Fayçal Hentati - Publications

Affiliations: 
Neurology Institut National de Neurologie, Tunis, Tunis, Tunisia 

178 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2015 Nabli F, Ben Sassi S, Amouri R, Duda JE, Farrer MJ, Hentati F. Motor phenotype of LRRK2-associated Parkinson's disease: a tunisian longitudinal study. Movement Disorders : Official Journal of the Movement Disorder Society. 30: 253-8. PMID 25487881 DOI: 10.1002/mds.26097  0.4
2015 Arous A, Riahi A, Walha K, Sebai R, Drissi C, Hammami N, Nagi S, Hentati F, Ben Hamouda M. 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. DOI: 10.1016/j.praneu.2015.02.004  0.4
2014 Trinh J, Gustavsson EK, Guella I, Vilariño-Güell C, Evans D, Encarnacion M, Sherman H, Hentati F, Farrer MJ. 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. PMID 25303626 DOI: 10.1111/ene.12489  0.4
2014 Sassi SB, Nabli F, Boubaker A, Ghorbel IB, Neji S, Hentati F. Pseudotumoral brain lesion as the presenting feature of primary Sjögren's syndrome. Journal of the Neurological Sciences. 339: 214-6. PMID 24507949 DOI: 10.1016/j.jns.2014.01.027  0.4
2014 El Euch-Fayache G, Bouhlal Y, Amouri R, Feki M, Hentati F. Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiency. Brain : a Journal of Neurology. 137: 402-10. PMID 24369383 DOI: 10.1093/brain/awt339  0.4
2014 Vilariño-Güell C, Rajput A, Milnerwood AJ, Shah B, Szu-Tu C, Trinh J, Yu I, Encarnacion M, Munsie LN, Tapia L, Gustavsson EK, Chou P, Tatarnikov I, Evans DM, Pishotta FT, ... ... Hentati F, et al. DNAJC13 mutations in Parkinson disease. Human Molecular Genetics. 23: 1794-801. PMID 24218364 DOI: 10.1093/hmg/ddt570  0.4
2014 Hammer MB, El Euch-Fayache G, Nehdi H, Feki M, Maamouri-Hicheri W, Hentati F, Amouri R. 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. PMID 24139731 DOI: 10.1016/j.jocn.2013.04.016  0.4
2013 Hentati F, Hentati E, Amouri R. Giant axonal neuropathy. Handbook of Clinical Neurology. 115: 933-8. PMID 23931822 DOI: 10.1016/B978-0-444-52902-2.00052-7  0.4
2013 Heckman MG, Soto-Ortolaza AI, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Carr J, Chartier-Harlin MC, Dardiotis E, Dickson DW, Diehl NN, ... ... Hentati F, et al. 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. PMID 23913756 DOI: 10.1002/mds.25600  0.4
2013 Trinh J, Vilariño-Güell C, Donald A, Shah B, Yu I, Szu-Tu C, Aasly JO, Wu RM, Hentati F, Rajput AH, Rajput A, Farrer MJ. STX6 rs1411478 is not associated with increased risk of Parkinson's disease. Parkinsonism & Related Disorders. 19: 563-5. PMID 23415606 DOI: 10.1016/j.parkreldis.2013.01.019  0.4
2013 Hammer MB, Eleuch-Fayache G, Schottlaender LV, Nehdi H, Gibbs JR, Arepalli SK, Chong SB, Hernandez DG, Sailer A, Liu G, Mistry PK, Cai H, Shrader G, Sassi C, Bouhlal Y, ... ... Hentati F, et al. Mutations in GBA2 cause autosomal-recessive cerebellar ataxia with spasticity. American Journal of Human Genetics. 92: 245-51. PMID 23332917 DOI: 10.1016/j.ajhg.2012.12.012  0.4
2013 Ben Ammar A, Soltanzadeh P, Bauché S, Richard P, Goillot E, Herbst R, Gaudon K, Huzé C, Schaeffer L, Yamanashi Y, Higuchi O, Taly A, Koenig J, Leroy JP, Hentati F, et al. A mutation causes MuSK reduced sensitivity to agrin and congenital myasthenia. Plos One. 8: e53826. PMID 23326516 DOI: 10.1371/journal.pone.0053826  0.4
2013 Hammer MB, Eleuch-Fayache G, Gibbs JR, Arepalli SK, Chong SB, Sassi C, Bouhlal Y, Hentati F, Amouri R, Singleton AB. 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. PMID 23043354 DOI: 10.1111/j.1468-1331.2012.03883.x  0.4
2012 Hammer MB, El Euch-Fayache G, Nehdi H, Saidi D, Nasri A, Nabli F, Bouhlal Y, Maamouri-Hicheri W, Hentati F, Amouri R. Clinical and molecular findings of ataxia with oculomotor apraxia type 2 (AOA2) in 5 Tunisian families. Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 21: 241-5. PMID 23111195 DOI: 10.1097/PDM.0b013e318257ad9a  0.4
2012 Herson S, Hentati F, Rigolet A, Behin A, Romero NB, Leturcq F, Laforêt P, Maisonobe T, Amouri R, Haddad H, Audit M, Montus M, Masurier C, Gjata B, Georger C, et al. A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C. Brain : a Journal of Neurology. 135: 483-92. PMID 22240777 DOI: 10.1093/brain/awr342  0.4
2012 Ben Sassi S, Nabli F, Hentati E, Nahdi H, Trabelsi M, Ben Ayed H, Amouri R, Duda JE, Farrer MJ, Hentati F. Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's disease. Parkinsonism & Related Disorders. 18: 243-6. PMID 22056842 DOI: 10.1016/j.parkreldis.2011.10.009  0.4
2012 Hentati F, El-Euch G, Bouhlal Y, Amouri R. Ataxia with vitamin E deficiency and abetalipoproteinemia. Handbook of Clinical Neurology. 103: 295-305. PMID 21827896 DOI: 10.1016/B978-0-444-51892-7.00018-8  0.4
2011 Chartier-Harlin MC, Dachsel JC, Vilariño-Güell C, Lincoln SJ, Leprêtre F, Hulihan MM, Kachergus J, Milnerwood AJ, Tapia L, Song MS, Le Rhun E, Mutez E, Larvor L, Duflot A, Vanbesien-Mailliot C, ... ... Hentati F, et al. Translation initiator EIF4G1 mutations in familial Parkinson disease. American Journal of Human Genetics. 89: 398-406. PMID 21907011 DOI: 10.1016/j.ajhg.2011.08.009  0.4
2011 Vilariño-Güell C, Wider C, Ross OA, Dachsel JC, Kachergus JM, Lincoln SJ, Soto-Ortolaza AI, Cobb SA, Wilhoite GJ, Bacon JA, Behrouz B, Melrose HL, Hentati E, Puschmann A, Evans DM, ... ... Hentati F, et al. VPS35 mutations in Parkinson disease. American Journal of Human Genetics. 89: 162-7. PMID 21763482 DOI: 10.1016/j.ajhg.2011.06.001  0.4
2011 Bouhlal Y, Amouri R, El Euch-Fayeche G, Hentati F. Autosomal recessive spastic ataxia of Charlevoix-Saguenay: an overview. Parkinsonism & Related Disorders. 17: 418-22. PMID 21450511 DOI: 10.1016/j.parkreldis.2011.03.005  0.4
2011 Bouhlal Y, Jennewein DM, Anderson B, Reynoldson J, Maamouri W, Hentati F, Amouri R, Lushbough C. Computational analysis of a novel SACS gene mutation with BioExtract server. Journal of Molecular Neuroscience : Mn. 44: 53-8. PMID 21416271 DOI: 10.1007/s12031-011-9512-8  0.4
2011 Maamouri W, Hammer MB, Bouhlel Y, Souilem S, Khmiri N, Nehdi H, Hentati F, Amouri R. Spinal muscular atrophy due to double gene conversion event. The International Journal of Neuroscience. 121: 107-11. PMID 21047176 DOI: 10.3109/00207454.2010.529209  0.4
2011 Souilem S, Chebel S, Mancuso M, Petrozzi L, Siciliano G, FrihAyed M, Hentati F, Amouri R. A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia. Journal of the Neurological Sciences. 300: 187-90. PMID 20884012 DOI: 10.1016/j.jns.2010.08.065  0.4
2011 H'mida-Ben Brahim D, M'zahem A, Assoum M, Bouhlal Y, Fattori F, Anheim M, Ali-Pacha L, Ferrat F, Chaouch M, Lagier-Tourenne C, Drouot N, Thibaut C, Benhassine T, Sifi Y, Stoppa-Lyonnet D, ... ... Hentati F, et al. Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays. Journal of Neurology. 258: 56-67. PMID 20798953 DOI: 10.1007/s00415-010-5682-5  0.4
2010 Vilariño-Güell C, Ross OA, Aasly JO, White LR, Rajput A, Rajput AH, Lynch T, Krygowska-Wajs A, Jasinska-Myga B, Opala G, Barcikowska M, Lee MC, Hentati F, Uitti RJ, Wszolek ZK, et al. An independent replication of PARK16 in Asian samples. Neurology. 75: 2248-9. PMID 21172849 DOI: 10.1212/WNL.0b013e318202031f  0.4
2010 Nishioka K, Vilariño-Güell C, Cobb SA, Kachergus JM, Ross OA, Hentati E, Hentati F, Farrer MJ. Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease. Parkinsonism & Related Disorders. 16: 686-7. PMID 20971673 DOI: 10.1016/j.parkreldis.2010.09.007  0.4
2010 Jasinska-Myga B, Kachergus J, Vilariño-Güell C, Wider C, Soto-Ortolaza AI, Kefi M, Middleton LT, Ishihara-Paul L, Gibson RA, Amouri R, Yahmed SB, Sassi SB, Zouari M, El Euch G, Ross OA, ... Hentati F, et al. Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa. Movement Disorders : Official Journal of the Movement Disorder Society. 25: 2052-8. PMID 20721913 DOI: 10.1002/mds.23283  0.4
2010 Dzamko N, Deak M, Hentati F, Reith AD, Prescott AR, Alessi DR, Nichols RJ. Inhibition of LRRK2 kinase activity leads to dephosphorylation of Ser(910)/Ser(935), disruption of 14-3-3 binding and altered cytoplasmic localization. The Biochemical Journal. 430: 405-13. PMID 20659021 DOI: 10.1042/BJ20100784  0.4
2010 Souilem S, Kefi M, Mancuso M, Nesti C, Hentati F, Amouri R. A novel heteroplasmic tRNA Ser(UCN) mtDNA point mutation associated with progressive ophthalmoplegia and dysphagia. Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B. 19: 28-32. PMID 20186009 DOI: 10.1097/PDM.0b013e3181b00f02  0.4
2010 Dachsel JC, Nishioka K, Vilariño-Güell C, Lincoln SJ, Soto-Ortolaza AI, Kachergus J, Hinkle KM, Heckman MG, Jasinska-Myga B, Taylor JP, Dickson DW, Gibson RA, Hentati F, Ross OA, Farrer MJ. Heterodimerization of Lrrk1-Lrrk2: Implications for LRRK2-associated Parkinson disease. Mechanisms of Ageing and Development. 131: 210-4. PMID 20144646 DOI: 10.1016/j.mad.2010.01.009  0.4
2010 Ben Ammar A, Petit F, Alexandri N, Gaudon K, Bauché S, Rouche A, Gras D, Fournier E, Koenig J, Stojkovic T, Lacour A, Petiot P, Zagnoli F, Viollet L, Pellegrini N, ... ... Hentati F, et al. Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7. Journal of Neurology. 257: 754-66. PMID 20012313 DOI: 10.1007/s00415-009-5405-y  0.4
2010 Nishioka K, Vilariño-Güell C, Cobb SA, Kachergus JM, Ross OA, Wider C, Gibson RA, Hentati F, Farrer MJ. Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa. Neuroscience Letters. 477: 57-60. PMID 19945510 DOI: 10.1016/j.neulet.2009.11.066  0.4
2010 Nishioka K, Kefi M, Jasinska-Myga B, Wider C, Vilariño-Güell C, Ross OA, Heckman MG, Middleton LT, Ishihara-Paul L, Gibson RA, Amouri R, Ben Yahmed S, Ben Sassi S, Zouari M, El Euch G, ... ... Hentati F, et al. A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry. 81: 391-5. PMID 19726410 DOI: 10.1136/jnnp.2009.185231  0.4
2010 Amara O, Bouzid K, Bahlous A, Sahli H, Sellami S, Hentati F, Abdelmoula J. Assessment of bone mineral status in boys with myopathies | Évaluation du statut minéral osseux au cours des myopathies Immuno-Analyse Et Biologie Specialisee. 25: 252-256. DOI: 10.1016/j.immbio.2010.06.002  0.4
2009 Amouri R, Nehdi H, Bouhlal Y, Kefi M, Larnaout A, Hentati F. Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosis. Journal of Molecular Neuroscience : Mn. 39: 337-41. PMID 19633821 DOI: 10.1007/s12031-009-9217-4  0.4
2009 Bouhlal Y, El Euch-Fayeche G, Hentati F, Amouri R. A novel SACS gene mutation in a Tunisian family. Journal of Molecular Neuroscience : Mn. 39: 333-6. PMID 19529988 DOI: 10.1007/s12031-009-9212-9  0.4
2009 Vilariño-Güell C, Wider C, Soto-Ortolaza AI, Cobb SA, Kachergus JM, Keeling BH, Dachsel JC, Hulihan MM, Dickson DW, Wszolek ZK, Uitti RJ, Graff-Radford NR, Boeve BF, Josephs KA, Miller B, ... ... Hentati F, et al. Characterization of DCTN1 genetic variability in neurodegeneration. Neurology. 72: 2024-8. PMID 19506225 DOI: 10.1212/WNL.0b013e3181a92c4c  0.4
2009 Vilariño-Güell C, Soto AI, Lincoln SJ, Ben Yahmed S, Kefi M, Heckman MG, Hulihan MM, Chai H, Diehl NN, Amouri R, Rajput A, Mash DC, Dickson DW, Middleton LT, Gibson RA, ... Hentati F, et al. ATP13A2 variability in Parkinson disease. Human Mutation. 30: 406-10. PMID 19085912 DOI: 10.1002/humu.20877  0.4
2008 Richard P, Gaudon K, Haddad H, Ammar AB, Genin E, Bauché S, Paturneau-Jouas M, Müller JS, Lochmüller H, Grid D, Hamri A, Nouioua S, Tazir M, Mayer M, Desnuelle C, ... ... Hentati F, et al. The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa. Neurology. 71: 1967-72. PMID 19064877 DOI: 10.1212/01.wnl.0000336921.51639.0b  0.4
2008 Larnaout A, Ammar N, Mourad Z, Naji S, Hentati F. Wilson's disease: appreciable improvement of sub-cortical white matter abnormalities after copper chelating treatment: five years follow-up. Neuropediatrics. 39: 176-8. PMID 18991198 DOI: 10.1055/s-0028-1085464  0.4
2008 Larnaout A, Amouri R, Kefi M, Hentati F. L-2-hydroxyglutaric aciduria: clinical and molecular study in three Tunisian families. Identification of a new mutation and inter-familial phenotype variability. Journal of Inherited Metabolic Disease. 31: S375-9. PMID 18780161 DOI: 10.1007/s10545-008-0934-6  0.4
2008 Ishihara-Paul L, Hulihan MM, Kachergus J, Upmanyu R, Warren L, Amouri R, Elango R, Prinjha RK, Soto A, Kefi M, Zouari M, Sassi SB, Yahmed SB, El Euch-Fayeche G, Matthews PM, ... ... Hentati F, et al. PINK1 mutations and parkinsonism. Neurology. 71: 896-902. PMID 18685134 DOI: 10.1212/01.wnl.0000323812.40708.1f  0.4
2008 Kefi M, Amouri R, Chabrak S, Mechmeche R, Hentati F. Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutations. Neuropediatrics. 39: 113-5. PMID 18671187 DOI: 10.1055/s-2008-1081465  0.4
2008 Hamzaoui K, Houman H, Hentati F, Hamzaoui A. BAFF is up-regulated in central nervous system of neuro-Behçet's disease. Journal of Neuroimmunology. 200: 111-4. PMID 18625522 DOI: 10.1016/j.jneuroim.2008.06.006  0.4
2008 Bouhlal Y, Zouari M, Kefi M, Ben Hamida C, Hentati F, Amouri R. Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family. Journal of Neurogenetics. 22: 139-48. PMID 18569450 DOI: 10.1080/01677060802025233  0.4
2008 Hulihan MM, Ishihara-Paul L, Kachergus J, Warren L, Amouri R, Elango R, Prinjha RK, Upmanyu R, Kefi M, Zouari M, Sassi SB, Yahmed SB, El Euch-Fayeche G, Matthews PM, Middleton LT, ... ... Hentati F, et al. LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study. The Lancet. Neurology. 7: 591-4. PMID 18539535 DOI: 10.1016/S1474-4422(08)70116-9  0.4
2008 Tsaousidou MK, Ouahchi K, Warner TT, Yang Y, Simpson MA, Laing NG, Wilkinson PA, Madrid RE, Patel H, Hentati F, Patton MA, Hentati A, Lamont PJ, Siddique T, Crosby AH. Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration. American Journal of Human Genetics. 82: 510-5. PMID 18252231 DOI: 10.1016/j.ajhg.2007.10.001  0.4
2008 Warren L, Gibson R, Ishihara L, Elango R, Xue Z, Akkari A, Ragone L, Pahwa R, Jankovic J, Nance M, Freeman A, Watts RL, Hentati F. A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease. Parkinsonism & Related Disorders. 14: 77-80. PMID 17433753 DOI: 10.1016/j.parkreldis.2007.02.001  0.4
2008 Farrer MJ, Gibson R, Hentati F. The ancestry of LRRK2 Gly2019Ser parkinsonism - Authors' reply The Lancet Neurology. 7: 770-771. DOI: 10.1016/S1474-4422(08)70179-0  0.4
2007 Larnaout A, Amouri R, Neji S, Zouari M, Kaabachi N, Hentati F. Osteoma of the calvaria in L-2-hydroxyglutaric aciduria. Journal of Inherited Metabolic Disease. 30: 980. PMID 17917788 DOI: 10.1007/s10545-007-0576-0  0.4
2007 Hammami N, Drissi C, Sebai R, Araar M, Maatallah Y, Belghith L, Nagi S, Hentati F, Ben Hamouda M. Reversible metronidazole-induced encephalopathy. Journal of Neuroradiology. Journal De Neuroradiologie. 34: 133-6. PMID 17368540 DOI: 10.1016/j.neurad.2007.01.127  0.4
2007 Ishihara L, Gibson RA, Warren L, Amouri R, Lyons K, Wielinski C, Hunter C, Swartz JE, Elango R, Akkari PA, Leppert D, Surh L, Reeves KH, Thomas S, Ragone L, ... ... Hentati F, et al. Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 55-61. PMID 17115391 DOI: 10.1002/mds.21180  0.4
2006 Charfi A, Ben Hadj Yahia S, Kharrat S, Zouari M, Bouchama J, Naziha K, Abdelmajid L, Hentati F, Hachicha S. [Study of dyslexia within school kids that suffer from epilepsia]. La Tunisie MéDicale. 84: 803-4. PMID 17288285  0.4
2006 Ishihara L, Warren L, Gibson R, Amouri R, Lesage S, Dürr A, Tazir M, Wszolek ZK, Uitti RJ, Nichols WC, Griffith A, Hattori N, Leppert D, Watts R, Zabetian CP, ... ... Hentati F, et al. Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations. Archives of Neurology. 63: 1250-4. PMID 16966502 DOI: 10.1001/archneur.63.9.1250  0.4
2006 Stum M, Davoine CS, Vicart S, Guillot-Noël L, Topaloglu H, Carod-Artal FJ, Kayserili H, Hentati F, Merlini L, Urtizberea JA, Hammouda el-H, Quan PC, Fontaine B, Nicole S. Spectrum of HSPG2 (Perlecan) mutations in patients with Schwartz-Jampel syndrome. Human Mutation. 27: 1082-91. PMID 16927315 DOI: 10.1002/humu.20388  0.4
2006 Ammar N, Gouider-Khouja N, Hentati F. [A comparative study of clinical and paramedical aspects of multiple sclerosis in Tunisia]. Revue Neurologique. 162: 729-33. PMID 16840981  0.4
2006 Hamzaoui K, Kamoun M, Houman H, Hentati F, Hamza M, Ayed K, Hamzaoui A. Discrepancies of NKT cells expression in peripheral blood and in cerebrospinal fluid from Behçet's disease. Journal of Neuroimmunology. 175: 160-8. PMID 16624421 DOI: 10.1016/j.jneuroim.2006.02.011  0.4
2006 Tomiyama H, Li Y, Funayama M, Hasegawa K, Yoshino H, Kubo S, Sato K, Hattori T, Lu CS, Inzelberg R, Djaldetti R, Melamed E, Amouri R, Gouider-Khouja N, Hentati F, et al. Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries. Movement Disorders : Official Journal of the Movement Disorder Society. 21: 1102-8. PMID 16622854 DOI: 10.1002/mds.20886  0.4
2006 Fendri K, Kefi M, Hentati F, Amouri R. Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes. Neuromuscular Disorders : Nmd. 16: 316-20. PMID 16616845 DOI: 10.1016/j.nmd.2006.02.007  0.4
2005 Bouhlal Y, El-Euch-Fayeche G, Amouri R, Hentati F. Distinct phenotypes within autosomal recessive ataxias not linked to already known loci. Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology / Edited by the Gaetano Conte Academy For the Study of Striated Muscle Diseases. 24: 155-61. PMID 16550933  0.4
2005 Aounallah Skhiri H, Ben Romdhane H, Haoula H, Kouni CM, Drissa H, Belhani A, Hentati F. [Secondary prevention of cardiovascular diseases: knowledge and practices of patients]. La Tunisie MéDicale. 83: 30-5. PMID 16094848  0.4
2005 Amouri R, Driss A, Murayama K, Kefi M, Nishino I, Hentati F. Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy. Neuromuscular Disorders : Nmd. 15: 361-3. PMID 15833430 DOI: 10.1016/j.nmd.2005.01.012  0.4
2005 Ben Ghorbel I, Ibnelhadj Z, Zouari M, Nagi S, Khanfir M, Hentati F, Houman MH. [Behçet's disease associated with peripheral neuropathy]. Revue Neurologique. 161: 218-20. PMID 15798522  0.4
2004 Amouri R, Moreira MC, Zouari M, El Euch G, Barhoumi C, Kefi M, Belal S, Koenig M, Hentati F. Aprataxin gene mutations in Tunisian families. Neurology. 63: 928-9. PMID 15365154  0.4
2004 El Bahri-Ben Mrad F, Gouider-Khouja N, Gabsi S, Larnaout A, Boughammoura A, Kefi M, Belal S, Hentati F. [Lateral gaze palsy and progressive scoliosis in 4 Tunisian families]. Revue Neurologique. 160: 307-10. PMID 15037843  0.4
2004 Hentati F. Autosomal recessive juvenile amyotrophic lateral sclerosis Handbook of Clinical Neurophysiology. 4: 563-567. DOI: 10.1016/S1567-4231(04)04032-8  0.4
2003 Turki I, Djaïet S, Boukhris S, Hentati F. [Acute polyradiculoneuropathy. Guillain-Barre syndrome]. La Tunisie MéDicale. 81: 781-7. PMID 17722794  0.4
2003 Kefi M, Amouri R, Driss A, Ben Hamida C, Ben Hamida M, Kunkel LM, Hentati F. Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation. Neuromuscular Disorders : Nmd. 13: 779-87. PMID 14678800 DOI: 10.1016/S0960-8966(03)00136-6  0.4
2003 Ammar N, Nelis E, Merlini L, Barisić N, Amouri R, Ceuterick C, Martin JJ, Timmerman V, Hentati F, De Jonghe P. Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease. Neuromuscular Disorders : Nmd. 13: 720-8. PMID 14561495 DOI: 10.1016/S0960-8966(03)00093-2  0.4
2003 El Euch-Fayache G, Lalani I, Amouri R, Turki I, Ouahchi K, Hung WY, Belal S, Siddique T, Hentati F. Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia. Archives of Neurology. 60: 982-8. PMID 12873855 DOI: 10.1001/archneur.60.7.982  0.4
2003 Gouider-Khouja N, Larnaout A, Amouri R, Sfar S, Belal S, Ben Hamida C, Ben Hamida M, Hattori N, Mizuno Y, Hentati F. Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study. Parkinsonism & Related Disorders. 9: 247-51. PMID 12781588 DOI: 10.1016/S1353-8020(03)00016-6  0.4
2003 Driss A, Noguchi S, Amouri R, Kefi M, Sasaki T, Sugie K, Souilem S, Hayashi YK, Shimizu N, Minoshima S, Kudoh J, Hentati F, Nishino I. Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I. Neurology. 60: 1341-4. PMID 12707439  0.4
2003 Hentati F, Gabsi-Gherairi S, Amouri R, Belal S, Feki M. Familial Ataxia with Isolated Vitamin E Deficiency (AVED) Genetics of Movement Disorders. 179-187. DOI: 10.1016/B978-012566652-7/50021-6  0.4
2002 Gouider-Khouja N, Mekaouar A, Larnaout A, Miladi N, Ben Khelifa F, Hentati F. Progressive encephalomyelitis with rigidity presenting as a stiff-person syndrome. Parkinsonism & Related Disorders. 8: 285-8. PMID 12039424 DOI: 10.1016/S1353-8020(01)00047-5  0.4
2002 Feki M, Belal S, Feki H, Souissi M, Frih-Ayed M, Kaabachi N, Hentati F, Ben Hamida M, Mebazaa A. Serum vitamin E and lipid-adjusted vitamin E assessment in Friedreich ataxia phenotype patients and unaffected family members. Clinical Chemistry. 48: 577-9. PMID 11861456  0.4
2002 Baxter RV, Ben Othmane K, Rochelle JM, Stajich JE, Hulette C, Dew-Knight S, Hentati F, Ben Hamida M, Bel S, Stenger JE, Gilbert JR, Pericak-Vance MA, Vance JM. Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21. Nature Genetics. 30: 21-2. PMID 11743579 DOI: 10.1038/ng796  0.4
2001 Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Pericak-Vance M, ... Hentati F, et al. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nature Genetics. 29: 160-5. PMID 11586297 DOI: 10.1038/ng1001-160  0.4
2001 Gabsi S, Gouider-Khouja N, Belal S, Fki M, Kefi M, Turki I, Ben Hamida M, Kayden H, Mebazaa R, Hentati F. Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 8: 477-81. PMID 11554913 DOI: 10.1046/j.1468-1331.2001.00273.x  0.4
2001 Marzouki N, Belal S, Benhamida C, Benlemlih M, Hentati F. Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families. Clinical Genetics. 59: 257-62. PMID 11298681 DOI: 10.1034/j.1399-0004.2001.590407.x  0.4
2001 Larnaout A, El-Euch G, Kchir N, Filali A, Hamida MB, Hentati F. Wernicke's encephalopathy in a patient with Crohn's disease: a pathological study. Journal of Neurology. 248: 57-60. PMID 11266021 DOI: 10.1007/s004150170270  0.4
2001 Barhoumi C, Amouri R, Ben Hamida C, Ben Hamida M, Machghoul S, Gueddiche M, Hentati F. Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3. Neuromuscular Disorders : Nmd. 11: 27-34. PMID 11166163 DOI: 10.1016/S0960-8966(00)00162-0  0.4
2001 Rochelle M, Stajich J, Dew-Knight S, Baxter R, Gilbert J, Ben Hamida M, Pericak-Vance MA, Hentati F, Vance JM. Construction of a sequence contig across the CMT4A region Acta Myologica. 20: 33-34.  0.4
2001 Vance JM, Middleton LT, Christodoulou K, Georghiou DM, Kyriakides T, Zamba E, Guilbot A, I-Petrusewicz H, Ben Hamida C, Ben Hamida M, Hentati F, Mubaidin A, Ozdemir C, Serdaroglu P, Sevilla T, et al. Editorial Acta Myologica. 20: 1-3.  0.4
2001 Hentati F, Ben Othmane K, Barhoumi C, Amouri R, Ben Hamida C, Ben Hamida M. Genotype phenotype relation analysis in autosomal recessive Charcot-Marie-Tooth disease in Tunisia Acta Myologica. 20: 25-28.  0.4
2000 Di Donna S, Renault V, Forestier C, Piron-Hamelin G, Thiesson D, Cooper RN, Ponsot E, Decary S, Amouri R, Hentati F, Butler-Browne GS, Mouly V. Regenerative capacity of human satellite cells: the mitotic clock in cell transplantation. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 21: S943-51. PMID 11382194  0.4
2000 Nicole S, Davoine CS, Topaloglu H, Cattolico L, Barral D, Beighton P, Hamida CB, Hammouda H, Cruaud C, White PS, Samson D, Urtizberea JA, Lehmann-Horn F, Weissenbach J, Hentati F, et al. Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia). Nature Genetics. 26: 480-3. PMID 11101850 DOI: 10.1038/82638  0.4
2000 Hentati A, Deng HX, Zhai H, Chen W, Yang Y, Hung WY, Azim AC, Bohlega S, Tandan R, Warner C, Laing NG, Cambi F, Mitsumoto H, Roos RP, Boustany RM, ... ... Hentati F, et al. Novel mutations in spastin gene and absence of correlation with age at onset of symptoms. Neurology. 55: 1388-90. PMID 11087788  0.4
2000 Bomont P, Cavalier L, Blondeau F, Ben Hamida C, Belal S, Tazir M, Demir E, Topaloglu H, Korinthenberg R, Tüysüz B, Landrieu P, Hentati F, Koenig M. The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy. Nature Genetics. 26: 370-4. PMID 11062483 DOI: 10.1038/81701  0.4
2000 Renault V, Piron-Hamelin G, Forestier C, DiDonna S, Decary S, Hentati F, Saillant G, Butler-Browne GS, Mouly V. Skeletal muscle regeneration and the mitotic clock. Experimental Gerontology. 35: 711-9. PMID 11053661 DOI: 10.1016/S0531-5565(00)00151-0  0.4
2000 Cavalier L, BenHamida C, Amouri R, Belal S, Bomont P, Lagarde N, Gressin L, Callen D, Demir E, Topaloglu H, Landrieu P, Ioos C, Hamida MB, Koenig M, Hentati F. Giant axonal neuropathy locus refinement to a < 590 kb critical interval. European Journal of Human Genetics : Ejhg. 8: 527-34. PMID 10909853 DOI: 10.1038/sj.ejhg.5200476  0.4
2000 Chaabane M, Larnaout A, Sebai R, Nagi S, Touibi S, Hentati F. Nasu-Hakola disease in two Tunisian siblings: new radiological findings. Neuroradiology. 42: 375-8. PMID 10872161  0.4
2000 Driss A, Amouri R, Ben Hamida C, Souilem S, Gouider-Khouja N, Ben Hamida M, Hentati F. A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3. Neuromuscular Disorders : Nmd. 10: 240-6. PMID 10838249 DOI: 10.1016/S0960-8966(00)00099-7  0.4
2000 Gouider-Khouja N, Miladi N, Belal S, Hentati F. Intrafamilial phenotypic variability of Hallervorden-Spätz syndrome in a Tunisian family. Parkinsonism & Related Disorders. 6: 175-179. PMID 10817958 DOI: 10.1016/S1353-8020(99)00060-7  0.4
2000 Gouider-Khouja N, Belal S, Hamida MB, Hentati F. Clinical and genetic study of familial Parkinson's disease in Tunisia. Neurology. 54: 1603-9. PMID 10762501  0.4
2000 Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F. Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family. Neurology. 54: 1408-14. PMID 10751248  0.4
2000 Decary S, Hamida CB, Mouly V, Barbet JP, Hentati F, Butler-Browne GS. Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children. Neuromuscular Disorders : Nmd. 10: 113-20. PMID 10714586 DOI: 10.1016/S0960-8966(99)00093-0  0.4
2000 Gouider-Khouja N, Gabsi S, Khouja N, Hentati F. Hemiparkinsonian syndrome due to a cerebral tumor infiltrating the substantia nigra. Parkinsonism & Related Disorders. 6: 115-117. PMID 10699394 DOI: 10.1016/S1353-8020(99)00054-1  0.4
1999 Gabsi S, Gouider-Khouja N, Mili-Boussen I, Miladi N, Hentati F. [Vermian agenesis: Report of a family and review of the literature]. La Tunisie MéDicale. 77: 655-8. PMID 10730159  0.4
1999 Othmane KB, Johnson E, Menold M, Graham FL, Hamida MB, Hasegawa O, Rogala AD, Ohnishi A, Pericak-Vance M, Hentati F, Vance JM. Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15. Genomics. 62: 344-9. PMID 10644431 DOI: 10.1006/geno.1999.6028  0.4
1999 Nicole S, White PS, Topaloglu H, Beigthon P, Salih M, Hentati F, Fontaine B. The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene. Human Genetics. 105: 98-103. PMID 10480361 DOI: 10.1007/s004390051069  0.4
1999 Miladi N, Bourguignon JP, Hentati F. Cognitive and psychological profile of a Tunisian population of limb girdle muscular dystrophy. Neuromuscular Disorders : Nmd. 9: 352-4. PMID 10407859 DOI: 10.1016/S0960-8966(99)00006-1  0.4
1999 Gouider-Khouja N, Turki I, Ben Hamida M, Hentati F. [Treatment of cervical dystonia with botulinum toxin]. La Tunisie MéDicale. 77: 101-4. PMID 10333707  0.4
1999 Gouider-Khouja N, Turki I, Ben Hamida M, Hentati F. [Hemifacial spasm and its treatment with botulinum toxin]. La Tunisie MéDicale. 77: 41-4. PMID 10333697  0.4
1999 Goebel HH, Schochet SS, Jaynes M, Brück W, Kohlschütter A, Hentati F. Progress in neuropathology of the neuronal ceroid lipofuscinoses. Molecular Genetics and Metabolism. 66: 367-72. PMID 10191130 DOI: 10.1006/mgme.1999.2808  0.4
1999 Copp RP, Wisniewski T, Hentati F, Larnaout A, Ben Hamida M, Kayden HJ. Localization of alpha-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders. Brain Research. 822: 80-7. PMID 10082886 DOI: 10.1016/S0006-8993(99)01090-2  0.4
1998 Larnaout A, Belal S, Miladi N, Kaabachi N, Mebazza A, Dhondt JL, Hentati F. Juvenile form of dihydropteridine reductase deficiency in 2 Tunisian patients. Neuropediatrics. 29: 322-3. PMID 10029353 DOI: 10.1055/s-2007-973586  0.4
1998 Hentati A, Ouahchi K, Pericak-Vance MA, Nijhawan D, Ahmad A, Yang Y, Rimmler J, Hung W, Schlotter B, Ahmed A, Ben Hamida M, Hentati F, Siddique T. Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers. Neurogenetics. 2: 55-60. PMID 9933301 DOI: 10.1007/s100480050052  0.4
1998 Hosler BA, Sapp PC, Berger R, O'Neill G, Bejaoui K, Hamida MB, Hentati F, Chin W, McKenna-Yasek D, Haines JL, Patterson D, Horvitz HR, Brown RH, Day CB. Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33. Neurogenetics. 2: 34-42. PMID 9933298 DOI: 10.1007/s100480050049  0.4
1998 Ben Othmane K, Rochelle JM, Ben Hamida M, Slotterbeck B, Rao N, Hentati F, Pericak-Vance MA, Vance JM. Fine localization of the CMT4A locus using a PAC contig and haplotype analysis. Neurogenetics. 2: 18-23. PMID 9933296 DOI: 10.1007/s100480050047  0.4
1998 Larnaout A, Ben Hamida M, Hentati F. A clinicopathological observation of Nyssen-van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entities. Acta Neurologica Scandinavica. 98: 452-7. PMID 9875626  0.4
1998 Miladi N, Larnaout A, Dhondt JL, Vincent MF, Kaabachi N, Hentati F. Dihydropteridine reductase deficiency in a large consanguineous Tunisian family: clinical, biochemical, and neuropathologic findings. Journal of Child Neurology. 13: 475-80. PMID 9796752  0.4
1998 Larnaout A, Mongalgi MA, Kaabachi N, Khiari D, Debbabi A, Mebazza A, Ben Hamida M, Hentati F. Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study. Journal of Inherited Metabolic Disease. 21: 639-44. PMID 9762599 DOI: 10.1023/A:1005428432730  0.4
1998 Liu J, Aoki M, Illa I, Wu C, Fardeau M, Angelini C, Serrano C, Urtizberea JA, Hentati F, Hamida MB, Bohlega S, Culper EJ, Amato AA, Bossie K, Oeltjen J, et al. Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nature Genetics. 20: 31-6. PMID 9731526 DOI: 10.1038/1682  0.4
1998 Zouari M, Feki M, Ben Hamida C, Larnaout A, Turki I, Belal S, Mebazaa A, Ben Hamida M, Hentati F. Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency. Neuromuscular Disorders : Nmd. 8: 416-25. PMID 9713861 DOI: 10.1016/S0960-8966(98)00051-0  0.4
1998 Bönnemann CG, Wong J, Ben Hamida C, Hamida MB, Hentati F, Kunkel LM. LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3. Neuromuscular Disorders : Nmd. 8: 193-7. PMID 9631401 DOI: 10.1016/S0960-8966(98)00014-5  0.4
1998 Larnaout A, Belal S, Ben Hamida C, Ben Hamida M, Hentati F. Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings. Journal of Neurology. 245: 231-5. PMID 9591225 DOI: 10.1007/s004150050210  0.4
1998 Liu J, Wu C, Bossie K, Bejaoui K, Hosler BA, Gingrich JC, Ben Hamida M, Hentati F, Schurr E, de Jong PJ, Brown RH. Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13. Genomics. 49: 23-9. PMID 9570945 DOI: 10.1006/geno.1998.5204  0.4
1998 Ménard A, Amouri R, Dobránsky T, Charriaut-Marlangue C, Pierig R, Cifuentes-Diaz C, Ghandour S, Belliveau J, Gascan H, Hentati F, Lyon-Caen O, Perron H, Rieger F. A gliotoxic factor and multiple sclerosis. Journal of the Neurological Sciences. 154: 209-21. PMID 9562313 DOI: 10.1016/S0022-510X(97)00231-1  0.4
1998 David G, Dürr A, Stevanin G, Cancel G, Abbas N, Benomar A, Belal S, Lebre AS, Abada-Bendib M, Grid D, Holmberg M, Yahyaoui M, Hentati F, Chkili T, Agid Y, et al. Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7). Human Molecular Genetics. 7: 165-70. PMID 9425222 DOI: 10.1093/hmg/7.2.165  0.4
1997 Ben Hamida C, Cavalier L, Belal S, Sanhaji H, Nadal N, Barhoumi C, M'Rissa N, Marzouki N, Mandel JL, Ben Hamida M, Koenig M, Hentati F. Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1. Neurogenetics. 1: 129-33. PMID 10732815  0.4
1997 Larnaout A, Belal S, Zouari M, Fki M, Ben Hamida C, Goebel HH, Ben Hamida M, Hentati F. Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient. Acta Neuropathologica. 93: 633-7. PMID 9194904 DOI: 10.1007/s004010050662  0.4
1997 Cancel G, Dürr A, Didierjean O, Imbert G, Bürk K, Lezin A, Belal S, Benomar A, Abada-Bendib M, Vial C, Guimarães J, Chneiweiss H, Stevanin G, Yvert G, Abbas N, ... ... Hentati F, et al. Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families. Human Molecular Genetics. 6: 709-15. PMID 9158145  0.4
1996 Ben Hamida M, Ben Hamida C, Zouari M, Belal S, Hentati F. Limb-girdle muscular dystrophy 2C: clinical aspects. Neuromuscular Disorders : Nmd. 6: 493-4. PMID 9027861 DOI: 10.1016/S0960-8966(96)00395-1  0.4
1996 Fontaine B, Nicole S, Topaloglu H, Ben Hamida C, Beighton P, Spaans F, Cantu JM, Bakouri S, Romero N, Ricker K, Barros-Nunez P, Ponsot G, Ben Hamida M, Weissenbach J, Hentati F, et al. Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval. Human Genetics. 98: 380-5. PMID 8707312 DOI: 10.1007/s004390050225  0.4
1996 Hamzaoui A, Hamzaoui K, Kooli C, Chabbou A, Hentati F, Ayed K. High levels of bcl-2 protein in the T lymphocytes of patients with Behçet's disease. Clinical and Experimental Rheumatology. 14: 106-7. PMID 8697647  0.4
1995 Ben Hamida M, Hentati F. Atypical amyotrophic lateral sclerosis. Advances in Neurology. 68: 153-5. PMID 8787225  0.4
1995 Nicole S, Hamida CB, Beighton P, Bakouri S, Belal S, Romero N, Viljoen D, Ponsot G, Sammoud A, Weissenbach J, Fardeau M, Hamida MB, Fontaine B, Hentati F. Localization of the schwartz-jampel syndrome (SJS) locus to chromosome 1p34-p36.1 by homozygosity mapping Human Molecular Genetics. 4: 1633-1636. PMID 8541852 DOI: 10.1093/hmg/4.9.1633  0.4
1995 Othmane KB, Loeb D, Hayworth-Hodgte R, Hentati F, Rao N, Roses AD, Ben Hamida M, Pericak-Vance MA, Vance JM. Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A. Genomics. 28: 286-90. PMID 8530038 DOI: 10.1006/geno.1995.1143  0.4
1995 Doerflinger N, Linder C, Ouahchi K, Gyapay G, Weissenbach J, Le Paslier D, Rigault P, Belal S, Ben Hamida C, Hentati F. Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families. American Journal of Human Genetics. 56: 1116-24. PMID 7726167  0.4
1995 Bejaoui K, Hirabayashi K, Hentati F, Haines JL, Ben Hamida C, Belal S, Miller RG, McKenna-Yasek D, Weissenbach J, Rowland LP. Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14. Neurology. 45: 768-72. PMID 7723968  0.4
1995 Ouahchi K, Arita M, Kayden H, Hentati F, Ben Hamida M, Sokol R, Arai H, Inoue K, Mandel JL, Koenig M. Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein. Nature Genetics. 9: 141-5. PMID 7719340 DOI: 10.1038/ng0295-141  0.4
1995 Ben Othmane K, Speer MC, Stauffer J, Blel S, Middleton L, Ben Hamida C, Etribi A, Loeb D, Hentati F, Roses AD. Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C) American Journal of Human Genetics. 57: 732-4. PMID 7668303  0.4
1995 Belal S, Hentati F, Ben Hamida C, Ben Hamida M. Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus. Clinical Neuroscience (New York, N.Y.). 3: 39-42. PMID 7614093  0.4
1995 Noguchi S, McNally EM, Ben Othmane K, Hagiwara Y, Mizuno Y, Yoshida M, Yamamoto H, Bönnemann CG, Gussoni E, Denton PH, Kyriakides T, Middleton L, Hentati F, Ben Hamida M, Nonaka I, et al. Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy. Science (New York, N.Y.). 270: 819-22. PMID 7481775  0.4
1995 Ben Hamida M, Ben Othmane K, Belal S, Hentati F. [Is there a single form of Charcot-Marie-Tooth disease, or are there several variations? A classification difficulty]. Revue Neurologique. 151: 221-4. PMID 7481371  0.4
1994 Rodius F, Duclos F, Wrogemann K, Le Paslier D, Ougen P, Billault A, Belal S, Musenger C, Brice A, Dürr A, Mignard C, Sirugo G, Weissenbach J, Cohen D, Hentati F, et al. Recombinations in individuals homozygous by descent localize the Friedreich ataxia locus in a cloned 450-kb interval American Journal of Human Genetics. 54: 1050-1059. PMID 8198128  0.4
1994 Ben Hamida C, Soussi-Yanicostas N, Butler-Browne GS, Bejaoui K, Hentati F, Ben Hamida M. Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy. Muscle & Nerve. 17: 400-10. PMID 8170486 DOI: 10.1002/mus.880170407  0.4
1994 Hamida CB, Soussi-Yanicostas N, Bejaoui K, Butler-Browne GS, Hentati F, Ben Hamida M. Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy. Journal of the Neurological Sciences. 123: 114-21. PMID 8064303 DOI: 10.1016/0022-510X(94)90212-7  0.4
1994 Belal S, Cancel G, Stevanin G, Hentati F, Khati C, Ben Hamida C, Auburger G, Agid Y, Ben Hamida M, Brice A. Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus. Neurology. 44: 1423-6. PMID 8058142  0.4
1994 Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity. Human Molecular Genetics. 3: 1263-7. PMID 7987300  0.4
1994 Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35. Nature Genetics. 7: 425-8. PMID 7920663 DOI: 10.1038/ng0794-425  0.4
1994 Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S. Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers. Human Molecular Genetics. 3: 1867-71. PMID 7849714  0.4
1994 Hamzaoui K, Hentati F, Hamzaoui A, Kahan A, Ben Hamida M, Chabbou A, Ayed K. CD11/CD18 bearing lymphocytes in cerebrospinal fluid from patients with active Behçet's disease. Clinical and Experimental Rheumatology. 12: 575-6. PMID 7842541  0.4
1994 Larnaout A, Hentati F, Ben Hamida C, Khrouf N, Ben Hamida M. [Congenital fibrolipoma of the mesencephalic protuberation area]. Archives De PéDiatrie : Organe Officiel De La SociéTe FrançAise De PéDiatrie. 1: 913-5. PMID 7842073  0.4
1994 Larnaout A, Hentati F, Belal S, Ben Hamida C, Kaabachi N, Ben Hamida M. Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria. Acta Neuropathologica. 88: 367-70. PMID 7839830 DOI: 10.1007/BF00310381  0.4
1994 Hillaire D, Leclerc A, Fauré S, Topaloglu H, Chiannilkulchaï N, Guicheney P, Grinas L, Legos P, Philpot J, Evangelista T, Routon MC, Mayer M, Pellissier JF, Estournet B, Barois A, ... Hentati F, et al. Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping Human Molecular Genetics. 3: 1657-1661. PMID 7833925 DOI: 10.1093/hmg/3.9.1657  0.4
1994 Hamzaoui K, Hamzaoui A, Hentati F, Kahan A, Ayed K, Chabbou A, Ben Hamida M, Hamza M. Phenotype and functional profile of T cells expressing gamma delta receptor from patients with active Behçet's disease. The Journal of Rheumatology. 21: 2301-6. PMID 7699633  0.4
1993 Ben Hamida M, Attia-Romdhane N, Hentati F, Triki C. Early onset ataxias in Tunisia. Intrafamilial heterogeneity. Advances in Neurology. 61: 105-14. PMID 8421961  0.4
1993 Kaabachi N, Larnaout A, Rabier D, Jakobs C, Belal S, Hentati F, Parvey P, Bardet J, Ben Hamida M, Mebazaa A. Familial encephalopathy and L-2-hydroxyglutaric aciduria. Journal of Inherited Metabolic Disease. 16: 893. PMID 8295407 DOI: 10.1007/BF00714285  0.4
1993 Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, Pericak-Vance MA, Ben Hamida M, Vance JM. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Human Molecular Genetics. 2: 1625-8. PMID 8268915  0.4
1993 Hamida CB, Doerflinger N, Belal S, Linder C, Reutenauer L, Dib C, Gyapay G, Vignal A, Le Paslier D, Cohen D, Pandolfo M, Mokini V, Novelli G, Hentati F, Hamida MB, et al. Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping Nature Genetics. 5: 195-200. PMID 8252047 DOI: 10.1038/ng1093-195  0.4
1993 Ben Hamida M, Belal S, Sirugo G, Ben Hamida C, Panayides K, Ionannou P, Beckmann J, Mandel JL, Hentati F, Koenig M. Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families. Neurology. 43: 2179-83. PMID 8232925  0.4
1993 Hamzaoui K, Hentati F, Hamzaoui A, Chabbou A, Ben Hamida M, Ayed K. C 02 Phenotype and functional profile of T cells expressing TCRγδ receptor from patients with active Behçet's disease (BD) La Revue De Medecine Interne. 14: 23s.  0.4
1993 Hentati F, Fredj M, Gharbi N, Ben Hamida M. P 037 Clinical and biological aspects of neuro-Behçet's in Tunisia La Revue De Medecine Interne. 14: 71s.  0.4
1992 Ben Hamida M, Hentati F, Ben Hamida C. [Juvenile amyotrophic lateral sclerosis. Study of 43 cases]. Bulletin De L'AcadéMie Nationale De MéDecine. 176: 213-9; discussion 21. PMID 1633561  0.4
1992 Belal S, Panayides K, Sirugo G, Ben Hamida C, Ioannou P, Hentati F, Beckmann J, Koenig M, Mandel JL, Ben Hamida M. Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus. American Journal of Human Genetics. 51: 1372-6. PMID 1463017  0.4
1992 Soussi-Yanicostas N, Ben Hamida C, Bejaoui K, Hentati F, Ben Hamida M, Butler-Browne GS. Evolution of muscle specific proteins in Werdnig-Hoffman's disease. Journal of the Neurological Sciences. 109: 111-20. PMID 1387678 DOI: 10.1016/0022-510X(92)90103-R  0.4
1992 Larnaout A, Mongalgi MA, Ben Ameur H, Hentati F, Debbabi A, Ben Hamida M. [Antenatal bilateral sylvian infarction and congenital syphilis]. Archives FrançAises De PéDiatrie. 49: 895-7. PMID 1304157  0.4
1992 Ben Othmane K, Ben Hamida M, Pericak-Vance MA, Ben Hamida C, Blel S, Carter SC, Bowcock AM, Petruhkin K, Gilliam TC, Roses AD. Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q. Nature Genetics. 2: 315-7. PMID 1303286 DOI: 10.1038/ng1292-315  0.4
1992 Hentati F, Ben Hamida C, Zeghal M, Kamoun M, Fezaa B, Ben Hamida M. Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum. Neuromuscular Disorders : Nmd. 2: 361-9. PMID 1300184 DOI: 10.1016/S0960-8966(06)80007-6  0.4
1992 Ben Jelloun-Dellagi S, Dellagi K, Burger D, Ben Younes-Chennoufi A, Hentati FF, Steck A, Ben Hamida M. Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein P0. Annals of Neurology. 32: 700-2. PMID 1280408 DOI: 10.1002/ana.410320515  0.4
1991 Soussi-Yanicostas N, Ben Hamida C, Butler-Browne GS, Hentati F, Bejaoui K, Ben Hamida M. Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome. Journal of the Neurological Sciences. 104: 64-73. PMID 1919599 DOI: 10.1016/0022-510X(91)90217-U  0.4
1991 Moalla M, Boussen K, Meddeb S, Gorgi Y, Khalfallah T, Hentati F, Ben Ayed H. [Fatal acute pancreatitis in systemic lupus erythematosus]. Annales De MéDecine Interne. 142: 230-2. PMID 1854139  0.4
1991 Ben Hamida M, Hentati F. Juvenile amyotrophic lateral sclerosis and related syndromes. Advances in Neurology. 56: 175-9. PMID 1853755  0.4
1991 Ben Hamida M, Attia-Romdhane N, Triki CH, Oueslati S, Hentati F. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias]. Revue Neurologique. 147: 798-808. PMID 1780608  0.4
1990 Ben Hamida M, Hentati F, Ben Hamida C. Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy. Brain : a Journal of Neurology. 113: 347-63. PMID 2328408  0.4
1990 Ben Jelloun-Dellagi S, Chaffey P, Hentati F, Ben Hamida C, Tome F, Colin H, Dellagi K, Kaplan JC, Fardeau M, Ben Hamida M. Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy. Neurology. 40: 1903. PMID 2247244  0.4
1990 Ben Hamida M, Hentati F, Ben Hamida C. Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindred. Neurology. 40: 245-50. PMID 2153943  0.4
1990 Jelloun-Dellagi SB, Chaffey P, Hentati F, Hamida CB, Tome F, Colin H, Dellagi K, Kaplan JC, Fardeau M, Hamida MB. Presence of normal dystrophin in tunisian severe childhood autosomal recessive muscular dystrophy Neurology. 40: 1903.  0.4
1989 Ben Hamida M, Hentati F. Tunisian severe childhood muscular dystrophy: a normal spinal cord and anterior horn neurons. Muscle & Nerve. 12: 156. PMID 2710148 DOI: 10.1002/mus.880120212  0.4
1988 Ben Hamida M, Hentati F, Chebbi N, Mhiri C, Ayed K, Hamzaoui K. [Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study]. Revue Neurologique. 144: 737-47. PMID 3231963  0.4
1987 Ben Hamida M, Hentati F, Ben Hamida C. [Multiminicore disease in a rigid spine syndrome]. Revue Neurologique. 143: 284-9. PMID 3629076  0.4
1987 Henderson CE, Hauser SL, Huchet M, Dessi F, Hentati F, Taguchi T, Changeux JP, Fardeau M. Extracts of muscle biopsies from patients with spinal muscular atrophies inhibit neurite outgrowth from spinal neurons. Neurology. 37: 1361-4. PMID 3614658  0.4
1987 Ben Hamida M, Letaief F, Hentati F, Ben Hamida C. Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosis. Journal of the Neurological Sciences. 78: 313-29. PMID 3585405 DOI: 10.1016/0022-510X(87)90045-1  0.4
1987 Ben Hamida M, Letaief F, Hentati F, Ben Hamida C. Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen cases. Acta Neuropathologica. 75: 51-61. PMID 3481153 DOI: 10.1007/BF00686793  0.4
1986 Ben Hamida M, Hentati F, Ben Hamida C, Slimane N, Ben Othman T, Chebbi N, Letaief F. [Case of the rigid spine syndrome in a female patient]. La Tunisie MéDicale. 64: 645-8. PMID 3787754  0.4
1985 Tomé FM, Brunet P, Fardeau M, Hentati F, Reix J. Familial disorder of the central and peripheral nervous systems with particular cytoplasmic lamellated inclusions in peripheral nerves, muscle satellite cells, and blood capillaries. Acta Neuropathologica. 68: 209-17. PMID 4082923 DOI: 10.1007/BF00690197  0.4
1984 Ben Hamida M, Hentati F. [Charcot's disease and juvenile amyotrophic lateral sclerosis]. Revue Neurologique. 140: 202-6. PMID 6729330  0.4
Show low-probability matches.