From | 2005-06-08 |
To | 2005-06-11 |
Course | No more fellowships available 15 fellowships from the Eumedis Program of the European Commission, covering tuition and living expenses (no travel), are available for citizens of the following States: Algeria, Cyprus, Egypt, Malta, Morocco, Israel, Jordan, Lebanon, the Palestinian Autonomous Territories, Syria, Tunisia and Turkey. Fee: ? 800 (including tuition, course material, room and board for the whole duration of the event, but NOT travel expenses). For participants without fellowships, whose citizenship is NOT European, North-American, Oceanian, Japanese and Korean, the course fee is ? 250 (including lunch meal, tuition and course material only). European School of Genetic Medicine 1st Course inNEUROGENETICS June 8th-11th, 2005 Rabat, MOROCCO Last update: May 6th, 2005 DIRECTOR: Al? Benomar (Rabat, MOROCCO) FACULTY: A.K. Abd El-Aleem (Cairo, EGYPT), M. Aguennouz (Messina, ITALY), N. Alami (Rabat, MOROCCO), N. Birouk (Rabat, MOROCCO), A. Bouhouche (Rabat, MOROCCO), A. Brice (Paris, FRANCE), A. Chabraoui (Rabat, MOROCCO), A. Filali (Rabat, MOROCCO), A. Filla (Napoli, ITALY), N. Gouider-Khouja (Tunis, TUNISIA), R. Gouider (Tunis, TUNISIA), A. Harouni (Cairo, EGYPT), F. Hentati (Tunis, TUNISIA), M. Jiddane (Rabat, MOROCCO), M. Koenig (Strasbourg, FRANCE), E. LeGuern (Paris, FRANCE), W. Messouak (F?s, MOROCCO), A. Saidi (Rabat, MOROCCO), A. Sefiani (Rabat, MOROCCO), G. Stevanin (Paris, FRANCE), M.Tazir (Algeri, Algeria), A. Toscano (Messina, ITALY), G. Vita (Messina, ITALY), M. Yahyaoui (Rabat, MOROCCO) Tuesday, June 7th ? Arrival at Hotel Ibis Moussafir, Rabat Wednesday, June 8th 08:00- 10:00 ? Reception and Registration at Universit? Mohammed V Souissi SESSION N?1: Trinucleotide repeat diseases Chairmen : M. Yahyaoui, A. Brice 10:00 M. Yahyaoui Autosomal dominant cerebellar ataxia type II 10:30 M. Jiddane Radiological aspects of cerebellar ataxia 11:00 A. Brice Clinical and genetic classification of autosomal dominant cerebellar ataxia 11:30 G. Stevanin Physiopathology of ADCA 12:00 A.K. Abd El -Aleem Fragile ? X and Kennedy diseases 12:30 ? DISCUSSION 13:00 ?Lunch Break SESSION N?2: Concurrent Workshops 15:00 G. Stevanin/A. Brice Linkage analysis (ROOM A) ? A. Filali/ M. Koenig Cloning and its applications (ROOM B) 17:00 ? Session end 17:30 OPEN CEREMONY ? Minister of health ? ?Minister of research ? President of the University Mohammed V Souissi ? ?Dean of Medicine and Pharmacy faculty ? European Coordinator of EUMEDIS project ? Local coordinator of EUMEDIS project 19:30 Refreshment Thursday, June 9th SESSION N?3: Autosomal recessive cerebellar ataxia Chairmen : M. Koenig, A. Filla 08:30 A. Filla Clinical Aspects of autosomal recessive cerebellar ataxias 09:00 M. Koenig Genetic aspects of Freidriech ataxia 09:30 ? DISCUSSION 09:45 A. Benomar Clinical and genetic aspects of Ataxia with vitamin E deficiency 10:15 ? DISCUSSION 10:30 Coffee Break SESSION N?4: Genetic Data of Movements Disorders Chairmen : A. Brice, N. Gouider Khouja 11:00 A. Brice Genetic aspects of Parkinson disease 11:30 N. Gouider-Khouja Clinical aspects of autosomal recessive Parkinson disease 12:00 W. Messouak Genetic aspects of Huntington disease 12:30 ? DISCUSSION 13:00 Lunch Break ? SESSION N?5: Concurrent Workshops 15:00 G. Stevanin/ A. Brice Linkage analysis (ROOM A) ? A. Filali/ M. Koenig Cloning and its applications (ROOM B) 17:00 ? Session end Friday, June 10th SESSION N?6: Genetic of Neuropathy Diseases Chairmen : N. Birouk, E. Leguern 08:30 N. Birouk Classification of Charcot Marie Tooth diseases and genetic aspects of autosomal recessive demyelinating forms 09:00 A. Bouhouche Genetic aspects of autosomal Recessive axonal forms of Charcot Marie Tooth Diseases 09:30 E. LeGuern Genetic aspects of autosomal dominant forms of Charcot Marie Tooth Diseases 10:00 ?R. Gouider Recurrent hereditay neuropathy 10:30 ? DISCUSSION 10:45 Coffee Break SESSION N?7: Genetic of Muscular Dystrophies Chairmen : A. Saidi, F. Hentati 11:00 A. Harouni Clinical and genetic aspects of dystrophinopathies 11:30 F. Hentati Sarcoglycanopathy: clinical and genetic aspects 12:00 G. Vita Nuclear factor-KappaB (NF-kB) in dystrophinopathies 12:30 M. Aguennouz Gene expression profile study investigation of acquired muscle disorder 13:00 M. Tazir Clinical and genetic aspects of congenital muscular dystrophy 13:30 ? DISCUSSION 13:45 Lunch Break SESSION N?8: Concurrent Workshops 15:00 E. LeGuern/ N. Alami/ A. Filla Gene therapy ? A. Sefiani/A. Brice Genetic council 17:00 ? Session end Saturday, June 11th SESSION N?9: Metabolic myopathy Chairmen : A. Chabraoui, G. Vita 08:30 ?A. Chabraoui Classification of metabolic myopathy 09:00 ?A. Saidi Anathomopathological aspects of metabolic myopathy disorders 10:00 A. Toscano Glycogen Storage Myopathies: from clinical features to treatment 10:30 Coffee Break 11:00 ? DISCUSSION 13:00 Lunch Break 14:30 Sightseeing of RABAT CITY 20:30 Gala Dinner Departure: Sunday Morning, June 12th |
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Programme | Rabat, MOROCCO June 8th-11th, 2005 DIRECTOR: AlÏ Benomar (Rabat, MOROCCO) FACULTY: A.K. Abd El-Aleem (Cairo, EGYPT), M. Aguennouz (Messina, ITALY), N. Alami (Rabat, MOROCCO), N. Birouk (Rabat, MOROCCO), A. Bouhouche (Rabat, MOROCCO), A. Brice (Paris, FRANCE), A. Chabraoui (Rabat, MOROCCO), A. Filali (Rabat, MOROCCO), A. Filla (Napoli, ITALY), N. Gouider-Khouja (Tunis, TUNISIA), R. Gouider (Tunis, TUNISIA), A. Harouni (Cairo, EGYPT), F. Hentati (Tunis, TUNISIA), M. Jiddane (Rabat, MOROCCO), M. Koenig (Strasbourg, FRANCE), E. LeGuern (Paris, FRANCE), W. Messouak (FËs, MOROCCO), A. Saidi (Rabat, MOROCCO), A. Sefiani (Rabat, MOROCCO), G. Stevanin (Paris, FRANCE), M.Tazir (Algeri, Algeria), A. Toscano (Messina, ITALY), G. Vita (Messina, ITALY), M. Yahyaoui (Rabat, MOROCCO) |