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Human Mutation|January 24, 2012
PCDH19-related infantile epileptic encephalopathy: an unusual X-linked inheritance disorderChristel Depienne, Eric LeGuernAmerican Journal of Human Genetics|April 3, 2021
30 years of repeat expansion disorders: What have we learned and what are the remaining challenges?Christel Depienne, Jean-Louis MandelMedizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
GC-rich repeat expansions: associated disorders and mechanismsChristopher Schröder, Bernhard Horsthemke, Christel DepienneMedizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Familial adult myoclonic epilepsy (FAME): clinical features, molecular characteristics, pathophysiological aspects and diagnostic work-upLorenz Peters, Christel Depienne, Stephan KlebeMedizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS): from clinical diagnosis towards genetic testingAndreas Thieme, Christel Depienne, Dagmar TimmannCurrent Opinion in Neurology|November 10, 2007
Hereditary spastic paraplegias: an updateChristel Depienne, Giovanni Stevanin, Alexis Brice, et al.F1000Research|May 9, 2022
Tourette syndrome research highlights from 2020Andreas Hartmann, Cyril Atkinson-Clement, Christel Depienne, et al.BMJ Neurology Open|December 26, 2025
Cerebellar ataxias and functional movement disorders: navigating clinical overlapFriedrich Erdlenbruch, Andreas Thieme, Christel Depienne, et al.Journal of Neurology|June 3, 2011
Congenital mirror movements: a clue to understanding bimanual motor controlCécile Galléa, Traian Popa, Ségolène Billot, et al.Human Mutation|December 25, 2018
A mutation update for the PCDH19 gene causing early-onset epilepsy in females with an unusual expression patternRojeen Niazi, Elizabeth A Fanning, Christel Depienne, et al.Pageof 18