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Pediatric immune thrombocytopenia: apoptotic markers may help in predicting the disease course

Pediatric research, 2021-07, Vol.90 (1), p.93-98

2021

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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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Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease

Haematologica (Roma), 2015-09, Vol.100 (9), p.1189

2015

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Asthma and hemoglobinopathy: When is supplemental oxygen required?

Pediatrics international, 2013-10, Vol.55 (5), p.e133-e135

2013

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STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds

Clinical immunology (Orlando, Fla.), 2017-08, Vol.181, p.32-42

2017

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Thiopurine Therapy for Inflammatory Bowel Disease During Pregnancy Is Not Associated with Anemia in the Infant

Digestive diseases and sciences, 2019-08, Vol.64 (8), p.2286-2290

2019

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Novel Insights Regarding Pediatric Essential Thrombocythemia

Blood, 2019-11, Vol.134 (Supplement_1), p.4191-4191

2019

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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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Quantification of specific T and B cells immunological markers in children with chronic and transient ITP

Pediatric blood & cancer, 2017-12, Vol.64 (12), p.n/a

2017

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Pediatric severe factor XI deficiency: A multicenter study

Pediatric blood & cancer, 2022-03, Vol.69 (3), p.e29545-n/a

2022

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

Blood, 2017-12, Vol.130, p.1182-1182

2017

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Neurologic manifestations of Fusobacterium infections in children

European journal of pediatrics, 2013, Vol.172 (1), p.77-83

2013

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

Blood, 2015-12, Vol.126 (23), p.2218-2218

2015

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Quantitation of bleeding symptoms in a national registry of patients with inherited platelet disorders

Blood cells, molecules, & diseases, 2017-09, Vol.67, p.59-62

2017

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Genetic analysis and clinical picture of severe congenital neutropenia in Israel

Pediatric blood & cancer, 2015-01, Vol.62 (1), p.103-108

2015

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Deferasirox treatment may be associated with reversible renal Fanconi syndrome

American journal of hematology, 2010-02, Vol.85 (2), p.132-134

2010

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Dysregulation of IL12 Signaling As a Novel Cause of an Autoimmune Lymphoproliferative like Syndrome

Blood, 2014-12, Vol.124 (21), p.1420-1420

2014

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Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients

European journal of haematology, 2005-02, Vol.74 (2), p.93-100

2005

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Preimplantation Genetic Diagnosis for Fetal Neonatal Alloimmune Thrombocytopenia Due to Antihuman Platelet Antigen Maternal Antibodies

Obstetrics and gynecology (New York. 1953), 2012-02, Vol.119 (2, Part 1), p.338-343

2012

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Respiratory failure and hypercoagulability in a toddler with Lemierre's syndrome

Pediatrics (Evanston), 2005-05, Vol.115 (5), p.e620

2005

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Mycoplasma pneumonia Infection: A Possible Trigger for Immune Thrombocytopenia

Indian journal of hematology & blood transfusion, 2011-03, Vol.27 (1), p.46-50

2011

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Prospective comparison of two flow cytometry methodologies for monitoring minimal residual disease in a multicenter treatment protocol of childhood acute lymphoblastic leukemia

Cytometry. Part B, Clinical cytometry, 2010-11, Vol.78B (6), p.365-371

2010

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Pediatric immune thrombocytopenia: apoptotic markers may help in predicting the disease course

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

Deregulation of Fas ligand expression as a novel cause of autoimmune lymphoproliferative syndrome-like disease

Asthma and hemoglobinopathy: When is supplemental oxygen required?

A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia

STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds

Thiopurine Therapy for Inflammatory Bowel Disease During Pregnancy Is Not Associated with Anemia in the Infant

Novel Insights Regarding Pediatric Essential Thrombocythemia

Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel

Quantification of specific T and B cells immunological markers in children with chronic and transient ITP

Pediatric severe factor XI deficiency: A multicenter study

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

Essential thrombocythemia A retrospective case series

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

Neurologic manifestations of Fusobacterium infections in children

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

Quantitation of bleeding symptoms in a national registry of patients with inherited platelet disorders

Genetic analysis and clinical picture of severe congenital neutropenia in Israel

Deferasirox treatment may be associated with reversible renal Fanconi syndrome

Dysregulation of IL12 Signaling As a Novel Cause of an Autoimmune Lymphoproliferative like Syndrome

Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients

Preimplantation Genetic Diagnosis for Fetal Neonatal Alloimmune Thrombocytopenia Due to Antihuman Platelet Antigen Maternal Antibodies

Respiratory failure and hypercoagulability in a toddler with Lemierre's syndrome

Mycoplasma pneumonia Infection: A Possible Trigger for Immune Thrombocytopenia

Prospective comparison of two flow cytometry methodologies for monitoring minimal residual disease in a multicenter treatment protocol of childhood acute lymphoblastic leukemia

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