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Journal Articles

Latent Myeloproliferative Neoplasm May Underlie Retinal Vein Occlusion In Older Patients

Katerina Zoi, PhD, Christine Zoi, Andreas Giannopoulos, MSc, Argyri Gialeraki, PhD, Kassiani Giannaki, MD, PhD, Niki Rougkala, Panagiotis Theodosiadis, MD, John Vergados, MD, Dimitris Loukopoulos, Nicholas C.P. Cross, PhD, FRCPath, Marianna Politou

Blood (2013) 122 (21): 5242.

https://doi.org/10.1182/blood.V122.21.5242.5242

Published: 2013

Journal Articles

The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: results of a 17-year, single-center trial (LaSHS)

Ersi Voskaridou, Dimitrios Christoulas, Antonios Bilalis, Eleni Plata, Konstantinos Varvagiannis, George Stamatopoulos, Klio Sinopoulou, Aggeliki Balassopoulou, Dimitris Loukopoulos, Evangelos Terpos

Blood (2010) 115 (12): 2354–2363.

https://doi.org/10.1182/blood-2009-05-221333

Published: 2010

Journal Articles

No Evidence for Increased Prevalence of JAK2 V617F in Women with a History of Recurrent Miscarriage

Issa J. Dahabreh, Amy V. Jones, Michael Voulgarelis, Christina Alafakis-Tzannatos, Stavroula Giannouli, Marighoula Varla-Leftherioti, Theodora Keramitsoglou, Christine Zoi, Dimitris Loukopoulos, Stelios Fotiou, Nicholas C.P. Cross, PhD, Katerina Zoi, PhD

Blood (2008) 112 (11): 5235.

https://doi.org/10.1182/blood.V112.11.5235.5235

Published: 2008

Journal Articles

Prolonged Administration of Hydroxyurea Reduces Morbidity and Mortality in Adult Patients with Sickle-Cell Syndromes: Long-Term Experience of a Single Center.

Ersi Voskaridou, Antonios Bilalis, Dimitrios Christoulas, Konstantinos Varvagiannis, Kleio Sinopoulou, Eleni Plata, Panagiotis Tsaftaridis, Dimitris Loukopoulos, Evangelos Terpos

Blood (2008) 112 (11): 1445.

https://doi.org/10.1182/blood.V112.11.1445.1445

Published: 2008

Journal Articles

Mutations in the Exon 12 of the JAK2 Gene Appeared To Be a Rare Event Essentially Clustered in V617F JAK2 Negative PV Patients.

Eirini Kouroupi, MD, Nathalie Parquet, MD, Christine Zoi, MD, Jean-Jacques Kiladjian, MD, Vassiliki Grigoraki, MD, Katerina Zoi, PhD, Linda Scott, PhD, Christine Dosquet, MD, Pierre Fenaux, MD, PhD, Dimitris Loukopoulos, MD, PhD, Christine Chomienne, MD, PhD, Bruno Cassinat, PharmD

Blood (2007) 110 (11): 2534.

https://doi.org/10.1182/blood.V110.11.2534.2534

Published: 2007

Journal Articles

Efficient Delivery of the A-Gamma Globin Gene in Human Hematopoietic and Non-Hematopoietic Cells by Cationic Phosphonolipid- and Lipophosphoramide-Mediated Transfection.

Daphne Koumbi, PhD, Jean C. Clement, PhD, Anna-Maria Psarra, PhD, Zili Sideratou, PhD, Jean-Jacques Yaouanc, PhD, Maria Chatzouli, BSc, Dimitris Loukopoulos, MD, Panagoula Kollia, PhD

Blood (2007) 110 (11): 5141.

https://doi.org/10.1182/blood.V110.11.5141.5141

Published: 2007

Journal Articles

Zoledronic Acid Is an Effective Treatment for Osteoporosis in Patients with Thalassemia Major: Results of a Randomized, Placebo-Controlled, Trial.

Ersi Voskaridou, MD, PhD, Dimitris Loukopoulos, MD, PhD, Eleni Stoupa, Eugenia Spyropoulou, John Meletis, Evangelos Terpos, MD, PhD

Blood (2005) 106 (11): 3656.

https://doi.org/10.1182/blood.V106.11.3656.3656

Published: 2005

Journal Articles

Osteoporosis in Sickle Cell/β-Thalassemia Is Primarily Caused by an Imbalance at the RANKL/OPG Pathway.

Ersi Voskaridou, MD, PhD, Ioannis Papassotiriou, PhD, Evangelos Premetis, PhD, John Meletis, MD, PhD, Dimitris Loukopoulos, MD, PhD, Evangelos Terpos, MD, PhD

Blood (2005) 106 (11): 3173.

https://doi.org/10.1182/blood.V106.11.3173.3173

Published: 2005

Journal Articles

Increased Expression of the PRV-1 Gene in Thalassemia Reflects the Rate of the Underlying Erythropoietic Activity.

Katerina Zoi, MSc, Christine Zoi, MSc, Ersi Voskaridou, MD, Evangelos Terpos, MD, Dimitris Loukopoulos, MD

Blood (2005) 106 (11): 2687.

https://doi.org/10.1182/blood.V106.11.2687.2687

Published: 2005

Journal Articles

Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders

Blood (2005) 106 (6): 2162–2168.

https://doi.org/10.1182/blood-2005-03-1320

Published: 2005

Journal Articles

Long Term Treatment with Hydroxyurea Does Not Prevent Development of Renal Dysfunction and Osteodystrophy in Patients with Sickle Cell Disease.

Ersi Voskaridou, Evangelos Terpos, Alexandra Margeli, Eugenia Hantzi, Eleni Stoupa, Aphroditi Loutradi, Ioannis Papassotiriou, Dimitris Loukopoulos

Blood (2004) 104 (11): 1675.

https://doi.org/10.1182/blood.V104.11.1675.1675

Published: 2004

Journal Articles

Elastic tissue abnormalities resembling pseudoxanthoma elasticum in β thalassemia and the sickling syndromes

Athanasios Aessopos, Dimitrios Farmakis, Dimitris Loukopoulos

Blood (2002) 99 (1): 30–35.

https://doi.org/10.1182/blood.V99.1.30

Published: 2002

Journal Articles

Cardiac involvement in thalassemia intermedia: a multicenter study

Athanasios Aessopos, Dimitrios Farmakis, Markisia Karagiorga, Ersi Voskaridou, Aphrodite Loutradi, Antonia Hatziliami, Jacqueline Joussef, John Rombos, Dimitris Loukopoulos

Blood (2001) 97 (11): 3411–3416.

https://doi.org/10.1182/blood.V97.11.3411

Published: 2001

Journal Articles

Healing of Chronic Leg Ulcers in the Hemoglobinopathies With Perilesional Injections of Granulocyte-Macrophage Colony-Stimulating Factor

Ersi Voskaridou, Maria-Christina Kyrtsonis, Aphrodite Loutradi-Anagnostou, Dimitris Loukopoulos

Blood (1999) 93 (10): 3568–3569.

https://doi.org/10.1182/blood.V93.10.3568.410a46c_3568_3569

Published: 1999

Journal Articles

Antigen Selection of Multiple Myeloma Clonogenic B Cells as Evidenced by V H and V L Gene Mutations

Christos Kosmas, Kostas Stamatopoulos, Dimitris Loukopoulos

Blood (1997) 90 (3): 1334.

https://doi.org/10.1182/blood.V90.3.1334

Published: 1997

Journal Articles

Brief Report: On the Chemical Abnormality of Hb "Alexandra," a Fetal Hemoglobin Variant

DIMITRIS LOUKOPOULOS, M.D., ANASTASIA KALTSOYA, M.D., PHAEDON FESSAS, M.D.

Blood (1969) 33 (1): 114–118.

https://doi.org/10.1182/blood.V33.1.114.114

Published: 1969

Journal Articles

Brief Report: Absorption Spectra of Inclusion Bodies in β-Thalassemia

PHAEDON FESSAS, M.D., DIMITRIS LOUKOPOULOS, M.D., BO THORELL, M.D.

Blood (1965) 25 (1): 105–109.

https://doi.org/10.1182/blood.V25.1.105.105

Published: 1965

NARROW

Latent Myeloproliferative Neoplasm May Underlie Retinal Vein Occlusion In Older Patients

The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: results of a 17-year, single-center trial (LaSHS)

No Evidence for Increased Prevalence of JAK2 V617F in Women with a History of Recurrent Miscarriage

Prolonged Administration of Hydroxyurea Reduces Morbidity and Mortality in Adult Patients with Sickle-Cell Syndromes: Long-Term Experience of a Single Center.

Mutations in the Exon 12 of the JAK2 Gene Appeared To Be a Rare Event Essentially Clustered in V617F JAK2 Negative PV Patients.

Efficient Delivery of the A-Gamma Globin Gene in Human Hematopoietic and Non-Hematopoietic Cells by Cationic Phosphonolipid- and Lipophosphoramide-Mediated Transfection.

Zoledronic Acid Is an Effective Treatment for Osteoporosis in Patients with Thalassemia Major: Results of a Randomized, Placebo-Controlled, Trial.

Osteoporosis in Sickle Cell/β-Thalassemia Is Primarily Caused by an Imbalance at the RANKL/OPG Pathway.

Increased Expression of the PRV-1 Gene in Thalassemia Reflects the Rate of the Underlying Erythropoietic Activity.

Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders

Long Term Treatment with Hydroxyurea Does Not Prevent Development of Renal Dysfunction and Osteodystrophy in Patients with Sickle Cell Disease.

Elastic tissue abnormalities resembling pseudoxanthoma elasticum in β thalassemia and the sickling syndromes

Cardiac involvement in thalassemia intermedia: a multicenter study

Healing of Chronic Leg Ulcers in the Hemoglobinopathies With Perilesional Injections of Granulocyte-Macrophage Colony-Stimulating Factor

Antigen Selection of Multiple Myeloma Clonogenic B Cells as Evidenced by V H and V L Gene Mutations

Brief Report: On the Chemical Abnormality of Hb "Alexandra," a Fetal Hemoglobin Variant

Brief Report: Absorption Spectra of Inclusion Bodies in β-Thalassemia

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American Society of Hematology

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American Society of Hematology

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