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.
147 related articles for article (PubMed ID: 38854909)
1. Careful Phenotypic Characterization of Tremor Phenomenology in a Patient with Spinocerebellar Ataxia Type 12-Tremor Features Do Not Match Those of Essential Tremor. Luo W; Zheng X; Lin Z; Luo W Tremor Other Hyperkinet Mov (N Y); 2024; 14():28. PubMed ID: 38854909 [TBL] [Abstract][Full Text] [Related]
2. Early-onset familial essential tremor is associated with nucleotide expansions of spinocerebellar ataxia in China. Zheng Z; Zhu Z; Pu J; Zhou C; Cao L; Lv D; Lu J; Zhao G; Chen Y; Tian J; Yin X; Zhang B; Yan Y; Zhao G Mol Biol Rep; 2024 Jan; 51(1):113. PubMed ID: 38227102 [TBL] [Abstract][Full Text] [Related]
3. Tremor in Spinocerebellar Ataxia: A Scoping Review. Mukherjee A; Pandey S Tremor Other Hyperkinet Mov (N Y); 2024; 14():31. PubMed ID: 38911333 [TBL] [Abstract][Full Text] [Related]
4. Unusual cerebral white matter change in a Chinese family with Spinocerebellar ataxia type 12. Hu T; Zhao B; Wei QQ; Shang H J Neurol Sci; 2015 Feb; 349(1-2):243-5. PubMed ID: 25586539 [TBL] [Abstract][Full Text] [Related]
5. Identification of FXTAS presenting with SCA 12 like phenotype in India. Faruq M; Srivastava AK; Suroliya V; Kumar D; Garg A; Shukla G; Behari M Parkinsonism Relat Disord; 2014 Oct; 20(10):1089-93. PubMed ID: 25085749 [TBL] [Abstract][Full Text] [Related]
6. The SCA12 mutation as a rare cause of spinocerebellar ataxia. Cholfin JA; Sobrido MJ; Perlman S; Pulst SM; Geschwind DH Arch Neurol; 2001 Nov; 58(11):1833-5. PubMed ID: 11708992 [TBL] [Abstract][Full Text] [Related]
7. Identification of 46 CAG repeats within PPP2R2B as probably the shortest pathogenic allele for SCA12. Dong Y; Wu JJ; Wu ZY Parkinsonism Relat Disord; 2015 Apr; 21(4):398-401. PubMed ID: 25634432 [TBL] [Abstract][Full Text] [Related]
8. Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia? Kuoppamäki M; Giunti P; Quinn N; Wood NW; Bhatia KP Mov Disord; 2003 Feb; 18(2):200-6. PubMed ID: 12539216 [TBL] [Abstract][Full Text] [Related]
9. Clinical, Radiological, and Genetic Profile of Spinocerebellar Ataxia 12: A Hospital-Based Cohort Analysis. Ganaraja VH; Holla VV; Stezin A; Kamble N; Yadav R; Purushottam M; Jain S; Pal PK Tremor Other Hyperkinet Mov (N Y); 2022; 12():13. PubMed ID: 35531119 [TBL] [Abstract][Full Text] [Related]
11. Clinical behaviour of spinocerebellar ataxia type 12 and intermediate length abnormal CAG repeats in PPP2R2B. Srivastava AK; Takkar A; Garg A; Faruq M Brain; 2017 Jan; 140(1):27-36. PubMed ID: 27864267 [TBL] [Abstract][Full Text] [Related]
12. Spasmodic dysphonia as a presenting symptom of spinocerebellar ataxia type 12. Rossi J; Cavallieri F; Giovannini G; Budriesi C; Gessani A; Carecchio M; Di Bella D; Sarto E; Mandrioli J; Contardi S; Meletti S Neurogenetics; 2019 Aug; 20(3):161-164. PubMed ID: 31190316 [TBL] [Abstract][Full Text] [Related]
13. Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes. Aydin G; Dekomien G; Hoffjan S; Gerding WM; Epplen JT; Arning L BMC Neurol; 2018 Jan; 18(1):3. PubMed ID: 29316893 [TBL] [Abstract][Full Text] [Related]
14. Essential Tremor Within the Broader Context of Other Forms of Cerebellar Degeneration. Louis ED; Faust PL Cerebellum; 2020 Dec; 19(6):879-896. PubMed ID: 32666285 [TBL] [Abstract][Full Text] [Related]
15. Familial essential tremor is not associated with SCA-12 mutation in southern Italy. Nicoletti G; Annesi G; Carrideo S; Tomaino C; Di Costanzo A; Zappia M; Quattrone A Mov Disord; 2002 Jul; 17(4):837-8. PubMed ID: 12210890 [TBL] [Abstract][Full Text] [Related]
16. Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism. Tan EK; Tong J; Pavanni R; Wong MC; Zhao Y Mov Disord; 2007 Oct; 22(13):1971-4. PubMed ID: 17712857 [TBL] [Abstract][Full Text] [Related]
17. Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia. Brussino A; Graziano C; Giobbe D; Ferrone M; Dragone E; Arduino C; Lodi R; Tonon C; Gabellini A; Rinaldi R; Miccoli S; Grosso E; Bellati MC; Orsi L; Migone N; Brusco A Mov Disord; 2010 Jul; 25(9):1269-73. PubMed ID: 20629122 [TBL] [Abstract][Full Text] [Related]
18. SCA12: an unusual mutation leads to an unusual spinocerebellar ataxia. Holmes SE; Hearn EO; Ross CA; Margolis RL Brain Res Bull; 2001 Oct-Nov 1; 56(3-4):397-403. PubMed ID: 11719278 [TBL] [Abstract][Full Text] [Related]
19. Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders. Robertson EE; Hall DA; McAsey AR; O'Keefe JA Clin Neuropsychol; 2016 Aug; 30(6):849-900. PubMed ID: 27414076 [TBL] [Abstract][Full Text] [Related]
20. Premutation alleles and fragile X-associated tremor/ataxia syndrome. Toft M; Farrer M JAMA; 2005 Jan; 293(3):296; author reply 296-7. PubMed ID: 15657320 [No Abstract] [Full Text] [Related] [Next] [New Search]