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Journal Articles

The Clinical Severity of Alpha-2 Globin Gene Variants: Homozygosity for Hb Agrinio ( HBA2 : c.89T>C) Leads to Severe Antenatal Anemia, about 8 Cases in 3 Families

Claire Berger, MD, Philippe Joly, PhD, Serge Pissard, PhD, Sandrine Baron-Joly, MD, Yoann Huguenin, MD, Aurélie Cantais, MD, Sophie Brun, MD, Cecile GED, MD, Catherine Badens, PhD PharmD, Muriel Giansily-Blaizot, MD, Aguilar-Martinez Patricia, MD PhD, Isabelle Thuret, MD

Blood (2020) 136 (Supplement 1): 3–4.

https://doi.org/10.1182/blood-2020-134894

Published: 2020

Journal Articles

A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H

Blood (2020) 136 (15): 1789–1793.

https://doi.org/10.1182/blood.2020005934

Published: 2020

Includes: Supplemental data

Journal Articles

Deciphering the Causal Diagnosis of Hydrops Fetalis or Unexplained Fetal Anemia Using Targeted Next Generation and Exome Sequencing

Julie Galimand, Helene Bourdeau, Odile Fenneteau, Sophie Dreux, Nathalie Couque, PharmD, Severine Drunat, PharmD, PhD, Serge Pissard, PhD, Thierry Leblanc, MD, Anne Lambilliotte, MD, Catherine Thong Vanh, Caroline Alby, jelena-Hélène martinovic-Bouriel, Chloé Quelin, Mohandas Narla, DSc, Anne Cortey, Lydie Da Costa

Blood (2019) 134 (Supplement_1): 3519.

https://doi.org/10.1182/blood-2019-127432

Published: 2019

Journal Articles

The First Two Years of Life in Sickle Cell Anemia Infants: Results of a Comprehensive Longitudinal Study

Blood (2017) 130 (Supplement 1): 688.

https://doi.org/10.1182/blood.V130.Suppl_1.688.688

Published: 2017

Journal Articles

Lesional Mechanism of Alpha Thalassemias : Towards a Common Mechanism Alpha Thal / Beta Thal

Serge Pissard, PhD, Flavia Guillem, PhD, Elisa Domingues-Hamdi, Michaël Dussiot, PhD, Thunwarat Suriyun, Olivier Hermine, MD PhD, Veronique Baudin creuza, Genevieve Courtois, PhD

Blood (2017) 130 (Supplement 1): 358.

https://doi.org/10.1182/blood.V130.Suppl_1.358.358

Published: 2017

Journal Articles

Biallelic Mutations in Hamp in Type 2b Hemochromatosis

Serge Pissard, MDPhD, Ka Chandran, Florence Houriez, Ichrache Benmaad, Martial Saunier, Thibault Lefebvre, Patricia Aguilar-Martinez, MD PhD, Patricia A. Bignell, Gerald Le Gac, MDPhD, Jacques Rochette, MB, DSc

Blood (2016) 128 (22): 1279.

https://doi.org/10.1182/blood.V128.22.1279.1279

Published: 2016

Journal Articles

Inherited and Acquired Modifiers of Iron Status May Dramatically Affect the Phenotypic Expression of Dehydrated Hereditary Stomatocytosis

Corentin Orvain, Lydie Da Costa, MD PhD, Richard van Wijk, PhD, Serge Pissard, MD PhD, Veronique Picard, MD PhD, Lamisse Mansour-Hendili, PharmD, Muriel Giansily-Blaizot, MD PhD, Guillaume Cartron, MD PhD, Jean-Francois Schved, MD PhD, Patricia Aguilar-Martinez, MD PhD

Blood (2016) 128 (22): 1281.

https://doi.org/10.1182/blood.V128.22.1281.1281

Published: 2016

Journal Articles

Impact of α-Gene Deletions and β-Globin Cluster Haplotypes on Biological Parameters at Baseline and on Hydroxyurea in Children with Sickle Cell Anemia

Francoise Bernaudin, MD, Cécile Arnaud, MD, Annie Kamdem, MD, Serge Pissard, MD PhD, Isabelle Hau, MD, Ralph Epaud, MD PhD, Corinne Pondarré, MD PhD

Blood (2016) 128 (22): 10.

https://doi.org/10.1182/blood.V128.22.10.10

Published: 2016

Journal Articles

Limits of Phenotype Analyses in the Diagnosis of HbS Heterozygosity. Example of a Hb S Carrier Phenocopy Due to Hb Arya (Alpha 1: codon 47 Asp>Asn) and a Gene Conversion

Serge Pissard, MD PhD, Adrien Pecriaux, Catherine Paillard, MD PhD, Anne Galoisy, PharmD, Jean Riou, Nathalie Le Metayer, Henri Wajcman, MD PhD

Blood (2016) 128 (22): 4850.

https://doi.org/10.1182/blood.V128.22.4850.4850

Published: 2016

Journal Articles

GATA 1: pArg202Thr, a New GATA 1 Mutation Involved in a Severe Dyserythropoietic Phenotype

Serge Pissard, MDPhD, Chadia Mekki, PharmD, Serge Hovhannisyan, MD, Lydie M. Da Costa, MD PhD, Valentine Brousse, MD, Carole Conejero, Stephane Giraudier, MD PhD, Mariane De Montalembert

Blood (2014) 124 (21): 1343.

https://doi.org/10.1182/blood.V124.21.1343.1343

Published: 2014

Journal Articles

Homozygous Southeast Asian ovalocytosis is a severe dyserythropoietic anemia associated with distal renal tubular acidosis

Véronique Picard, Alexis Proust, Marion Eveillard, Joanna F. Flatt, Marie-Laure Couec, Gaêlle Caillaux, Madeleine Fénéant-Thibault, Arie Finkelstein, Martine Raphaël, Jean Delaunay, Lesley J. Bruce, Serge Pissard, Caroline Thomas

Blood (2014) 123 (12): 1963–1965.

https://doi.org/10.1182/blood-2014-01-548149

Published: 2014

Journal Articles

Early Clinical Manifestations, Presence Of a Single Bantou Haplotype and High Baseline Reticulocyte Count Predict Severity In a Sickle Cell Anemia Newborn Cohort

Corinne Pondarre, MD, PHD, Annie Kamdem, MD, Cécile Arnaud, MD, Serge Pissard, PhD, Josiane Michau, PHD, Clément Tassel, MD, Isabelle Hau, MD, Ralph Epaud, MD, PHD, Francoise Bernaudin, MD

Blood (2013) 122 (21): 2213.

https://doi.org/10.1182/blood.V122.21.2213.2213

Published: 2013

Journal Articles

Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysis

Pablo Bartolucci, Carlo Brugnara, Armando Teixeira-Pinto, Serge Pissard, Kamran Moradkhani, Hélène Jouault, Frederic Galacteros

Blood (2012) 120 (15): 3136–3141.

https://doi.org/10.1182/blood-2012-04-424184

Published: 2012

Journal Articles

The First Reported Case of Prenatal Diagnosis for Pyruvate Kinase Deficiency in a Chinese Family

Jason CC So, MBBS, Mary Tang, MBBS, Rever Li, MBBS, Shau Yin Ha, MBBS, Serge Pissard, PhD, Li Chong Chan, MBChB, PhD

Blood (2011) 118 (21): 5276.

https://doi.org/10.1182/blood.V118.21.5276.5276

Published: 2011

Journal Articles

Beta-Globin Cluster Cis-ACTING Sequence and BCL11A Variants in the Control of Hemoglobin F Expression

Elyes Slim Ghedira, Laure Lecerf, Emmanuelle Faubert, Nathalie Lemetayer, Christian Vasseur, Frederic Galacteros, Serge Pissard, PhD

Blood (2011) 118 (21): 1091.

https://doi.org/10.1182/blood.V118.21.1091.1091

Published: 2011

Journal Articles

Gallstones in a Newborn-Cohort with Sickle Cell Anemia (SCA): Cumulative Risk and Predictive Factors

Annie Kamdem, Cécile Arnaud, Nadia Médejel, Clément Tassel, Isabelle Hau, Serge Pissard, Francoise Bernaudin

Blood (2011) 118 (21): 513.

https://doi.org/10.1182/blood.V118.21.513.513

Published: 2011

Journal Articles

Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolome

Dhouha Darghouth, Bérengère Koehl, Geoffrey Madalinski, Jean-François Heilier, Petra Bovee, Ying Xu, Marie-Françoise Olivier, Pablo Bartolucci, Malika Benkerrou, Serge Pissard, Yves Colin, Frederic Galacteros, Giel Bosman, Christophe Junot, Paul-Henri Roméo

Blood (2011) 117 (6): e57–e66.

https://doi.org/10.1182/blood-2010-07-299636

Published: 2011

Includes: Supplemental data

Journal Articles

Analysis of Rare deletional Thalassemia Using Custom CGH Array DNA Chip

Serge Pissard, PhD, Raphael Ceccaldi, PhD, Emmanuelle Faubert-Laugé, PhD, Valerie Velayoudane, PhD, Valerie Delattre, PhD, Laure Lecerf, PhD

Blood (2010) 116 (21): 4278.

https://doi.org/10.1182/blood.V116.21.4278.4278

Published: 2010

Journal Articles

Unstable Alpha Hemoglobin Stabilizing Protein as a Cause of Thalassemia: Proof of Concept.

Serge Pissard, Corinne Vasseur, Fabienne Toutain, Muriel Silva, Emmanuelle Faubert-Laugé, Elisa Domingues, Michael Marden, Henri Wajcman, Véronique Baudin-Creuza

Blood (2009) 114 (22): 462.

https://doi.org/10.1182/blood.V114.22.462.462

Published: 2009

Journal Articles

Evolution of Transfusion Requirement in Algerian Thalassemic Major (TM) and Intermediate (TI) Patients Treated with Hydroxyurea (HU).

Mohamed Bradai, MD, Serge Pissard, MD, Mohand Tayeb Abad, MD, Agnes Dechartres, MD, Jean-Antoine Ribeil, MD, Paul Landais, MD, Mariane De Montalembert, MD

Blood (2006) 108 (11): 1588.

https://doi.org/10.1182/blood.V108.11.1588.1588

Published: 2006

NARROW

The Clinical Severity of Alpha-2 Globin Gene Variants: Homozygosity for Hb Agrinio ( HBA2 : c.89T>C) Leads to Severe Antenatal Anemia, about 8 Cases in 3 Families

A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H

Deciphering the Causal Diagnosis of Hydrops Fetalis or Unexplained Fetal Anemia Using Targeted Next Generation and Exome Sequencing

The First Two Years of Life in Sickle Cell Anemia Infants: Results of a Comprehensive Longitudinal Study

Lesional Mechanism of Alpha Thalassemias : Towards a Common Mechanism Alpha Thal / Beta Thal

Biallelic Mutations in Hamp in Type 2b Hemochromatosis

Inherited and Acquired Modifiers of Iron Status May Dramatically Affect the Phenotypic Expression of Dehydrated Hereditary Stomatocytosis

Impact of α-Gene Deletions and β-Globin Cluster Haplotypes on Biological Parameters at Baseline and on Hydroxyurea in Children with Sickle Cell Anemia

Limits of Phenotype Analyses in the Diagnosis of HbS Heterozygosity. Example of a Hb S Carrier Phenocopy Due to Hb Arya (Alpha 1: codon 47 Asp>Asn) and a Gene Conversion

GATA 1: pArg202Thr, a New GATA 1 Mutation Involved in a Severe Dyserythropoietic Phenotype

Homozygous Southeast Asian ovalocytosis is a severe dyserythropoietic anemia associated with distal renal tubular acidosis

Early Clinical Manifestations, Presence Of a Single Bantou Haplotype and High Baseline Reticulocyte Count Predict Severity In a Sickle Cell Anemia Newborn Cohort

Erythrocyte density in sickle cell syndromes is associated with specific clinical manifestations and hemolysis

The First Reported Case of Prenatal Diagnosis for Pyruvate Kinase Deficiency in a Chinese Family

Beta-Globin Cluster Cis-ACTING Sequence and BCL11A Variants in the Control of Hemoglobin F Expression

Gallstones in a Newborn-Cohort with Sickle Cell Anemia (SCA): Cumulative Risk and Predictive Factors

Pathophysiology of sickle cell disease is mirrored by the red blood cell metabolome

Analysis of Rare deletional Thalassemia Using Custom CGH Array DNA Chip

Unstable Alpha Hemoglobin Stabilizing Protein as a Cause of Thalassemia: Proof of Concept.

Evolution of Transfusion Requirement in Algerian Thalassemic Major (TM) and Intermediate (TI) Patients Treated with Hydroxyurea (HU).

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American Society of Hematology

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American Society of Hematology

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