Fayçal Hentati

Affiliations: 
Neurology Institut National de Neurologie, Tunis, Tunis, Tunisia 
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"Fayçal Hentati"
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Publications

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Nabli F, Ben Sassi S, Amouri R, et al. (2015) Motor phenotype of LRRK2-associated Parkinson's disease: a tunisian longitudinal study. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 253-8
Arous A, Riahi A, Walha K, et al. (2015) Acute oculomotor nerve palsy revealing a neurovascular conflict: Contribution of MRI | Paralysie brutale du nerf oculomoteur commun révélant un conflit vasculo-nerveux: Intérêt de l'IRM Pratique Neurologique - Fmc. 6: 274-276
Trinh J, Gustavsson EK, Guella I, et al. (2014) The role of SNCA and MAPT in Parkinson disease and LRRK2 parkinsonism in the Tunisian Arab-Berber population. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 21: e91-2
Sassi SB, Nabli F, Boubaker A, et al. (2014) Pseudotumoral brain lesion as the presenting feature of primary Sjögren's syndrome. Journal of the Neurological Sciences. 339: 214-6
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
Hentati F, Hentati E, Amouri R. (2013) Giant axonal neuropathy. Handbook of Clinical Neurology. 115: 933-8
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
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