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.
133 related articles for article (PubMed ID: 36635135)
1. A subtle presentation of a treatable cause of predominant hemidystonia with minimal ataxia: Expert commentary. Teive HAG Parkinsonism Relat Disord; 2023 Feb; 107():105275. PubMed ID: 36635135 [No Abstract] [Full Text] [Related]
2. A subtle presentation of a treatable cause of predominant hemidystonia with minimal ataxia. Wrigley SM; O'Sullivan SS; Ryan AM Parkinsonism Relat Disord; 2023 Feb; 107():104909. PubMed ID: 34823986 [No Abstract] [Full Text] [Related]
3. Autopsy case of severe generalized dystonia and static ataxia with marked cerebellar atrophy. Miyamoto R; Sumikura H; Takeuchi T; Sanada M; Fujita K; Kawarai T; Mure H; Morigaki R; Goto S; Murayama S; Izumi Y; Kaji R Neurology; 2015 Oct; 85(17):1522-4. PubMed ID: 26408497 [No Abstract] [Full Text] [Related]
4. Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 (FAM36A) mutation. Doss S; Lohmann K; Seibler P; Arns B; Klopstock T; Zühlke C; Freimann K; Winkler S; Lohnau T; Drungowski M; Nürnberg P; Wiegers K; Lohmann E; Naz S; Kasten M; Bohner G; Ramirez A; Endres M; Klein C J Neurol; 2014 Jan; 261(1):207-12. PubMed ID: 24202787 [TBL] [Abstract][Full Text] [Related]
5. Recurrent Ataxia and Dystonia with Anti-Neurochondrin Autoantibodies. Barrea C; Depierreux F Neuropediatrics; 2021 Jun; 52(3):228-229. PubMed ID: 33445194 [No Abstract] [Full Text] [Related]
6. Hypocortisolism as an unusual but treatable cause of dystonia-parkinsonism. Desjardins C; Mongin M; de Liège A; Degos B J Neurol; 2023 Apr; 270(4):2314-2316. PubMed ID: 36496545 [No Abstract] [Full Text] [Related]
7. The pathogenetic basis for a disease continuum in early- and late-onset ataxia-dystonia supports a unified genetic diagnostic approach. Garofalo M; Vansenne F; Verbeek DS; Sival DA Eur J Paediatr Neurol; 2023 Mar; 43():44-51. PubMed ID: 36905829 [TBL] [Abstract][Full Text] [Related]
8. Familial leukoencephalopathy with slowly progressive dystonia and ataxia. Blumkin L; Mandel H; Anca-Herschkovitsch M; Kivity S; Lev D; Lerman-Sagie T Eur J Paediatr Neurol; 2009 Nov; 13(6):530-3. PubMed ID: 19071044 [TBL] [Abstract][Full Text] [Related]
9. Subacute tremor and ataxia: Diligence in pursuit of a diagnosis: Expert commentary. Reich SG Parkinsonism Relat Disord; 2022 Nov; 104():132-133. PubMed ID: 36323593 [No Abstract] [Full Text] [Related]
10. Dystonia with myoclonus and vertical supranuclear gaze palsy associated with a rare GNB1 variant. Reyes NGD; Di Luca DG; McNiven V; Lang AE Parkinsonism Relat Disord; 2023 Jan; 106():105239. PubMed ID: 36521323 [TBL] [Abstract][Full Text] [Related]
11. Movement Disorders in Treatable Inborn Errors of Metabolism. Ebrahimi-Fakhari D; Van Karnebeek C; Münchau A Mov Disord; 2019 May; 34(5):598-613. PubMed ID: 30557456 [TBL] [Abstract][Full Text] [Related]
12. KIF1C Variants Are Associated with Hypomyelination, Ataxia, Tremor, and Dystonia in Fraternal Twins. Marchionni E; Méneret A; Keren B; Melki J; Denier C; Durr A; Apartis E; Boespflug-Tanguy O; Mochel F Tremor Other Hyperkinet Mov (N Y); 2019; 9():. PubMed ID: 31413903 [TBL] [Abstract][Full Text] [Related]
13. [The acute cerebro-cerebellar ataxic form of epilepsy in childhood]. Tets IS Zh Nevropatol Psikhiatr Im S S Korsakova; 1969; 69(11):1672-8. PubMed ID: 5369968 [No Abstract] [Full Text] [Related]