Results 181 to 185 of about 34,320 (185)

Case Report: Acute hepatitis A virus infection presenting with direct antiglobulin test-negative autoimmune hemolytic anemia and α-thalassemia trait. [PDF]

F1000Res
Debbabi H, Chakroun E, Hassine H, Kchir H, Cherif D, Yacoub H, Maamouri N.   +6 more
europepmc   +1 more source

Use of HSC-targeted LNP to generate a mouse model of lethal α-thalassemia and treatment via lentiviral gene therapy.

Blood
Chappell ME, Breda L, Tricoli L, Guerra A, Jarocha D, Castruccio Castracani C, Papp TE, Tanaka N, Hamilton N, Triebwasser MP, Ghiaccio V, Fedorky MT, Gollomp KL, Bochenek V, Roche AM, Everett JK, Cook EJ, Bushman FD, Teawtrakul N, Glentis S, Kattamis A, Mui BL, Tam YK, Weissman D, Abdulmalik O, Parhiz H, Rivella S.   +26 more
europepmc   +1 more source

Molecular Basis of α-Thalassemia in Iran [PDF]

Iran Biomed J, 2018
Valaei A, Karimipoor M, Kordafshari A, Zeinali S.   +3 more
europepmc   +1 more source

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Rapid and simultaneous detection of β- thalassemia point mutations by reverse hybridization strip assay among Egyptian patients

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, Moustafa Sakr, Ahmed Daif, Khalil Elhalfawy   +3 more
openaire   +1 more source