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.
193 related articles for article (PubMed ID: 30849405)
21. The neurophysiological features of myoclonus-dystonia and differentiation from other dystonias. Popa T; Milani P; Richard A; Hubsch C; Brochard V; Tranchant C; Sadnicka A; Rothwell J; Vidailhet M; Meunier S; Roze E JAMA Neurol; 2014 May; 71(5):612-9. PubMed ID: 24638021 [TBL] [Abstract][Full Text] [Related]
22. Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype. Asmus F; Zimprich A; Tezenas Du Montcel S; Kabus C; Deuschl G; Kupsch A; Ziemann U; Castro M; Kühn AA; Strom TM; Vidailhet M; Bhatia KP; Dürr A; Wood NW; Brice A; Gasser T Ann Neurol; 2002 Oct; 52(4):489-92. PubMed ID: 12325078 [TBL] [Abstract][Full Text] [Related]
23. Genomic deletion size at the epsilon-sarcoglycan locus determines the clinical phenotype. Asmus F; Hjermind LE; Dupont E; Wagenstaller J; Haberlandt E; Munz M; Strom TM; Gasser T Brain; 2007 Oct; 130(Pt 10):2736-45. PubMed ID: 17898012 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. 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]
26. SGCZ mutations are unlikely to be associated with myoclonus dystonia. Peall KJ; Ritz K; Waite AJ; Groen JL; Morris HR; Baas F; Blake DJ; Tijssen MA Neuroscience; 2014 Jul; 272():88-91. PubMed ID: 24792710 [TBL] [Abstract][Full Text] [Related]
27. A novel SGCE gene mutation causing myoclonus dystonia in a family with an unusual phenotype. Tedroff K; Rolfs A; Norling A Acta Paediatr; 2012 Feb; 101(2):e90-2. PubMed ID: 22026499 [TBL] [Abstract][Full Text] [Related]
29. The epsilon-sarcoglycan gene in myoclonic syndromes. Valente EM; Edwards MJ; Mir P; DiGiorgio A; Salvi S; Davis M; Russo N; Bozi M; Kim HT; Pennisi G; Quinn N; Dallapiccola B; Bhatia KP Neurology; 2005 Feb; 64(4):737-9. PubMed ID: 15728306 [TBL] [Abstract][Full Text] [Related]
30. Cortical neuronal hyperexcitability and synaptic changes in SGCE mutation-positive myoclonus dystonia. Sperandeo A; Tamburini C; Noakes Z; de la Fuente DC; Keefe F; Petter O; Plumbly W; Clifton NE; Li M; Peall KJ Brain; 2023 Apr; 146(4):1523-1541. PubMed ID: 36204995 [TBL] [Abstract][Full Text] [Related]
31. Psychiatric symptoms in myoclonus-dystonia syndrome are just concomitant features regardless of the SGCE gene mutation. Kim JY; Lee WW; Shin CW; Kim HJ; Park SS; Chung SJ; Cho JW; Ryu HS; Son TO; Jeon B Parkinsonism Relat Disord; 2017 Sep; 42():73-77. PubMed ID: 28690014 [TBL] [Abstract][Full Text] [Related]
32. 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]
33. Earlier onset of motor deficits in mice with double mutations in Dyt1 and Sgce. Yokoi F; Yang G; Li J; DeAndrade MP; Zhou T; Li Y J Biochem; 2010 Oct; 148(4):459-66. PubMed ID: 20627944 [TBL] [Abstract][Full Text] [Related]
34. Pallidal deep brain stimulation for patients with myoclonus-dystonia without SGCE mutations. Ikezawa J; Yokochi F; Okiyama R; Isoo A; Agari T; Kamiyama T; Yugeta A; Tojima M; Kawasaki T; Watanabe K; Kumada S; Takahashi K J Neurol; 2024 Jun; 271(6):2948-2954. PubMed ID: 38575756 [TBL] [Abstract][Full Text] [Related]
36. Myoclonus-dystonia due to maternal uniparental disomy. Guettard E; Portnoi MF; Lohmann-Hedrich K; Keren B; Rossignol S; Winkler S; El Kamel I; Leu S; Apartis E; Vidailhet M; Klein C; Roze E Arch Neurol; 2008 Oct; 65(10):1380-5. PubMed ID: 18852357 [TBL] [Abstract][Full Text] [Related]
37. Delineating the motor phenotype of SGCE-myoclonus dystonia syndrome. Vanegas MI; Marcé-Grau A; Martí-Sánchez L; Mellid S; Baide-Mairena H; Correa-Vela M; Cazurro A; Rodríguez C; Toledo L; Fernández-Ramos JA; Pons R; Aguilera-Albesa S; Martí MJ; Eiris J; Iglesias G; De Fabregues O; Maqueda E; Garriz-Luis M; Madruga M; Espinós C; Macaya A; Cabrera JC; Pérez-Dueñas B Parkinsonism Relat Disord; 2020 Nov; 80():165-174. PubMed ID: 33022436 [TBL] [Abstract][Full Text] [Related]
38. Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation. Maréchal L; Raux G; Dumanchin C; Lefebvre G; Deslandre E; Girard C; Campion D; Parain D; Frebourg T; Hannequin D Am J Med Genet B Neuropsychiatr Genet; 2003 May; 119B(1):114-7. PubMed ID: 12707948 [TBL] [Abstract][Full Text] [Related]
39. Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers. Hess CW; Raymond D; Aguiar Pde C; Frucht S; Shriberg J; Heiman GA; Kurlan R; Klein C; Bressman SB; Ozelius LJ; Saunders-Pullman R Neurology; 2007 Feb; 68(7):522-4. PubMed ID: 17296918 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]