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Fayçal Hentati

Affiliations: 
Neurology Institut National de Neurologie, Tunis, Tunis, Tunisia 
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"Fayçal Hentati"
Mean distance: 20 (cluster 3)
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Parents

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Mongi Ben Hamida grad student Institut National de Neurologie

Children

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Senda Ajroud-Driss grad student Institut National de Neurologie

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BETA: Related publications

Publications

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Hammer MB, Ding J, Mochel F, et al. (2017) SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families. Neuro-Degenerative Diseases. 17: 208-212
Trinh J, Gustavsson EK, Vilariño-Güell C, et al. (2016) DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study. The Lancet. Neurology
El Euch-Fayache G, Bouhlal Y, Amouri R, et al. (2014) Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency. Brain : a Journal of Neurology. 137: 402-10
Vilariño-Güell C, Rajput A, Milnerwood AJ, et al. (2014) DNAJC13 mutations in Parkinson disease. Human Molecular Genetics. 23: 1794-801
Hammer MB, El Euch-Fayache G, Nehdi H, et al. (2014) Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 21: 311-5
Heckman MG, Soto-Ortolaza AI, Aasly JO, et al. (2013) Population-specific frequencies for LRRK2 susceptibility variants in the Genetic Epidemiology of Parkinson's Disease (GEO-PD) Consortium. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 1740-4
Trinh J, Vilariño-Güell C, Donald A, et al. (2013) STX6 rs1411478 is not associated with increased risk of Parkinson's disease. Parkinsonism & Related Disorders. 19: 563-5
Hammer MB, Eleuch-Fayache G, Schottlaender LV, et al. (2013) Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity. American Journal of Human Genetics. 92: 245-51
Ben Ammar A, Soltanzadeh P, Bauché S, et al. (2013) A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia. Plos One. 8: e53826
Hammer MB, Eleuch-Fayache G, Gibbs JR, et al. (2013) Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 20: 486-92
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