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European Journal of Neurology|October 1, 2010
TWINKLE gene mutation: report of a French family with an autosomal dominant progressive external ophthalmoplegia and literature reviewM-L Martin-Negrier, G Sole, C Jardel, et al.La Revue De Medecine Interne|July 31, 2003
[Rituximab in cold agglutinin disease]F Camou, J-F Viallard, J-L PellegrinLa Revue De Medecine Interne|January 31, 2021
[Common variable immunodeficiency disorders: Part 2. Updated clinical manifestations and therapeutic management]J F Viallard, B Lebail, H Begueret, et al.La Revue De Medecine Interne|April 14, 2000
[Schnitzler syndrome: a rare cause of systemic urticaria]P Germain, J Fach, N Bui, et al.Clinical Neuropathology|July 1, 1994
Lhermitte-Duclos type cerebellum hamartoma and Cowden diseaseA Vital, C Vital, M L Martin-Negrier, et al.La Revue De Medecine Interne|December 13, 2021
[HHV-8 Related immunological and hematological diseases]F Blaison, J Galtier, M Parrens, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1994
Colony-stimulating factors and cell cycle in the chemotherapy of acute myelogenous leukemiaJ F Viallard, M Puntous, C Grosset, et al.La Revue De Medecine Interne|May 24, 2003
[Multiple pseudo-cellulitis plaques and Koplick's sign: a particular form of parvovirus B19 primo-infection in adults]X Delbrel, V Sibaud, O Cogrel, et al.Journal of Clinical Pathology|December 29, 2000
Unusual manifestations of type II cryoglobulinaemia associated with Waldenström's macroglobulinaemiaP Blanco, J F Viallard, J Rivel, et al.Pageof 18