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Journal Articles

A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene

Bernard Grandchamp, Gilles Hetet, Caroline Kannengiesser, Claire Oudin, Carole Beaumont, Sylvie Rodrigues-Ferreira, Robert Amson, Adam Telerman, Peter Nielsen, Elisabeth Kohne, Christina Balser, Hermann Heimpel

Blood (2011) 118 (25): 6660–6666.

https://doi.org/10.1182/blood-2011-01-329011

Published: 2011

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

Two New Human DMT1 Mutations in a Compound Heterozygous Patient with Microcytic Anemia and Low Iron Stores.

Carole Beaumont, PhD, Jean Delaunay, MD, PhD, Gilles Hetet, Mariane de Montalembert, MD, Bernard Grandchamp, MD, PhD, Gilbert J. Tchernia, MD, PhD

Blood (2005) 106 (11): 3540.

https://doi.org/10.1182/blood.V106.11.3540.3540

Published: 2005

Journal Articles

Analysis of JAK2 Mutation in Essential Thrombocythemia (ET) Patients with Monoclonal and Polyclonal X-Chromosome Inactivation Patterns (XCIPs).

Jean-Jacques Kiladjian, MD, Nahed Elkassar, MD, Gilles Hetet, Nicole Balitrand, Carole Conejero, Stephane Giraudier, MD, Bruno Cassinat, MD, Claude Gardin, MD, Pierre Fenaux, MD, Christine Chomienne, MD, Bernard Grandchamp, MD

Blood (2005) 106 (11): 2603.

https://doi.org/10.1182/blood.V106.11.2603.2603

Published: 2005

Journal Articles

Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations

Gilles Hetet, Isabelle Devaux, Nadem Soufir, Bernard Grandchamp, Carole Beaumont

Blood (2003) 102 (5): 1904–1910.

https://doi.org/10.1182/blood-2003-02-0439

Published: 2003

Includes: Supplemental data

Journal Articles

Clonality Analysis of Hematopoiesis in Essential Thrombocythemia: Advantages of Studying T Lymphocytes and Platelets

Nahed El-Kassar, Gilles Hetet, Jean Brière, Bernard Grandchamp

Blood (1997) 89 (1): 128–134.

https://doi.org/10.1182/blood.V89.1.128

Published: 1997

NARROW

A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene

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

Two New Human DMT1 Mutations in a Compound Heterozygous Patient with Microcytic Anemia and Low Iron Stores.

Analysis of JAK2 Mutation in Essential Thrombocythemia (ET) Patients with Monoclonal and Polyclonal X-Chromosome Inactivation Patterns (XCIPs).

Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations

Clonality Analysis of Hematopoiesis in Essential Thrombocythemia: Advantages of Studying T Lymphocytes and Platelets

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ASH Publications

American Society of Hematology

A novel type of congenital hypochromic anemia associated with a nonsense mutation in the STEAP3/TSAP6 gene

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

Two New Human DMT1 Mutations in a Compound Heterozygous Patient with Microcytic Anemia and Low Iron Stores.

Analysis of JAK2 Mutation in Essential Thrombocythemia (ET) Patients with Monoclonal and Polyclonal X-Chromosome Inactivation Patterns (XCIPs).

Molecular analyses of patients with hyperferritinemia and normal serum iron values reveal both L ferritin IRE and 3 new ferroportin (slc11A3) mutations

Clonality Analysis of Hematopoiesis in Essential Thrombocythemia: Advantages of Studying T Lymphocytes and Platelets

Email alerts

ASH Publications

American Society of Hematology

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