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Depot Institutionnel de l'UMBB >
Browsing by Author Benhassine, Traki
Showing results 1 to 4 of 4
| Date de publication | Titre | Auteur(s) | | 2014 | Intragenic deletion patterns of dystrophin gene in duchenne and becker muscular dystrophy patients from algeria | Cherrallah, Amira; Benhassine, Traki; Nouioua, Sonia; MakriAffiliated, Samira; Chaouch, Malika; Tazir, Meriem; Hamadouche, Tarik |
| 2010 | LRRK2 G2019S mutation in parkinson's disease : a neuropsychological and neuropsychiatric study in a large algerian cohort | Belarbi, Soreya; Hecham, Nassima; Lesage, Suzanne; Kediha, Mohamed I.; Smail, Nourredine; Benhassine, Traki; Ysmail-Dahlouk, Farida; Lohman, Ebba; Benhabyles, Badia; Hamadouche, Tarik; Assami, Salima; Brice, Alexis; Tazir, Meriem |
| 2011 | Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes | Nouioua, Sonia; Hamadouche, Tarik; Funalot, Benoit; Bernard, Rafaëlle; Bellatache, Nora; Bouderba, Radia; Grid, Djamel; Assami, Salima; Benhassine, Traki; Levy, Nicolas; Vallat, Jean-Michel; Tazir, Meriem |
| 2010 | Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans | Lesage, Suzanne; Patin, Etienne; Condroyer, Christel; Leutenegger, Anne-Louise; Lohmann, Ebba; Giladi, Nir; Bar-Shira, Anat; Belarbi, Soraya; Hecham, Nassima; Pollak, Pierre; Ouvrard-Hernandez, Anne-Marie; Bardien, Soraya; Carr, Jonathan; Benhassine, Traki; Tomiyama, Hiroyuki; Pirkevi, Caroline; Hamadouche, Tarik; Cazeneuve, Cécile; Basak, A. Nazli; Hattori, Nobutaka; Dürr, Alexandra; Tazir, Meriem; Orr-Urtreger, Avi; Quintana-Murci, Lluis; Brice, Alexis |
Showing results 1 to 4 of 4
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