1. RyR1-related myopathy mutations in ATP and calcium binding sites impair channel regulation Yuan, Qi; Dridi, Haikel; Clarke, Oliver B.; Reiken, Steven; Melville, Zephan; Wronska, Anetta; Kushnir, Alexander; Zalk, Ran; Sittenfeld, Leah; Marks, Andrew R. 2021 Articles Muscles--DiseasesCytologyBiology
2. Cervical Dystonia Mimics: A Case Series and Review of the Literature Raju, Srinivas; Ravi, Amogh; Prashanth, L.K. 2019 Articles DystoniaMuscles--DiseasesDiagnostic errorsTorticollisNeurosciences
3. Generalized Dystonia and Paroxysmal Dystonic Attacks due to a Novel ATP1A3 Variant Zúñiga-Ramírez, Carlos; Kramis-Hollands, Mirelle; Mercado-Pimente, Rodrigo; González-Usigli, Héctor Alberto; Sáenz-Farret, Michel; Soto-Escageda, Alberto; Fasano, Alfonso 2019 Articles Movement disorders--EtiologyDystoniaMuscles--DiseasesNervous system--Diseases--Genetic aspectsParkinson's disease
4. Dystonia Associated with Idiopathic Slow Orthostatic Tremor Kobylecki, Christopher; Silverdale, Monty A.; Dick, Jeremy P. R.; Kellett, Mark W.; Marshall, Andrew G. 2016 Articles Movement disordersElectrophysiologyDystoniaMuscles--DiseasesNeurophysiologyTremorNeurosciencesMedicine
5. A Wide Range of 3243A>G/tRNALeu(UUR) (MELAS) Mutation Loads May Segregate in Offspring through the Female Germline Bottleneck Pallotti, Francesco; Binelli, Giorgio; Fabbri, Raffaella; Valentino, Maria L.; Vicenti, Rossella; Macciocca, Maria; Cevoli, Sabina; Baruzzi, Agostino; DiMauro, Salvatore; Carelli, Valerio 2014 Articles OvumMuscles--DiseasesMusculoskeletal systemEpitheliumMitochondrial DNAGenetics