These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
134 related articles for article (PubMed ID: 28899475)
1. [Gene mutations in a newborn infant with hypermethioninemia]. Yang YQ; Wang HY; Jiang LH; Zhang YP; Yu B; Zhu W; Qin ZQ Zhongguo Dang Dai Er Ke Za Zhi; 2017 Sep; 19(9):1020-1021. PubMed ID: 28899475 [No Abstract] [Full Text] [Related]
2. [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]
3. 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]
4. 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]
5. 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]
6. 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]
7. Adenosine kinase deficiency: Three new cases and diagnostic value of hypermethioninemia. Becker PH; Demir Z; Mozer Glassberg Y; Sevin C; Habes D; Imbard A; Mussini C; Rozenfeld Bar Lev M; Davit-Spraul A; Benoist JF; Thérond P; Slama A; Jacquemin E; Gonzales E; Gaignard P Mol Genet Metab; 2021 Jan; 132(1):38-43. PubMed ID: 33309011 [TBL] [Abstract][Full Text] [Related]
8. 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]
10. HYPERMETHIONINEMIA: A METABOLIC DISORDER ASSOCIATED WITH CIRRHOSIS, ISLET CELL HYPERPLASIA, AND RENAL TUBULAR DEGENERATION. PERRY TL; HARDWICK DF; DIXON GH; DOLMAN CL; HANSEN S Pediatrics; 1965 Aug; 36():236-50. PubMed ID: 14320034 [No Abstract] [Full Text] [Related]
11. A Turkish patient with novel AHCY variants and presumed diagnosis of S-adenosylhomocysteine hydrolase deficiency. Bas H; Cilingir O; Tekin N; Saylisoy S; Durak Aras B; Uzay E; Erzurumluoglu Gokalp E; Artan S Am J Med Genet A; 2020 Apr; 182(4):740-745. PubMed ID: 31957987 [TBL] [Abstract][Full Text] [Related]
12. [Clinical investigation and mutation analysis of a child with citrin deficiency complicated with purpura, convulsive seizures and methioninemia]. Wen PQ; Wang GB; Chen ZL; Liu XH; Cui D; Shang Y; Li CR Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):649-53. PubMed ID: 24327139 [TBL] [Abstract][Full Text] [Related]
13. Abnormal Hypermethylation at Imprinting Control Regions in Patients with S-Adenosylhomocysteine Hydrolase (AHCY) Deficiency. Motzek A; Knežević J; Switzeny OJ; Cooper A; Barić I; Beluzić R; Strauss KA; Puffenberger EG; Mudd SH; Vugrek O; Zechner U PLoS One; 2016; 11(3):e0151261. PubMed ID: 26974671 [TBL] [Abstract][Full Text] [Related]