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Genetic backgrounds and clinical characteristics of congenital neutropenias in Israel.
- Published in:
- European Journal of Haematology, 2024, v. 113, n. 2, p. 146, doi. 10.1111/ejh.14197
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- Article
Symptomatic corpus luteum hemorrhage in adolescent females with ITP.
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- European Journal of Pediatrics, 2024, v. 183, n. 7, p. 2893, doi. 10.1007/s00431-024-05560-0
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- Article
Support Vector Machine-Based Formula for Detecting Suspected α Thalassemia Carriers: A Path toward Universal Screening.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 12, p. 6446, doi. 10.3390/ijms25126446
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- Article
The Impact of Ca 2+ on Intracellular Distribution of Hemoglobin in Human Erythrocytes.
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- Cells (2073-4409), 2023, v. 12, n. 18, p. 2280, doi. 10.3390/cells12182280
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- Article
Associations between red blood cell indices and iron status and neurocognitive function in young adults: Evidence from memory and executive function tests and event‐related potentials.
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- Annals of the New York Academy of Sciences, 2022, v. 1517, n. 1, p. 300, doi. 10.1111/nyas.14877
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- Article
The protective effect of the spleen in sickle cell patients. A comparative study between patients with asplenia/hyposplenism and hypersplenism.
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- Frontiers in Physiology, 2022, v. 13, p. 1, doi. 10.3389/fphys.2022.796837
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- Article
Resolution of iron deficiency following successful eradication of Helicobacter pylori in children.
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- Acta Paediatrica, 2022, v. 111, n. 5, p. 1075, doi. 10.1111/apa.16255
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- Article
Characterization of acquired anemia in children by iron metabolism parameters.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-06574-0
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- Article
Back to the "Gold Standard": How Precise is Hematocrit Detection Today?
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- Mediterranean Journal of Hematology & Infectious Diseases, 2022, v. 14, n. 1, p. 1, doi. 10.4084/MJHID.2022.049
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- Article
Renal function in β-thalassemia major patients treated with two different iron-chelation regimes.
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- 2021
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- Publication type:
- journal article
Extracellular Vesicle MicroRNA That Are Involved in β-Thalassemia Complications.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 18, p. 9760, doi. 10.3390/ijms22189760
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- Article
Do We Store Packed Red Blood Cells under "Quasi-Diabetic" Conditions?
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- Biomolecules (2218-273X), 2021, v. 11, n. 7, p. 992, doi. 10.3390/biom11070992
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- Article
Severe Protein C Deficiency due to Novel Biallelic Variants in PROC and Their Phenotype Correlation.
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- Acta Haematologica, 2021, v. 144, n. 3, p. 327, doi. 10.1159/000509968
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- Article
Pediatric Otogenic Cerebral Sinus Vein Thrombosis and Thrombophilia.
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- Israel Medical Association Journal, 2021, v. 23, n. 2, p. 99
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- Article
Primary autoimmune myelofibrosis: A case report in a child.
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- EJHaem, 2020, v. 1, n. 1, p. 1, doi. 10.1002/jha2.38
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- Article
Immune Thrombocytopenia Secondary to Hodgkin's Lymphoma in Children: Case Reports and Review of the Literature.
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- Israel Medical Association Journal, 2020, v. 22, n. 4, p. 224
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- Article
Attention, response inhibition and brain event‐related potential alterations in adults with beta‐thalassaemia major.
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- British Journal of Haematology, 2019, v. 186, n. 4, p. 580, doi. 10.1111/bjh.15957
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- Article
Extracellular Vesicle Characteristics in β-thalassemia as Potential Biomarkers for Spleen Functional Status and Ineffective Erythropoiesis.
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- Frontiers in Physiology, 2018, p. N.PAG, doi. 10.3389/fphys.2018.01214
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- Publication type:
- Article
Detection of β-Thalassemia Carriers by Red Cell Parameters Obtained from Automatic Counters using Mathematical Formulas.
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- Mediterranean Journal of Hematology & Infectious Diseases, 2018, v. 10, n. 1, p. 1, doi. 10.4084/MJHID.2018.008
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- Publication type:
- Article
Executive function and neural activation in adults with β-thalassemia major: an event-related potentials study.
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- Annals of the New York Academy of Sciences, 2016, v. 1386, n. 1, p. 16, doi. 10.1111/nyas.13279
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- Article
Hb TAYBE: clinical and morphological findings IN 43 patients.
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- European Journal of Haematology, 2016, v. 97, n. 2, p. 137, doi. 10.1111/ejh.12694
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- Article
Cognitive functions in adults with β-thalassemia major: before and after blood transfusion and comparison with healthy controls.
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- Annals of the New York Academy of Sciences, 2016, v. 1375, n. 1, p. 19, doi. 10.1111/nyas.13103
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- Article
Genetic analysis and clinical picture of severe congenital neutropenia in Israel.
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- Pediatric Blood & Cancer, 2015, v. 62, n. 1, p. 103, doi. 10.1002/pbc.25251
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- Article
Extracellular Vesicles in Hematological Disorders.
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- Rambam Maimonides Medical Journal, 2014, v. 5, n. 4, p. 1, doi. 10.5041/RMMJ.10166
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- Article
Spontaneous intestinal perforation and multiple thrombotic events in a neonate with thrombophilia.
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- Case Reports in Perinatal Medicine, 2014, v. 3, n. 2, p. 155, doi. 10.1515/crpm-2013-0081
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- Article
Immune-mediated mechanism for thrombocytopenia after Loxosceles spider bite.
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- Pediatric Blood & Cancer, 2014, v. 61, n. 8, p. 1466, doi. 10.1002/pbc.24959
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- Publication type:
- Article
Small-platelet thrombocytopenia in a family with autosomal recessive inheritance pattern.
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- Pediatric Blood & Cancer, 2013, v. 60, n. 10, p. E128, doi. 10.1002/pbc.24581
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- Publication type:
- Article
Non-transferrin bound iron in Thalassemia: Differential detection of redox active forms in children and older patients.
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- American Journal of Hematology, 2012, v. 87, n. 1, p. 55, doi. 10.1002/ajh.22203
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- Article
Healing of Refractory Leg Ulcer in a Patient with Thalassemia Intermedia and Hypercoagulability after 14 Years of Unresponsive Therapy.
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- Israel Medical Association Journal, 2011, v. 13, n. 5, p. 316
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- Article
Migraine and hypercoagulability, are they related? A clinical study of thrombophilia in children with migraine.
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- British Journal of Haematology, 2011, v. 152, n. 3, p. 349, doi. 10.1111/j.1365-2141.2010.08464.x
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- Article
No evidence for myocardial iron overload and free iron species in multitransfused patients with sickle/β<sup>0</sup>-thalassaemia.
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- European Journal of Haematology, 2010, v. 84, n. 1, p. 59, doi. 10.1111/j.1600-0609.2009.01355.x
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- Publication type:
- Article
Non-transferrin bound labile plasma iron and iron overload in Sickle Cell Disease: a comparative study between Sickle Cell Disease and β thalassemic patients.
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- European Journal of Haematology, 2010, v. 84, n. 1, p. 72, doi. 10.1111/j.1600-0609.2009.01342.x
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- Article
Pylephlebitis due to perforated appendicitis in a teenager.
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- 2009
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- Publication type:
- journal article
Renal function in children with β-thalassemia major and thalassemia intermedia.
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- Pediatric Nephrology, 2008, v. 23, n. 10, p. 1847, doi. 10.1007/s00467-008-0897-8
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- Article
Response to hydroxyurea therapy in β-thalassemia.
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- American Journal of Hematology, 2008, v. 83, n. 5, p. 366, doi. 10.1002/ajh.21120
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- Article
Downregulation of hepcidin and haemojuvelin expression in the hepatocyte cell-line HepG2 induced by thalassaemic sera.
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- British Journal of Haematology, 2006, v. 135, n. 1, p. 129, doi. 10.1111/j.1365-2141.2006.06258.x
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- Article
Red blood cells, platelets and polymorphonuclear neutrophils of patients with sickle cell disease exhibit oxidative stress that can be ameliorated by antioxidants.
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- British Journal of Haematology, 2006, v. 132, n. 1, p. 108, doi. 10.1111/j.1365-2141.2005.05834.x
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- Article