Hentati F - Search Results

1

Hentati F, Hentati E, Amouri R. Hentati F, et al. Among authors: hentati e. Handb Clin Neurol. 2013;115:933-8. doi: 10.1016/B978-0-444-52902-2.00052-7. Handb Clin Neurol. 2013. PMID: 23931822 Review.

2

Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency.

El Euch-Fayache G, Bouhlal Y, Amouri R, Feki M, Hentati F. El Euch-Fayache G, et al. Among authors: hentati f. Brain. 2014 Feb;137(Pt 2):402-10. doi: 10.1093/brain/awt339. Epub 2013 Dec 25. Brain. 2014. PMID: 24369383

3

Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.

El Euch-Fayache G, Lalani I, Amouri R, Turki I, Ouahchi K, Hung WY, Belal S, Siddique T, Hentati F. El Euch-Fayache G, et al. Among authors: hentati f. Arch Neurol. 2003 Jul;60(7):982-8. doi: 10.1001/archneur.60.7.982. Arch Neurol. 2003. PMID: 12873855

4

Ataxia with vitamin E deficiency and abetalipoproteinemia.

Hentati F, El-Euch G, Bouhlal Y, Amouri R. Hentati F, et al. Handb Clin Neurol. 2012;103:295-305. doi: 10.1016/B978-0-444-51892-7.00018-8. Handb Clin Neurol. 2012. PMID: 21827896 Review. No abstract available.

5

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study.

Trinh J, Gustavsson EK, Vilariño-Güell C, Bortnick S, Latourelle J, McKenzie MB, Tu CS, Nosova E, Khinda J, Milnerwood A, Lesage S, Brice A, Tazir M, Aasly JO, Parkkinen L, Haytural H, Foroud T, Myers RH, Sassi SB, Hentati E, Nabli F, Farhat E, Amouri R, Hentati F, Farrer MJ. Trinh J, et al. Among authors: hentati e, hentati f. Lancet Neurol. 2016 Nov;15(12):1248-1256. doi: 10.1016/S1474-4422(16)30203-4. Epub 2016 Sep 28. Lancet Neurol. 2016. PMID: 27692902

6

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.

Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F. Mrissa N, et al. Among authors: hentati f. Neurology. 2000 Apr 11;54(7):1408-14. doi: 10.1212/wnl.54.7.1408. Neurology. 2000. PMID: 10751248 Clinical Trial.

7

Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3.

Barhoumi C, Amouri R, Ben Hamida C, Ben Hamida M, Machghoul S, Gueddiche M, Hentati F. Barhoumi C, et al. Among authors: hentati f. Neuromuscul Disord. 2001 Jan;11(1):27-34. doi: 10.1016/s0960-8966(00)00162-0. Neuromuscul Disord. 2001. PMID: 11166163

8

Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.

Bouhlal Y, Zouari M, Kefi M, Ben Hamida C, Hentati F, Amouri R. Bouhlal Y, et al. Among authors: hentati f. J Neurogenet. 2008;22(2):139-48. doi: 10.1080/01677060802025233. J Neurogenet. 2008. PMID: 18569450

9

A novel SACS gene mutation in a Tunisian family.

Bouhlal Y, El Euch-Fayeche G, Hentati F, Amouri R. Bouhlal Y, et al. Among authors: hentati f. J Mol Neurosci. 2009 Nov;39(3):333-6. doi: 10.1007/s12031-009-9212-9. Epub 2009 Jun 16. J Mol Neurosci. 2009. PMID: 19529988

10

Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosis.

Amouri R, Nehdi H, Bouhlal Y, Kefi M, Larnaout A, Hentati F. Amouri R, et al. Among authors: hentati f. J Mol Neurosci. 2009 Nov;39(3):337-41. doi: 10.1007/s12031-009-9217-4. Epub 2009 Jul 25. J Mol Neurosci. 2009. PMID: 19633821

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