Hanna Shalev

Meir Medical Center — Israel

Medicine · Health Sciences

23h-index2.6kcitations59works0.02yr avg
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Research Topics

Erythrocyte Function and Pathophysiology(19), Hemoglobinopathies and Related Disorders(14), Iron Metabolism and Disorders(10), Ion Transport and Channel Regulation(9), Blood properties and coagulation(8)

Publications59 total

P-724 Long-term health outcomes of 19 years follow-up of mothers conceived after oocyte donation based on the registry of a large healthcare organization
Human Reproduction·2024Open Access
P-778 Same mother-different Oocyte: Comparison of obstetric and perinatal outcomes between pregnancies achieved through oocyte donation versus those achieved through spontaneous conception for the same mother
Human Reproduction·2023Open Access
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
Blood·2020· 57 citedOpen Access
Prevalence of left ventricular hypertrabeculation/noncompaction among patients with congenital dyserythropoietic anemia Type 1 (CDA1)
International Journal of Cardiology·2020· 3 cited
Treatment of transfusion‐dependent congenital dyserythropoietic anemia Type I patients with pegylated interferon alpha‐2a
European Journal Of Haematology·2020· 6 cited
Novel manifestations of immune dysregulation and granule defects in gray platelet syndrome
2020· 6 citedOpen Access
A novel <i>SLC12A1</i> mutation in Bedouin kindred with antenatal Bartter syndrome type I
Annals of Human Genetics·2019· 6 cited
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)
Human Molecular Genetics·2018· 53 citedOpen Access
Issue Information
European Journal Of Haematology·2017Open Access
Morphological features of congenital dyserythropoietic anemia type I: The role of electron microscopy in diagnosis
European Journal Of Haematology·2017· 10 cited
SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome
Brain·2017· 100 citedOpen Access
Proton pump inhibitors use suppresses iron absorption in congenital dyserythropoietic anemia
Pediatric Hematology and Oncology·2016· 7 cited
Morbidity and mortality of adult patients with congenital dyserythropoietic anemia type I
European Journal Of Haematology·2016· 18 cited
Persistent Pulmonary Hypertension of the Newborn Associated With Severe Congenital Anemia of Various Etiologies
Journal of Pediatric Hematology/Oncology·2013· 13 cited
TRPM6 and Hypomagnesaemia/Hypocalcaemia
2013· 1 cited
A novel epsilon gamma delta beta thalassemia presenting with pregnancy complications and severe neonatal anemia
European Journal Of Haematology·2012· 21 cited
High levels of soluble serum hemojuvelin in patients with congenital dyserythropoietic anemia type I
European Journal Of Haematology·2012· 15 cited
Urine metabolomics reveals novel physiologic functions of human aldehyde oxidase and provides biomarkers for typing xanthinuria
Metabolomics·2011· 25 cited
High Levels of Soluble Serum Hemojuvelin in Patients with Congenital Dyserythropoietic Anemia Type I,
Blood·2011
Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2
Nephrology Dialysis Transplantation·2011· 55 cited
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Frequent Co-authors

Hannah Tamary(18), Daniel Landau(16), Joseph Kapelushnik(10), Orly Dgany(8), Rina Zaizov(5), Isaac Yaniv(5), Asher Moser(5), Rivka Carmi(4), Itai Levi(4), Ohad S. Birk(4), Val C. Sheffield(3), Lea Shalmon(3), Tatyana Krasnov(3), Meira Zoldan(3), Ruth Schreiber(3), Melly Ohali(3), P Resnitzky(3), Tanya Krasnov(3), Dina Shaft(3), Josef Kapelushnik(3)