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Depot Institutionnel de l'UMBB >
Browsing by Author Hamadouche, Tarik
Showing results 2 to 8 of 8
Date de publication | Titre | Auteur(s) | 2014 | Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases : an update | Tazir, Meriem; Hamadouche, Tarik; Nouioua, Sonia; Mathis, Stephane; Vallat, Jean-Michel |
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 |
2015 | Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia | Hamza, Wahiba; Ali Pacha, Lamia; Hamadouche, Tarik; Muller, Jean; Drouot, Nathalie; Ferrat, Farida; Makri, Samira; Chaouch, Malika; Tazir, Meriem; Koenig, Michel |
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 |
2012 | Two novel missense mutations in FGD4/FRABIN cause Charcot-Marie-Tooth type 4H (CMT4H) | Baudot, Cécile; Esteve, Clothilde; Castro, Christel; Poitelon, Yannick; Mas, Camille; Hamadouche, Tarik; El-Rajab, Maryam; Lévy, Nicolas; Megarbané, André; Delague, Valérie |
Showing results 2 to 8 of 8
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