Shalev, Hanna

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1

Dgany, O., Avidan, N., Delaunay, J., Krasnov, T., Shalmon, L., Shalev, H., Eidelitz-Markus, T., Kapelushnik, J., Cattan, D., Pariente, A., et al. (2002) · The American Journal of Human Genetics

Hemoglobinopathies and Related DisordersErythrocyte Function and Pathophysiology

Cited by 168

Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I

Tamary, H., Shalev, H., Perez-Avraham, G., Zoldan, M., Levi, I., Swinkels, D. W., Tanno, T., & Miller, J. L. (2008) · Blood

GDF15 and Related BiomarkersIron Metabolism and Disorders

Cited by 135

SLC30A9 mutation affecting intracellular zinc homeostasis causes a novel cerebro-renal syndrome

Perez, Y., Shorer, Z., Liani-Leibson, K., Chabosseau, P., Kadir, R., Volodarsky, M., Halperin, D., Barber-Zucker, S., Shalev, H., Schreiber, R., et al. (2017) · Brain

Trace Elements in HealthNeurological diseases and metabolism

Cited by 99