156 related articles for article (PubMed ID: 37116293)
1. A novel ANO3 variant in two siblings with different phenotypes.
Esposito M; Trinchillo A; Piceci-Sparascio F; D'Asdia MC; Consoli F; De Luca A
Parkinsonism Relat Disord; 2023 Jun; 111():105413. PubMed ID: 37116293
[TBL] [Abstract][Full Text] [Related]
2. The phenotypic spectrum of DYT24 due to ANO3 mutations.
Stamelou M; Charlesworth G; Cordivari C; Schneider SA; Kägi G; Sheerin UM; Rubio-Agusti I; Batla A; Houlden H; Wood NW; Bhatia KP
Mov Disord; 2014 Jun; 29(7):928-34. PubMed ID: 24442708
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. The Clinical Spectrum of ANO3-Report of a New Family and Literature Review.
Percetti M; Zini M; Soliveri P; Cogiamanian F; Ferrara M; Orunesu E; Ranghetti A; Ferrarese C; Pezzoli G; Garavaglia B; Isaias IU; Sacilotto G
Mov Disord Clin Pract; 2024 Mar; 11(3):289-297. PubMed ID: 38284143
[TBL] [Abstract][Full Text] [Related]
5. Tremor in Primary Monogenic Dystonia.
Pandey S; Bhattad S; Dinesh S
Curr Neurol Neurosci Rep; 2021 Jul; 21(9):48. PubMed ID: 34264428
[TBL] [Abstract][Full Text] [Related]
6. Reply to: "Heterogeneous Phenotypic Evolution in ANO3-Related Dystonia Due to the Recurrent p.Glu510Lys Variant".
Romito LM; Leta V; Garavaglia B; Panteghini C; Zorzi G; Elia AE; Colucci F; Carecchio M; Eleopra R
Mov Disord; 2024 Mar; 39(3):632-633. PubMed ID: 38525607
[No Abstract] [Full Text] [Related]
7. Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review.
Lange LM; Junker J; Loens S; Baumann H; Olschewski L; Schaake S; Madoev H; Petkovic S; Kuhnke N; Kasten M; Westenberger A; Domingo A; Marras C; König IR; Camargos S; Ozelius LJ; Klein C; Lohmann K
Mov Disord; 2021 May; 36(5):1086-1103. PubMed ID: 33502045
[TBL] [Abstract][Full Text] [Related]
8. ANO3 and early-onset dyskinetic encephalopathy.
Jiménez de Domingo A; Lopez-Martín S; Albert J; Jiménez de la Peña M; Tirado P; Fernández-Mayoralas DM; Fernández-Perrone AL; Calleja-Pérez B; Martínez-García M; Álvarez S; Fernández-Jaén A
Eur J Med Genet; 2020 Dec; 63(12):104085. PubMed ID: 33045406
[TBL] [Abstract][Full Text] [Related]
9. Isolated dystonia: clinical and genetic updates.
Domingo A; Yadav R; Ozelius LJ
J Neural Transm (Vienna); 2021 Apr; 128(4):405-416. PubMed ID: 33247415
[TBL] [Abstract][Full Text] [Related]
10. A novel ANO3 variant identified in a 53-year-old woman presenting with hyperkinetic dysarthria, blepharospasm, hyperkinesias, and complex motor tics.
Blackburn PR; Zimmermann MT; Gass JM; Harris KG; Cousin MA; Boczek NJ; Ross OA; Klee EW; Brazis PW; Van Gerpen JA; Atwal PS
BMC Med Genet; 2016 Dec; 17(1):93. PubMed ID: 27919237
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. ANO3 as a Cause of Early-Onset Chorea Combined with Dystonia: Illustration of Phenotypic Evolution.
Romito LM; Leta V; Garavaglia B; Panteghini C; Zorzi G; Elia AE; Colucci F; Carecchio M; Eleopra R
Mov Disord; 2024 Jan; 39(1):220-221. PubMed ID: 38073131
[No Abstract] [Full Text] [Related]
13. A novel variant in the transmembrane 4 domain of ANO3 identified in a two-year-old girl with developmental delay and tremor.
Aihara Y; Shirota M; Kikuchi A; Katata Y; Abe Y; Niihori T; Funayama R; Nakayama K; Aoki Y; Kure S
J Hum Genet; 2023 Jan; 68(1):51-54. PubMed ID: 36167772
[TBL] [Abstract][Full Text] [Related]
14. Heterogeneous Phenotypic Evolution in ANO3-Related Dystonia Due to the Recurrent p.Glu510Lys Variant.
Indelicato E; Boesch S; Zech M
Mov Disord; 2024 Mar; 39(3):631-632. PubMed ID: 38525591
[No Abstract] [Full Text] [Related]
15. Genetic spectrum and clinical features in a cohort of Chinese patients with isolated dystonia.
Li LX; Liu Y; Huang JH; Yang Y; Pan YG; Zhang XL; Pan LZ; Jin LJ
Clin Genet; 2023 Apr; 103(4):459-465. PubMed ID: 36648081
[TBL] [Abstract][Full Text] [Related]
16. Early-onset generalized dystonia starting in the lower extremities in a patient with a novel ANO3 variant.
Yoo D; Kim HJ; Lee JS; Lee S; Kim SY; Choi M; Chae JH; Jeon B
Parkinsonism Relat Disord; 2018 May; 50():124-125. PubMed ID: 29449182
[No Abstract] [Full Text] [Related]
17. Role of ANO3 mutations in dystonia: A large-scale mutational screening study.
Olschewski L; Jesús S; Kim HJ; Tunc S; Löns S; Junker J; Zeuner KE; Kühn AA; Kuhlenbäumer G; Schäffer E; Berg D; Kasten M; Ferbert A; Altenmüller E; Brüggemann N; Bauer P; Rolfs A; Jeon B; Bäumer T; Mir P; Klein C; Lohmann K
Parkinsonism Relat Disord; 2019 May; 62():196-200. PubMed ID: 30712998
[TBL] [Abstract][Full Text] [Related]
18. Dystonic Tremor in Adult-onset DYT-KMT2B.
Shimazaki R; Ikezawa J; Okiyama R; Azuma K; Akagawa H; Takahashi K
Intern Med; 2022 Aug; 61(15):2357-2360. PubMed ID: 35022352
[TBL] [Abstract][Full Text] [Related]
19. Craniocervical dystonia with levodopa-responsive parkinsonism co-segregating with a pathogenic ANO3 mutation in a Taiwanese family.
Kuo MC; Lin HI; Lin CH
Parkinsonism Relat Disord; 2019 May; 62():236-238. PubMed ID: 30692049
[No Abstract] [Full Text] [Related]
20. Broadening the clinical spectrum: molecular mechanisms and new phenotypes of ANO3-dystonia.
Ousingsawat J; Talbi K; Gómez-Martín H; Koy A; Fernández-Jaén A; Tekgül H; Serdaroğlu E; Schreiber R; Ortigoza-Escobar JD; Kunzelmann K
Brain; 2023 Dec; ():. PubMed ID: 38079528
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
