169 related articles for article (PubMed ID: 29801903)
1. Targeted gene capture sequencing in diagnosis of dystonia patients.
Ma J; Wang L; Yang YM; Wan XH
J Neurol Sci; 2018 Jul; 390():36-41. PubMed ID: 29801903
[TBL] [Abstract][Full Text] [Related]
2. A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan.
Wu MC; Chang YY; Lan MY; Chen YF; Tai CH; Lin YF; Tsai SF; Chen PL; Lin CH
J Mol Diagn; 2022 Mar; 24(3):262-273. PubMed ID: 35041927
[TBL] [Abstract][Full Text] [Related]
3. Whole exome sequencing and clinical investigation of young onset dystonia: What can we learn?
Ahn JH; Kim AR; Park WY; Cho JW; Park J; Youn J
Parkinsonism Relat Disord; 2023 Oct; 115():105814. PubMed ID: 37607452
[TBL] [Abstract][Full Text] [Related]
4. Clinical exome sequencing in early-onset generalized dystonia and large-scale resequencing follow-up.
Zech M; Boesch S; Jochim A; Weber S; Meindl T; Schormair B; Wieland T; Lunetta C; Sansone V; Messner M; Mueller J; Ceballos-Baumann A; Strom TM; Colombo R; Poewe W; Haslinger B; Winkelmann J
Mov Disord; 2017 Apr; 32(4):549-559. PubMed ID: 27666935
[TBL] [Abstract][Full Text] [Related]
5. SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype.
Peall KJ; Kurian MA; Wardle M; Waite AJ; Hedderly T; Lin JP; Smith M; Whone A; Pall H; White C; Lux A; Jardine PE; Lynch B; Kirov G; O'Riordan S; Samuel M; Lynch T; King MD; Chinnery PF; Warner TT; Blake DJ; Owen MJ; Morris HR
J Neurol; 2014 Dec; 261(12):2296-304. PubMed ID: 25209853
[TBL] [Abstract][Full Text] [Related]
6. DRD1 rare variants associated with tardive-like dystonia: a pilot pathway sequencing study in dystonia.
Groen JL; Ritz K; Warner TT; Baas F; Tijssen MA
Parkinsonism Relat Disord; 2014 Jul; 20(7):782-5. PubMed ID: 24768614
[TBL] [Abstract][Full Text] [Related]
7. Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes.
Kumar KR; Davis RL; Tchan MC; Wali GM; Mahant N; Ng K; Kotschet K; Siow SF; Gu J; Walls Z; Kang C; Wali G; Levy S; Phua CS; Yiannikas C; Darveniza P; Chang FCF; Morales-Briceño H; Rowe DB; Drew A; Gayevskiy V; Cowley MJ; Minoche AE; Tisch S; Hayes M; Kummerfeld S; Fung VSC; Sue CM
Parkinsonism Relat Disord; 2019 Dec; 69():111-118. PubMed ID: 31731261
[TBL] [Abstract][Full Text] [Related]
8. Clinical and genetic profile of patients with dystonia: An experience from a tertiary neurology center from India.
Dhar D; Holla VV; Kumari R; Yadav R; Kamble N; Muthusamy B; Pal PK
Parkinsonism Relat Disord; 2024 Mar; 120():105986. PubMed ID: 38219528
[TBL] [Abstract][Full Text] [Related]
9.
Li S; Wang L; Yang Y; Ma J; Wan X
Front Neurol; 2019; 10():1351. PubMed ID: 32116979
[No Abstract] [Full Text] [Related]
10. Novel Dystonia Genes: Clues on Disease Mechanisms and the Complexities of High-Throughput Sequencing.
Domingo A; Erro R; Lohmann K
Mov Disord; 2016 Apr; 31(4):471-7. PubMed ID: 26991507
[TBL] [Abstract][Full Text] [Related]
11. Prenatal Genetic Testing for Dopa-Responsive Dystonia - Clinical Judgment in the Context of Next Generation Sequencing.
Nedelea F; Veduta A; Duta S; Vayna AM; Panaitescu A; Peltecu G; Duba HC
J Med Life; 2018; 11(4):343-345. PubMed ID: 30894892
[TBL] [Abstract][Full Text] [Related]
12. Clinically relevant copy-number variants in exome sequencing data of patients with dystonia.
Zech M; Boesch S; Škorvánek M; Necpál J; Švantnerová J; Wagner M; Dincer Y; Sadr-Nabavi A; Serranová T; Rektorová I; Havránková P; Ganai S; Mosejová A; Příhodová I; Šarláková J; Kulcsarová K; Ulmanová O; Bechyně K; Ostrozovičová M; Haň V; Ventosa JR; Shariati M; Shoeibi A; Weber S; Mollenhauer B; Trenkwalder C; Berutti R; Strom TM; Ceballos-Baumann A; Mall V; Haslinger B; Jech R; Winkelmann J
Parkinsonism Relat Disord; 2021 Mar; 84():129-134. PubMed ID: 33611074
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. The expanding clinical and genetic spectrum of ANO3 dystonia.
Jiang LT; Li LX; Liu Y; Zhang XL; Pan YG; Wang L; Wan XH; Jin LJ
Neurosci Lett; 2021 Feb; 746():135590. PubMed ID: 33388357
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited.
Dobričić V; Kresojević N; Žarković M; Tomić A; Marjanović A; Westenberger A; Cvetković D; Svetel M; Novaković I; Kostić VS
Parkinsonism Relat Disord; 2015 Oct; 21(10):1256-9. PubMed ID: 26297380
[TBL] [Abstract][Full Text] [Related]
17. [A childhood-onset rapid-onset dystonia parkinsonism family with ATP1A3 gene mutation and literatures review].
Zhang CL; Yin F; He F; Gai N; Shi ZQ; Peng J
Zhonghua Er Ke Za Zhi; 2017 Apr; 55(4):288-293. PubMed ID: 28441826
[No Abstract] [Full Text] [Related]
18. Genetics in dystonia.
Klein C
Parkinsonism Relat Disord; 2014 Jan; 20 Suppl 1():S137-42. PubMed ID: 24262166
[TBL] [Abstract][Full Text] [Related]
19. Common polymorphisms in dystonia-linked genes and susceptibility to the sporadic primary dystonias.
Newman JR; Sutherland GT; Boyle RS; Limberg N; Blum S; O'Sullivan JD; Silburn PA; Mellick GD
Parkinsonism Relat Disord; 2012 May; 18(4):351-7. PubMed ID: 22172551
[TBL] [Abstract][Full Text] [Related]
20. Increased diagnostic yield in complex dystonia through exome sequencing.
Wirth T; Tranchant C; Drouot N; Keren B; Mignot C; Cif L; Lefaucheur R; Lion-François L; Méneret A; Gras D; Roze E; Laroche C; Burbaud P; Bannier S; Lagha-Boukbiza O; Spitz MA; Laugel V; Bereau M; Ollivier E; Nitschke P; Doummar D; Rudolf G; Anheim M; Chelly J
Parkinsonism Relat Disord; 2020 May; 74():50-56. PubMed ID: 32334381
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
