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Blood Cells, Molecules & Diseases|February 8, 2002
Acute intermittent porphyria: heterogeneity of mutations in the hydroxymethylbilane synthase gene in ItalyF Martinez di Montemuros, E Di Pierro, G Biolcati, et al.Blood Cells, Molecules & Diseases|February 8, 2002
Pathophysiology of a sickle cell trait mouse model: human alpha(beta)(S) transgenes with one mouse beta-globin alleleC T Noguchi, M Gladwin, B Diwan, et al.Blood Cells, Molecules & Diseases|July 30, 2019
Elevated surface-bound complement FH alters the function of platelets and monocytes in FHR1/3 null healthy individualsAngika Bhasym, Teena Bhakuni, Prasenjit GuchhaitBlood Cells, Molecules & Diseases|March 16, 2011
Thalassemia intermedia is associated with a proatherogenic biochemical phenotypeMaria Eliana Lai, Stefania Vacquer, Maria Paola Carta, et al.Blood Cells, Molecules & Diseases|April 16, 2011
A comprehensive molecular characterization of beta thalassemia in a highly heterogeneous populationHaleh Akhavan-Niaki, Poupak Derakhshandeh-Peykar, Ali Banihashemi, et al.Blood Cells, Molecules & Diseases|April 26, 2011
Lack of iron-related phenotype in Sp6 intestinal knockout micePavle Matak, Jean-Christophe Deschemin, Carole Peyssonnaux, et al.Blood Cells, Molecules & Diseases|June 7, 2011
Engineering erythrocytes to be erythrosensors: first stepsMark A Milanick, Sarah Ritter, Kenith MeissnerBlood Cells, Molecules & Diseases|November 26, 2010
Characterization of the ERAD process of the L444P mutant glucocerebrosidase variantInna Bendikov-Bar, Idit Ron, Mirella Filocamo, et al.Blood Cells, Molecules & Diseases|December 31, 2010
Application of MLPA assay to characterize unsolved α-globin gene rearrangementsAlessia Colosimo, Valentina Gatta, Valentina Guida, et al.Blood Cells, Molecules & Diseases|February 11, 2011
Polymorphonuclear neutrophils from JAK2(V617F) positive MPD patients do not support hypercoagulability: A study with calibrated automated thrombography (CAT)Julien Perrin, Dana Ranta, Fabienne Empereur, et al.Pageof 220