Results 181 to 190 of about 34,912 (203)
Molecular Basis of α-Thalassemia in Iran [PDF]
Iran Biomed J, 2018 Valaei A +3 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Journal of Biochemistry, Microbiology and Biotechnology, 2016
Thalassemia is a wide range hereditary disease with high incidence in Egypt along with the high frequency of consanguineous marriages. Investigation the heterogeneity, molecular basis, and natural history are the most effective methods to deal with the thalassemia to develop effective method for management and prevention including the prenatal ...
Osama Shalaan +3 more
openaire +1 more source
Thalassemia is a wide range hereditary disease with high incidence in Egypt along with the high frequency of consanguineous marriages. Investigation the heterogeneity, molecular basis, and natural history are the most effective methods to deal with the thalassemia to develop effective method for management and prevention including the prenatal ...
Osama Shalaan +3 more
openaire +1 more source
CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia
New England Journal of Medicine, 2021David M Altshuler +2 more
exaly
A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia
New England Journal of Medicine, 2020Maria Domenica Cappellini +2 more
exaly
Survival in Medically Treated Patients with Homozygous β-Thalassemia
New England Journal of Medicine, 1994Nancy F Olivieri, Alan R Cohen
exaly
Gene Therapy in Patients with Transfusion-Dependent β-Thalassemia
New England Journal of Medicine, 2018Alexis A Thompson +2 more
exaly
Bone Marrow Transplantation in Patients with Thalassemia
New England Journal of Medicine, 1990Emanuele Angelucci, Donatella Baronciani
exaly