BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

107 related articles for article (PubMed ID: 28247119)

  • 1. Attenuated brain lesion on magnetic resonance imaging in an adult patient with methionine adenosyltransferase I/III deficiency.
    Maruta U; Shimono T; Tokuhara D; Hanayama Y; Miki Y
    Neurol Sci; 2017 Jun; 38(6):1131-1133. PubMed ID: 28247119
    [No Abstract]   [Full Text] [Related]  

  • 2. Reversible white matter lesion in methionine adenosyltransferase I/III deficiency.
    Tada H; Takanashi J; Barkovich AJ; Yamamoto S; Kohno Y
    AJNR Am J Neuroradiol; 2004; 25(10):1843-5. PubMed ID: 15569761
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 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. 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]  

  • 7. 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]  

  • 8. Methionine adenosyltransferase (MAT) I/III deficiency with concurrent hyperhomocysteinaemia: two novel cases.
    Linnebank M; Lagler F; Muntau AC; Röschinger W; Olgemöller B; Fowler B; Koch HG
    J Inherit Metab Dis; 2005; 28(6):1167-8. PubMed ID: 16435220
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hepatic methionine adenosyltransferase deficiency in a 31-year-old man.
    Gahl WA; Finkelstein JD; Mullen KD; Bernardini I; Martin JJ; Backlund P; Ishak KG; Hoofnagle JH; Mudd SH
    Am J Hum Genet; 1987 Jan; 40(1):39-49. PubMed ID: 3812486
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. Normal brain myelination in a patient homozygous for a mutation that encodes a severely truncated methionine adenosyltransferase I/III.
    Hazelwood S; Bernardini I; Shotelersuk V; Tangerman A; Guo J; Mudd H; Gahl WA
    Am J Med Genet; 1998 Feb; 75(4):395-400. PubMed ID: 9482646
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hypermethioninemia associated with methionine adenosyltransferase deficiency: clinical, morphologic, and biochemical observations on four patients.
    Gaull GE; Tallan HH; Lonsdale D; Przyrembel H; Schaffner F; von Bassewitz DB
    J Pediatr; 1981 May; 98(5):734-41. PubMed ID: 7229751
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Characteristic MR imaging changes in severe hypermethioninemic states.
    Braverman NE; Mudd SH; Barker PB; Pomper MG
    AJNR Am J Neuroradiol; 2005; 26(10):2705-6. PubMed ID: 16286426
    [No Abstract]   [Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene.
    Chamberlin ME; Ubagai T; Mudd SH; Levy HL; Chou JY
    Am J Hum Genet; 1997 Mar; 60(3):540-6. PubMed ID: 9042912
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.