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Hemoglobin|September 29, 2011
α-Hemoglobin stabilizing protein: a modulating factor in thalassemias?Henri Wajcman, Corinne Vasseur, Serge Pissard, et al.
Molecular Diagnosis : a Journal Devoted to the Understanding of Human Disease Through the Clinical Application of Molecular Biology|October 8, 2003
A one-step real-time PCR assay for rapid prenatal diagnosis of sickle cell disease and detection of maternal contaminationCatherine Costa, Serge Pissard, Emmanuelle Girodon, et al.
Hemoglobin|October 16, 2004
Compound heterozygosity for two new mutations in the beta-globin gene [codon 9 (+TA) and polyadenylation site (AATAAA-->AAAAAA)] leads to thalassemia intermedia in a Tunisian patientAurelia Jacquette, Geneviève Le Roux, Chantal Lacombe, et al.
Hemoglobin|May 26, 2016
Hb Savaria [α49(CE7)Ser→Arg; HBA2: c.150C > A]: A New Case and Complete DescriptionThi Hai Yen Tran Houangkeo, Virginie Bodereau, Jean Riou, 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.
Blood Cells, Molecules & Diseases|March 4, 2014
Variability of hemoglobin F expression in hemoglobin EE disease: hematological and molecular analysisNaruwat Pakdee, Supawadee Yamsri, Goonnapa Fucharoen, et al.
Blood|April 19, 2003
Hydroxyurea can eliminate transfusion requirements in children with severe beta-thalassemiaMohamed Bradai, Mohand Tayeb Abad, Serge Pissard, et al.
Journal of Pediatric Hematology/Oncology|May 20, 2026
A Rare Case of Homozygous HbE With Coinherited Alpha-Thalassemia and Hb Constant Spring in a Neonate Reveals a Mild Hematologic PhenotypeVictor Bobée, Maïssa Souissi, Cécile Dumesnil, et al.
Hemoglobin|March 23, 2011
A second observation of the rare frameshift mutation in the β-globin gene: codon 46 (+A) (Hbb:c.138_139insA)Elyes Slim Ghedira, Delphine Dupin-Deguine, Denis Duffilot, et al.
American Journal of Hematology|January 26, 2011
Evaluation of the free α-hemoglobin pool in red blood cells: a new test providing a scale of β-thalassemia severityCorinne Vasseur, Serge Pissard, Elisa Domingues-Hamdi, et al.
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