142 related articles for article (PubMed ID: 16286426)
1. 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]
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. [Disorders of transsulfuration; disorders of sulfur-aminoacids metabolism].
Hase Y
Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):205-18. PubMed ID: 9590029
[No Abstract] [Full Text] [Related]
4. Elevated plasma total homocysteine in severe methionine adenosyltransferase I/III deficiency.
Stabler SP; Steegborn C; Wahl MC; Oliveriusova J; Kraus JP; Allen RH; Wagner C; Mudd SH
Metabolism; 2002 Aug; 51(8):981-8. PubMed ID: 12145770
[TBL] [Abstract][Full Text] [Related]
5. Cystathionine-synthase-deficient patients do not use the transamination pathway of methionine to reduce hypermethioninemia and homocystinemia.
Blom HJ; Boers GH; Trijbels JM; van Roessel JJ; Tangerman A
Metabolism; 1989 Jun; 38(6):577-82. PubMed ID: 2725296
[TBL] [Abstract][Full Text] [Related]
6. Methionine adenosyltransferase, cystathionine beta-synthase and cystathionine gamma-lyase activity of rat liver subcellular particles, human blood cells and mixed white cells from rat bone marrow.
Allsop J; Watts RW
Clin Sci Mol Med Suppl; 1975 Jun; 48(6):509-13. PubMed ID: 1056281
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. 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]
10. 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]
11. 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]
12. Long follow up of betaine therapy in two Japanese siblings with cystathionine beta-synthase deficiency.
Yokoi K; Ito T; Ohkubo Y; Sumi S; Ueta A; Sugiyama N; Togari H
Pediatr Int; 2008 Oct; 50(5):694-5. PubMed ID: 19261122
[No 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 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]
15. 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]
16. Two siblings with vitamin B6-nonresponsive cystathionine beta-synthase deficiency and differing blood methionine levels during the neonatal period.
Watanabe T; Ito M; Naito E; Yokota I; Matsuda J; Kuroda Y
J Med Invest; 1997 Aug; 44(1-2):95-7. PubMed ID: 9395725
[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. 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]
19. 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]
20. Intermittent hypermethioninaemia associated with normal hepatic methionine adenosyltransferase activity: report of a case.
Jhaveri BM; Buist NR; Gaull GE; Tallan HH
J Inherit Metab Dis; 1982; 5(2):101-5. PubMed ID: 6820418
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]