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.
158 related articles for article (PubMed ID: 25868953)
1. Japanese familial case of myoclonus-dystonia syndrome with a splicing mutation in SGCE. Wada T; Takano K; Tsurusaki Y; Miyake N; Nakashima M; Saitsu H; Matsumoto N; Osaka H Pediatr Int; 2015 Apr; 57(2):324-6. PubMed ID: 25868953 [TBL] [Abstract][Full Text] [Related]
2. Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes. Tezenas du Montcel S; Clot F; Vidailhet M; Roze E; Damier P; Jedynak CP; Camuzat A; Lagueny A; Vercueil L; Doummar D; Guyant-Maréchal L; Houeto JL; Ponsot G; Thobois S; Cournelle MA; Durr A; Durif F; Echenne B; Hannequin D; Tranchant C; Brice A; J Med Genet; 2006 May; 43(5):394-400. PubMed ID: 16227522 [TBL] [Abstract][Full Text] [Related]
3. [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]
4. Screening for SGCE mutations in Moroccan sporadic patients with Myoclonus-Dystonia syndrome. Rachad L; El Otmani H; Karkar A; El Moutawakil B; El Kadmiri N; Nadifi S Neurosci Lett; 2019 Jun; 703():1-4. PubMed ID: 30849405 [TBL] [Abstract][Full Text] [Related]
5. Gait Impairment in Myoclonus-Dystonia (DYT- Haeri G; Shahidi G; Fasano A; Rohani M Tremor Other Hyperkinet Mov (N Y); 2019; 9():. PubMed ID: 31413899 [TBL] [Abstract][Full Text] [Related]
6. SGCE missense mutations that cause myoclonus-dystonia syndrome impair epsilon-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA. Esapa CT; Waite A; Locke M; Benson MA; Kraus M; McIlhinney RA; Sillitoe RV; Beesley PW; Blake DJ Hum Mol Genet; 2007 Feb; 16(3):327-42. PubMed ID: 17200151 [TBL] [Abstract][Full Text] [Related]
7. Delayed Diagnoses of Varga MG; Nand NP; LeDoux MS Tremor Other Hyperkinet Mov (N Y); 2020 Jul; 10():23. PubMed ID: 32775037 [TBL] [Abstract][Full Text] [Related]
8. Pediatric writer's cramp in myoclonus-dystonia: maternal imprinting hides positive family history. Gerrits MC; Foncke EM; Koelman JH; Tijssen MA Eur J Paediatr Neurol; 2009 Mar; 13(2):178-80. PubMed ID: 18571946 [TBL] [Abstract][Full Text] [Related]
9. A novel SGCE variant is associated with myoclonus-dystonia with phenotypic variability. Delgado-Alvarado M; Matilla-Dueñas A; Altadill-Bermejo A; Setién S; Misiego-Peral M; Sánchez-de la Torre JR; Corral-Juan M; Riancho J Neurol Sci; 2020 Dec; 41(12):3779-3781. PubMed ID: 32955639 [TBL] [Abstract][Full Text] [Related]
11. Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome. Zimprich A; Grabowski M; Asmus F; Naumann M; Berg D; Bertram M; Scheidtmann K; Kern P; Winkelmann J; Müller-Myhsok B; Riedel L; Bauer M; Müller T; Castro M; Meitinger T; Strom TM; Gasser T Nat Genet; 2001 Sep; 29(1):66-9. PubMed ID: 11528394 [TBL] [Abstract][Full Text] [Related]
12. A mixed-ethnicity myoclonus-dystonia patient with a novel SGCE nonsense mutation: a case report. de Leon MAJ; Rosales RL; Klein C; Westenberger A BMC Neurol; 2022 Jan; 22(1):11. PubMed ID: 34986800 [TBL] [Abstract][Full Text] [Related]
13. A novel conserved mutation in SGCE gene in 3 unrelated patients with classical phenotype myoclonus-dystonia syndrome. Szubiga M; Rudzińska M; Bik-Multanowski M; Pietrzyk JJ; Szczudlik A Neurol Res; 2013 Jul; 35(6):659-62. PubMed ID: 23561547 [TBL] [Abstract][Full Text] [Related]
14. 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]
17. Mutation in ε-Sarcoglycan Induces a Myoclonus-Dystonia Syndrome-Like Movement Disorder in Mice. Li J; Liu Y; Li Q; Huang X; Zhou D; Xu H; Zhao F; Mi X; Wang R; Jia F; Xu F; Yang J; Liu D; Deng X; Zhang Y Neurosci Bull; 2021 Mar; 37(3):311-322. PubMed ID: 33355901 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. Abnormal nuclear envelopes in the striatum and motor deficits in DYT11 myoclonus-dystonia mouse models. Yokoi F; Dang MT; Zhou T; Li Y Hum Mol Genet; 2012 Feb; 21(4):916-25. PubMed ID: 22080833 [TBL] [Abstract][Full Text] [Related]
20. A novel mutation of the epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome. Chen XP; Zhang YW; Zhang SS; Chen Q; Burgunder JM; Wu SH; Yang Y; Luo ZM; Shang HF Mov Disord; 2008 Jul; 23(10):1472-5. PubMed ID: 18581468 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]