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Journal Articles

A phase 3 randomized trial of mavorixafor, a CXCR4 antagonist, for WHIM syndrome

Blood (2024) 144 (1): 35–45.

https://doi.org/10.1182/blood.2023022658

Published: 2024

Includes: Supplemental data

Journal Articles

A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia

Blood (2022) 139 (17): 2642–2652.

https://doi.org/10.1182/blood.2021013674

Published: 2022

Includes: Supplemental data

Journal Articles

Global Phase 3, Randomized, Placebo-Controlled Trial with Open-Label Extension Evaluating the Oral CXCR4 Antagonist Mavorixafor in Patients with WHIM Syndrome (4WHIM): Trial Design and Enrollment

Blood (2021) 138 (Supplement 1): 4310.

https://doi.org/10.1182/blood-2021-153346

Published: 2021

Journal Articles

Double-Blind, Randomized Study of Canakinumab Treatment in Pediatric and Young Adult Patients with Sickle Cell Anemia

Blood (2019) 134 (Supplement_1): 615.

https://doi.org/10.1182/blood-2019-123355

Published: 2019

Journal Articles

Renal Function in Transfusion-Dependent β-Thalassemia Patients: A Decade of Follow-up and Comparison between Chelation Regimes

Osama Tanous, MD, Yossi Azulay, MD, Tal Dujovny, MD, Netta Schwarz, PhD, Raul Colodner, PhD, Ariel Koren, MD, Carina Levin, MDPhD

Blood (2017) 130 (Supplement 1): 949.

https://doi.org/10.1182/blood.V130.Suppl_1.949.949

Published: 2017

Journal Articles

Leptin Is Associated with the Degree of Anemia and the Erythropoietin Levels in β Thalassemia Patients

Lila Mahagna, MSc, Osama Tanous, MD, Tal Dujovny, MD, Harel Eitam, PhD, Refaat Masalha, MSc, Raul Colodner, PhD, Ariel Koren, MD, Carina Levin, MDPhD

Blood (2017) 130 (Supplement 1): 950.

https://doi.org/10.1182/blood.V130.Suppl_1.950.950

Published: 2017

Journal Articles

Characterization and Genotype-Phenotype Correlation of Fanconi Anemia Patients in Israel

Orna Steinberg Shemer, MD MSc, Tracie Goldberg, MD, Joanne Yacobovich, MD, Carina Levin, MDPhD, Ariel Koren, MD, Shoshana Revel-Vilk, MD, Tal Ben-Ami, MD, Amir A Kuperman, MD, Vered Shkalim, MD, Amos Toren, MD PhD, Joseph Kapelushnik, Ayelet Ben-Barak, MD, Hagit Miskin, MD, Tanya Krasnov, MSc, Sharon Noy-Lotan, PhD, Orly Dgany, PhD, Hannah Tamary, MD

Blood (2017) 130 (Supplement 1): 1182.

https://doi.org/10.1182/blood.V130.Suppl_1.1182.1182

Published: 2017

Journal Articles

HSP70 Is Increased in Circulating Extracellular Vesicles from Transfusion-Dependent β-Thalassemia Patients: Potential Biomarker for Ineffective Erythropoiesis

Carina Levin, MD, Annie Rebibo-Sabbah, Ariel Koren, MD, Benjamin Brenner, MD, Anat Aharon, PhD

Blood (2016) 128 (22): 1010.

https://doi.org/10.1182/blood.V128.22.1010.1010

Published: 2016

Journal Articles

Regulatory Mechanisms for Iron Homeostasis Are Present in Small Preterm Newborns

Carina Levin, MD, Marina Marina Peniakov, MD, Dan Reich, MD, Scott Weiner, MD, Jamal Hasnein, MD, Raul Colodner, PhD, Ariel Koren, MD, Clari Felszer, MD

Blood (2016) 128 (22): 2460.

https://doi.org/10.1182/blood.V128.22.2460.2460

Published: 2016

Journal Articles

Non Transferrin Bound Labile Plasma Iron and Iron Overload in Sickle Cell Disease: a Comparative Study Between Sickle Cell Disease and β Thalassemic Patients.

Ariel Koren, MD, Daniel Fink, Osnat Admoni, Yardena Tennenbaum-Rakover, Carina Levin

Blood (2009) 114 (22): 4625.

https://doi.org/10.1182/blood.V114.22.4625.4625

Published: 2009

Journal Articles

Frequency and Natural History of Inherited Bone Marrow Failure Syndromes: The Israeli Inherited Bone Marrow Failure Registry

Hannah Tamary, MD, Daniella Nishri, MD, Joanne Yacobovich, MD, Rama Zilber, RN, Shraga Aviner, MD, PhD, Polina Stepensky, MD, Shoshana S Vilk- Ravel, Menachem Bitan, Chaim Kaplinsky, MD, Ayelet Ben Barak, MD, Joseph Kapelusnik, MD, Ariel Koren, MD, Carina Levin, MD, Isaac Yaniv, MD, Philip S Rosenberg, PhD, Blanche P. Alter, MD

Blood (2008) 112 (11): 1045.

https://doi.org/10.1182/blood.V112.11.1045.1045

Published: 2008

Journal Articles

T2* MRI Provides No Evidence for Myocardial and Pancreatic Iron Overload in Multitransfused Patients with Sickle/β-Thalassemia.

Hussam Ghoti, Orly Goitein, Elie Konen, Ariel Koren, MD, Carina Levin, Alan Berebi, Pinhas Stark, MD, Eliezer Rachmilewitz, MD

Blood (2008) 112 (11): 1422.

https://doi.org/10.1182/blood.V112.11.1422.1422

Published: 2008

Journal Articles

Down Regulation of Hepcidin and Haemojuvelin Expression in the Hepatocyte Cell-Line HepG2 Induced by Thalassaemic Sera.

Orly Weizer-Stern, Konstantin Adamsky, PhD, Ninette Amariglio, PhD, Carina Levin, MD, Ariel Koren, MD, William Breuer, PhD, Eliezer Rachmilewitz, MD, Sara Gardenghi, Stefano Rivella, PhD, Yoav Cabantchik, PhD, Gideon Rechavi, MD, PhD

Blood (2006) 108 (11): 1556.

https://doi.org/10.1182/blood.V108.11.1556.1556

Published: 2006

Journal Articles

Hepcidin Expression in Cultured Liver Cells Responds Differently to Iron Overloaded Sera Derived from Patients with Thalassemia and Hemochromatosis.

Orly Weizer, Konstantin Adamsky, PhD, Laura Breda, Ioav Cabantchik, MD, PhD, Eliezer Rachmilewitz, MD, William Breuer, PhD, Alon Harmelin, DVM, Carina Levin, MD, Ariel Koren, MD, Ninette Amariglio, PhD, Stefano Rivella, PhD, Gideon Rechavi, MD, PhD

Blood (2004) 104 (11): 3196.

https://doi.org/10.1182/blood.V104.11.3196.3196

Published: 2004

NARROW

A phase 3 randomized trial of mavorixafor, a CXCR4 antagonist, for WHIM syndrome

A randomized, placebo-controlled, double-blind trial of canakinumab in children and young adults with sickle cell anemia

Global Phase 3, Randomized, Placebo-Controlled Trial with Open-Label Extension Evaluating the Oral CXCR4 Antagonist Mavorixafor in Patients with WHIM Syndrome (4WHIM): Trial Design and Enrollment

Double-Blind, Randomized Study of Canakinumab Treatment in Pediatric and Young Adult Patients with Sickle Cell Anemia

Renal Function in Transfusion-Dependent β-Thalassemia Patients: A Decade of Follow-up and Comparison between Chelation Regimes

Leptin Is Associated with the Degree of Anemia and the Erythropoietin Levels in β Thalassemia Patients

Characterization and Genotype-Phenotype Correlation of Fanconi Anemia Patients in Israel

HSP70 Is Increased in Circulating Extracellular Vesicles from Transfusion-Dependent β-Thalassemia Patients: Potential Biomarker for Ineffective Erythropoiesis

Regulatory Mechanisms for Iron Homeostasis Are Present in Small Preterm Newborns

Non Transferrin Bound Labile Plasma Iron and Iron Overload in Sickle Cell Disease: a Comparative Study Between Sickle Cell Disease and β Thalassemic Patients.

Frequency and Natural History of Inherited Bone Marrow Failure Syndromes: The Israeli Inherited Bone Marrow Failure Registry

T2* MRI Provides No Evidence for Myocardial and Pancreatic Iron Overload in Multitransfused Patients with Sickle/β-Thalassemia.

Down Regulation of Hepcidin and Haemojuvelin Expression in the Hepatocyte Cell-Line HepG2 Induced by Thalassaemic Sera.

Hepcidin Expression in Cultured Liver Cells Responds Differently to Iron Overloaded Sera Derived from Patients with Thalassemia and Hemochromatosis.

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American Society of Hematology

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American Society of Hematology

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