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Journal Articles

Cancer Risk in Patients with Gaucher Disease Using Real-World Data

Shoshana Revel-Vilk, Ari Zimran, Majdolen Istaiti, Orly Manor, Varda Shalev, Litat Azani, Gabriel Chodick, Ora Paltiel

Blood (2023) 142 (Supplement 1): 488.

https://doi.org/10.1182/blood-2023-179459

Published: 2023

Journal Articles

EBV-driven lymphoid neoplasms associated with pediatric ALL maintenance therapy

Blood (2023) 141 (7): 743–755.

https://doi.org/10.1182/blood.2022016975

Published: 2023

Includes: Supplemental data

Journal Articles

Study Design: Development of an Advanced Machine Learning Algorithm for the Early Diagnosis of Gaucher Disease Using Real-World Data

Shoshana Revel-Vilk, MDMSc, Gabriel Chodick, PhD, Varda Shalev, MD, Noga Gadir, PhD

Blood (2020) 136 (Supplement 1): 13–14.

https://doi.org/10.1182/blood-2020-134414

Published: 2020

Journal Articles

Under-Diagnosed and Under-Treated Menorrhagia in Young Women Produce Suboptimal Performance

Dvora Bauman, MD, Adir Sommer, MD, Dar Noy, Tal Hammer, Shoshana Revel-Vilk, MDMSc

Blood (2020) 136 (Supplement 1): 38.

https://doi.org/10.1182/blood-2020-139354

Published: 2020

Journal Articles

Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders

Blood (2019) 134 (23): 2082–2091.

https://doi.org/10.1182/blood.2018891192

Published: 2019

Includes: Supplemental data

Journal Articles

Not All Patients with Mild Phenotype of Gaucher Disease (GD) Need Disease Specific Treatment As Reflected By Patients Reported Outcomes Measures

Shoshana Revel-Vilk, MD, Tama Dinur, PhD, Majdolen Istaiti, Dafna Frydman, DMV, Michal Becker-Cohen, MSc, Ari Zimran, MD

Blood (2019) 134 (Supplement_1): 4712.

https://doi.org/10.1182/blood-2019-123000

Published: 2019

Journal Articles

Bone Marrow Involvement in Patients with Type 1 Gaucher Disease Receiving Low-Dose Long Term Enzyme Replacement Therapy (median 18 years)

Shoshana Revel-Vilk, MD, Jeffrey Szer, MBBS, Michal Becker Cohen, Ari Zimran, MD

Blood (2019) 134 (Supplement_1): 4862.

https://doi.org/10.1182/blood-2019-131013

Published: 2019

Journal Articles

Novel Insights Regarding Pediatric Essential Thrombocythemia

Assaf Arie Barg, Gili Kenet, Tami Livnat, PhD, Gal Goldstein, MD, Joanne Yacobovich, MD, Oded Gilad, MD, Orna Steinberg Shemer, MD MSc, Shoshana Revel-Vilk, MD, Hagit Miskin, MD, Amos Toren, MD PhD, Vered Shkalim, MD

Blood (2019) 134 (Supplement_1): 4191.

https://doi.org/10.1182/blood-2019-123865

Published: 2019

Journal Articles

GNE variants causing autosomal recessive macrothrombocytopenia without associated muscle wasting

Blood (2018) 132 (17): 1851–1854.

https://doi.org/10.1182/blood-2018-04-845545

Published: 2018

Includes: Supplemental data

Journal Articles

Reduction in Intravenous Infusion Duration of Enzyme Replacement Therapy to Ten Minutes with Velaglucerase Alfa in Adult Patients with Type 1 Gaucher Disease

Ari Zimran, MD, Shoshana Revel-Vilk, MD, Deborah Elstein, PhD, Naama Arbel, Michal Becker-Cohen, MSc, Gaya Chicco, Jeff Szer, MB, BS, FRACP

Blood (2017) 130 (Supplement 1): 2101.

https://doi.org/10.1182/blood.V130.Suppl_1.2101.2101

Published: 2017

Journal Articles

Epstein Barr Virus-Associated Lymphoproliferative Disorder during Maintenance Therapy of Childhood Acute Lymphoblastic Leukemia

Sarah Elitzur, MD, Andishe Attarbaschi, MD, Susan Baird, MD, Miri Ben Harosh, MD, Lisa Hjalgrim, PhD, Shai Izraeli, MD, Michaela Kuhlen, MD, Anja Moricke, MD, Shoshana Revel-Vilk, MD, Kjeld Schmiegelow, MD, Martin Schrappe, MD PhD, Melanie Tamesberger, MD, Ajay Vora, MD, Arndt Borkhardt, Prof MD

Blood (2017) 130 (Supplement 1): 1292.

https://doi.org/10.1182/blood.V130.Suppl_1.1292.1292

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

Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding

Blood (2017) 130 (8): 1026–1030.

https://doi.org/10.1182/blood-2017-03-776773

Published: 2017

Includes: Supplemental data

Journal Articles

Are We Choosing Wisely with Blood Use? an Assessment of Transfusion Practices

Shoshana Revel-Vilk, MD MSc, Barak Karavany, Revital Saban, MD, Orly Zelig, MD, Mira Naamad, PhD, Meir Turniansky, MIHA, Bela Savitsky, MSc, Hagit Hochner, PhD

Blood (2016) 128 (22): 1003.

https://doi.org/10.1182/blood.V128.22.1003.1003

Published: 2016

Journal Articles

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

Ilenia Simeoni, Jonathan C. Stephens, Fengyuan Hu, Sri V. V. Deevi, Karyn Megy, Tadbir K. Bariana, Claire Lentaigne, Sol Schulman, Suthesh Sivapalaratnam, Minka J. A. Vries, Sarah K. Westbury, Daniel Greene, Sofia Papadia, Marie-Christine Alessi, Antony P. Attwood, Matthias Ballmaier, Gareth Baynam, Emilse Bermejo, Marta Bertoli, Paul F. Bray, Loredana Bury, Marco Cattaneo, Peter Collins, Louise C. Daugherty, Rémi Favier, Deborah L. French, Bruce Furie, Michael Gattens, Manuela Germeshausen, Cedric Ghevaert, Anne C. Goodeve, Jose A. Guerrero, Daniel J. Hampshire, Daniel P. Hart, Johan W. M. Heemskerk, Yvonne M. C. Henskens, Marian Hill, Nancy Hogg, Jennifer D. Jolley, Walter H. Kahr, Anne M. Kelly, Ron Kerr, Myrto Kostadima, Shinji Kunishima, Michele P. Lambert, Ri Liesner, José A. López, Rutendo P. Mapeta, Mary Mathias, Carolyn M. Millar, Amit Nathwani, Marguerite Neerman-Arbez, Alan T. Nurden, Paquita Nurden, Maha Othman, Kathelijne Peerlinck, David J. Perry, Pawan Poudel, Pieter Reitsma, Matthew T. Rondina, Peter A. Smethurst, William Stevenson, Artur Szkotak, Salih Tuna, Christel van Geet, Deborah Whitehorn, David A. Wilcox, Bin Zhang, Shoshana Revel-Vilk, Paolo Gresele, Daniel B. Bellissimo, Christopher J. Penkett, Michael A. Laffan, Andrew D. Mumford, Augusto Rendon, Keith Gomez, Kathleen Freson, Willem H. Ouwehand, Ernest Turro

Blood (2016) 127 (23): 2791–2803.

https://doi.org/10.1182/blood-2015-12-688267

Published: 2016

Includes: Supplemental data

Journal Articles

Activating Mutation of STAT3 Protects Lymphocytes from Apoptosis and Leads to a Clinical Phenotype Resembling the Autoimmune Lymphoproliferative Syndrome

Schafiq Nabhani, PhD, Hagit Miskin, MD, Cyrill Schipp, MSc, Dan Harlev, Shoshana Revel-Vilk, MD MSc, Michael Gombert, PhD, Sebastian Ginzel, MSc, Arndt Borkhardt, MD, Polina Stepensky, MD, Ute Fischer, PhD

Blood (2015) 126 (23): 2218.

https://doi.org/10.1182/blood.V126.23.2218.2218

Published: 2015

Journal Articles

Iron Deficiency Anemia As a Leading Cause of Severe Anemia in Children May be Associated with Unnecessary Red Blood Cells (RBCs) Transfusion

Tal Ben-Ami, MD, Mohammad Natour, MD, David Rekhtman, MD, Tenenbaum Ariel, MD, Shoshana Revel-Vilk, MD MSc

Blood (2015) 126 (23): 4454.

https://doi.org/10.1182/blood.V126.23.4454.4454

Published: 2015

Journal Articles

Effects of eltrombopag on platelet count and platelet activation in Wiskott-Aldrich syndrome/X-linked thrombocytopenia

Anja J. Gerrits, Emily A. Leven, Andrew L. Frelinger, III, Sophie L. Brigstocke, Michelle A. Berny-Lang, W. Beau Mitchell, Shoshana Revel-Vilk, Hannah Tamary, Sabrina L. Carmichael, Marc R. Barnard, Alan D. Michelson, James B. Bussel

Blood (2015) 126 (11): 1367–1378.

https://doi.org/10.1182/blood-2014-09-602573

Published: 2015

Journal Articles

Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency

Blood (2015) 125 (5): 753–761.

https://doi.org/10.1182/blood-2014-08-593202

Published: 2015

Includes: Supplemental data

Journal Articles

New Mutation in Chromosome 9 Associated with Familial Autosomal Recessive Macrothrombocytopenia

Shoshana Revel-Vilk, MD MSc, Ela Shai, PhD, Nivin Gashem, MSc, Esti Hyam, Galia Spectre, MD, Orly Elpeleg, MD, David Varon, MD

Blood (2014) 124 (21): 2776.

https://doi.org/10.1182/blood.V124.21.2776.2776

Published: 2014

NARROW

Cancer Risk in Patients with Gaucher Disease Using Real-World Data

EBV-driven lymphoid neoplasms associated with pediatric ALL maintenance therapy

Study Design: Development of an Advanced Machine Learning Algorithm for the Early Diagnosis of Gaucher Disease Using Real-World Data

Under-Diagnosed and Under-Treated Menorrhagia in Young Women Produce Suboptimal Performance

Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders

Not All Patients with Mild Phenotype of Gaucher Disease (GD) Need Disease Specific Treatment As Reflected By Patients Reported Outcomes Measures

Bone Marrow Involvement in Patients with Type 1 Gaucher Disease Receiving Low-Dose Long Term Enzyme Replacement Therapy (median 18 years)

Novel Insights Regarding Pediatric Essential Thrombocythemia

GNE variants causing autosomal recessive macrothrombocytopenia without associated muscle wasting

Reduction in Intravenous Infusion Duration of Enzyme Replacement Therapy to Ten Minutes with Velaglucerase Alfa in Adult Patients with Type 1 Gaucher Disease

Epstein Barr Virus-Associated Lymphoproliferative Disorder during Maintenance Therapy of Childhood Acute Lymphoblastic Leukemia

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

Expanded repertoire of RASGRP2 variants responsible for platelet dysfunction and severe bleeding

Are We Choosing Wisely with Blood Use? an Assessment of Transfusion Practices

A high-throughput sequencing test for diagnosing inherited bleeding, thrombotic, and platelet disorders

Activating Mutation of STAT3 Protects Lymphocytes from Apoptosis and Leads to a Clinical Phenotype Resembling the Autoimmune Lymphoproliferative Syndrome

Iron Deficiency Anemia As a Leading Cause of Severe Anemia in Children May be Associated with Unnecessary Red Blood Cells (RBCs) Transfusion

Effects of eltrombopag on platelet count and platelet activation in Wiskott-Aldrich syndrome/X-linked thrombocytopenia

Early-onset Evans syndrome, immunodeficiency, and premature immunosenescence associated with tripeptidyl-peptidase II deficiency

New Mutation in Chromosome 9 Associated with Familial Autosomal Recessive Macrothrombocytopenia

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American Society of Hematology

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ASH Publications

American Society of Hematology

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