CoA dehydrogenase gene.
    Yokota I; Coates PM; Hale DE; Rinaldo P; Tanaka K
    Prog Clin Biol Res; 1992; 375():425-40. PubMed ID: 1359563
    [No Abstract]   [Full Text] [Related]  

  • 3. Characterization of medium-chain acyl-CoA dehydrogenase (MCAD) with a point mutation associated with MCAD deficiency.
    Bross P; Jensen T; Kräutle F; Winter V; Andresen BS; Engst S; Bolund L; Kølvraa S; Ghisla S; Rasched I
    Prog Clin Biol Res; 1992; 375():473-8. PubMed ID: 1438390
    [No Abstract]   [Full Text] [Related]  

  • 4. Mutations causing medium-chain acyl-CoA dehydrogenase deficiency: a collaborative compilation of the data from 172 patients. Workshop on Molecular Aspects of MCAD Deficiency.
    Prog Clin Biol Res; 1992; 375():499-506. PubMed ID: 1438394
    [No Abstract]   [Full Text] [Related]  

  • 5. Prevalence of K329E mutation in the medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards.
    Matsubara Y; Narisawa K; Tada K; Ikeda H; Yeqi Y; Danks DM; Green A; McCabe ER
    Prog Clin Biol Res; 1992; 375():453-62. PubMed ID: 1359564
    [No Abstract]   [Full Text] [Related]  

  • 6. Molecular analysis of medium-chain acyl-CoA dehydrogenase deficiency: a diagnostic approach.
    Gregersen N; Winter V; Kølvraa S; Andresen BS; Bross P; Blakemore A; Curtis D; Bolund L
    Prog Clin Biol Res; 1992; 375():441-52. PubMed ID: 1438387
    [No Abstract]   [Full Text] [Related]  

  • 7. Medium chain acyl-CoA dehydrogenase deficiency in the United Kingdom.
    Curtis D; Blakemore AI; Engel PC; Kolvraa S; Gregersen N; Pollitt RJ
    Prog Clin Biol Res; 1992; 375():489-94. PubMed ID: 1438392
    [No Abstract]   [Full Text] [Related]  

  • 8. Frequency of medium-chain acyl-CoA dehydrogenase deficiency G-985 mutation in sudden infant death syndrome.
    Miller ME; Brooks JG; Forbes N; Insel R
    Pediatr Res; 1992 Apr; 31(4 Pt 1):305-7. PubMed ID: 1570195
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Historical perspective of medium-chain acyl-CoA dehydrogenase deficiency: a decade of discovery.
    Coates PM
    Prog Clin Biol Res; 1992; 375():409-23. PubMed ID: 1438385
    [No Abstract]   [Full Text] [Related]  

  • 10. Medium-chain acyl-CoA dehydrogenase deficiency.
    Egidio RJ; Francis GL; Coates PM; Hale DE; Roesel A
    Am Fam Physician; 1989 May; 39(5):221-6. PubMed ID: 2718899
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a novel mutation in patients with medium-chain acyl-CoA dehydrogenase deficiency.
    Yang BZ; Ding JH; Zhou C; Dimachkie MM; Sweetman L; Dasouki MJ; Wilkinson J; Roe CR
    Mol Genet Metab; 2000 Mar; 69(3):259-62. PubMed ID: 10767181
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Medium chain acyl-CoA dehydrogenase deficiency].
    Matsubara Y; Ikeda Y; Tanaka K
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):560-3. PubMed ID: 3270863
    [No Abstract]   [Full Text] [Related]  

  • 13. [Medium chain Acyl-Coa Dehydrogenase deficiency. A diagnostic challenge for clinicians and laboratory].
    Heinonen OJ; Iitiä A; Irjala K; Pulkki K
    Duodecim; 1996; 112(1):35-41. PubMed ID: 10590599
    [No Abstract]   [Full Text] [Related]  

  • 14. Frequency of G-985 mutation in medium chain acyl-coenzyme A dehydrogenase (MCAD) deficiency in sudden infant death syndrome (SIDS).
    Miller M; Brooks J; Forbes N; Insel R
    Prog Clin Biol Res; 1992; 375():495-8. PubMed ID: 1438393
    [No Abstract]   [Full Text] [Related]  

  • 15. Molecular analysis of medium chain acyl-CoA dehydrogenase deficiency.
    Strauss AW; Duran M; Zhang ZF; Alpers R; Kelly DP
    Prog Clin Biol Res; 1990; 321():609-23. PubMed ID: 2326315
    [No Abstract]   [Full Text] [Related]  

  • 16. Is the medium-chain acyl-CoA dehydrogenase G985 mutation involved in sudden infant death in Norway?
    Opdal SH; Vege A; Saugstad OD; Rognum TO
    Eur J Pediatr; 1995 Feb; 154(2):166-7. PubMed ID: 7720752
    [No Abstract]   [Full Text] [Related]  

  • 17. Molecular cloning and nucleotide sequence of cDNAs encoding human short chain acyl-CoA dehydrogenase and study of the molecular basis of human short chain acyl-CoA dehydrogenase deficiency.
    Naito E; Ozasa H; Ikeda Y; Tanaka K
    Prog Clin Biol Res; 1990; 321():625-32. PubMed ID: 2326316
    [No Abstract]   [Full Text] [Related]  

  • 18. A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death.
    Brackett JC; Sims HF; Steiner RD; Nunge M; Zimmerman EM; deMartinville B; Rinaldo P; Slaugh R; Strauss AW
    J Clin Invest; 1994 Oct; 94(4):1477-83. PubMed ID: 7929823
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular diagnosis and characterization of medium-chain acyl-CoA dehydrogenase deficiency.
    Andresen BS; Bross P; Jensen TG; Knudsen I; Winter V; Kølvraa S; Bolund L; Gregersen N
    Scand J Clin Lab Invest Suppl; 1995; 220():9-25. PubMed ID: 7652482
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Medium chain acyl CoA dehydrogenase deficiency.
    Lancet; 1991 Aug; 338(8766):544-5. PubMed ID: 1678805
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 10.