1 - 25 of 34 results for author:"Hentati F." in Literature citations
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| Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's disease. Ben Sassi S., Nabli F., Hentati E., Nahdi H., Trabelsi M., Ben Ayed H., Amouri R., Duda J.E., Farrer M.J., Hentati F. Parkinsonism Relat. Disord. 18:243-246(2012) · Mapped (4) |
| Translation initiator EIF4G1 mutations in familial Parkinson disease. Chartier-Harlin M.C., Dachsel J.C., Vilarino-Guell C., Lincoln S.J., Lepretre F., Hulihan M.M., Kachergus J., Milnerwood A.J., Tapia L., Song M.S. et al. Am. J. Hum. Genet. 89:398-406(2011) · UniProtKB (1) · Mapped (9) |
| VPS35 mutations in Parkinson disease. Vilarino-Guell C., Wider C., Ross O.A., Dachsel J.C., Kachergus J.M., Lincoln S.J., Soto-Ortolaza A.I., Cobb S.A., Wilhoite G.J., Bacon J.A. et al. Am. J. Hum. Genet. 89:162-167(2011) · UniProtKB (2) · Mapped (2) |
| Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease. Nishioka K., Vilarino-Guell C., Cobb S.A., Kachergus J.M., Ross O.A., Hentati E., Hentati F., Farrer M.J. Parkinsonism Relat. Disord. 16:686-687(2010) · Mapped (6) |
| Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa. Jasinska-Myga B., Kachergus J., Vilarino-Guell C., Wider C., Soto-Ortolaza A.I., Kefi M., Middleton L.T., Ishihara-Paul L., Gibson R.A., Amouri R. et al. Mov. Disord. 25:2052-2058(2010) · Mapped (4) |
| Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7. Ben Ammar A., Petit F., Alexandri N., Gaudon K., Bauche S., Rouche A., Gras D., Fournier E., Koenig J., Stojkovic T. et al. |
| Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa. Nishioka K., Vilarino-Guell C., Cobb S.A., Kachergus J.M., Ross O.A., Wider C., Gibson R.A., Hentati F., Farrer M.J. Neurosci. Lett. 477:57-60(2010) · Mapped (1) |
| A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease. Nishioka K., Kefi M., Jasinska-Myga B., Wider C., Vilarino-Guell C., Ross O.A., Heckman M.G., Middleton L.T., Ishihara-Paul L., Gibson R.A. et al. J. Neurol. Neurosurg. Psychiatr. 81:391-395(2010) · Mapped (22) |
| A novel SACS gene mutation in a Tunisian family. Bouhlal Y., El Euch-Fayeche G., Hentati F., Amouri R. J. Mol. Neurosci. 39:333-336(2009) · UniProtKB (1) |
| Characterization of DCTN1 genetic variability in neurodegeneration. Vilarino-Gueell C., Wider C., Soto-Ortolaza A.I., Cobb S.A., Kachergus J.M., Keeling B.H., Dachsel J.C., Hulihan M.M., Dickson D.W., Wszolek Z.K. et al. |
| ATP13A2 variability in Parkinson disease. Vilarino-Guell C., Soto A.I., Lincoln S.J., Ben Yahmed S., Kefi M., Heckman M.G., Hulihan M.M., Chai H., Diehl N.N., Amouri R. et al. |
| The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa. Richard P., Gaudon K., Haddad H., Ammar A.B., Genin E., Bauche S., Paturneau-Jouas M., Muller J.S., Lochmuller H., Grid D. et al. Neurology 71:1967-1972(2008) · Mapped (2) |
| L-2-hydroxyglutaric aciduria: clinical and molecular study in three Tunisian families. Identification of a new mutation and inter-familial phenotype variability. Larnaout A., Amouri R., Kefi M., Hentati F. J. Inherit. Metab. Dis. 31 Suppl 2:S375-9(2008) · Mapped (2) |
| PINK1 mutations and parkinsonism. Ishihara-Paul L., Hulihan M.M., Kachergus J., Upmanyu R., Warren L., Amouri R., Elango R., Prinjha R.K., Soto A., Kefi M. et al. Neurology 71:896-902(2008) · Mapped (1) |
| Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutations. Kefi M., Amouri R., Chabrak S., Mechmeche R., Hentati F. Neuropediatrics 39:113-115(2008) · Mapped (1) |
| LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study. Hulihan M.M., Ishihara-Paul L., Kachergus J., Warren L., Amouri R., Elango R., Prinjha R.K., Upmanyu R., Kefi M., Zouari M. et al. Lancet Neurol 7:591-594(2008) · Mapped (4) |
| Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration. Tsaousidou M.K., Ouahchi K., Warner T.T., Yang Y., Simpson M.A., Laing N.G., Wilkinson P.A., Madrid R.E., Patel H., Hentati F. et al. Am. J. Hum. Genet. 82:510-515(2008) · UniProtKB (1) · Mapped (1) |
| A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease. Warren L., Gibson R., Ishihara L., Elango R., Xue Z., Akkari A., Ragone L., Pahwa R., Jankovic J., Nance M. et al. Parkinsonism Relat. Disord. 14:77-80(2008) · Mapped (4) |
| Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families. Ishihara L., Gibson R.A., Warren L., Amouri R., Lyons K., Wielinski C., Hunter C., Swartz J.E., Elango R., Akkari P.A. et al. Mov. Disord. 22:55-61(2007) · Mapped (4) |
| Phospholipid-hydroperoxide glutathione peroxidase (GPx-4) localization in resting platelets, and compartmental change during platelet activation. Januel C., El Hentati F.Z., Carreras M., Arthur J.R., Calzada C., Lagarde M., Vericel E. Biochim. Biophys. Acta 1761:1228-1234(2006) · Mapped (4) |
| Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations. Ishihara L., Warren L., Gibson R., Amouri R., Lesage S., Durr A., Tazir M., Wszolek Z.K., Uitti R.J., Nichols W.C. et al. Arch. Neurol. 63:1250-1254(2006) · Mapped (4) |
| Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries. Tomiyama H., Li Y., Funayama M., Hasegawa K., Yoshino H., Kubo S., Sato K., Hattori T., Lu C.S., Inzelberg R. et al. Mov. Disord. 21:1102-1108(2006) · Mapped (4) |
| Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy. Amouri R., Driss A., Murayama K., Kefi M., Nishino I., Hentati F. Neuromuscul. Disord. 15:361-363(2005) · Mapped (6) |
| Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease. Ammar N., Nelis E., Merlini L., Barisic N., Amouri R., Ceuterick C., Martin J.J., Timmerman V., Hentati F., De Jonghe P. Neuromuscul. Disord. 13:720-728(2003) · Mapped (6) |
| 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 W.Y., Belal S., Siddique T., Hentati F. Arch. Neurol. 60:982-988(2003) · UniProtKB (1) |