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Journal Articles

A Deletion Of About 11kb Starting From 0.5 Kb 5’ To The β-Globin Gene Reactivates Foetal Haemoglobin and Leads To β Thalassemia Intermedia When Associated To a β-Zero Thalassemic Mutation

Photis Beris, MD, Tanguy Araud, Lorella Clerici, Anne-Pascale Grandjean, MD, Georgios Georgiou, MD, Frédéric Guerry, Kaveh Samii, MD, Pierre-Alain Menoud, MD

Blood (2013) 122 (21): 4702.

https://doi.org/10.1182/blood.V122.21.4702.4702

Published: 2013

Journal Articles

Iron Overload Diagnosis and Management Among Clinicians: International Survey Showing Gaps In Knowledge and Need for Continuing Educational Programs

Maria Domenica Cappellini, MD, Photis Beris, Pierre Brissot, MD, John B. Porter, MD, Ali Taher, MD, Patty Peterson, CCMEP, Elaine Rudell, CCMEP

Blood (2010) 116 (21): 2562.

https://doi.org/10.1182/blood.V116.21.2562.2562

Published: 2010

Journal Articles

Low Bone Mineral Density and High Bone Turnover In Patients with Non-Hodgkin's Lymphoma (NHL) Who Receive Frontline Therapy: Results of a Multicenter Prospective Study

Konstantinos Anargyrou, Theodoros P. Vassilakopoulos, Konstantinos Tsionos, Panayiotis Kokkoris, Georgios Boutsikas, Maria K. Angelopoulou, Dimitrios Christoulas, Stavroula Masouridou, Maria Dimou, Athanasios Papatheodorou, Danos N. Chatzifotiadis, Panayiotis Panayiotidis, Gerasimos A. Pangalis, Photis Beris, Evangelos Terpos

Blood (2010) 116 (21): 5071.

https://doi.org/10.1182/blood.V116.21.5071.5071

Published: 2010

Journal Articles

Efficacy and Safety of 1 Year’s Treatment with Deferasirox (Exjade ® ): Assessment of Regularly Transfused Patients with Diamond-Blackfan Anemia Enrolled in the EPIC Study.

John B Porter, Gian Luca Forni, Photis Beris, Ali Taher, Dany Habr, Gabor Domokos, Abdel Hmissi, Maria Domenica Cappellini

Blood (2008) 112 (11): 1048.

https://doi.org/10.1182/blood.V112.11.1048.1048

Published: 2008

Journal Articles

Growth Differentiation Factor-15 Is Not Responsible for Decreased Hepcidin Expression in Cases of Ineffective Eythropoiesis.

Photis Beris, MD, Olivier Golaz, PhD, Nouri Mensi, Thomas Matthes, MD, Christophe Chardot, MD, Isabelle Tchou, PhD

Blood (2007) 110 (11): 2674.

https://doi.org/10.1182/blood.V110.11.2674.2674

Published: 2007

Journal Articles

Development of a Model for the Study of PU.1 Function in Primary Human Hematopoietic Cells.

Stephane Durual, PhD, Alexandra Rideau, Maciej Wiznerowics, PhD, Sylvie Ruault, Photis Beris, MD, Vincent Piguet, MD, Thomas Matthes, MD

Blood (2005) 106 (11): 4234.

https://doi.org/10.1182/blood.V106.11.4234.4234

Published: 2005

Journal Articles

GATA-1 Overexpression Does Not Restore Deficient Erythropoiesis in Myelodysplastic Syndromes.

Alexandra Rideau, Stephane Durual, PhD, Maciej Wiznerowics, PhD, Sylvie Ruault, Vincent Piguet, MD, PhD, Photis Beris, MD, Thomas Matthes, MD

Blood (2005) 106 (11): 3430.

https://doi.org/10.1182/blood.V106.11.3430.3430

Published: 2005

Journal Articles

Molecular Mechanism of Hepcidin Deficiency in a Patient with Juvenile Hemochromatosis.

Alexandra Rideau, BSc, Bastien Mangeat, BSc, Thomas Matthes, MD, Didier Trono, MD, PhD, Photis Beris, MD

Blood (2004) 104 (11): 3194.

https://doi.org/10.1182/blood.V104.11.3194.3194

Published: 2004

Journal Articles

Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5′-UTR of the HAMP gene

Thomas Matthes, Patricia Aguilar-Martinez, Loredana Pizzi-Bosman, Régis Darbellay, Laura Rubbia-Brandt, Emilio Giostra, Martine Michel, Tomas Ganz, Photis Beris

Blood (2004) 104 (7): 2181–2183.

https://doi.org/10.1182/blood-2004-01-0332

Published: 2004

Journal Articles

Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome

Samuel Deutsch, Alexandra Rideau, Marie-Luce Bochaton-Piallat, Giuseppe Merla, Antoine Geinoz, Giulio Gabbiani, Torsten Schwede, Thomas Matthes, Stylianos E. Antonarakis, Photis Beris

Blood (2003) 102 (2): 529–534.

https://doi.org/10.1182/blood-2002-09-2783

Published: 2003

NARROW

A Deletion Of About 11kb Starting From 0.5 Kb 5’ To The β-Globin Gene Reactivates Foetal Haemoglobin and Leads To β Thalassemia Intermedia When Associated To a β-Zero Thalassemic Mutation

Iron Overload Diagnosis and Management Among Clinicians: International Survey Showing Gaps In Knowledge and Need for Continuing Educational Programs

Low Bone Mineral Density and High Bone Turnover In Patients with Non-Hodgkin's Lymphoma (NHL) Who Receive Frontline Therapy: Results of a Multicenter Prospective Study

Efficacy and Safety of 1 Year’s Treatment with Deferasirox (Exjade ® ): Assessment of Regularly Transfused Patients with Diamond-Blackfan Anemia Enrolled in the EPIC Study.

Growth Differentiation Factor-15 Is Not Responsible for Decreased Hepcidin Expression in Cases of Ineffective Eythropoiesis.

Development of a Model for the Study of PU.1 Function in Primary Human Hematopoietic Cells.

GATA-1 Overexpression Does Not Restore Deficient Erythropoiesis in Myelodysplastic Syndromes.

Molecular Mechanism of Hepcidin Deficiency in a Patient with Juvenile Hemochromatosis.

Severe hemochromatosis in a Portuguese family associated with a new mutation in the 5′-UTR of the HAMP gene

Asp1424Asn MYH9 mutation results in an unstable protein responsible for the phenotypes in May-Hegglin anomaly/Fechtner syndrome

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American Society of Hematology

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American Society of Hematology

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