Mario Kahale

One‐year results from a prospective randomized trial comparing phlebotomy with deferasirox for the treatment of iron overload in pediatric patients with thalassemia major following curative stem cell transplantation

M. Cappellini, A. Inati, A. Taher, 2017, Pediatric blood & cancer.

A phase 2 study of HQK‐1001, an oral fetal haemoglobin inducer, in β‐thalassaemia intermedia

A. Inati, A. Taher, S. Perrine, 2014, British Journal of Haematology.

One-year results from a prospective randomized trial comparing phlebotomywith deferasirox for the treatment of iron overload in pediatric patients with thalassemiamajor following curative stem cell transplantation

M. Cappellini, A. Inati, A. Taher, 2016 .

Identification of the First Mutation in a Bre Motif of the β-Globin Gene and its Inheritance with two Other α-Globin Gene Mutations in a Lebanese Family

A. Inati, D. Chui, Hong‐yuan Luo, 2013, Hemoglobin.