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Faut-il avoir peur des OGM = Should we be afraid of GMOs ?HENTATI, Faycal.MHA (Sousse). 2003, Vol juillet, pp 50-51, issn 0330-8030, 2 p., HSConference Paper

Les polyradiculonevrites aiguës «syndrome de Guillain-Barré» : Expérience de l'Institut National de Neurologie (INN) = Acute polyradiculoneuropathy. Guillain-Barre syndromeTURKI, Ilhem; DJAÏET, Salwa; BOUKHRIS, S et al.Tunisie médicale. 2003, Vol 81, Num 10, pp 781-787, issn 0041-4131, 7 p.Article

Molecular, clinical and peripheral neuropathy study of Tunisian patients with ataxia with vitamin E deficiencyEL EUCH-FAYACHE, Ghada; BOUHLAL, Yosr; AMOURI, Rim et al.Brain. 2014, Vol 137, pp 402-410, issn 0006-8950, 9 p., 2Article

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21BAXTER, Rachel V; KAMEL BEN OTHMANE; GILBERT, John R et al.Nature genetics. 2002, Vol 30, Num 1, pp 21-22, issn 1061-4036Article

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathyBOMONT, Pascale; CAVALIER, Laurent; LANDRIEU, Pierre et al.Nature genetics. 2000, Vol 26, Num 3, pp 370-374, issn 1061-4036Article

Etude de la dyslexie chez les enfants épileptiques scolarisés = Study of dyslexia within school kids that suffer from epilepsiaCHARFI, Afifa; SIHEM BEN HADJ YAHIA; KHARRAT, Salima et al.Tunisie médicale. 2006, Vol 84, Num 12, pp 803-804, issn 0041-4131, 2 p.Article

A novel mitochondrial tRNA^Ile point mutation associated with chronic progressive external ophthalmoplegia and hyperCKemiaSOUILEM, Sihem; CHEBEL, Saber; MANCUSO, Michelangelo et al.Journal of the neurological sciences. 2011, Vol 300, Num 1-2, pp 187-190, issn 0022-510X, 4 p.Article

Prevention secondaire des maladies cardiovasculaires : Connaissances et pratiques des malades = Secondary prevention of cardiovascular diseases : Knowledge and practices of patientsHAJER AOUNALLAH SKHIRI; HABIBA BEN ROMDHANE; HAOULA, Habib et al.Tunisie médicale. 2005, Vol 83, Num 5, pp 30-35, issn 0041-4131, 6 p., SUPArticle

Serum vitamin E and lipid-adjusted vitamin E assessment in Friedreich ataxia phenotype patients and unaffected family membersFEKI, Moncef; BELAL, Samir; FEKI, Habib et al.Clinical chemistry (Baltimore, Md.). 2002, Vol 48, Num 3, pp 577-579, issn 0009-9147Article

Translation Initiator EIF4G1 Mutations in Familial Parkinson DiseaseCHARTIER-HARLIN, Marie-Christine; DACHSEL, Justus C; LE RHUN, Emilie et al.American journal of human genetics. 2011, Vol 89, Num 3, pp 398-406, issn 0002-9297, 9 p.Article

Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North AfricaNISHIOKA, Kenya; VILARINO-GÜELL, Carles; COBB, Stephanie A et al.Neuroscience letters. 2010, Vol 477, Num 2, pp 57-60, issn 0304-3940, 4 p.Article

Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutationsISHIHARA, Lianna; WARREN, Liling; GRIFFITH, Alida et al.Archives of neurology (Chicago). 2006, Vol 63, Num 9, pp 1250-1254, issn 0003-9942, 5 p.Article

VPS35 Mutations in Parkinson DiseaseVILARINO-GÜELL, Carles; WIDER, Christian; BEHROUZ, Bahareh et al.American journal of human genetics. 2011, Vol 89, Num 1, pp 162-167, issn 0002-9297, 6 p.Article

A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's diseaseNISHIOKA, Kenya; KEFI, Mounir; AMOURI, Rim et al.Journal of neurology, neurosurgery and psychiatry. 2010, Vol 81, Num 4, pp 391-395, issn 0022-3050, 5 p.Article

Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countriesTOMIYAMA, Hiroyuki; YUANZHE LI; DJALDETTI, Ruth et al.Movement disorders. 2006, Vol 21, Num 8, pp 1102-1108, issn 0885-3185, 7 p.Article

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisYI YANG; HENTATI, Afif; COLE, Natalie et al.Nature genetics. 2001, Vol 29, Num 2, pp 160-165, issn 1061-4036Article

A phase I trial of adeno-associated virus serotype 1-γ-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2CHERSON, Serge; HENTATI, Faycal; AUDIT, Muriel et al.Brain. 2012, Vol 135, pp 483-492, issn 0006-8950, 10 p., 2Article

Comprehensive Sequencing of the LRRK2 Gene in Patients with Familial Parkinson's Disease from North AfricaJASINSKA-MYGA, Barbara; KACHERGUS, Jennifer; SAMIA BEN YAHMED et al.Movement disorders. 2010, Vol 25, Num 13, pp 2052-2058, issn 0885-3185, 7 p.Article

Heterodimerization of Lrrk1-Lrrk2: Implications for LRRK2-associated Parkinson diseaseDACHSEL, Justus C; NISHIOKA, Kenya; DICKSON, Dennis W et al.Mechanisms of ageing and development. 2010, Vol 131, Num 3, pp 210-214, issn 0047-6374, 5 p.Article

Sequence Alterations within CYP7B1 Implicate Defective Cholesterol Homeostasis in Motor-Neuron DegenerationTSAOUSIDOU, Maria K; OUAHCHI, Karim; PATTON, Michael A et al.American journal of human genetics. 2008, Vol 82, Num 2, pp 510-515, issn 0002-9297, 6 p.Article

Screening for Lrrk2 G2019S and clinical comparison of tunisian and North American caucasian Parkinson's disease familiesISHIHARA, Lianna; GIBSON, Rachel A; LEPPERT, David et al.Movement disorders. 2007, Vol 22, Num 1, pp 55-61, issn 0885-3185, 7 p.Article

Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in TunisiaEL EUCH-FAYACHE, Ghada; LALANI, Irfan; AMOURI, Rim et al.Archives of neurology (Chicago). 2003, Vol 60, Num 7, pp 982-988, issn 0003-9942, 7 p.Article

Perlecan, the major proteoglycan of basement membranes, is altered in patients with Schwartz-Jampel syndrome (chondrodystrophic myotonia)NICOLE, Sophie; DAVOINE, Claire-Sophie; SAMSON, Delphine et al.Nature genetics. 2000, Vol 26, Num 4, pp 480-483, issn 1061-4036Article