Articles | Posters et présentations orales
- Charrier L, Driss A, Yan Y, Nduati V, Klapproth JM, Sitaraman SV, Merlin D. hpepT1 mediates bacterial tripeptide fMLP uptake in human monocytes. Laboratory Investigation, Lab Invest. 2006 May;86(5):490-503.
- Driss A, Charrier L, Yan Y, Nduati V and Merlin D. Dystroglycan Receptor is Involved in Integrin Activation in Intestinal Epithelia. American Journal of Physiology, Am J Physiol Gastrointest Liver Physiol. 2005 Dec 15.
- Kucharzik T, Lugering A, Yan Y, Driss A, Charrier L, Sitaraman S and Merlin D. Activation of Epithelial CD98 Glycoprotein Enhances Colonic Inflammation. Laboratory Investigation, 2005, 85(7): 932-41.
- Amouri R, Driss A, Murayama K, Kefi M, Nishino I, Hentati F. Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathy. Neuromuscular Disorders. 2005; 15: 361–363.
- Charrier L, Yan Y, Driss A, Laboisse CL, Sitaraman SV, Merlin D. ADAM-15 Inhibits Wound Healing in Human Intestinal Epithelial Cell Monolayers. Am J Physiol Gastrointestinal and Liver Physiology. 2005 Feb;288(2):G346-53. Epub 2004 Sep.
- Kefi M, Amouri R, Driss A, Ben Hamida C, Ben Hamida M, Kunkel LM, Hentati F. Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation. Neuromuscular Disorders. 2003 Dec;13(10):779-87.
- Driss A, Noguchi S, Sasaki T, Amouri R, Sugie K, Hayashi Y, Shimizu N, Minoshima S, Kudoh J, Hentati F and Nishino I. Fukutin-related protein gene mutations in the original limb-girdle muscular dystrophy 2I. Neurology 2003; 60: 1341-1344.
- Nishino I, Noguchi S, Murayama K, Driss A, Sugie K, Oya Y, Nagata T, Chida K, Takahashi T, Takusa Y, Ohi T, Nishimiya J, Sunohara N, Ciafaloni E, Kawai M, Aoki M, Nonaka I. Distal myopathy with rimmed vacuoles is allelic tohereditary inclusion body myopathy. Neurology 2002 59: 1689-1693.
- Driss A, Amouri R, Ben Hamida C, Souilem S, Gouider-Khouja N, Ben Hamida M, Hentati F. A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3. Neuromuscular Disorders 2000;10(4-5): 240-246.
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Last update... June 2006
- A. Driss, , R. Amouri, S. Souilem, S. Kobbi, S. Masmoudi, F. Hentati. Aspects Cliniques et Histopathologiques d’une nouvelle forme génétique de dystrophie musculaire des ceintures. Réunion de la Société Française de Neuropathologie, Tunis 1998, Tunisie. Présentation orale.
- R. Amouri, M. Zouari, A. Driss, S. Gabsi, M. Ben Hamida, F. Hentati. Genetic heterogeneity of autosomal racessive inclusion body myopathy in Tunisia. Filaments et Myopathies, a symposium in honore of FMS Tomé – Institut de myologie, Hôpital de la Salpetrière – Paris, 1998 – France. Présentation orale.
- Driss A, Amouri R, Ben Hamida C, Souilem S et al. A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family. Word Muscle Society, IVth International Congress – Antalia 1999 – Turquie. Presentation orale.
- M. Kefi, R. Amouri, A. Driss, C. Ben hamida, M. Ben hamida, F. Hentati. Etude de corrélation phénotype génotype des gamma-sarcoglycanopathies en Tunisie. Congres de Psychiatrie et de Neurologie de langue française, Hammamet 2001, Tunisie. Présentation orale.
- A. Driss, S. Noguchi, T. Sasaki, I. Nishino. Limb Girdle Muscular Dystrophy 2 I. The annual meeting of the DNA academy, Tokyo 2001, Japan. Présentation orale.
- A. Driss, S. Noguchi, T. Sasaki, I. Nishino. Progress in the research of the Limb Girdle Muscular Dystrophy 2 I. The annual meeting of Keio University, Tokyo 2002, Japan. Présentation orale.
- A. Driss, S. Noguchi, R. Amouri, F. Hentati, I. Nishino. FKRP (Fukutin Related Protein) Gene Mutated in Limb Girdle Muscular Dystrophy 2I. Xth International Congress on Neuromuscular Disorders, Vancouver 2002, Canada. Poster.
- F. Hentati, R. Amouri, A. Driss, M. Zouari, K. Muruyama, I. Nishino, M. Ben Hamida. Allelic Heterogeneity of Autosomal Recessive Inclusion Body Myopathy in Tunisia. Xth International Congress on Neuromuscular Disorders, Vancouver 2002, Canada. Poster.
- F. Hentati, M. Kefi, R. Amouri, A. Driss, C. Ben Hamida, M. Ben Hamida. Muscle Biopsy Sarcoglycan Expression is not Related to the Clinical Phenotype in Tunisian LGMD 2C Patients Sharing the Same DEL521-T Mutation. Xth International Congress on Neuromuscular Disorders, Vancouver 2002, Canada. Poster.
- A. Driss, L.N. Charrier, Y Yan, V. Nduati, D. Merlin. The Non-Integrin Laminin Receptor Dystroglycan is expressed in Intestinal Epithelia. 44th annual meeting of the American Society for Cell Biology, Washington, DC, USA, 2004.
Last update August 2006