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Hannah Tamary

Tel Aviv University

180

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3435

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Mutations in RASGRP2 gene identified in patients misdiagnosed as Glanzmann thrombasthenia patients.

2021 Blood Cells Molecules and Diseases
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Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome.

2021 Pediatric Blood & Cancer
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Cdan1 Is Essential for Primitive Erythropoiesis

2021 Frontiers in Physiology
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Recommendations for Pregnancy in Rare Inherited Anemias

2020
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Essential thrombocythemia A retrospective case series

2020 Pediatric Blood & Cancer
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Table 5. [Possible Parental Genotypes and Corresponding Outcomes in Sibs of a Proband with HbH Disease].

2020
- Hannah Tamary
- Orly Dgany
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Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Congenital Anemias.

2020 Molecular Diagnosis & Therapy
- Orna Steinberg-Shemer
- Hannah Tamary
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Alpha-Thalassemia Carrier due to –α 3.7 Deletion: Not So Silent

2020 Acta Haematologica
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Splenectomy and emerging novel treatments in rare inherited hemolytic anemias

2019
- Joanne Yacobovich
- Hannah Tamary
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Endoscopic findings and esophageal cancer incidence among Fanconi Anemia patients participating in an endoscopic surveillance program

2019 Digestive and Liver Disease
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