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Movement Disorders : Official Journal of the Movement Disorder Society|September 8, 2006
Developments in neuroacanthocytosis: expanding the spectrum of choreatic syndromesRuth H Walker, Adrian Danek, Carol Dobson-Stone, et al.
Archives of Neurology|October 12, 2011
Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindredAntonio Velayos-Baeza, Elke Holinski-Feder, Birgit Neitzel, et al.
Investigative Ophthalmology & Visual Science|April 13, 2026
The Genetic Landscape of Inherited Retinal Diseases in the Israeli PopulationSapir Shalom, Libe Gradstein, Eran Pras, et al.
Medrxiv : the Preprint Server for Health Sciences|March 17, 2025
Lesion network localization of functional and somatic symptomsBeatrice Annunziata Milano, Stephan Palm, Matthew J Burke, et al.
Developmental Medicine and Child Neurology|November 3, 2010
Mirror movements in healthy humans across the lifespan: effects of development and ageingInga Koerte, Lara Eftimov, Ruediger Paul Laubender, et al.
Frontiers in Physiology|April 11, 2025
Red blood cell lipid distribution in the pathophysiology and laboratory evaluation of chorea-acanthocytosis and McLeod syndrome patientsAnne-Sophie Cloos, Marine Ghodsi, Amaury Stommen, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|June 25, 2017
Frontotemporal lobar degeneration and social behaviour: Dissociation between the knowledge of its consequences and its conceptual meaningRoland Zahn, Sophie Green, Helen Beaumont, et al.
Journal of Geriatric Psychiatry and Neurology|November 7, 2022
Demographic and Symptom Correlates of Initial Idiopathic Psychiatric Diagnosis in Frontotemporal DementiaCorinne Sejourne, Jordan D Dworkin, Megan S Barker, et al.
Neuro-Degenerative Diseases|March 7, 2008
In vivo and postmortem clinicoanatomical correlations in frontotemporal dementia and parkinsonism linked to chromosome 17Bernardino Ghetti, Salvatore Spina, Jill R Murrell, et al.
European Journal of Human Genetics : EJHG|February 7, 2019
SCAPER localizes to primary cilia and its mutation affects cilia length, causing Bardet-Biedl syndromeOhad Wormser, Libe Gradstein, Yuval Yogev, et al.
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