154 related articles for article (PubMed ID: 35885946)
1. 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]
2. 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]
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. 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]
5. 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]
6. Methionine adenosyltransferase I/III deficiency: Long-term follow-up and treatment of 3 adult siblings.
Bannick A; Chase S; Miner A; Seeterlin M; Conway RL
Eur J Med Genet; 2020 Dec; 63(12):104076. PubMed ID: 32980525
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. Genomic analysis of 9 infants with hypermethioninemia by whole-exome sequencing among in Henan, China.
Zhao D; Ni M; Jia C; Li X; Zhu X; Liu S; Su L; Lv S; Wang L; Jia L
Clin Chim Acta; 2022 Aug; 533():109-113. PubMed ID: 35760084
[TBL] [Abstract][Full Text] [Related]
15. [Analysis of MAT1A gene mutations in a child affected with simple hypermethioninemia].
Sun Y; Ma D; Wang Y; Yang B; Jiang T
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb; 34(1):98-101. PubMed ID: 28186605
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. [Newborn screening and variant analysis for methionine adenosyltransferase I/III deficiency].
Lin C; Zheng Q; Jiang M; Lin Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 May; 37(5):527-531. PubMed ID: 32335878
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Methionine adenosyltransferase I/III deficiency: two Korean compound heterozygous siblings with a novel mutation.
Kim SZ; Santamaria E; Jeong TE; Levy HL; Mato JM; Corrales FJ; Mudd SH
J Inherit Metab Dis; 2002 Dec; 25(8):661-71. PubMed ID: 12705496
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
