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Gynecologie, Obstetrique & Fertilite|October 25, 2011
[Don't forget fallopian tubes! A morphologic and immunohistochemical study about Fallopian tubes with genetic risk (BRCA mutation)]G Chêne, I Raoelfils, A Cayre, et al.Human Genetics|January 1, 1990
Dual genotype in cutaneous T-cell lymphomas and pseudolymphomasY J Bignon, P Souteyrand, H Roger, et al.Advances in Therapy|December 9, 1995
Equally efficacious asthma management with budesonide 800 micrograms administered by Turbuhaler or with beclomethasone dipropionate > or = 1500 micrograms given through a pressurized metered-dose inhaler with spacer. The French Budesonide Trial GroupJ Piquet, P Zuck, G Dennewald, et al.Revue Des Maladies Respiratoires|January 1, 1992
[Sequential administration of a reduced dose of almitrine to patients with chronic obstructive bronchopneumopathies. A controlled multicenter study]E Weitzenblum, F Arnaud, J Bignon, et al.Revue D'Epidemiologie Et De Sante Publique|January 1, 1995
[Longitudinal study of radiologic anomalies in subjects working in asbestos-insulated buildings]N Pierre, Y Iwatsubo, J Ameille, et al.American Journal of Industrial Medicine|September 5, 2002
Estimation of the incidence of pleural mesothelioma according to death certificates in FranceY Iwatsubo, M Matrat, E Michel, et al.Journal of Chromatography. B, Biomedical Sciences and Applications|March 3, 1999
Isolation, purification and quantification of BRCA1 protein from tumour cells by affinity perfusion chromatographyC Hizel, J C Maurizis, P Rio, et al.Annals of the Rheumatic Diseases|June 1, 1986
Angioimmunoblastic lymphadenopathy with dysproteinaemia (AILD) and sicca syndromeY J Bignon, A Janin-Mercier, J J Dubost, et al.Disease Markers|December 14, 1999
Four years analysis of cancer genetic clinics activity in France from 1994 to 1997: a survey on 801 patients. French Cooperative Network/Groupe Génétique et Cancer de la Fédération Nationale des Centres de Lutte Contre le CancerH Sobol, Y J Bignon, C Bonaiti, et al.Human Mutation|April 17, 1999
The 1396del A mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer. Mutations in brief no. 136. OnlineV Vidal, J O Bay, F Champomier, et al.Pageof 37