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Splenectomy in childhood for non‐malignant haematologic disorders – long‐term follow‐up shows minimal adverse effects

British journal of haematology, 2020-09, Vol.190 (6), p.909-915

2020

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Excellent response to treatment with hydroxychloroquine in pediatric patients with SLE‐related immune thrombocytopenia

Pediatric blood & cancer, 2024-05, Vol.71 (5), p.e30911-n/a

2024

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Cerebral sinus venous thrombosis in children with inherited bleeding disorders: A case series

Pediatric blood & cancer, 2022-10, Vol.69 (10), p.e29902-n/a

2022

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Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias

British journal of haematology, 2021-05, Vol.193 (3), p.570-580

2021

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

British journal of haematology, 2024-03, Vol.204 (3), p.1067-1071

2024

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Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene

Pediatric blood & cancer, 2020-06, Vol.67 (6), p.e28237-n/a

2020

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Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel

European journal of haematology, 2024-08, Vol.113 (2), p.146-162

2024

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Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome

Pediatric blood & cancer, 2021-10, Vol.68 (10), p.e29138-n/a

2021

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Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias

European journal of haematology, 2018-09, Vol.101 (3), p.297-304

2018

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Essential thrombocythemia A retrospective case series

Pediatric blood & cancer, 2020-05, Vol.67 (5), p.e28183-n/a

2020

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Evaluating platelet function disorders in children with bleeding tendency - A single center study

Platelets (Edinburgh), 2017-10, Vol.28 (7), p.676-681

2017

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Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1

Proceedings of the National Academy of Sciences - PNAS, 2018-05, Vol.115 (20), p.5241-5246

2018

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

Haematologica (Roma), 2020-07, Vol.105 (7), p.1825

2020

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Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells

Cell stem cell, 2016-01, Vol.18 (1), p.73-78

2016

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Congenital thrombocytopenia associated with a heterozygous variant in the MEIS1 gene encoding a transcription factor essential for megakaryopoiesis

Platelets (Edinburgh), 2022-05, Vol.33 (4), p.645-648

2022

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Cdan1 Is Essential for Primitive Erythropoiesis

Frontiers in physiology, 2021-06, Vol.12, p.685242-685242

2021

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

Blood, 2018-06, Vol.131 (24), p.2737-2737

2018

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Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Congenital Anemias

Molecular diagnosis & therapy, 2020-08, Vol.24 (4), p.397-407

2020

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GENETIC PANELS FOR THE DIAGNOSIS OF RARE CONGENITAL HEMATOLOGICAL DISORDERS

הרפואה, 2023-01, Vol.162 (1), p.52

2023

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Cytopenias in pediatric kidney transplant recipients: preceding factors and clinical consequences

Pediatric nephrology (Berlin, West), 2023-10, Vol.38 (10), p.3445-3454

2023

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When Less Is More: Intravenous Immune Globulin for the Treatment of New-Onset Pediatric Immune Thrombocytopenia

Blood, 2022-11, Vol.140 (Supplement 1), p.2681-2682

2022

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Neonatal Thrombocytopenia: Differing Characteristics of NAIT Versus Non-NAIT

Journal of pediatric hematology/oncology, 2023-08, Vol.45 (6), p.e728

2023

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Symptomatic corpus luteum hemorrhage in adolescent females with ITP

European journal of pediatrics, 2024-07, Vol.183 (7), p.2893-2897

2024

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Autoimmune Neutropenia of Infancy- Unexpected Prevalence of Pseudomonas Skin Infections

Blood, 2018-11, Vol.132 (Supplement 1), p.4940-4940

2018

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Characterization of Fanconi Anemia Patients with Head and Neck Squamous Cell Carcinoma: Israel Fanconi Registry

The Israel Medical Association journal, 2022-08, Vol.24 (8), p.491-496

2022

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Splenectomy in childhood for non‐malignant haematologic disorders – long‐term follow‐up shows minimal adverse effects

Excellent response to treatment with hydroxychloroquine in pediatric patients with SLE‐related immune thrombocytopenia

Cerebral sinus venous thrombosis in children with inherited bleeding disorders: A case series

Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias

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

Congenital neutropenia with variable clinical presentation in novel mutation of the SRP54 gene

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel

Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome

Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias

Essential thrombocythemia A retrospective case series

Evaluating platelet function disorders in children with bleeding tendency - A single center study

Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1

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

Targeted Application of Human Genetic Variation Can Improve Red Blood Cell Production from Stem Cells

Congenital thrombocytopenia associated with a heterozygous variant in the MEIS1 gene encoding a transcription factor essential for megakaryopoiesis

Cdan1 Is Essential for Primitive Erythropoiesis

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

Impact of Next-Generation Sequencing on the Diagnosis and Treatment of Congenital Anemias

GENETIC PANELS FOR THE DIAGNOSIS OF RARE CONGENITAL HEMATOLOGICAL DISORDERS

Cytopenias in pediatric kidney transplant recipients: preceding factors and clinical consequences

When Less Is More: Intravenous Immune Globulin for the Treatment of New-Onset Pediatric Immune Thrombocytopenia

Neonatal Thrombocytopenia: Differing Characteristics of NAIT Versus Non-NAIT

Symptomatic corpus luteum hemorrhage in adolescent females with ITP

Autoimmune Neutropenia of Infancy- Unexpected Prevalence of Pseudomonas Skin Infections

Characterization of Fanconi Anemia Patients with Head and Neck Squamous Cell Carcinoma: Israel Fanconi Registry

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