Showing results (1-10 of 87) with videos related to
Sort By:
Pageof 9
British Journal of Haematology|June 30, 2016
Advances in understanding the pathogenesis of the red cell volume disordersCatherine Badens, Hélène GuizouarnIntractable & Rare Diseases Research|October 25, 2014
Human Mendelian diseases related to abnormalities of the RNA exosome or its cofactorsAlexandre Fabre, Catherine BadensAnnales De Biologie Clinique|December 9, 2014
[Beta-thalassemias: molecular, epidemiological, diagnostical and clinical aspects]Philippe Joly, Corinne Pondarre, Catherine BadensCells|August 27, 2020
Molecular and Mechanobiological Pathways Related to the Physiopathology of FPLD2Alice-Anaïs Varlet, Emmanuèle Helfer, Catherine BadensOrphanet Journal of Rare Diseases|January 11, 2013
Syndromic diarrhea/Tricho-hepato-enteric syndromeAlexandre Fabre, Christine Martinez-Vinson, Olivier Goulet, et al.Hemoglobin|April 18, 2009
The rare codon 24 (T>A) (beta+) mutation in association with the common codon 39 (C> T) (beta0) mutation causes transfusion-dependent beta-thalassemia in a Moroccan patientImane Agouti, Mohcine Bennani, Nicolas Levy, et al.Genetic Testing|November 4, 2008
Molecular basis of beta-thalassemia in Morocco: possible origins of the molecular heterogeneityImane Agouti, Catherine Badens, Ahmed Abouyoub, et al.Frontiers in Physiology|January 24, 2022
Dynamics of Individual Red Blood Cells Under Shear Flow: A Way to Discriminate Deformability AlterationsScott Atwell, Catherine Badens, Anne Charrier, et al.Haematologica|January 18, 2005
Compound heterozygosity for unstable hemoglobin Genova and beta(o)-thalassemia associated with early onset of thalassemia major syndromeCatherine Badens, Chantal Paolasso, Chantal Fossat, et al.European Journal of Haematology|December 18, 2007
Beta-thalassemia intermedia due to two novel mutations in the promoter region of the beta-globin geneImane Agouti, Mohcine Bennani, Meyer Nezri, et al.Pageof 9