Results 201 to 210 of about 136,995 (252)

Gene Therapy of Beta Hemoglobinopathies. [PDF]

Biomedicines
Testa U, Pelosi E, Castelli G.
europepmc   +1 more source

PCA-Based Database Mining Enables the Discovery of Bacterial Carbene Transferases for Stereodivergent Cyclopropanation. [PDF]

Angew Chem Int Ed Engl
Kato S, Takeuchi K, Umeda K, Kudo H, Hasunuma T, Hayashi T.   +5 more
europepmc   +1 more source

ACMG/AMP-Based Variant Classification of a Novel HBA2 Variant (HBA2: C.297del, Hb Taiping) in Compound Heterozygosity With Hb Adana (HBA2:C.179G>A) Causing Non-Deletional Hb H Disease. [PDF]

Int J Lab Hematol
Yasin NM, Somasundram S, Hassan S, Aziz NA, Hamid FSA, Zulkefli ES, Mohamad NN, Lee CM, Darawi MN, Papasavva T, Stephanou C, Kountouris P, Arkesteijn SJG, Koopman T, Harteveld CL.   +14 more
europepmc   +1 more source

Genetic variations and clinical implications of B-thalassemia in Iraqi population. [PDF]

PLoS One
Jawad AZ, Chelly M, Al-Zuhairy SH, Bouaziz H.   +3 more
europepmc   +1 more source

Clinical and Hematological Characteristics of Vietnamese Heterozygous Hb Tak/β-Thalassemia Patients: A Four-Case Series. [PDF]

Mediterr J Hematol Infect Dis
Nguyen TC, Nguyen TTH, Phi TNA, Le XH, Vu DL, Nguyen ND.   +5 more
europepmc   +1 more source

Subtype Distribution and Mutation Spectrum of Thalassemia in Children Under 10 Years in Northern Vietnam. [PDF]

Mediterr J Hematol Infect Dis
Nguyen HT, Nguyen TTH, Nguyen TC, Phi TNA, Le TTH, Hoang PL, Vu DB, Nguyen ND.   +7 more
europepmc   +1 more source

Revisiting hemoglobin constant spring: molecular insights, pathophysiological mechanisms, and clinical perspectives. [PDF]

Orphanet J Rare Dis
Wongkhammul N, Khamphikham P, Maneekesorn S, Charoenkwan P.   +3 more
europepmc   +1 more source

A novel HBD gene mutation associated with normal-range hb A2 in β-thalassemia carriers. [PDF]

Ann Hematol
Zhang L, Yang J, Li X, Liu Y, Liu C, Duan S, Zhang L, Liu W, Chang M.   +8 more
europepmc   +1 more source