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Faycal Hentati

Research Profile

Geographic Areas

Tunisia

Concepts & Ideas

Physiology

Genes & Molecular Sequences

Recessive Genes

Procedures

Disorders

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Publications

TOP 3
Joanne Trinh; Carles vilarino-guell; Ruey-Meei Wu; Irene Yu; Faycal Hentati; Alex Rajput; Ali H Rajput; Brinda Shah; Chelsea Szu-Tu; Jan O Aasly; Alan Donald; Matthew J Farrer
STX6 rs1411478 is not associated with increased risk of Parkinson's disease.
M B Hammer; Faycal Hentati; C Sassi; Rim Amouri; Sampath Arepalli; YOSR BOUHLAL; S B Chong; G Eleuch-Fayache; J Raphael Gibbs; Andrew B Singleton
Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders.
Monia Benhamed Hammer; Faycal Hentati; Wieme Maamouri-Hicheri; Fatma Nabli; Amira Nasri; Houda Nehdi; Dalel Saidi; YOSR BOUHLAL; Ghada El Euch-Fayache; Rim Amouri
Clinical and molecular findings of ataxia with oculomotor apraxia type 2 (AOA2) in 5 Tunisian families.

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All Publications

2013: Joanne Trinh; Carles vilarino-guell; Ruey-Meei Wu; Irene Yu; Faycal Hentati; Alex Rajput; Ali H Rajput; Brinda Shah; Chelsea Szu-Tu; Jan O Aasly; Alan Donald; Matthew J Farrer
STX6 rs1411478 is not associated with increased risk of Parkinson's disease.
Parkinsonism & related disorders 2013;19(5):563-5.
2013: M B Hammer; Faycal Hentati; C Sassi; Rim Amouri; Sampath Arepalli; YOSR BOUHLAL; S B Chong; G Eleuch-Fayache; J Raphael Gibbs; Andrew B Singleton
Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2013;20(3):486-92.
2012: Monia Benhamed Hammer; Faycal Hentati; Wieme Maamouri-Hicheri; Fatma Nabli; Amira Nasri; Houda Nehdi; Dalel Saidi; YOSR BOUHLAL; Ghada El Euch-Fayache; Rim Amouri
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 2012;21(4):241-5.
2012: Serge Herson; Jean-Yves Hogrel; David Klatzmann; Pascal Laforêt; François M Lemoine; France Leturcq; Thierry Maisonobe; Carole Masurier; Marie Montus; Richard C Mulligan; A Rigolet; Norma B Romero; H Lee Sweeney; Thomas Voït; Didier Caizergues; Pierre Carlier; Mustapha Cheraï; Bruno Eymard; Christophe Georger; Bernard Gjata; Hafedh Haddad; Faycal Hentati; Ariane Herson; Yves Allenbach; Rim Amouri; Muriel Audit; Anthony Behin; Olivier Benveniste
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 2012;135(Pt 2):483-92.
2011: Sihem Souilem; Saber Chebel; Michelangelo Mancuso; Lucia Petrozzi; Gabriele Siciliano; Mahbouba FrihAyed; Faycal Hentati; Rim Amouri
A novel mitochondrial tRNA(Ile) point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemia.
Journal of the neurological sciences 2011;300(1-2):187-90.
2011: D H'mida-Ben Brahim; A M'zahem; M Assoum; YOSR BOUHLAL; F Fattori; Mathieu Anheim; L Ali-Pacha; F Ferrat; M Chaouch; Clotilde Lagier-Tourenne; N Drouot; C Thibaut; Traki Benhassine; Y Sifi; Dominique Stoppa-Lyonnet; K N'Guyen; J Poujet; A Hamri; Faycal Hentati; Rim Amouri; F M Santorelli; Meriem Tazir; Michel Koenig
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays.
Journal of neurology 2011;258(1):56-67.
2010: Kenya Nishioka; Carles vilarino-guell; Stephanie A Cobb; Jennifer Kachergus; Owen A Ross; Emna Hentati; Faycal Hentati; Matthew J Farrer
Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease.
Parkinsonism & related disorders 2010;16(10):686-7.
2010: Barbara Jasinska-Myga; Jennifer Kachergus; Carles vilarino-guell; Christian Wider; Alexandra I Soto-Ortolaza; Mounir Kefi; Lefkos T Middleton; Lianna Ishihara-Paul; Rachel A Gibson; Rim Amouri; Samia Ben Yahmed; Samia Ben Sassi; Mourad Zouari; Ghada El Euch; Owen A Ross; Faycal Hentati; Matthew J Farrer
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 2010;25(13):2052-8.
2010: Nicolas Dzamko; Maria Deak; Faycal Hentati; Alastair D Reith; Alan R Prescott; Dario R Alessi; R Jeremy Nichols
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 2010;430(3):405-13.
2010: Kenya Nishioka; Carles vilarino-guell; Stephanie A Cobb; Jennifer Kachergus; Owen A Ross; Christian Wider; Rachel A Gibson; Faycal Hentati; Matthew J Farrer
Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa.
Neuroscience letters 2010;477(2):57-60.
2010: Kenya Nishioka; Mounir Kefi; Barbara Jasinska-Myga; Christian Wider; Carles vilarino-guell; Owen A Ross; Michael G Heckman; Lefkos T Middleton; Lianna Ishihara-Paul; Rachel A Gibson; Rim Amouri; Samia Ben Yahmed; Samia Ben Sassi; Mourad Zouari; Ghada El Euch; Matthew J Farrer; Faycal Hentati
A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease.
Journal of neurology, neurosurgery, and psychiatry 2010;81(4):391-5.
2010: Sihem Souilem; Mounir Kefi; Michelangelo Mancuso; Claudia Nesti; Faycal Hentati; Rim Amouri
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 2010;19(1):28-32.
2010: Justus C Dachsel; Kenya Nishioka; Carles vilarino-guell; Sarah J Lincoln; Alexandra I Soto-Ortolaza; Jennifer Kachergus; Kelly M Hinkle; Michael G Heckman; Barbara Jasinska-Myga; Julie P Taylor; dennis dickson; Rachel A Gibson; Faycal Hentati; Owen A Ross; Matthew J Farrer
Heterodimerization of Lrrk1-Lrrk2: Implications for LRRK2-associated Parkinson disease.
Mechanisms of ageing and development 2010;131(3):210-4.
2009: Rim Amouri; Houda Nehdi; YOSR BOUHLAL; Mounir Kefi; Abdelmajid Larnaout; Faycal Hentati
Allelic ROBO3 heterogeneity in Tunisian patients with horizontal gaze palsy with progressive scoliosis.
Journal of molecular neuroscience : MN 2009;39(3):337-41.
2009: YOSR BOUHLAL; Ghada El Euch-Fayeche; Faycal Hentati; Rim Amouri
A novel SACS gene mutation in a Tunisian family.
Journal of molecular neuroscience : MN 2009;39(3):333-6.
2009: Carles vilarino-guell; C Wider; A I Soto-Ortolaza; Stephanie A Cobb; Jennifer Kachergus; B H Keeling; J C Dachsel; Mary Hulihan; dennis dickson; Zbigniew K Wszolek; Ryan Uitti; Neill R Graff-Radford; Bradley Boeve; Keith A Josephs; Bruce L Miller; K B Boylan; Katrina Gwinn-Hardy; Charles H Adler; Jan Aasly; Faycal Hentati; Alain Destée; Anna Krygowska-Wajs; Marie-Christine Chartier-Harlin; Owen A Ross; Rosa Rademakers; Matthew J Farrer
Characterization of DCTN1 genetic variability in neurodegeneration.
Neurology 2009;72(23):2024-8.
2009: Carles vilarino-guell; Alexandra I Soto; Sarah J Lincoln; Samia Ben Yahmed; Mounir Kefi; Michael G Heckman; Mary Hulihan; Hua Chai; Nancy N Diehl; Rim Amouri; Alex Rajput; Deborah C Mash; dennis dickson; Lefkos T Middleton; Rachel A Gibson; Faycal Hentati; Matthew J Farrer
ATP13A2 variability in Parkinson disease.
Human mutation 2009;30(3):406-10.
2009: Samia Ben Sassi; Lamia Kallel; Sawssen Ben Romdhane; Jalel Boubaker; Azza Filali; Faycal Hentati
Peripheral neuropathy in inflammatory bowel disease patients: a prospective cohort study.
Scandinavian journal of gastroenterology 2009;44(10):1268-9.
2009: S Ben Sassi; G El Euch; A Regaieg; T Mabrouk; M Zouari; N Ben Romdhane; Faycal Hentati
Man-in-the-barrel syndrome with combination of infarctions in the anterior spinal artery and posterior inferior cerebellar artery territories.
Cerebrovascular diseases (Basel, Switzerland) 2009;27(2):201-2.
2008: P Richard; K Gaudon; H Haddad; A Ben Ammar; E Genin; S Bauché; M Paturneau-Jouas; J S Müller; H Lochmüller; D Grid; A Hamri; S Nouioua; M Tazir; M Mayer; C Desnuelle; A Barois; B Chabrol; J Pouget; J Koenig; N Gouider-Khouja; Faycal Hentati; B Eymard; D Hantaï
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa.
Neurology 2008;71(24):1967-72.
2008: Abdelmajid Larnaout; Mounir Kefi; Rim Amouri; Faycal Hentati
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 2008;31 Suppl 2():S375-9.
2008: L Ishihara-Paul; Mary Hulihan; Jennifer Kachergus; R Upmanyu; L Warren; R Amouri; R Elango; Rab Prinjha; A Soto; M Kefi; M Zouari; S B Sassi; S B Yahmed; G El Euch-Fayeche; Paul Matthews; L T Middleton; R A Gibson; Faycal Hentati; Matthew J Farrer
PINK1 mutations and parkinsonism.
Neurology 2008;71(12):896-902.
2008: Kamel Hamzaoui; Habib Houman; Faycal Hentati; Agnes Hamzaoui
BAFF is up-regulated in central nervous system of neuro-Behçet's disease.
Journal of neuroimmunology 2008;200(1-2):111-4.
2008: Mary Hulihan; Lianna Ishihara-Paul; Jennifer Kachergus; Liling Warren; Rim Amouri; Ramu Elango; Rab Prinjha; Ruchi Upmanyu; Mounir Kefi; Mourad Zouari; Samia Ben Sassi; Samia Ben Yahmed; Ghada El Euch-Fayeche; Paul Matthews; Lefkos T Middleton; Rachel A Gibson; Faycal Hentati; Matthew J Farrer
LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study.
Lancet neurology 2008;7(7):591-4.
2008: A Larnaout; N Ammar; Z Mourad; S Naji; Faycal Hentati
Wilson's disease: appreciable improvement of sub-cortical white matter abnormalities after copper chelating treatment: five years follow-up.
Neuropediatrics 2008;39(3):176-8.
2008: M Kefi; R Amouri; S Chabrak; R Mechmeche; Faycal Hentati
Variable cardiac involvement in Tunisian siblings harboring FKRP gene mutations.
Neuropediatrics 2008;39(2):113-5.
2008: YOSR BOUHLAL; Mourad Zouari; Mounir Kefi; Christiane Ben Hamida; Faycal Hentati; Rim Amouri
Autosomal recessive ataxia caused by three distinct gene defects in a single consanguineous family.
Journal of neurogenetics 2008;22(2):139-48.
2008: L Warren; R Gibson; Lianna Ishihara; R Elango; Z Xue; A Akkari; L Ragone; Rajesh Pahwa; Joseph Jankovic; Martha Nance; Alan Freeman; Ray L Watts; Faycal Hentati
A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease.
Parkinsonism & related disorders 2008;14(1):77-80.
2007: Abdelmajid Larnaout; Rim Amouri; S Neji; Mourad Zouari; Neziha Kaabachi; Faycal Hentati
Osteoma of the calvaria in L-2-hydroxyglutaric aciduria.
Journal of inherited metabolic disease 2007;30(6):980.
2007: N Hammami; Cyrine Drissi; Rim Sebai; M Araar; Y Maatallah; Lotfi Belghith; Sonia Nagi; Faycal Hentati; Mohamed Ben Hamouda
Reversible metronidazole-induced encephalopathy.
Journal of neuroradiology. Journal de neuroradiologie 2007;34(2):133-6.
2007: Lianna Ishihara; Rachel A Gibson; Liling Warren; Rim Amouri; Kelly E Lyons; Catherine Wielinski; Christine Hunter; Jina Swartz; Ramu Elango; P Anthony Akkari; David Leppert; Linda Surh; Kevin H Reeves; Siwan Thomas; Leigh Ragone; Nobutaka Hattori; Rajesh Pahwa; Joseph Jankovic; Martha Nance; Alan Freeman; Neziha Gouider-Khouja; Mounir Kefi; Mourad Zouari; Samia Ben Sassi; Samia Ben Yahmed; Ghada El Euch-Fayeche; Lefkos T Middleton; David J Burn; Ray L Watts; Faycal Hentati
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 2007;22(1):55-61.
2006: Afifa Charfi; Sihem Ben Hadj Yahia; Salima Kharrat; Mourad Zouari; Jihen Bouchama; Khouja Naziha; Larnaout Abdelmajid; Faycal Hentati; Slah Hachicha
[Study of dyslexia within school kids that suffer from epilepsia].
La Tunisie médicale 2006;84(12):803-4.
2006: Imed Ben Ghorbel; Waffa Chebbi; Mourad Zouari; Faycal Hentati; Mohamed Miled; Mohamed Habib Houman
[Ureteral stenosis in Wegener's granulomatosis. Case report].
Presse médicale (Paris, France : 1983) 2006;35(11 Pt 1):1659-63.
2006: Morgane Stum; Claire-Sophie Davoine; Savine Vicart; Léna Guillot-Noël; Haluk Topaloglu; Francisco Javier Carod-Artal; Hulya Kayserili; Faycal Hentati; Luciano Merlini; J Andoni Urtizberea; El-Hadi Hammouda; Phuc Canh Quan; Bertrand Fontaine; Sophie Nicole
Spectrum of HSPG2 (Perlecan) mutations in patients with Schwartz-Jampel syndrome.
Human mutation 2006;27(11):1082-91.
2006: Lianna Ishihara; Liling Warren; Rachel Gibson; Rim Amouri; Suzanne Lesage; Alexandra Dürr; Meriem Tazir; Zbigniew K Wszolek; Ryan Uitti; William C Nichols; Alida Griffith; Nobutaka Hattori; David Leppert; Ray L Watts; Cyrus Zabetian; Tatiana Foroud; Matthew J Farrer; Alexis Brice; Lefkos T Middleton; Faycal Hentati
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
Archives of neurology 2006;63(9):1250-4.
2006: Ridha Mrad; Imen Dorboz; Lamia Ben Jemaa; Faouzi Maazoul; Madiha Trabelsi; Mohamed Chaabouni; Brahim Mlaiki; Nakjoua Miladi; Faycal Hentati; Habiba Chaabouni
Molecular analysis of the SMN1 and NAIP genes in 60 Tunisian spinal muscular atrophy patients.
La Tunisie médicale 2006;84(8):465-9.
2006: Hiroyuki Tomiyama; Yuanzhe Li; Manabu Funayama; Kazuko Hasegawa; Hiroyo Yoshino; Shin-Ichiro Kubo; Kenichi Sato; Tatsuya Hattori; Chin-Song Lu; Rivka Inzelberg; Ruth Djaldetti; Eldad Melamed; Rim Amouri; Neziha Gouider-Khouja; Faycal Hentati; Yasuko Hatano; Mei Wang; Yoko Imamichi; Koichi Mizoguchi; Hiroaki Miyajima; Fumiya Obata; Tatsushi Toda; Matthew J Farrer; Yoshikuni Mizuno; Nobutaka Hattori
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 2006;21(8):1102-8.
2006: Sonia Chabrak; S Ammar; Nadia Ammar; S Ouali; F Mghaieth; N Larbi; Naceur Kafsi; Faycal Hentati; Rachid Mechmeche
[Cardiac involvement in Emery-Dreifuss muscular dystrophy: a case report].
La Tunisie médicale 2006;84(6):361-4.
2006: Nadia Ammar; Neziha Gouider-Khouja; Faycal Hentati
[A comparative study of clinical and paramedical aspects of multiple sclerosis in Tunisia].
Revue neurologique 2006;162(6-7):729-33.
2006: Kamel Hamzaoui; Mariam Kamoun; Habib Houman; Faycal Hentati; M'hamed Hamza; Khaled Ayed; Agnes Hamzaoui
Discrepancies of NKT cells expression in peripheral blood and in cerebrospinal fluid from Behçet's disease.
Journal of neuroimmunology 2006;175(1-2):160-8.
2006: K Fendri; Mounir Kefi; Faycal Hentati; Rim Amouri
Genetic heterogeneity within a consanguineous family involving the LGMD 2D and the LGMD 2C genes.
Neuromuscular disorders : NMD 2006;16(5):316-20.
2005: YOSR BOUHLAL; G El-Euch-Fayeche; Rim Amouri; Faycal Hentati
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 2005;24(2):155-61.
2005: Hajer Aounallah Skhiri; Habiba Ben Romdhane; Habib Haoula; Chahed Mohamed Kouni; Habiba Drissa; Ali Belhani; Faycal Hentati
[Secondary prevention of cardiovascular diseases: knowledge and practices of patients].
La Tunisie médicale 2005;83 Suppl 5():30-5.
2005: Rim Amouri; Adel Driss; Kumiko Murayama; Mounir Kefi; Ichizo Nishino; Faycal Hentati
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy.
Neuromuscular disorders : NMD 2005;15(5):361-3.
2005: Imed Ben Ghorbel; Zied ibn elhadj; Mourad Zouari; Sonia Nagi; Monia Khanfir; Faycal Hentati; Mohamed Habib Houman
[Behçet's disease associated with peripheral neuropathy].
Revue neurologique 2005;161(2):218-20.
2004: Rim Amouri; MC Moreira; Mourad Zouari; G El Euch; C Barhoumi; Mounir Kefi; Samir Belal; Michel Koenig; Faycal Hentati
Aprataxin gene mutations in Tunisian families.
Neurology 2004;63(5):928-9.
2004: F El Bahri-Ben Mrad; Neziha Gouider-Khouja; S Gabsi; Abdelmajid Larnaout; A Boughammoura; Mounir Kefi; Samir Belal; Faycal Hentati
[Lateral gaze palsy and progressive scoliosis in 4 Tunisian families].
Revue neurologique 2004;160(3):307-10.
2003: Mounir Kefi; Rim Amouri; Adel Driss; Christiane Ben Hamida; Mongi Ben Hamida; Louis Kunkel; Faycal Hentati
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation.
Neuromuscular disorders : NMD 2003;13(10):779-87.
2003: Nadia Ammar; Eva Nelis; Luciano Merlini; Nina Barisić; Rim Amouri; Chantal Ceuterick; Jean-Jacques Martin; Vincent Timmerman; Faycal Hentati; Peter De Jonghe
Identification of novel GDAP1 mutations causing autosomal recessive Charcot-Marie-Tooth disease.
Neuromuscular disorders : NMD 2003;13(9):720-8.
2003: Ilhem Turki; Salwa Djaïet; S Boukhris; Faycal Hentati
[Acute polyradiculoneuropathy. Guillain-Barre syndrome].
La Tunisie médicale 2003;81(10):781-7.
2003: Ghada El Euch-Fayache; Irfan Lalani; Rim Amouri; Ilhem Turki; Karim Ouahchi; Wu-Yen Hung; Samir Belal; Teepu Siddique; Faycal Hentati
Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.
Archives of neurology 2003;60(7):982-8.
2003: Neziha Gouider-Khouja; Abdelmajid Larnaout; Rim Amouri; Sana Sfar; Samir Belal; Christiane Ben Hamida; Mongi Ben Hamida; Nobutaka Hattori; Yoshikuni Mizuno; Faycal Hentati
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
Parkinsonism & related disorders 2003;9(5):247-51.
2003: Adel Driss; Satoru Noguchi; Rim Amouri; Mounir Kefi; T Sasaki; Kazuma Sugie; S Souilem; Yukiko K Hayashi; N Shimizu; S Minoshima; J Kudoh; Faycal Hentati; Ichizo Nishino
Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2I.
Neurology 2003;60(8):1341-4.
2002: Neziha Gouider-Khouja; Aouatef Mekaouar; Abdelmajid Larnaout; Nakjoua Miladi; Fethi Ben Khelifa; Faycal Hentati
Progressive encephalomyelitis with rigidity presenting as a stiff-person syndrome.
Parkinsonism & related disorders 2002;8(4):285-8.
2002: Moncef Feki; Samir Belal; Habib Feki; Malek Souissi; Mahbouba Frih-Ayed; Neziha Kaabachi; Faycal Hentati; Mongi Ben Hamida; Abderraouf Mebazaa
Serum vitamin E and lipid-adjusted vitamin E assessment in Friedreich ataxia phenotype patients and unaffected family members.
Clinical chemistry 2002;48(3):577-9.
2002: Rachel V Baxter; Kamel Ben Othmane; Julie M Rochelle; Jason E Stajich; Christine M Hulette; Susan Dew-Knight; Faycal Hentati; Mongi Ben Hamida; S Bel; Judith E Stenger; John Gilbert; Margaret Pericak-Vance; Jeffery Vance
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.
Nature genetics 2002;30(1):21-2.
2001: Y Yang; A Hentati; H X Deng; Omar Dabbagh; T Sasaki; M Hirano; Wu-Yen Hung; Karim Ouahchi; J Yan; anser azim; N Cole; GG Gascon; A Yagmour; Mongi Ben Hamida; Margaret Pericak-Vance; Faycal Hentati; Teepu Siddique
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 2001;29(2):160-5.
2001: S Gabsi; Neziha Gouider-Khouja; Samir Belal; M Fki; Mounir Kefi; Ilhem Turki; Mongi Ben Hamida; HJ Kayden; R Mebazaa; Faycal Hentati
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 2001;8(5):477-81.
2001: MARZOUKI NAIMA; Samir Belal; C Benhamida; Mohamed Benlemlih; Faycal Hentati
Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families.
Clinical genetics 2001;59(4):257-62.
2001: Abdelmajid Larnaout; G El-Euch; N Kchir; Azza Filali; MB Hamida; Faycal Hentati
Wernicke's encephalopathy in a patient with Crohn's disease: a pathological study.
Journal of neurology 2001;248(1):57-60.
2001: C Barhoumi; Rim Amouri; Christiane Ben Hamida; Mongi Ben Hamida; Salem Machghoul; M Gueddiche; Faycal Hentati
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3.
Neuromuscular disorders : NMD 2001;11(1):27-34.
2000: Sophie Nicole; Claire-Sophie Davoine; Haluk Topaloglu; Laurence Cattolico; D Barral; P Beighton; CB Hamida; H Hammouda; Corinne Cruaud; Peter White; D Samson; J Andoni Urtizberea; Frank Lehmann-Horn; Jean Weissenbach; Faycal Hentati; Bertrand Fontaine
Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia).
Nature genetics 2000;26(4):480-3.
2000: A Hentati; Han-Xiang Deng; H Zhai; W Chen; Y Yang; Wu-Yen Hung; anser azim; Saeed Bohlega; Rup Tandan; C Warner; N G Laing; F Cambi; Hiroshi Mitsumoto; Raymond P Roos; Rose-Mary N Boustany; Mongi Ben Hamida; Faycal Hentati; Teepu Siddique
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms.
Neurology 2000;55(9):1388-90.
2000: Pascale Bomont; L Cavalier; Francois Blondeau; Christiane Ben Hamida; Samir Belal; Meriem Tazir; Ercan Demir; Haluk Topaloglu; R Korinthenberg; B Tüysüz; P Landrieu; Faycal Hentati; Michel Koenig
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy.
Nature genetics 2000;26(3):370-4.
2000: Valerie Renault; G Piron-Hamelin; C Forestier; S DiDonna; S Decary; Faycal Hentati; G Saillant; Gillian Butler-Browne; Vincent Mouly
Skeletal muscle regeneration and the mitotic clock.
Experimental gerontology 2000;35(6-7):711-9.
2000: L Cavalier; C BenHamida; Rim Amouri; Samir Belal; Pascale Bomont; N Lagarde; L Gressin; D Callen; Ercan Demir; Haluk Topaloglu; P Landrieu; C Ioos; MB Hamida; Michel Koenig; Faycal Hentati
Giant axonal neuropathy locus refinement to a < 590 kb critical interval.
European journal of human genetics : EJHG 2000;8(7):527-34.
2000: Adel Driss; Rim Amouri; Christiane Ben Hamida; S Souilem; Neziha Gouider-Khouja; Mongi Ben Hamida; Faycal Hentati
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3.
Neuromuscular disorders : NMD 2000;10(4-5):240-6.
2000: M Chaabane; Abdelmajid Larnaout; Rim Sebai; Sonia Nagi; Slaheddine Touibi; Faycal Hentati
Nasu-Hakola disease in two Tunisian siblings: new radiological findings.
Neuroradiology 2000;42(5):375-8.
2000: Neziha Gouider-Khouja; Samir Belal; MB Hamida; Faycal Hentati
Clinical and genetic study of familial Parkinson's disease in Tunisia.
Neurology 2000;54(8):1603-9.
2000: N Mrissa; Samir Belal; CB Hamida; Rim Amouri; Ilhem Turki; R Mrissa; MB Hamida; Faycal Hentati
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.
Neurology 2000;54(7):1408-14.
2000: S Decary; CB Hamida; Vincent Mouly; J P Barbet; Faycal Hentati; Gillian Butler-Browne
Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children.
Neuromuscular disorders : NMD 2000;10(2):113-20.
2000: Silvia Di Donna; Valerie Renault; C Forestier; G Piron-Hamelin; D Thiesson; Racquel N Cooper; E Ponsot; S Decary; Rim Amouri; Faycal Hentati; Gillian Butler-Browne; Vincent Mouly
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 2000;21(5 Suppl):S943-51.
1999: K B Othmane; E Johnson; Marisa M Menold; Felicia L Graham; MB Hamida; O Hasegawa; A D Rogala; A Ohnishi; Margaret Pericak-Vance; Faycal Hentati; Jeffery Vance
Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15.
Genomics 1999;62(3):344-9.
1999: S Gabsi; Neziha Gouider-Khouja; I Mili-Boussen; Nakjoua Miladi; Faycal Hentati
[Vermian agenesis: Report of a family and review of the literature].
La Tunisie médicale 1999;77(12):655-8.
1999: Abdelmajid Larnaout; M T De Lattore; G Lyon; Faycal Hentati
Prognostic factors in congenital hemiplegia in full-term and preterm children.
La Tunisie médicale 1999;77(12):644-7.
1999: Sophie Nicole; Peter White; Haluk Topaloglu; P Beigthon; Mustafa Salih; Faycal Hentati; Bertrand Fontaine
The human CDC42 gene: genomic organization, evidence for the existence of a putative pseudogene and exclusion as a SJS1 candidate gene.
Human genetics 1999;105(1-2):98-103.
1999: Nakjoua Miladi; J P Bourguignon; Faycal Hentati
Cognitive and psychological profile of a Tunisian population of limb girdle muscular dystrophy.
Neuromuscular disorders : NMD 1999;9(5):352-4.
1999: Hans H Goebel; Sydney S Schochet; ME Jaynes; W Brück; Alfried Kohlschuetter; Faycal Hentati
Progress in neuropathology of the neuronal ceroid lipofuscinoses.
Molecular genetics and metabolism 1999;66(4):367-72.
1999: R P Copp; Thomas Wisniewski; Faycal Hentati; Abdelmajid Larnaout; Mongi Ben Hamida; HJ Kayden
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 1999;822(1-2):80-7.
1999: Neziha Gouider-Khouja; Ilhem Turki; Mongi Ben Hamida; Faycal Hentati
[Treatment of cervical dystonia with botulinum toxin].
La Tunisie médicale 1999;77(2):101-4.
1999: Neziha Gouider-Khouja; Ilhem Turki; Mongi Ben Hamida; Faycal Hentati
[Hemifacial spasm and its treatment with botulinum toxin].
La Tunisie médicale 1999;77(1):41-4.
1998: Abdelmajid Larnaout; Samir Belal; Nakjoua Miladi; Neziha Kaabachi; A Mebazza; J L Dhondt; Faycal Hentati
Juvenile form of dihydropteridine reductase deficiency in 2 Tunisian patients.
Neuropediatrics 1998;29(6):322-3.
1998: A Hentati; Karim Ouahchi; Margaret Pericak-Vance; D Nijhawan; A Ahmad; Y Yang; Jacqueline B Rimmler; W Hung; B Schlotter; A Ahmed; Mongi Ben Hamida; Faycal Hentati; Teepu Siddique
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.
Neurogenetics 1998;2(1):55-60.
1998: Betsy A Hosler; Peter C Sapp; R Berger; Gilmore O'Neill; Khemissa Bejaoui; MB Hamida; Faycal Hentati; Wendy Chin; Diane McKenna-Yasek; Jonathan L Haines; D Patterson; H Robert Horvitz; Robert H Brown; C B Day
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33.
Neurogenetics 1998;2(1):34-42.
1998: K Ben Othmane; Julie M Rochelle; Mongi Ben Hamida; BD Slotterbeck; N Rao; Faycal Hentati; Margaret Pericak-Vance; Jeffery Vance
Fine localization of the CMT4A locus using a PAC contig and haplotype analysis.
Neurogenetics 1998;2(1):18-23.
1998: Abdelmajid Larnaout; Mongi Ben Hamida; Faycal Hentati
A clinicopathological observation of Nyssen-van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entities.
Acta neurologica Scandinavica 1998;98(6):452-7.
1998: Nakjoua Miladi; Abdelmajid Larnaout; J L Dhondt; M F Vincent; Neziha Kaabachi; Faycal Hentati
Dihydropteridine reductase deficiency in a large consanguineous Tunisian family: clinical, biochemical, and neuropathologic findings.
Journal of child neurology 1998;13(10):475-80.
1998: J Liu; M Aoki; Isabel Illa; C Wu; M Fardeau; Corrado Angelini; C Serrano; J Andoni Urtizberea; Faycal Hentati; MB Hamida; Saeed Bohlega; E J Culper; A A Amato; K Bossie; J Oeltjen; Khemissa Bejaoui; Diane McKenna-Yasek; Betsy A Hosler; E Schurr; Kiichi Arahata; P J de Jong; Robert H Brown
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy.
Nature genetics 1998;20(1):31-6.
1998: Abdelmajid Larnaout; MA Mongalgi; Neziha Kaabachi; D Khiari; Ali Debbabi; A Mebazza; Mongi Ben Hamida; Faycal Hentati
Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study.
Journal of inherited metabolic disease 1998;21(6):639-44.
1998: Mourad Zouari; Moncef Feki; Christiane Ben Hamida; Abdelmajid Larnaout; Ilhem Turki; Samir Belal; Abderraouf Mebazaa; Mongi Ben Hamida; Faycal Hentati
Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency.
Neuromuscular disorders : NMD 1998;8(6):416-25.
1998: C G Bönnemann; J Wong; Christiane Ben Hamida; MB Hamida; Faycal Hentati; Louis Kunkel
LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3.
Neuromuscular disorders : NMD 1998;8(3-4):193-7.
1998: Abdelmajid Larnaout; Samir Belal; Christiane Ben Hamida; Mongi Ben Hamida; Faycal Hentati
Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings.
Journal of neurology 1998;245(4):231-5.
1998: J Liu; C Wu; K Bossie; Khemissa Bejaoui; Betsy A Hosler; J C Gingrich; Mongi Ben Hamida; Faycal Hentati; E Schurr; P J de Jong; Robert H Brown
Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13.
Genomics 1998;49(1):23-9.
1998: Armelle Ménard; Rim Amouri; T Dobránsky; Christiane Charriaut-Marlangue; Régine Pierig; Carmen Cifuentes-Diaz; S Ghandour; J Belliveau; H Gascan; Faycal Hentati; O Lyon-Caen; Hervé Perron; François Rieger
A gliotoxic factor and multiple sclerosis.
Journal of the neurological sciences 1998;154(2):209-21.
1998: G David; Alexandra Dürr; Giovanni Stevanin; G Cancel; Nacer Abbas; Ali Benomar; Samir Belal; Anne-Sophie Lebre; M Abada-Bendib; Djamel Grid; M Holmberg; Mohamed Yahyaoui; Faycal Hentati; Taïeb Chkili; Yves Agid; Alexis Brice
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7).
Human molecular genetics 1998;7(2):165-70.
1997: Christiane Ben Hamida; L Cavalier; Samir Belal; H Sanhaji; N Nadal; C Barhoumi; N M'Rissa; MARZOUKI NAIMA; J L Mandel; Mongi Ben Hamida; Michel Koenig; Faycal Hentati
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1.
Neurogenetics 1997;1(2):129-33.
1997: Abdelmajid Larnaout; Samir Belal; Mourad Zouari; M Fki; Christiane Ben Hamida; H H Goebel; Mongi Ben Hamida; Faycal Hentati
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient.
Acta neuropathologica 1997;93(6):633-7.
1997: G Cancel; Alexandra Dürr; O Didierjean; G Imbert; Katrin Bürk; Agnes Lezin; Samir Belal; Ali Benomar; M Abada-Bendib; C Vial; J Guimarães; H Chneiweiss; Giovanni Stevanin; Gaël Yvert; Nacer Abbas; Frédéric Saudou; Anne-Sophie Lebre; Mohamed Yahyaoui; Faycal Hentati; JC Vernant; Thomas Klockgether; Jean-Louis Mandel; Yves Agid; Alexis Brice
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 families.
Human molecular genetics 1997;6(5):709-15.
1996: Mongi Ben Hamida; Christiane Ben Hamida; Mourad Zouari; Samir Belal; Faycal Hentati
Limb-girdle muscular dystrophy 2C: clinical aspects.
Neuromuscular disorders : NMD 1996;6(6):493-4.
1996: B Fontaine; S Nicole; Haluk Topaloglu; Christiane Ben Hamida; P Beighton; F Spaans; J M Cantu; S Bakouri; N Romero; K Ricker; P Barros-Nunez; G Ponsot; M Ben Hamida; Jean Weissenbach; Faycal Hentati; F Lehmann-Horn
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 1996;98(3):380-5.
1996: Agnes Hamzaoui; Kamel Hamzaoui; C Kooli; A Chabbou; Faycal Hentati; Khaled Ayed
High levels of bcl-2 protein in the T lymphocytes of patients with Behçet's disease.
Clinical and experimental rheumatology 1996;14(1):106-7.
1995: Satoru Noguchi; Elizabeth McNally; K Ben Othmane; Y Hagiwara; Y Mizuno; Mikiharu Yoshida; H Yamamoto; Carsten G Bönnemann; Emanuela Gussoni; P H Denton; T Kyriakides; Lefkos T Middleton; Faycal Hentati; Mongi Ben Hamida; I Nonaka; Jeffery Vance; Louis Kunkel; Eijiro Ozawa
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy.
Science (New York, N.Y.) 1995;270(5237):819-22.
1995: K Ben Othmane; M C Speer; J Stauffer; S Blel; Lefkos T Middleton; Christiane Ben Hamida; A Etribi; D Loeb; Faycal Hentati; Allen D Roses
Evidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)
American journal of human genetics 1995;57(3):732-4.
1995: K B Othmane; D Loeb; R Hayworth-Hodgte; Faycal Hentati; N Rao; Allen D Roses; Mongi Ben Hamida; Margaret Pericak-Vance; Jeffery Vance
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.
Genomics 1995;28(2):286-90.
1995: N Doerflinger; C Linder; K Ouahchi; Gabor Gyapay; Jean Weissenbach; D Le Paslier; P Rigault; Samir Belal; Christiane Ben Hamida; Faycal Hentati
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 1995;56(5):1116-24.
1995: Khemissa Bejaoui; K Hirabayashi; Faycal Hentati; Jonathan L Haines; Christiane Ben Hamida; Samir Belal; R G Miller; Diane McKenna-Yasek; J Weissenbach; L P Rowland
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14.
Neurology 1995;45(4):768-72.
1995: Mongi Ben Hamida; K Ben Othmane; S Belal; Faycal Hentati
[Is there a single form of Charcot-Marie-Tooth disease, or are there several variations? A classification difficulty].
Revue neurologique 1995;151(4):221-4.
1995: K Ouahchi; M Arita; H Kayden; Faycal Hentati; M Ben Hamida; Ronald Sokol; H Arai; K Inoue; Jean-Louis Mandel; Michel Koenig
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer protein.
Nature genetics 1995;9(2):141-5.
1995: M Ben Hamida; Faycal Hentati
Atypical amyotrophic lateral sclerosis.
Advances in neurology 1995;68():153-5.
1995: Samir Belal; Faycal Hentati; Christiane Ben Hamida; Mongi Ben Hamida
Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus.
Clinical neuroscience (New York, N.Y.) 1995;3(1):39-42.
1994: Kamel Hamzaoui; Agnes Hamzaoui; Faycal Hentati; A Kahan; Khaled Ayed; A Chabbou; Mongi Ben Hamida; M Hamza
Phenotype and functional profile of T cells expressing gamma delta receptor from patients with active Behçet's disease.
The Journal of rheumatology 1994;21(12):2301-6.
1994: A Hentati; Margaret Pericak-Vance; F Lennon; B Wasserman; Faycal Hentati; T Juneja; M H Angrist; Wu-Yen Hung; Rose-Mary N Boustany; S Bohlega
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers.
Human molecular genetics 1994;3(10):1867-71.
1994: Abdelmajid Larnaout; Faycal Hentati; Christiane Ben Hamida; N Khrouf; Mongi Ben Hamida
[Congenital fibrolipoma of the mesencephalic protuberation area].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1994;1(10):913-5.
1994: Kamel Hamzaoui; Faycal Hentati; Agnes Hamzaoui; A Kahan; Mongi Ben Hamida; A Chabbou; Khaled Ayed
CD11/CD18 bearing lymphocytes in cerebrospinal fluid from patients with active Behçet's disease.
Clinical and experimental rheumatology 1994;12(5):575-6.
1994: Samir Belal; G Cancel; Giovanni Stevanin; Faycal Hentati; C Khati; Christiane Ben Hamida; Georg Auburger; Yves Agid; Mongi Ben Hamida; Alexis Brice
Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus.
Neurology 1994;44(8):1423-6.
1994: A Hentati; Margaret Pericak-Vance; Wu-Yen Hung; S Belal; N Laing; Rose-Mary N Boustany; Faycal Hentati; M Ben Hamida; Teepu Siddique
Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.
Human molecular genetics 1994;3(8):1263-7.
1994: A Hentati; Khemissa Bejaoui; Margaret Pericak-Vance; Faycal Hentati; M C Speer; Wu-Yen Hung; Denise A Figlewicz; Jonathan L Haines; J Rimmler; Christiane Ben Hamida
Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.
Nature genetics 1994;7(3):425-8.
1994: C B Hamida; Nadia Soussi-Yanicostas; Khemissa Bejaoui; Gillian Butler-Browne; Faycal Hentati; M Ben Hamida
Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy.
Journal of the neurological sciences 1994;123(1-2):114-21.
1994: Christiane Ben Hamida; Nadia Soussi-Yanicostas; Gillian Butler-Browne; Khemissa Bejaoui; Faycal Hentati; M Ben Hamida
Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy.
Muscle & nerve 1994;17(4):400-10.
1994: Abdelmajid Larnaout; Faycal Hentati; Samir Belal; Christiane Ben Hamida; Neziha Kaabachi; Mongi Ben Hamida
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria.
Acta neuropathologica 1994;88(4):367-70.
1993: Mongi Ben Hamida; Samir Belal; Giorgio Sirugo; Christiane Ben Hamida; Kyproula Christodoulou; P Ionannou; Jacques Beckmann; Jean-Louis Mandel; Faycal Hentati; Michel Koenig
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families.
Neurology 1993;43(11):2179-83.
1993: K Ben Othmane; Faycal Hentati; F Lennon; Christiane Ben Hamida; S Blel; Allen D Roses; Margaret Pericak-Vance; Mongi Ben Hamida; Jeffery Vance
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.
Human molecular genetics 1993;2(10):1625-8.
1993: Mongi Ben Hamida; N Attia-Romdhane; Faycal Hentati; C Triki
Early onset ataxias in Tunisia. Intrafamilial heterogeneity.
Advances in neurology 1993;61():105-14.
1993: Neziha Kaabachi; Abdelmajid Larnaout; D Rabier; C Jakobs; Samir Belal; Faycal Hentati; P Parvey; J Bardet; Mongi Ben Hamida; Abderraouf Mebazaa
Familial encephalopathy and L-2-hydroxyglutaric aciduria.
Journal of inherited metabolic disease 1993;16(5):893.
1992: Samir Belal; Kyproula Christodoulou; Giorgio Sirugo; Christiane Ben Hamida; P Ioannou; Faycal Hentati; Jacques Beckmann; Michel Koenig; Jean-Louis Mandel; Mongi Ben Hamida
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.
American journal of human genetics 1992;51(6):1372-6.
1992: Abdelmajid Larnaout; MA Mongalgi; H Ben Ameur; Faycal Hentati; Ali Debbabi; Mongi Ben Hamida
[Antenatal bilateral sylvian infarction and congenital syphilis].
Archives françaises de pédiatrie 1992;49(10):895-7.
1992: S Ben Jelloun-Dellagi; Koussay Dellagi; D Burger; A Ben Younes-Chennoufi; Faycal Hentati; A Steck; M Ben Hamida
Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein P0.
Annals of neurology 1992;32(5):700-2.
1992: Nadia Soussi-Yanicostas; Christiane Ben Hamida; Khemissa Bejaoui; Faycal Hentati; M Ben Hamida; Gillian Butler-Browne
Evolution of muscle specific proteins in Werdnig-Hoffman's disease.
Journal of the neurological sciences 1992;109(1):111-20.
1992: M Ben Hamida; Faycal Hentati; Christiane Ben Hamida
[Juvenile amyotrophic lateral sclerosis. Study of 43 cases].
Bulletin de l'Académie nationale de médecine 1992;176(2):213-9; discussion 219-22.
1992: Abdelmajid Larnaout; M Haddad; Faycal Hentati; Mongi Ben Hamida
[Candida albicans meningitis and neurosarcoidosis].
Revue neurologique 1992;148(12):762-6.
1992: Faycal Hentati; Christiane Ben Hamida; M Zeghal; M Kamoun; B Fezaa; Mongi Ben Hamida
Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum.
Neuromuscular disorders : NMD 1992;2(5-6):361-9.
1991: Nadia Soussi-Yanicostas; Christiane Ben Hamida; Gillian Butler-Browne; Faycal Hentati; Khemissa Bejaoui; M Ben Hamida
Modification in the expression and localization of contractile and cytoskeletal proteins in Schwartz-Jampel syndrome.
Journal of the neurological sciences 1991;104(1):64-73.
1991: M Moalla; K Boussen; S Meddeb; Yousr Gorgi; T Khalfallah; Faycal Hentati; H Ben Ayed
[Fatal acute pancreatitis in systemic lupus erythematosus].
Annales de médecine interne 1991;142(3):230-2.
1991: M Ben Hamida; Faycal Hentati
Juvenile amyotrophic lateral sclerosis and related syndromes.
Advances in neurology 1991;56():175-9.
1991: Mongi Ben Hamida; N Attia-Romdhane; C H Triki; S Oueslati; Faycal Hentati
[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
Revue neurologique 1991;147(12):798-808.
1990: S Ben Jelloun-Dellagi; P Chaffey; Faycal Hentati; Christiane Ben Hamida; F Tome; H Colin; K Dellagi; Jean-Claude Kaplan; M Fardeau; M Ben Hamida
Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy.
Neurology 1990;40(12):1903.
1990: M F Ben Dridi; A Samoud; N Tebib; M Slim; M Taktak; Faycal Hentati; S Boubaker
[Pompe's disease: a report of 3 cases (clinical, biochemical, anatomo-pathological study].
La Tunisie médicale 1990;68(6-7):463-7.
1990: Mongi Ben Hamida; Faycal Hentati; Christiane Ben Hamida
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 1990;113 ( Pt 2)():347-63.
1990: M Ben Hamida; Faycal Hentati; Christiane Ben Hamida
Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindred.
Neurology 1990;40(2):245-50.
1989: M Ben Hamida; Faycal Hentati
Tunisian severe childhood muscular dystrophy: a normal spinal cord and anterior horn neurons.
Muscle & nerve 1989;12(2):156.
1988: Mongi Ben Hamida; Faycal Hentati; N Chebbi; C Mhiri; Khaled Ayed; Kamel Hamzaoui
[Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study].
Revue neurologique 1988;144(11):737-47.
1987: Christopher E Henderson; S L Hauser; M Huchet; F Dessi; Faycal Hentati; T Taguchi; Jean-Pierre Changeux; M Fardeau
Extracts of muscle biopsies from patients with spinal muscular atrophies inhibit neurite outgrowth from spinal neurons.
Neurology 1987;37(8):1361-4.
1987: Mongi Ben Hamida; F Letaief; Faycal Hentati; Christiane Ben Hamida
Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosis.
Journal of the neurological sciences 1987;78(3):313-29.
1987: M Ben Hamida; Faycal Hentati; Christiane Ben Hamida
[Multiminicore disease in a rigid spine syndrome].
Revue neurologique 1987;143(4):284-9.
1987: Mongi Ben Hamida; F Letaief; Faycal Hentati; Christiane Ben Hamida
Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen cases.
Acta neuropathologica 1987;75(1):51-61.
1986: Mongi Ben Hamida; H Chaabouni; S Madani; S Boussen; S Samoud; F Letaief; Amel Mrabet; Faycal Hentati; Nakjoua Miladi
[Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence].
Journal de génétique humaine 1986;34(3-4):267-74.
1986: Mongi Ben Hamida; Faycal Hentati; Christiane Ben Hamida; N Slimane; T Ben Othman; N Chebbi; F Letaief
[Case of the rigid spine syndrome in a female patient].
La Tunisie médicale 1986;64(6-7):645-8.
1985: F M Tomé; P Brunet; M Fardeau; Faycal Hentati; J Reix
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 1985;68(3):209-17.
1984: M Ben Hamida; Faycal Hentati
[Charcot's disease and juvenile amyotrophic lateral sclerosis].
Revue neurologique 1984;140(3):202-6.