197 related articles for article (PubMed ID: 23993429)
21. Persistent hypermethioninaemia with dominant inheritance.
Blom HJ; Davidson AJ; Finkelstein JD; Luder AS; Bernardini I; Martin JJ; Tangerman A; Trijbels JM; Mudd SH; Goodman SI
J Inherit Metab Dis; 1992; 15(2):188-97. PubMed ID: 1527987
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. 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]
24. 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]
25. 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]
26. [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]
27. [Still another cause of hypermethioninemia in children: S-adenosylmethionine synthetase deficiency].
Gout JP; Serre JC; Dieterlen M; Antener I; Frappat P; Bost M; Beaudoing A
Arch Fr Pediatr; 1977 May; 34(5):416-23. PubMed ID: 889406
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. 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]
30. 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]
31. Newborn screening for homocystinurias: Recent recommendations versus current practice.
Keller R; Chrastina P; Pavlíková M; Gouveia S; Ribes A; Kölker S; Blom HJ; Baumgartner MR; Bártl J; Dionisi-Vici C; Gleich F; Morris AA; Kožich V; Huemer M; ; Barić I; Ben-Omran T; Blasco-Alonso J; Bueno Delgado MA; Carducci C; Cassanello M; Cerone R; Couce ML; Crushell E; Delgado Pecellin C; Dulin E; Espada M; Ferino G; Fingerhut R; Garcia Jimenez I; Gonzalez Gallego I; González-Irazabal Y; Gramer G; Juan Fita MJ; Karg E; Klein J; Konstantopoulou V; la Marca G; Leão Teles E; Leuzzi V; Lilliu F; Lopez RM; Lund AM; Mayne P; Meavilla S; Moat SJ; Okun JG; Pasquini E; Pedron-Giner CC; Racz GZ; Ruiz Gomez MA; Vilarinho L; Yahyaoui R; Zerjav Tansek M; Zetterström RH; Zeyda M
J Inherit Metab Dis; 2019 Jan; 42(1):128-139. PubMed ID: 30740731
[TBL] [Abstract][Full Text] [Related]
32. Pleiotropic effects of methionine adenosyltransferases deregulation as determinants of liver cancer progression and prognosis.
Frau M; Feo F; Pascale RM
J Hepatol; 2013 Oct; 59(4):830-41. PubMed ID: 23665184
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. 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]
35. Structural basis of the dominant inheritance of hypermethioninemia associated with the Arg264His mutation in the MAT1A gene.
Panmanee J; Antonyuk SV; Hasnain SS
Acta Crystallogr D Struct Biol; 2020 Jun; 76(Pt 6):594-607. PubMed ID: 32496220
[TBL] [Abstract][Full Text] [Related]
36. Methionine Adenosyltransferase I/III Deficiency in Portugal: High Frequency of a Dominantly Inherited Form in a Small Area of Douro High Lands.
Martins E; Marcão A; Bandeira A; Fonseca H; Nogueira C; Vilarinho L
JIMD Rep; 2012; 6():107-12. PubMed ID: 23430947
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. A new type of hypermethioninemia in neonates.
Tsuchiyama A; Oyanagi K; Nakata F; Uetsuji N; Tsugawa S; Nakao T; Mori M
Tohoku J Exp Med; 1982 Nov; 138(3):281-8. PubMed ID: 7157356
[TBL] [Abstract][Full Text] [Related]
39. Determination of Autosomal Dominant or Recessive Methionine Adenosyltransferase I/III Deficiencies Based on Clinical and Molecular Studies.
Kim YM; Kim JH; Choi J; Gu-Hwan K; Kim JM; Kang M; Choi IH; Cheon CK; Sohn YB; Maccarana M; Yoo HW; Lee BH
Mol Med; 2016 Sep; 22():147-155. PubMed ID: 26933843
[TBL] [Abstract][Full Text] [Related]
40. Hypermethioninemia in Campania: Results from 10 years of newborn screening.
Villani GRD; Albano L; Caterino M; Crisci D; Di Tommaso S; Fecarotta S; Fisco MG; Frisso G; Gallo G; Mazzaccara C; Marchese E; Nolano A; Parenti G; Pecce R; Redi A; Salvatore F; Strisciuglio P; Turturo MG; Vallone F; Ruoppolo M
Mol Genet Metab Rep; 2019 Dec; 21():100520. PubMed ID: 31641591
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
