Wafa Bashir

Mutation of FA2H underlies a complicated form of hereditary spastic paraplegia (SPG35)

Katherine Dick, Matthias Eckhardt, Coro Paisán‐Ruíz et al. · Human Mutation · 2010 · 197 citations

Life Sciences, Genetics, Neurology +17

Thiamine responsive megaloblastic anemia: The puzzling phenotype

Ismail Beshlawi, Shoaib Al Zadjali, Wafa Bashir et al. · Pediatric Blood & Cancer · 2013 · 26 citations

Life Sciences, Genetics, Hematology +15

Cytogenetic Profile of Childhood Acute Lymphoblastic Leukemia in Oman

A.M. Udayakumar, Wafa Bashir, Anil Pathare et al. · Archives of Medical Research · 2007 · 15 citations

Medicine, Oncology, Pediatrics +14

Spectrum of external catheter-related infections in children with acute leukemia—Single-center experience

Mathew Zachariah, Laila Al-Yazidi, Wafa Bashir et al. · Journal of Infection and Public Health · 2013 · 12 citations · Full text

Medicine, Infectious Diseases, Pediatrics +13

Comparative Assessment of Deferiprone and Deferasirox in Thalassemia Major Patients in the First Two Decades-Single Centre Experience

Mathew Zachariah, Surekha Tony, Wafa Bashir et al. · Pediatric Hematology and Oncology · 2013 · 10 citations

Medicine, Hematology, Pharmacotherapy +17