158 related articles for article (PubMed ID: 31922275)
1. 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]
2. TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model.
Lüthy K; Mei D; Fischer B; De Fusco M; Swerts J; Paesmans J; Parrini E; Lubarr N; Meijer IA; Mackenzie KM; Lee WT; Cittaro D; Aridon P; Schoovaerts N; Versées W; Verstreken P; Casari G; Guerrini R
Brain; 2019 Aug; 142(8):2319-2335. PubMed ID: 31257402
[TBL] [Abstract][Full Text] [Related]
3. Child Neurology: Genetically determined dystonias with childhood onset.
Larsh T; Friedman N; Fernandez H
Neurology; 2020 May; 94(20):892-895. PubMed ID: 32033988
[No Abstract] [Full Text] [Related]
4. Increased risk for recurrent major depression in DYT1 dystonia mutation carriers.
Duane DD
Neurology; 2005 May; 64(10):1821-2; author reply 1821-2. PubMed ID: 15911830
[No Abstract] [Full Text] [Related]
5. PRKRA Mutation Causing Early-Onset Generalized Dystonia-Parkinsonism (DYT16) in an Italian Family.
Quadri M; Olgiati S; Sensi M; Gualandi F; Groppo E; Rispoli V; Graafland J; Breedveld GJ; Fabbrini G; Berardelli A; Bonifati V
Mov Disord; 2016 May; 31(5):765-7. PubMed ID: 26990861
[No Abstract] [Full Text] [Related]
6. Novel GNAL mutations in two German patients with sporadic dystonia.
Ziegan J; Wittstock M; Westenberger A; Dobričić V; Wolters A; Benecke R; Klein C; Kamm C
Mov Disord; 2014 Dec; 29(14):1833-4. PubMed ID: 25382112
[No Abstract] [Full Text] [Related]
7. Screening of mutations in GNAL in sporadic dystonia patients.
Dufke C; Sturm M; Schroeder C; Moll S; Ott T; Riess O; Bauer P; Grundmann K
Mov Disord; 2014 Aug; 29(9):1193-6. PubMed ID: 24408567
[TBL] [Abstract][Full Text] [Related]
8. Genetic Aspects of Myoclonus-Dystonia Syndrome (MDS).
Rachad L; El Kadmiri N; Slassi I; El Otmani H; Nadifi S
Mol Neurobiol; 2017 Mar; 54(2):939-942. PubMed ID: 26790671
[TBL] [Abstract][Full Text] [Related]
9. De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.
Dobričić V; Kresojević N; Westenberger A; Svetel M; Tomić A; Ralić V; Petrović I; Lukić MJ; Lohmann K; Novaković I; Klein C; Kostić VS
Mov Disord; 2014 Aug; 29(9):1190-3. PubMed ID: 24729450
[TBL] [Abstract][Full Text] [Related]
10. Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.
Tian WT; Huang XJ; Mao X; Liu Q; Liu XL; Zeng S; Guo XN; Shen JY; Xu YQ; Tang HD; Yin XM; Zhang M; Tang WG; Liu XR; Tang BS; Chen SD; Cao L
Mov Disord; 2018 Mar; 33(3):459-467. PubMed ID: 29356177
[TBL] [Abstract][Full Text] [Related]
11. Reply to: "Early Onset Nonprogressive Generalized Dystonia Is Caused by Biallelic SHQ1 Variants".
Indelicato E; Boesch S; Zech M
Mov Disord; 2023 Jun; 38(6):1119-1120. PubMed ID: 37475612
[No Abstract] [Full Text] [Related]
12. [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]
13. Novel THAP1 variants in Brazilian patients with idiopathic isolated dystonia.
da Silva-Junior FP; dos Santos CO; Silva SM; Barbosa ER; Borges V; Ferraz HB; Limongi JC; Rocha MS; de Carvalho Aguiar P
J Neurol Sci; 2014 Sep; 344(1-2):190-2. PubMed ID: 24976531
[TBL] [Abstract][Full Text] [Related]
14. Molecular diversity of combined and complex dystonia: insights from diagnostic exome sequencing.
Zech M; Jech R; Wagner M; Mantel T; Boesch S; Nocker M; Jochim A; Berutti R; Havránková P; Fečíková A; Kemlink D; Roth J; Strom TM; Poewe W; Růžička E; Haslinger B; Winkelmann J
Neurogenetics; 2017 Dec; 18(4):195-205. PubMed ID: 28849312
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. A novel heterozygous ANO3 mutation responsible for myoclonic dystonia.
Laurencin C; Broussolle E; Danaila T; Anheim M; Chelly J; Thobois S
J Neurol Sci; 2019 Aug; 403():65-66. PubMed ID: 31228765
[No Abstract] [Full Text] [Related]
17. The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?
Brüggemann N; Kock N; Lohmann K; König IR; Rakovic A; Hagenah J; Schmidt A; Ziegler A; Jabusch HC; Siebner H; Altenmüller E; Münchau A; Klein C
Neurology; 2009 Apr; 72(16):1441-3. PubMed ID: 19380705
[No Abstract] [Full Text] [Related]
18. Update on KMT2B-Related Dystonia.
Zech M; Lam DD; Winkelmann J
Curr Neurol Neurosci Rep; 2019 Nov; 19(11):92. PubMed ID: 31768667
[TBL] [Abstract][Full Text] [Related]
19. Risk Factor Genes in Patients with Dystonia: A Comprehensive Review.
Siokas V; Aloizou AM; Tsouris Z; Michalopoulou A; Mentis AA; Dardiotis E
Tremor Other Hyperkinet Mov (N Y); 2018; 8():559. PubMed ID: 30643666
[TBL] [Abstract][Full Text] [Related]
20. Truncating VPS16 Mutations Are Rare in Early Onset Dystonia.
Pott H; Brüggemann N; Reese R; Zeuner KE; Gandor F; Gruber D; ; Klein C; Volkmann J; Lohmann K
Ann Neurol; 2021 Mar; 89(3):625-626. PubMed ID: 33305852
[No Abstract] [Full Text] [Related]
[Next] [New Search]