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.
160 related articles for article (PubMed ID: 30911858)
21. Novel mutation in the replication focus targeting sequence domain of DNMT1 causes hereditary sensory and autonomic neuropathy IE. Yuan J; Higuchi Y; Nagado T; Nozuma S; Nakamura T; Matsuura E; Hashiguchi A; Sakiyama Y; Yoshimura A; Takashima H J Peripher Nerv Syst; 2013 Mar; 18(1):89-93. PubMed ID: 23521649 [TBL] [Abstract][Full Text] [Related]
22. Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment. Davis KN; Qu PP; Ma S; Lin L; Plastini M; Dahl N; Plazzi G; Pizza F; O'Hara R; Wong WH; Hallmayer J; Mignot E; Zhang X; Urban AE Hum Mol Genet; 2023 Oct; 32(21):3105-3120. PubMed ID: 37584462 [TBL] [Abstract][Full Text] [Related]
23. First Portuguese patient presenting with hereditary sensory and autonomic neuropathy type 1E associated with a novel mutation in DNMT1 gene. Coelho P; Oliveira Santos M Neurol Sci; 2020 May; 41(5):1289-1290. PubMed ID: 31807999 [No Abstract] [Full Text] [Related]
24. [A case of hereditary sensory and autonomic neuropathy type 1E with frontal lobe dysfunction as an initial symptom]. Watanabe M; Matsumoto Y; Okamoto K; Okuda B; Mizuta I; Mizuno T Rinsho Shinkeigaku; 2017 Dec; 57(12):753-758. PubMed ID: 29187684 [TBL] [Abstract][Full Text] [Related]
25. DNMT1 mutations found in HSANIE patients affect interaction with UHRF1 and neuronal differentiation. Smets M; Link S; Wolf P; Schneider K; Solis V; Ryan J; Meilinger D; Qin W; Leonhardt H Hum Mol Genet; 2017 Apr; 26(8):1522-1534. PubMed ID: 28334952 [TBL] [Abstract][Full Text] [Related]
26. Cataplexy and ataxia: red flags for the diagnosis of DNA methyltransferase 1 mutation. Postiglione E; Antelmi E; Pizza F; Vandi S; La Morgia C; Carelli V; Nassetti S; Seri M; Plazzi G J Clin Sleep Med; 2020 Jan; 16(1):143-147. PubMed ID: 31957642 [TBL] [Abstract][Full Text] [Related]
27. Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report. Kume K; Morino H; Miyamoto R; Matsuda Y; Ohsawa R; Kanaya Y; Tada Y; Kurashige T; Kawakami H BMC Med Genet; 2020 Mar; 21(1):68. PubMed ID: 32234020 [TBL] [Abstract][Full Text] [Related]
28. Novel de novo DNMT1 gene mutation associated with hereditary sensory and autonomic neuropathy 1E (HSAN1E). Parissis D; Christodoulou K; Kleopa KA Neurol Sci; 2023 Jun; 44(6):2199-2201. PubMed ID: 36746843 [No Abstract] [Full Text] [Related]
29. Novel pregnancy-triggered episodes of CAPOS syndrome. Chang IJ; Adam MP; Jayadev S; Bird TD; Natarajan N; Glass IA Am J Med Genet A; 2018 Jan; 176(1):235-240. PubMed ID: 29090527 [TBL] [Abstract][Full Text] [Related]
30. [Clinical, multimodal electrophysiological study of a family with progressive cerebellar ataxia and late deafness and an autosomal recessive inheritance]. Ragno M; Curatola L; Rossi R; Salvolini U Acta Neurol (Napoli); 1992; 14(4-6):431-9. PubMed ID: 1293986 [TBL] [Abstract][Full Text] [Related]
32. Clinical spectrum of AIFM1-associated disease in an Irish family, from mild neuropathy to severe cerebellar ataxia with colour blindness. Bogdanova-Mihaylova P; Alexander MD; Murphy RP; Chen H; Healy DG; Walsh RA; Murphy SM J Peripher Nerv Syst; 2019 Dec; 24(4):348-353. PubMed ID: 31523922 [TBL] [Abstract][Full Text] [Related]
33. Mutations in DNMT1 cause hereditary sensory neuropathy with dementia and hearing loss. Klein CJ; Botuyan MV; Wu Y; Ward CJ; Nicholson GA; Hammans S; Hojo K; Yamanishi H; Karpf AR; Wallace DC; Simon M; Lander C; Boardman LA; Cunningham JM; Smith GE; Litchy WJ; Boes B; Atkinson EJ; Middha S; B Dyck PJ; Parisi JE; Mer G; Smith DI; Dyck PJ Nat Genet; 2011 Jun; 43(6):595-600. PubMed ID: 21532572 [TBL] [Abstract][Full Text] [Related]
34. Identification of a novel mutation in the CACNA1C gene in a Chinese family with autosomal dominant cerebellar ataxia. Chen J; Sun Y; Liu X; Li J BMC Neurol; 2019 Jul; 19(1):157. PubMed ID: 31291898 [TBL] [Abstract][Full Text] [Related]
35. Generation of a transgenic mouse embryonic stem cell line expressing Dnmt1 Choudhury S; Mohan KN Stem Cell Res; 2021 Oct; 56():102561. PubMed ID: 34634759 [TBL] [Abstract][Full Text] [Related]
36. Classifications of neurogenetic diseases: An increasingly complex problem. Vallat JM; Goizet C; Tazir M; Couratier P; Magy L; Mathis S Rev Neurol (Paris); 2016; 172(6-7):339-49. PubMed ID: 27240993 [TBL] [Abstract][Full Text] [Related]
37. Early Diagnosis of CAPOS Syndrome Before Acute-Onset Ataxia-Review of the Literature and a New Family. Duat Rodriguez A; Prochazkova M; Santos Santos S; Rubio Cabezas O; Cantarin Extremera V; Gonzalez-Gutierrez-Solana L Pediatr Neurol; 2017 Jun; 71():60-64. PubMed ID: 28483396 [TBL] [Abstract][Full Text] [Related]