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Neurology. Genetics|December 30, 2020
Who and Why? Requests for Presymptomatic Genetic Testing for Amyotrophic Lateral Sclerosis/Frontotemporal Dementia vs Huntington DiseaseMaria Del Mar Amador, Marcela Gargiulo, Christilla Boucher, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|August 16, 2014
Cerebellar abnormalities in Huntington's disease: a role in motor and psychiatric impairment?Elin M Rees, Ruth Farmer, James H Cole, et al.
Brain : a Journal of Neurology|June 14, 2003
Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genesGiovanni Stevanin, Hiroto Fujigasaki, Anne-Sophie Lebre, et al.
Plos One|March 26, 2009
Neuroendocrine disturbances in Huntington's diseaseNadine Saleh, Stéphane Moutereau, Alexandra Durr, et al.
Neurogenetics|June 29, 2007
A de novo SPAST mutation leading to somatic mosaicism is associated with a later age at onset in HSPChristel Depienne, Estelle Fedirko, Jean-Marc Faucheux, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 28, 2024
Digital Gait Measures Capture 1-Year Progression in Early-Stage Spinocerebellar Ataxia Type 2Jens Seemann, Lina Daghsen, Matthieu Cazier, et al.
Annals of Neurology|March 24, 2005
Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28)Naima Bouslam, Ali Benomar, Hamid Azzedine, et al.
Archives of Neurology|April 17, 2008
Rapid eye movement sleep disturbances in Huntington diseaseIsabelle Arnulf, Jørgen Nielsen, Ebba Lohmann, et al.
Human Mutation|October 15, 2008
Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10Cyril Goizet, Amir Boukhris, Emeline Mundwiller, et al.
Frontiers in Neurology|October 26, 2017
Recommendations for the Use of Automated Gray Matter Segmentation Tools: Evidence from Huntington's DiseaseEileanoir B Johnson, Sarah Gregory, Hans J Johnson, et al.
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