BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

225 related articles for article (PubMed ID: 21963049)

  • 1. Adenosine kinase deficiency disrupts the methionine cycle and causes hypermethioninemia, encephalopathy, and abnormal liver function.
    Bjursell MK; Blom HJ; Cayuela JA; Engvall ML; Lesko N; Balasubramaniam S; Brandberg G; Halldin M; Falkenberg M; Jakobs C; Smith D; Struys E; von Döbeln U; Gustafsson CM; Lundeberg J; Wedell A
    Am J Hum Genet; 2011 Oct; 89(4):507-15. PubMed ID: 21963049
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia.
    Becker PH; Demir Z; Mozer Glassberg Y; Sevin C; Habes D; Imbard A; Mussini C; Rozenfeld Bar Lev M; Davit-Spraul A; Benoist JF; Thérond P; Slama A; Jacquemin E; Gonzales E; Gaignard P
    Mol Genet Metab; 2021 Jan; 132(1):38-43. PubMed ID: 33309011
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hypermethioninemias of genetic and non-genetic origin: A review.
    Mudd SH
    Am J Med Genet C Semin Med Genet; 2011 Feb; 157C(1):3-32. PubMed ID: 21308989
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Adenosine kinase deficiency: expanding the clinical spectrum and evaluating therapeutic options.
    Staufner C; Lindner M; Dionisi-Vici C; Freisinger P; Dobbelaere D; Douillard C; Makhseed N; Straub BK; Kahrizi K; Ballhausen D; la Marca G; Kölker S; Haas D; Hoffmann GF; Grünert SC; Blom HJ
    J Inherit Metab Dis; 2016 Mar; 39(2):273-83. PubMed ID: 26642971
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Liver transplantation for treatment of severe S-adenosylhomocysteine hydrolase deficiency.
    Strauss KA; Ferreira C; Bottiglieri T; Zhao X; Arning E; Zhang S; Zeisel SH; Escolar ML; Presnick N; Puffenberger EG; Vugrek O; Kovacevic L; Wagner C; Mazariegos GV; Mudd SH; Soltys K
    Mol Genet Metab; 2015; 116(1-2):44-52. PubMed ID: 26095522
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Adult-onset liver disease and hepatocellular carcinoma in S-adenosylhomocysteine hydrolase deficiency.
    Stender S; Chakrabarti RS; Xing C; Gotway G; Cohen JC; Hobbs HH
    Mol Genet Metab; 2015 Dec; 116(4):269-74. PubMed ID: 26527160
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Demyelination of the brain is associated with methionine adenosyltransferase I/III deficiency.
    Chamberlin ME; Ubagai T; Mudd SH; Wilson WG; Leonard JV; Chou JY
    J Clin Invest; 1996 Aug; 98(4):1021-7. PubMed ID: 8770875
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Lessons Learned from Inherited Metabolic Disorders of Sulfur-Containing Amino Acids Metabolism.
    Kožich V; Stabler S
    J Nutr; 2020 Oct; 150(Suppl 1):2506S-2517S. PubMed ID: 33000152
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Adenosine Kinase Deficiency in the Brain Results in Maladaptive Synaptic Plasticity.
    Sandau US; Colino-Oliveira M; Jones A; Saleumvong B; Coffman SQ; Liu L; Miranda-Lourenço C; Palminha C; Batalha VL; Xu Y; Huo Y; Diógenes MJ; Sebastião AM; Boison D
    J Neurosci; 2016 Nov; 36(48):12117-12128. PubMed ID: 27903722
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spectrum of hypermethioninemia in neonatal screening.
    Chien YH; Chiang SC; Huang A; Hwu WL
    Early Hum Dev; 2005 Jun; 81(6):529-33. PubMed ID: 15935930
    [TBL] [Abstract][Full Text] [Related]  

  • 11. S-adenosylmethionine treatment in methionine adenosyltransferase deficiency, a case report.
    Furujo M; Kinoshita M; Nagao M; Kubo T
    Mol Genet Metab; 2012 Mar; 105(3):516-8. PubMed ID: 22178350
    [TBL] [Abstract][Full Text] [Related]  

  • 12. S-adenosylhomocysteine hydrolase deficiency in a human: a genetic disorder of methionine metabolism.
    Baric I; Fumic K; Glenn B; Cuk M; Schulze A; Finkelstein JD; James SJ; Mejaski-Bosnjak V; Pazanin L; Pogribny IP; Rados M; Sarnavka V; Scukanec-Spoljar M; Allen RH; Stabler S; Uzelac L; Vugrek O; Wagner C; Zeisel S; Mudd SH
    Proc Natl Acad Sci U S A; 2004 Mar; 101(12):4234-9. PubMed ID: 15024124
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders.
    Barić I; Staufner C; Augoustides-Savvopoulou P; Chien YH; Dobbelaere D; Grünert SC; Opladen T; Petković Ramadža D; Rakić B; Wedell A; Blom HJ
    J Inherit Metab Dis; 2017 Jan; 40(1):5-20. PubMed ID: 27671891
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Familial hypermethioninemia partially responsive to dietary restriction.
    Labrune P; Perignon JL; Rault M; Brunet C; Lutun H; Charpentier C; Saudubray JM; Odievre M
    J Pediatr; 1990 Aug; 117(2 Pt 1):220-6. PubMed ID: 2380820
    [TBL] [Abstract][Full Text] [Related]  

  • 15. S-Adenosylmethionine and S-adenosylhomocystein metabolism in isolated rat liver. Effects of L-methionine, L-homocystein, and adenosine.
    Hoffman DR; Marion DW; Cornatzer WE; Duerre JA
    J Biol Chem; 1980 Nov; 255(22):10822-7. PubMed ID: 7430157
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Isolated hypermethioninemia: measurements of S-adenosylmethionine and choline.
    Mudd SH; Jenden DJ; Capdevila A; Roch M; Levy HL; Wagner C
    Metabolism; 2000 Dec; 49(12):1542-7. PubMed ID: 11145114
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Adenosine kinase deficiency with neurodevelopemental delay and recurrent hepatic dysfunction: A case report.
    Shakiba M; Mahjoub F; Fazilaty H; Rezagholizadeh F; Shakiba A; Ziadlou M; Gahl WA; Behnam B
    Adv Rare Dis; 2016; 3():. PubMed ID: 27500280
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Clinical utility of methionine restriction in adenosine kinase deficiency.
    Almuhsen N; Guay SP; Lefrancois M; Gauvin C; Al Bahlani AQ; Ahmed N; Saint-Martin C; Gagnon T; Waters P; Braverman N; Buhas D
    JIMD Rep; 2021 Sep; 61(1):52-59. PubMed ID: 34485018
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Methionine adenosyltransferase deficiency: new enzymatic defect associated with hypermethioninemia.
    Gaull GE; Tallan HH
    Science; 1974 Oct; 186(4158):59-60. PubMed ID: 4421454
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neurologically normal development of a patient with severe methionine adenosyltransferase I/III deficiency after continuing dietary methionine restriction.
    Hirabayashi K; Shiohara M; Yamada K; Sueki A; Ide Y; Takeuchi K; Hagimoto R; Kinoshita T; Yabuhara A; Mudd SH; Koike K
    Gene; 2013 Nov; 530(1):104-8. PubMed ID: 23973726
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.