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Hemoglobin|November 13, 2007
Thalassemia intermedia due to a novel mutation in the second intervening sequence of the beta-globin geneImane Agouti, Mohcine Bennani, Abouyoub Ahmed, et al.
Journal of Clinical Apheresis|August 15, 2015
Comparative evaluation of the depletion-red cell exchange program with the Spectra Optia and the isovolemic hemodilution-red cell exchange method with the COBE Spectra in sickle cell disease patientsPascale Poullin, Frederick Sanderson, Emmanuelle Bernit, et al.
Cardiovascular Research|January 12, 2024
Perilipin 1: a systematic review on its functions on lipid metabolism and atherosclerosis in mice and humansCamille Desgrouas, Tabea Thalheim, Mathieu Cerino, et al.
American Journal of Medical Genetics. Part A|February 24, 2007
Intractable diarrhea with "phenotypic anomalies" and tricho-hepato-enteric syndrome: two names for the same disorderAlexandre Fabre, Nicolas André, Anne Breton, et al.
Hemoglobin|October 25, 2012
A new ATRX mutation in a patient with acquired α-thalassemia myelodysplastic syndromeCharles Herbaux, Catherine Badens, Stéphanie Guidez, et al.
Intractable & Rare Diseases Research|September 26, 2017
Management of syndromic diarrhea/tricho-hepato-enteric syndrome: A review of the literatureAlexandre Fabre, Patrice Bourgeois, Marie-Edith Coste, et al.
European Journal of Haematology|July 31, 2023
Transfusion requirements and complication rate in β-thalassemia intermedia due to heterozygous β-globin gene mutation and triplicated α-globin genesNathalie Bonello-Palot, Audrey Benoit, Imane Agouti, et al.
Hemoglobin|March 26, 2015
Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte IslandMathias Muszlak, Serge Pissard, Catherine Badens, et al.
Frontiers in Cell and Developmental Biology|April 27, 2019
Rare BANF1 Alleles and Relatively Frequent EMD Alleles Including 'Healthy Lipid' Emerin p.D149H in the ExAC CohortTejas Dharmaraj, Youchen Guan, Julie Liu, et al.
Clinical Biochemistry|January 4, 2011
Analytical evaluation of the Tosoh HLC-723 G8 automated HPLC analyzer for hemoglobin analysis in beta-thalassemia modeFrançoise Merono, Imane Agouti, Nathalie Bonello-Palot, et al.
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