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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

138 related articles for article (PubMed ID: 37131084)

  • 1. Perampanel as a novel treatment for subcortical myoclonus in myoclonus-dystonia syndrome.
    Belli E; Del Prete E; Unti E; Mazzucchi S; Palermo G; Ceravolo R
    Neurol Sci; 2023 Aug; 44(8):2943-2945. PubMed ID: 37131084
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A Case Report of Myoclonus-Dystonia with Isolated Myoclonus Phenotype and Novel Mutation Successfully Treated with Deep Brain Stimulation.
    Besa Lehmann V; Rosenbaum M; Bulman DE; Read T; Verhagen Metman L
    Neurol Ther; 2020 Jun; 9(1):187-191. PubMed ID: 32274660
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [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]  

  • 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. Myoclonus-dystonia and epilepsy in a family with a novel epsilon-sarcoglycan mutation.
    Haugarvoll K; Tzoulis C; Tran GT; Karlsen B; Engelsen BA; Knappskog PM; Bindoff LA
    J Neurol; 2014 Feb; 261(2):358-62. PubMed ID: 24297365
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Bilateral Pallidal Stimulation in a Family With Myoclonus Dystonia Syndrome Due to a Mutation in the Sarcoglycan Gene.
    Sobstyl M; Stapińska-Syniec A; Zaremba J; Jurek M; Kupryjaniuk A; Rylski M
    Neuromodulation; 2022 Aug; 25(6):918-924. PubMed ID: 33497502
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Improvement of Isolated Myoclonus Phenotype in Myoclonus Dystonia after Pallidal Deep Brain Stimulation.
    Ramdhani RA; Frucht SJ; Behnegar A; Kopell BH
    Tremor Other Hyperkinet Mov (N Y); 2016; 6():369. PubMed ID: 26989574
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Twenty years on: Myoclonus-dystonia and ε-sarcoglycan - neurodevelopment, channel, and signaling dysfunction.
    Menozzi E; Balint B; Latorre A; Valente EM; Rothwell JC; Bhatia KP
    Mov Disord; 2019 Nov; 34(11):1588-1601. PubMed ID: 31449710
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myoclonus-dystonia: clinical and electrophysiologic pattern related to SGCE mutations.
    Roze E; Apartis E; Clot F; Dorison N; Thobois S; Guyant-Marechal L; Tranchant C; Damier P; Doummar D; Bahi-Buisson N; André-Obadia N; Maltete D; Echaniz-Laguna A; Pereon Y; Beaugendre Y; Dupont S; De Greslan T; Jedynak CP; Ponsot G; Dussaule JC; Brice A; Dürr A; Vidailhet M
    Neurology; 2008 Mar; 70(13):1010-6. PubMed ID: 18362280
    [TBL] [Abstract][Full Text] [Related]  

  • 13. ε-Sarcoglycan: Unraveling the Myoclonus-Dystonia Gene.
    Cazurro-Gutiérrez A; Marcé-Grau A; Correa-Vela M; Salazar A; Vanegas MI; Macaya A; Bayés À; Pérez-Dueñas B
    Mol Neurobiol; 2021 Aug; 58(8):3938-3952. PubMed ID: 33886091
    [TBL] [Abstract][Full Text] [Related]  

  • 14. "Jerky" dystonia in children: spectrum of phenotypes and genetic testing.
    Asmus F; Langseth A; Doherty E; Nestor T; Munz M; Gasser T; Lynch T; King MD
    Mov Disord; 2009 Apr; 24(5):702-9. PubMed ID: 19117362
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical and neurophysiological improvement of SGCE myoclonus-dystonia with GPi deep brain stimulation.
    Kurtis MM; San Luciano M; Yu Q; Goodman RR; Ford B; Raymond D; Pullman SL; Saunders-Pullman R
    Clin Neurol Neurosurg; 2010 Feb; 112(2):149-52. PubMed ID: 19896264
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Distribution and Coexistence of Myoclonus and Dystonia as Clinical Predictors of SGCE Mutation Status: A Pilot Study.
    Zutt R; Dijk JM; Peall KJ; Speelman H; Dreissen YE; Contarino MF; Tijssen MA
    Front Neurol; 2016; 7():72. PubMed ID: 27242657
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Add-on perampanel in Lance-Adams syndrome.
    Steinhoff BJ; Bacher M; Kurth C; Staack AM; Kornmeier R
    Epilepsy Behav Case Rep; 2016; 6():28-9. PubMed ID: 27437182
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.