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Therapeutic Advances in Rare Disease|July 31, 2024
Koolen-de Vries Syndrome: a journey from diagnosis to treatmentsAnna C Pfalzer, Blake Ivers, Alayna Haynam, et al.
Angiology|April 8, 2003
The LONFLIT4--Concorde Deep Venous Thrombosis and Edema Study: prevention with travel stockingsMaria Rosaria Cesarone, Gianni Belcaro, Bruno M Errichi, et al.
Journal of Neurology|April 29, 2023
The phenotypic spectrum of epilepsy associated with periventricular nodular heterotopiaKarina Paliotti, Christelle Dassi, Saoussen Berrahmoune, et al.
Epilepsy Research|January 9, 2021
Contribution of rare genetic variants to drug response in absence epilepsyKenneth A Myers, Mark F Bennett, Bronwyn E Grinton, et al.
European Journal of Human Genetics : EJHG|November 25, 2025
Identification of an episignature for the MEF2C-associated syndromeAnanília Silva, Sadegheh Haghshenas, Liselot van der Laan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 5, 2024
Defining the Genetic Landscape of Congenital Mirror Movements in 80 Affected IndividualsMeagan L Collins Hutchinson, Judith St-Onge, Sabrina Schlienger, et al.
Annals of Neurology|October 17, 2019
The Genetic Landscape of Epilepsy of Infancy with Migrating Focal SeizuresRosemary Burgess, Shuyu Wang, Amy McTague, et al.
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