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Journal Articles

Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study

Thomas Pincez, Corinne Guitton, Frédéric Gauthier, Guénolée de Lambert, Véronique Picard, Madeleine Fénéant-Thibault, Ali Turhan, Narla Mohandas, Gil Tchernia, Loïc Garçon

Blood (2016) 127 (12): 1616–1618.

https://doi.org/10.1182/blood-2015-11-679357

Published: 2016

Journal Articles

Long-Term Follow up of the Beneficial Effects and of Issues in Subtotal Splenectomy for Hereditary Spherocytosis

Thomas Pincez, Corinne Guitton, Frederic Gauthier, Guenolee Lambert, Veronique Picard, PhDMD, Madeleine feneant Thibault, Narla Mohandas, DSc, Gil Tchernia, MD, Loic Garcon

Blood (2015) 126 (23): 276.

https://doi.org/10.1182/blood.V126.23.276.276

Published: 2015

Journal Articles

The Cerebral Vasculopathy In Malian Sickle Cell Anemia Children: Lesson From Routine Transcranial Doppler Screening

Dapa Aly Diallo, MD, Aldiouma Guindo, PhD, Alain Dorie, MD, Boubacari Ali Touré, MD, Baba Fané, MD, Yaya Sarro, PharmD, Gil Tchernia, MD

Blood (2013) 122 (21): 4687.

https://doi.org/10.1182/blood.V122.21.4687.4687

Published: 2013

Journal Articles

Activation of p53 Pathway In Erythroid Precursor Cells of Diamond-Blackfan Anemia Leads to Two Distinct Phenotypes

Hélène Moniz, Aurore Crétien, Corinne Hurtaud, Thierry Leblanc, Isabelle Marie, Gil Tchernia, William Vainchenker, MD, PhD, Mohandas Narla, DSc, Lydie M. Da Costa, MD, PhD

Blood (2010) 116 (21): 2225.

https://doi.org/10.1182/blood.V116.21.2225.2225

Published: 2010

Journal Articles

Distinct Differences in in Vitro Erythroid Proliferation and Differentiation, p53 and Apoptosis Pathways in Diamond-Blackfan Anemia in Conjunction with Depletion of RPS19, RPL5 and RPL11 mRNA.

Hélène Moniz, Corinne Hurtaud, Thierry Leblanc, MD, Gil Tchernia, MD, Narla Mohandas, DSc, Lydie Da Costa, MD, PhD

Blood (2009) 114 (22): 176.

https://doi.org/10.1182/blood.V114.22.176.176

Published: 2009

Journal Articles

A Somatic Mutation in the G6PD Gene in Hematopoietic Cells Causes a Chronic Haemolytic Anemia.

Loïc Garçon, Gérard Tertian, Audrey Boutron, Françoise Driss, Stéphane Giraudier, William Vainchenker, MD, PhD, Michel Goossens, MD, Frederic Galacteros, MD, PhD, Gil Tchernia, MD, Claude Préhu

Blood (2009) 114 (22): 4033.

https://doi.org/10.1182/blood.V114.22.4033.4033

Published: 2009

Journal Articles

Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A

Ashley M. Toye, Rosalind C. Williamson, Moudji Khanfar, Brigitte Bader-Meunier, Thérèse Cynober, Madeleine Thibault, Gil Tchernia, Michèle Déchaux, Jean Delaunay, Lesley J. Bruce

Blood (2008) 111 (11): 5380–5389.

https://doi.org/10.1182/blood-2007-07-099473

Published: 2008

Includes: Supplemental data

Journal Articles

Two Distinct Mechanisms Are Responsible for Regulation of Ribosomal Protein S19 Expression Level in Diamond-Blackfan Anemia by NF-κB Pathway.

Corinne Hurtaud, PhD, Aurore Cretien, PhD, Valerie Clayette, PhD, Didier Pisani, PhD, Stephane Giraudier, MD, PhD, Thierry Leblanc, MD, Jean Delaunay, MD, PhD, Gil Tchernia, MD, Narla Mohandas, PhD, Lydie Da Costa, MD, PhD

Blood (2007) 110 (11): 1684.

https://doi.org/10.1182/blood.V110.11.1684.1684

Published: 2007

Journal Articles

Impaired ribosome biogenesis in Diamond-Blackfan anemia

Valérie Choesmel, Daniel Bacqueville, Jacques Rouquette, Jacqueline Noaillac-Depeyre, Sébastien Fribourg, Aurore Crétien, Thierry Leblanc, Gil Tchernia, Lydie Da Costa, Pierre-Emmanuel Gleizes

Blood (2006) 109 (3): 1275–1283.

https://doi.org/10.1182/blood-2006-07-038372

Published: 2006

Includes: Supplemental data

Journal Articles

Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload

Carole Beaumont, Jean Delaunay, Gilles Hetet, Bernard Grandchamp, Mariane de Montalembert, Gil Tchernia

Blood (2006) 107 (10): 4168–4170.

https://doi.org/10.1182/blood-2005-10-4269

Published: 2006

Includes: Supplemental data

Journal Articles

The First Homozygous RPS19 Mutation Identified in a Diamond-Blackfan Anemia Patient Is Not Deleterious.

Aurore Cretien, Patricia Rince, Thierry Leblanc, MD, Rolande Ducrocq, MD, Alexis Proust, Isabelle Marie, Jean Delaunay, MD, PhD, Mohandas Narla, MD, PhD, Gil Tchernia, MD, Lydie Da Costa, MD, PhD

Blood (2005) 106 (11): 3548.

https://doi.org/10.1182/blood.V106.11.3548.3548

Published: 2005

Journal Articles

High Risk Pregnancies in Women with Diamond Blackfan Anaemia: A Survey of 64 Pregnancies from the French and German Registries.

Thierry Leblanc, MD, Laurence Faivre, MD, Jorg Meerpohl, MD, Lydie Da Costa, MD, PhD, Christian Nouvel, MD, Francis Bauters, MD, Bertrand Coiffier, MD, Pierre-Yves Peaud, MD, Patrick Rispal, MD, Alain Berrebi, MD, Claire Berger, MD, Bruno Varet, MD, Charlotte Niemeyer, MD, PhD, Gil Tchernia, MD

Blood (2005) 106 (11): 3549.

https://doi.org/10.1182/blood.V106.11.3549.3549

Published: 2005

Journal Articles

Proteasome Inhibitors Restore to Normal the Decreased Levels of Protein Expression and Nucleolar Localization of Various Mutant Ribosomal S19 Proteins Identified in DBA Patients.

Aurore Cretien, Alexis Proust, Hanna Gazda, MD, PhD, Jorg Meerpohl, MD, Charlotte Marie Niemeyer, MD, PhD, Jean Delaunay, MD, PhD, Gil Tchernia, MD, Mohandas Narla, MD, PhD, Lydie Da Costa, MD, PhD

Blood (2005) 106 (11): 185.

https://doi.org/10.1182/blood.V106.11.185.185

Published: 2005

Journal Articles

Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP–sialic acid transporter

Ivan Martinez-Duncker, Thierry Dupré, Véronique Piller, Friedrich Piller, Jean-Jacques Candelier, Catherine Trichet, Gil Tchernia, Rafael Oriol, Rosella Mollicone

Blood (2005) 105 (7): 2671–2676.

https://doi.org/10.1182/blood-2004-09-3509

Published: 2005

Journal Articles

Human blood IgM “memory” B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire

Sandra Weller, Moritz C. Braun, Bruce K. Tan, Andreas Rosenwald, Corinne Cordier, Mary Ellen Conley, Alessandro Plebani, Dinakhanta S. Kumararatne, Damien Bonnet, Olivier Tournilhac, Gil Tchernia, Birte Steiniger, Louis M. Staudt, Jean-Laurent Casanova, Claude-Agnès Reynaud, Jean-Claude Weill

Blood (2004) 104 (12): 3647–3654.

https://doi.org/10.1182/blood-2004-01-0346

Published: 2004

Includes: Supplemental data

Journal Articles

Metoclopramide Treatment in Patients with Diamond-Blackfan Anemia: Preliminary Results of a French Prospective Trial.

Thierry Leblanc, MD, Isabelle Marie, Marianne Debre, MD, Lydie Da Costa, MD, PhD, Pierre Bordigoni, MD, Pierre Demolis, MD, Gil Tchernia, MD, the SHIP DBA Working Group

Blood (2004) 104 (11): 2843.

https://doi.org/10.1182/blood.V104.11.2843.2843

Published: 2004

Journal Articles

Molecular Basis of Congenital Dyserythropoietic Anemia Type I in French Patients.

Hannah Tamary, MD, Orly Dgany, PhD, Alexis Proust, MSc, Tanya Krasnov, MSc, Nili Avidan, PhD, Gil Tchernia, MD, David Geneviève, MD, Valérie Comier-Darre, MD, Martine Le Merrer, MD, Brigitte Bader-Meunier, MD, Corinne Ferrero-Vacher, MD, Isaac Yaniv, MD, Jean Delaunay, MD

Blood (2004) 104 (11): 3709.

https://doi.org/10.1182/blood.V104.11.3709.3709

Published: 2004

Journal Articles

Nucleolar localization of RPS19 protein in normal cells and mislocalization due to mutations in the nucleolar localization signals in 2 Diamond-Blackfan anemia patients: potential insights into pathophysiology

Lydie Da Costa, Gil Tchernia, Philippe Gascard, Annie Lo, Joerg Meerpohl, Charlotte Niemeyer, Joel-Anne Chasis, Jason Fixler, Narla Mohandas

Blood (2003) 101 (12): 5039–5045.

https://doi.org/10.1182/blood-2002-12-3878

Published: 2003

Journal Articles

Ribosomal protein S19 expression during erythroid differentiation

Lydie Da Costa, Goutham Narla, Thiébaut-Noel Willig, Luanne L. Peters, Marilyn Parra, Jason Fixler, Gil Tchernia, Narla Mohandas

Blood (2003) 101 (1): 318–324.

https://doi.org/10.1182/blood-2002-04-1131

Published: 2003

Journal Articles

A splicing alteration of 4.1R pre-mRNA generates 2 protein isoforms with distinct assembly to spindle poles in mitotic cells

François Delhommeau, Corinne Vasseur-Godbillon, Philippe Leclerc, Pierre-Olivier Schischmanoff, Laure Croisille, Patricia Rince, Madeleine Morinière, Edward J. Benz, Jr, Gil Tchernia, Gabriel Tamagnini, Leticia Ribeiro, Jean Delaunay, Faouzi Baklouti

Blood (2002) 100 (7): 2629–2636.

https://doi.org/10.1182/blood.V100.7.2629

Published: 2002

NARROW

Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study

Long-Term Follow up of the Beneficial Effects and of Issues in Subtotal Splenectomy for Hereditary Spherocytosis

The Cerebral Vasculopathy In Malian Sickle Cell Anemia Children: Lesson From Routine Transcranial Doppler Screening

Activation of p53 Pathway In Erythroid Precursor Cells of Diamond-Blackfan Anemia Leads to Two Distinct Phenotypes

Distinct Differences in in Vitro Erythroid Proliferation and Differentiation, p53 and Apoptosis Pathways in Diamond-Blackfan Anemia in Conjunction with Depletion of RPS19, RPL5 and RPL11 mRNA.

A Somatic Mutation in the G6PD Gene in Hematopoietic Cells Causes a Chronic Haemolytic Anemia.

Band 3 Courcouronnes (Ser667Phe): a trafficking mutant differentially rescued by wild-type band 3 and glycophorin A

Two Distinct Mechanisms Are Responsible for Regulation of Ribosomal Protein S19 Expression Level in Diamond-Blackfan Anemia by NF-κB Pathway.

Impaired ribosome biogenesis in Diamond-Blackfan anemia

Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overload

The First Homozygous RPS19 Mutation Identified in a Diamond-Blackfan Anemia Patient Is Not Deleterious.

High Risk Pregnancies in Women with Diamond Blackfan Anaemia: A Survey of 64 Pregnancies from the French and German Registries.

Proteasome Inhibitors Restore to Normal the Decreased Levels of Protein Expression and Nucleolar Localization of Various Mutant Ribosomal S19 Proteins Identified in DBA Patients.

Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP–sialic acid transporter

Human blood IgM “memory” B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire

Metoclopramide Treatment in Patients with Diamond-Blackfan Anemia: Preliminary Results of a French Prospective Trial.

Molecular Basis of Congenital Dyserythropoietic Anemia Type I in French Patients.

Nucleolar localization of RPS19 protein in normal cells and mislocalization due to mutations in the nucleolar localization signals in 2 Diamond-Blackfan anemia patients: potential insights into pathophysiology

Ribosomal protein S19 expression during erythroid differentiation

A splicing alteration of 4.1R pre-mRNA generates 2 protein isoforms with distinct assembly to spindle poles in mitotic cells

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American Society of Hematology

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American Society of Hematology

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