Lucia Zalman

Deleterious mutation in the FYB gene is associated with congenital autosomal recessive small‐platelet thrombocytopenia

Carina Levin, Ariel Koren, Etheresia Pretorius et al. · Journal of Thrombosis and Haemostasis · 2015 · 68 citations · Full text

Life Sciences, Genetics, Hematology +16

Response to hydroxyurea therapy in β‐thalassemia

Ariel Koren, Carina Levin, Orly Dgany et al. · American Journal of Hematology · 2008 · 64 citations · Full text

Medicine, Hematology, Molecular Medicine +11

EFFECT OF HYDROXYUREA IN SICKLE CELL ANEMIA: A Clinical Trial in Children and Teenagers with Severe Sickle Cell Anemia and Sickle Cell beta-Thalassemia

Ariel Koren, Dora Segal-Kupershmit, Lucia Zalman et al. · Pediatric Hematology and Oncology · 1999 · 56 citations

Medicine, Hematology, Pediatrics +14

Leishmania tropica in northern Israel: A clinical overview of an emerging focus

Ayelet Shani‐Adir, Stephanie Kamil, Dganit Rozenman et al. · Journal of the American Academy of Dermatology · 2005 · 42 citations

Veterinary Medicine, Infectious Diseases, Pathobiology +16

A <i>PIGN</i> mutation responsible for multiple congenital anomalies–hypotonia–seizures syndrome 1 (MCAHS1) in an Israeli–Arab family

Morad Khayat, Joseph M. Tilghman, Ilana Chervinsky et al. · American Journal of Medical Genetics Part A · 2015 · 29 citations

Life Sciences, Genetics, Molecular Genetics +17