Hanna Shalev
Meir Medical Center(IL)
Publications by Year
Research Areas
Erythrocyte Function and Pathophysiology, Hemoglobinopathies and Related Disorders, Iron Metabolism and Disorders, Ion Transport and Channel Regulation, Blood properties and coagulation
Most-Cited Works
- → Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia(2002)562 cited
- → CATSPER2, a human autosomal nonsyndromic male infertility gene(2003)206 cited
- → Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1(2002)171 cited
- → Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I(2008)139 cited
- → Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis(2006)133 cited
- → Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic Syndrome(1999)123 cited
- → Transient neonatal hyperkalemia in the antenatal (ROMK defective) Bartter syndrome(2003)118 cited
- → SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome(2017)101 cited
- → Hypocholesterolemia in chronic anemias with increased erythropoietic activity(2006)95 cited
- → Hypocomplementemic autosomal recessive hemolytic uremic syndrome with decreased factor H(1998)89 cited