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Scientific Reports|March 6, 2019
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's DiseaseEman Al Yemni, Dorota Monies, Thamer Alkhairallah, et al.
Surgical Neurology International|July 5, 2021
Effect of cranioplasty timing on the functional neurological outcome and postoperative complicationsAhmed Aloraidi, Ali Alkhaibary, Ahoud Alharbi, et al.
Nature Genetics|September 6, 2003
Mutations in NHLRC1 cause progressive myoclonus epilepsyElayne M Chan, Edwin J Young, Leonarda Ianzano, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 16, 2015
Strategies for treatment of dystoniaDirk Dressler, Eckart Altenmueller, Roongroj Bhidayasiri, et al.
American Journal of Human Genetics|November 26, 2008
Mutations in C2orf37, encoding a nucleolar protein, cause hypogonadism, alopecia, diabetes mellitus, mental retardation, and extrapyramidal syndromeAnas M Alazami, Amr Al-Saif, Abdulaziz Al-Semari, et al.
Journal of Movement Disorders|June 13, 2023
Nine Hereditary Movement Disorders First Described in Asia: Their History and EvolutionPriya Jagota, Yoshikazu Ugawa, Zakiyah Aldaajani, et al.
Journal of Neurology|February 10, 2018
Defining spasticity: a new approach considering current movement disorders terminology and botulinum toxin therapyDirk Dressler, Roongroj Bhidayasiri, Saeed Bohlega, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|February 26, 2021
Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticityDirk Dressler, Maria Concetta Altavista, Eckart Altenmueller, et al.
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