Hannah Tamary

Kaplan St 14, 4920235
Petah Tiqwa, M 49202, Israel

Last Updated: 09/26/2026

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Found 88 publications

A Nationwide Analysis of the Phenotype/Genotype Landscape of Hemophagocytic Lymphohistiocytosis: UNC13D Associates with Poor Prognosis.

A Nationwide Analysis of the Phenotype/Genotype Landscape of Hemophagocytic Lymphohistiocytosis: UNC13D Associates with Poor Prognosis.

Journal: Genes
Published: August 22, 2025

Fanconi anemia patients with head and neck squamous cell carcinoma - a multi-center study.

Fanconi anemia patients with head and neck squamous cell carcinoma - a multi-center study.

Journal: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery
Published: February 01, 2025

Erratum to: Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population.

Erratum to: Characterization and genotype-phenotype correlation of patients with Fanconi anemia in a multi-ethnic population.

Journal: Haematologica
Published: January 01, 2025

European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action based on a systematic evidence review.

European guidelines on treatment and supportive measures in chronic neutropenias: A consensus between the European Hematology Association and the EuNet-INNOCHRON COST Action based on a systematic evidence review.

Journal: HemaSphere
Published: November 03, 2024

A Variable Clinical Presentation of Hemoglobin City of Hope.

A Variable Clinical Presentation of Hemoglobin City of Hope.

Journal: Clinical genetics
Published: September 27, 2024

Codanin-1, defective in congenital dyserythropoietic anemia I (CDA-I), regulates erythroid differentiation.

Codanin-1, defective in congenital dyserythropoietic anemia I (CDA-I), regulates erythroid differentiation.

Journal: Annals of hematology
Published: August 12, 2024

Clinical and Laboratory Characteristics of Pediatric Patients With ACKR1/DARC-Associated Neutropenia.

Clinical and Laboratory Characteristics of Pediatric Patients With ACKR1/DARC-Associated Neutropenia.

Journal: Pediatric blood & cancer
Published: June 16, 2024

Symptomatic corpus luteum hemorrhage in adolescent females with ITP.

Symptomatic corpus luteum hemorrhage in adolescent females with ITP.

Journal: European journal of pediatrics
Published: February 17, 2024

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.

Journal: European journal of haematology
Published: December 19, 2023

A Need for a Novel Survival Risk Scoring System for Intensive Care Admissions Due to Sepsis in Pediatric Hematology/Oncology Patients.

A Need for a Novel Survival Risk Scoring System for Intensive Care Admissions Due to Sepsis in Pediatric Hematology/Oncology Patients.

Journal: Journal of intensive care medicine
Published: November 20, 2023

Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2.

Biallelic hypomorphic variants in CAD cause uridine-responsive macrocytic anaemia with elevated haemoglobin-A2.

Journal: British journal of haematology
Published: August 28, 2023

GENETIC PANELS FOR THE DIAGNOSIS OF RARE CONGENITAL HEMATOLOGICAL DISORDERS

GENETIC PANELS FOR THE DIAGNOSIS OF RARE CONGENITAL HEMATOLOGICAL DISORDERS

Journal: Harefuah
Published: January 30, 2023
Showing 1-12 of 88

Last Updated: 09/26/2026