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Journal Articles

Clinical and Laboratory Characteristics of Pediatric Patients with ACKR1/Darc -Associated Neutropenia

Lital Oz-Alcalay, Orna Steinberg-Shemer, Sarah Elitzur, Dafna Brik Simon, Hannah Tamary, Shai Izraeli, Joanne Yacobovich, Oded Gilad

Blood (2024) 144 (Supplement 1): 2532.

https://doi.org/10.1182/blood-2024-200343

Published: 2024

Journal Articles

The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia

Blood (2023) 141 (23): 2853–2866.

https://doi.org/10.1182/blood.2022019425

Published: 2023

Includes: Supplemental data

Journal Articles

Multinational Study on the Clinical and Genetic Features of the ERCC6L2-Disease

Marja Hakkarainen, Suvi P. M. Douglas, Tom Vulliamy, Inderjeet Dokal, Jean Soulier, Lise Larcher, Riitta Niinimäki, Timo Siitonen, Eva Hellstrom Lindberg, Gisela Barbany, Bianca Tesi, Amir Asher Kuperman, Hannah Tamary, Sharon Jackson, Outi Kilpivaara, Ulla Wartiovaara-Kautto

Blood (2021) 138 (Supplement 1): 864.

https://doi.org/10.1182/blood-2021-145039

Published: 2021

Journal Articles

Autoimmune Neutropenia of Infancy- Unexpected Prevalence of Pseudomonas Skin Infections

Joanne Yacobovich, MD, Neta Aviran Dagan, MD, Tracie Goldberg, MD, Orna Steinberg Shemer, MD MSc, Hannah Tamary, MD

Blood (2018) 132 (Supplement 1): 4940.

https://doi.org/10.1182/blood-2018-99-113408

Published: 2018

Journal Articles

Towards an External Quality Assessment for Next Generation Sequencing in the Diagnosis of Rare Inherited Anaemias

Blood (2018) 132 (Supplement 1): 4936.

https://doi.org/10.1182/blood-2018-99-111609

Published: 2018

Journal Articles

Gray platelet syndrome mimicking atypical autoimmune lymphoproliferative syndrome: the key is in the blood smear

Orna Steinberg-Shemer, Hannah Tamary

Blood (2018) 131 (24): 2737.

https://doi.org/10.1182/blood-2018-03-841940

Published: 2018

Journal Articles

Mutations in Ribosomal Protein Genes L9 and L15 Link to DBA with Specific Clinical Phenotypes

Marcin W. Wlodarski, MD PhD, Lydie M. Da Costa, MD PhD, Marie-Francoise O'-Donohue, Marc Gastou, Ina Hainmann, Enikoe Amina Szvetnik, Thierry Leblanc, MD, Marc Bierings, MD PhD, Nathalie Montel-Lehry, Hannah Tamary, MD, Charlotte M. Niemeyer, MD, Pierre-Emmanuel Gleizes, Alyson W. MacInnes

Blood (2017) 130 (Supplement 1): 1172.

https://doi.org/10.1182/blood.V130.Suppl_1.1172.1172

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

Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin

Blood (2017) 130 (7): 875–880.

https://doi.org/10.1182/blood-2017-02-768036

Published: 2017

Includes: Supplemental data

Journal Articles

Long Term Outcome of Splenectomy in Pediatric Patients with Non-Malignant Hematological Diseases: Four Decades of Follow up

Joanne Yacobovich, MD, Shlomit Barzilai-Birenboim, MD, Pinhas Stark, MD, Idit Pazgal, MD, Orna Steinberg-Shemer, MD, Hannah Tamary, MD

Blood (2016) 128 (22): 3585.

https://doi.org/10.1182/blood.V128.22.3585.3585

Published: 2016

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

Triallelic and epigenetic-like inheritance in human disorders of telomerase

Laura C. Collopy, Amanda J. Walne, Shirleny Cardoso, Josu de la Fuente, Mahfuzah Mohamed, Helga Toriello, Hannah Tamary, Adam J. Y. V. Ling, Timothy Lloyd, Rebecca Kassam, Hemanth Tummala, Thomas J. Vulliamy, Inderjeet Dokal

Blood (2015) 126 (2): 176–184.

https://doi.org/10.1182/blood-2015-03-633388

Published: 2015

Includes: Supplemental data

Journal Articles

Nephrolithiasis in Transfusion-Dependent Pediatric Patients

Joanne Yacobovich, MD, Irit Krause, MD, Rotem Semo-Oz, MD, Hannah Tamary, MD

Blood (2014) 124 (21): 4895.

https://doi.org/10.1182/blood.V124.21.4895.4895

Published: 2014

Journal Articles

Codanin-1 Binds to Key Erythroid Genes and Its Knockdown Coupled with Ectopic Mutant Expression Recapitulates the Congenital Dyserythropoietic Anemia Type I (CDA I) Phenotype

Linette Bosques, Caroline Tang, MD, Diane Krause, MD PhD, Sherman M. Weissman, MD, Patrick G Gallagher, MD, Mitchell J. Weiss, MD PhD, Hannah Tamary, MD, Gary M. Kupfer, MD

Blood (2014) 124 (21): 360.

https://doi.org/10.1182/blood.V124.21.360.360

Published: 2014

Journal Articles

Effects Of Eltrombopag On Thrombocytopenia, Platelet Function and Bleeding In Patients With Wiskott-Aldrich Syndrome/X-Linked Thrombocytopenia

Anja J Gerrits, PhD, Emily Leven, Andrew L. Frelinger, III, PhD, Michelle A. Berny-Lang, PhD, Hannah Tamary, MD, Shoshana Revel-Vilk, MD, MSc, Sabrina L. Carmichael, BS, W. Beau Mitchell, MD, Alan D. Michelson, MD, James B Bussel, MD

Blood (2013) 122 (21): 3536.

https://doi.org/10.1182/blood.V122.21.3536.3536

Published: 2013

Journal Articles

Congenital dyserythropoietic anemias: molecular insights and diagnostic approach

Achille Iolascon, Hermann Heimpel, Anders Wahlin, Hannah Tamary

Blood (2013) 122 (13): 2162–2166.

https://doi.org/10.1182/blood-2013-05-468223

Published: 2013

Journal Articles

Modeling Congenital Dyserythropoietic Anemia Type I Through Patient-Derived Induced Pluripotent Stem Cells

Orna Steinberg Shemer, MD, MSc, Yu Yao, Gary M. Kupfer, MD, Hannah Tamary, MD, Mitchell J. Weiss, MD, PhD

Blood (2012) 120 (21): 3196.

https://doi.org/10.1182/blood.V120.21.3196.3196

Published: 2012

Journal Articles

High Levels of Soluble Serum Hemojuvelin in Patients with Congenital Dyserythropoietic Anemia Type I,

Hannah Tamary, MD, Joseph Kapelushnik, M.D, Galit Perez-Avraham, MD, Itai Levi, MD, Carole Brasse-Lagnel, MD, Hanna Shalev, MD

Blood (2011) 118 (21): 3179.

https://doi.org/10.1182/blood.V118.21.3179.3179

Published: 2011

Journal Articles

How Rare Is Rare? Carrier Frequencies for Fanconi Anemia In the United States and Israel

Philip S Rosenberg, PhD, Hannah Tamary, MD, Blanche P. Alter, MD, MPH

Blood (2010) 116 (21): 2229.

https://doi.org/10.1182/blood.V116.21.2229.2229

Published: 2010

Journal Articles

Platelet Function and Response to Thrombopoietin Mimetics In Wiskott-Aldrich Syndrome/X-Linked Thrombocytopenia.

James B. Bussel, MD, Andrew L Frelinger, III, PhD, William B Mitchell, MD, Mariana P Pinheiro, MD, Marc R Barnard, MS, Michael Lampa, BS, Bethan Psaila, MD, PhD, Nayla Boulad, BA, Hannah Tamary, MD, Alan D. Michelson, MD

Blood (2010) 116 (21): 1429.

https://doi.org/10.1182/blood.V116.21.1429.1429

Published: 2010

NARROW

Clinical and Laboratory Characteristics of Pediatric Patients with ACKR1/Darc -Associated Neutropenia

The clinical picture of ERCC6L2 disease: from bone marrow failure to acute leukemia

Multinational Study on the Clinical and Genetic Features of the ERCC6L2-Disease

Autoimmune Neutropenia of Infancy- Unexpected Prevalence of Pseudomonas Skin Infections

Towards an External Quality Assessment for Next Generation Sequencing in the Diagnosis of Rare Inherited Anaemias

Gray platelet syndrome mimicking atypical autoimmune lymphoproliferative syndrome: the key is in the blood smear

Mutations in Ribosomal Protein Genes L9 and L15 Link to DBA with Specific Clinical Phenotypes

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

Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin

Long Term Outcome of Splenectomy in Pediatric Patients with Non-Malignant Hematological Diseases: Four Decades of Follow up

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

Triallelic and epigenetic-like inheritance in human disorders of telomerase

Nephrolithiasis in Transfusion-Dependent Pediatric Patients

Codanin-1 Binds to Key Erythroid Genes and Its Knockdown Coupled with Ectopic Mutant Expression Recapitulates the Congenital Dyserythropoietic Anemia Type I (CDA I) Phenotype

Effects Of Eltrombopag On Thrombocytopenia, Platelet Function and Bleeding In Patients With Wiskott-Aldrich Syndrome/X-Linked Thrombocytopenia

Congenital dyserythropoietic anemias: molecular insights and diagnostic approach

Modeling Congenital Dyserythropoietic Anemia Type I Through Patient-Derived Induced Pluripotent Stem Cells

High Levels of Soluble Serum Hemojuvelin in Patients with Congenital Dyserythropoietic Anemia Type I,

How Rare Is Rare? Carrier Frequencies for Fanconi Anemia In the United States and Israel

Platelet Function and Response to Thrombopoietin Mimetics In Wiskott-Aldrich Syndrome/X-Linked Thrombocytopenia.

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American Society of Hematology

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ASH Publications

American Society of Hematology

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