164 related articles for article (PubMed ID: 33497487)
21. [Genetic dissection of dystonia].
Tamiya G
No To Shinkei; 2005 Nov; 57(11):935-44. PubMed ID: 16363633
[No Abstract] [Full Text] [Related]
22. [KMT2B variants responsible for children dystonia 28: report of two cases].
Dai LF; Ding CH; Fang T; Xie ZH; Liu TH; Zhang WH; Wang XH; Ren XT; Liu M; Tian XJ; Wu HS; Fang F
Zhonghua Er Ke Za Zhi; 2019 Jul; 57(7):564-566. PubMed ID: 31269560
[TBL] [Abstract][Full Text] [Related]
23. Early-Onset Dystonia, Exacerbation With Fever, and Striatal Signal Changes: Emerging Phenotype of DYT-
Bhowmick SS; Raha S; Bohora A
Neurology; 2022 Aug; 99(5):206-207. PubMed ID: 35914940
[No Abstract] [Full Text] [Related]
24. Dystonia genes and their biological pathways.
Jinnah HA; Sun YV
Neurobiol Dis; 2019 Sep; 129():159-168. PubMed ID: 31112762
[TBL] [Abstract][Full Text] [Related]
25. Update on the Genetics of Dystonia.
Lohmann K; Klein C
Curr Neurol Neurosci Rep; 2017 Mar; 17(3):26. PubMed ID: 28283962
[TBL] [Abstract][Full Text] [Related]
26. AOPEP Homozygous Loss-of-Function Variant in an Indian Patient with Early-Onset Generalized Dystonia.
Fevga C; Ferraro F; Breedveld GJ; Savant Sankhla C; Bonifati V
Mov Disord; 2022 Apr; 37(4):874-875. PubMed ID: 35072283
[No Abstract] [Full Text] [Related]
27. Expanded Genetic Spectrum and Variable Disease Onset in AOPEP-Associated Dystonia.
Menden B; Gutschalk A; Wunderlich G; Haack TB
Mov Disord; 2022 May; 37(5):1113-1115. PubMed ID: 35587627
[No Abstract] [Full Text] [Related]
28. Prevalence of dystonia in Akita Prefecture in Northern Japan.
Sugawara M; Watanabe S; Toyoshima I
Mov Disord; 2006 Jul; 21(7):1047-9. PubMed ID: 16602106
[TBL] [Abstract][Full Text] [Related]
29. Biallelic mutations of TBC1D24 in exercise-induced paroxysmal dystonia.
Steel D; Heim J; Kruer MC; Sanchis-Juan A; Raymond LF; Eunson P; Kurian MA
Mov Disord; 2020 Feb; 35(2):372-373. PubMed ID: 31922275
[No Abstract] [Full Text] [Related]
30. A novel presentation of DYT 16: acute onset in infancy and association with MRI abnormalities.
Lemmon ME; Lavenstein B; Applegate CD; Hamosh A; Tekes A; Singer HS
Mov Disord; 2013 Dec; 28(14):1937-8. PubMed ID: 24142417
[No Abstract] [Full Text] [Related]
31. Phenotype of the DYT1 mutation in the TOR1A gene in a Polish population of patients with dystonia. A preliminary report.
Gajos A; Piaskowski S; Sławek J; Ochudło S; Opala G; Łobińska A; Honczarenko K; Budrewicz S; Koszewicz M; Pełszyńska B; Liberski PP; Bogucki A
Neurol Neurochir Pol; 2007; 41(6):487-94. PubMed ID: 18224570
[TBL] [Abstract][Full Text] [Related]
32. Molecular mechanisms of hereditary progressive dystonia with marked diurnal fluctuation, Segawa's disease.
Ichinose H; Inagaki H; Suzuki T; Ohye T; Nagatsu T
Brain Dev; 2000 Sep; 22 Suppl 1():S107-10. PubMed ID: 10984669
[TBL] [Abstract][Full Text] [Related]
33. Untwisting dystonia: stepping-up genetics, shifting pathophysiology, and strategizing care.
Rosales RL; Westenberger A
J Neural Transm (Vienna); 2021 Apr; 128(4):393-394. PubMed ID: 33928446
[No Abstract] [Full Text] [Related]
34. Harnessing Transcriptomics to Decipher Dystonia Pathogenesis.
Fellner A; Kumar KR
Mov Disord; 2022 May; 37(5):891. PubMed ID: 35277998
[No Abstract] [Full Text] [Related]
35. [Clinical and genetic analysis of childhood-onset myoclonus dystonia syndrome caused by SGCE variants].
Tian XJ; Ding CH; Zhang YH; Dai LF; Chen CH; Li JW; Wang X; Han TL; Wang XH; Deng J
Zhonghua Er Ke Za Zhi; 2020 Feb; 58(2):123-128. PubMed ID: 32102149
[No Abstract] [Full Text] [Related]
36. Dystonia: genetics, phenomenology, and pathophysiology.
Vidailhet M; Méneret A; Roze E
Lancet Neurol; 2020 Nov; 19(11):881-882. PubMed ID: 33098786
[No Abstract] [Full Text] [Related]
37. A Recurrent EIF2AK2 Missense Variant Causes Autosomal-Dominant Isolated Dystonia.
Musacchio T; Zech M; Reich MM; Winkelmann J; Volkmann J
Ann Neurol; 2021 Jun; 89(6):1257-1258. PubMed ID: 33866603
[No Abstract] [Full Text] [Related]
38. Ethnic Differences in Dystonia Prevalence and Phenotype.
Mulroy E; Macerollo A; Scotton S; Cociasu I; Di Lazzaro G; Bashir S; Doherty J; Hamid S; Mooney N; Batla A; Morgante F; Bhatia KP
Mov Disord; 2022 Jun; 37(6):1323-1325. PubMed ID: 35500158
[No Abstract] [Full Text] [Related]
39. Neurodevelopmental Gene-Related Dystonia: A Pediatric Case with NAA15 Variant.
Yubero D; Martorell L; Nunes T; Lyon GJ; Ortigoza-Escobar JD
Mov Disord; 2022 Nov; 37(11):2320-2321. PubMed ID: 36221186
[No Abstract] [Full Text] [Related]
40. Review of the phenotype of early-onset generalised progressive dystonia due to mutations in KMT2B.
Gorman KM; Meyer E; Kurian MA
Eur J Paediatr Neurol; 2018 Mar; 22(2):245-256. PubMed ID: 29289525
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
