BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 22178350)

  • 1. 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]  

  • 2. Methionine adenosyltransferase I/III deficiency: neurological manifestations and relevance of S-adenosylmethionine.
    Furujo M; Kinoshita M; Nagao M; Kubo T
    Mol Genet Metab; 2012 Nov; 107(3):253-6. PubMed ID: 22951388
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Spectrum of mutations associated with methionine adenosyltransferase I/III deficiency among individuals identified during newborn screening in Japan.
    Nagao M; Tanaka T; Furujo M
    Mol Genet Metab; 2013 Dec; 110(4):460-4. PubMed ID: 24231718
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening.
    Couce ML; Bóveda MD; García-Jimémez C; Balmaseda E; Vives I; Castiñeiras DE; Fernández-Marmiesse A; Fraga JM; Mudd SH; Corrales FJ
    Mol Genet Metab; 2013 Nov; 110(3):218-21. PubMed ID: 23993429
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Molecular mechanisms of an inborn error of methionine pathway. Methionine adenosyltransferase deficiency.
    Ubagai T; Lei KJ; Huang S; Mudd SH; Levy HL; Chou JY
    J Clin Invest; 1995 Oct; 96(4):1943-7. PubMed ID: 7560086
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Neonatal methionine adenosyltransferase I/III deficiency with abnormal signal intensity in the central tegmental tract.
    Kido J; Sawada T; Momosaki K; Suzuki Y; Uetani H; Kitajima M; Mitsubuchi H; Nakamura K; Matsumoto S
    Brain Dev; 2019 Apr; 41(4):382-388. PubMed ID: 30389272
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Analysis of five cases of hypermethioninemia diagnosed by neonatal screening.
    Zhang Z; Wang Y; Ma D; Cheng W; Sun Y; Jiang T
    J Pediatr Endocrinol Metab; 2020 Jan; 33(1):47-52. PubMed ID: 31851615
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Molecular genetics of hepatic methionine adenosyltransferase deficiency.
    Chou JY
    Pharmacol Ther; 2000 Jan; 85(1):1-9. PubMed ID: 10674710
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Methionine adenosyltransferase I/III deficiency: novel mutations and clinical variations.
    Chamberlin ME; Ubagai T; Mudd SH; Thomas J; Pao VY; Nguyen TK; Levy HL; Greene C; Freehauf C; Chou JY
    Am J Hum Genet; 2000 Feb; 66(2):347-55. PubMed ID: 10677294
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Molecular pathology and DNA diagnosis of phenylketonuria and hypermethioninemia].
    Nagao M
    Tanpakushitsu Kakusan Koso; 1998 May; 43(6):762-9. PubMed ID: 9612070
    [No Abstract]   [Full Text] [Related]  

  • 15. Mudd's disease (MAT I/III deficiency): a survey of data for MAT1A homozygotes and compound heterozygotes.
    Chien YH; Abdenur JE; Baronio F; Bannick AA; Corrales F; Couce M; Donner MG; Ficicioglu C; Freehauf C; Frithiof D; Gotway G; Hirabayashi K; Hofstede F; Hoganson G; Hwu WL; James P; Kim S; Korman SH; Lachmann R; Levy H; Lindner M; Lykopoulou L; Mayatepek E; Muntau A; Okano Y; Raymond K; Rubio-Gozalbo E; Scholl-Bürgi S; Schulze A; Singh R; Stabler S; Stuy M; Thomas J; Wagner C; Wilson WG; Wortmann S; Yamamoto S; Pao M; Blom HJ
    Orphanet J Rare Dis; 2015 Aug; 10():99. PubMed ID: 26289392
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hypermethioninaemia due to methionine adenosyltransferase I/III (MAT I/III) deficiency: diagnosis in an expanded neonatal screening programme.
    Couce ML; Bóveda MD; Castiñeiras DE; Corrales FJ; Mora MI; Fraga JM; Mudd SH
    J Inherit Metab Dis; 2008 Dec; 31 Suppl 2():S233-9. PubMed ID: 18500573
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Genetic analysis of isolated persistent hypermethioninemia with dominant inheritance.
    Nagao M; Oyanagi K
    Acta Paediatr Jpn; 1997 Oct; 39(5):601-6. PubMed ID: 9363660
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Enzymatic activity of methionine adenosyltransferase variants identified in patients with persistent hypermethioninemia.
    Fernández-Irigoyen J; Santamaría E; Chien YH; Hwu WL; Korman SH; Faghfoury H; Schulze A; Hoganson GE; Stabler SP; Allen RH; Wagner C; Mudd SH; Corrales FJ
    Mol Genet Metab; 2010; 101(2-3):172-7. PubMed ID: 20675163
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Methionine Adenosyltransferase I/III Deficiency Detected by Newborn Screening.
    Hübner V; Hannibal L; Janzen N; Grünert SC; Freisinger P
    Genes (Basel); 2022 Jun; 13(7):. PubMed ID: 35885946
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.