Font Size: a A A
Keyword [thalassemia]
Result: 141 - 160 | Page: 8 of 10
141. Combined Use Of Astragalus Polysaccharide With Sodium Butyrate In The Induction Of HbF Synthesis On K562 Cells And Human Erthroid Progenitor Cells
142. The Body Development, Growth And Iron Overload In Child With β-Thalassemia Major In The Western Of Guangxi
143. The Clinical Researching On The B Thalassemia Mutation IVS-â…¡-5 Gâ†'C
144. The Changes Of The Level Of Blood Routine And Sf And The Influence On Pregnancy Outcome For Women With Alpha Thalassemia
145. The Study Of Middle Cerebral Artery Peak Systolic Velovity In Fetuses With α-Thalassaemia In The First Trimester
146. Quality Of Life In Patients With Thalassemia Major After Hematopoietic Stem-Cell Transplantation
147. The Clinical Study Of Qi And Jing Supplement Formula For Children With β-thalassemia Intermedia And "Weakness Of Spleen And Kidney"
148. The Biological Mechanism Of Symptoms Seasonal Variation Based On Hemolysis Of Erythrocyte And Anemia Of Patients With Thalassemia Disease
149. Development Of An Electrochemical DNA Sensor For The Detection Of α-thalassemia And β-thalassemia
150. Influence Of Pretransplantation Serum Ferritin On Beta-thalassemia Major Undergoing Allogeneic Hematopoietic Stem Cell Transplantation
151. Development Of A Capillary Zone Electrophoresis Method For Rapid Determining Human Globin Chains
152. A New Method To Detect α-thalassemia Deletions Using Nextgeneration Sequencing
153. Economic Cost Investigation And Counter Measure Research On Thalassemia Major Patients Guangxi
154. The Study Of β-thalassemia Major Patients’ Treatment Status And The Cost-effective Analysis Of Iron Chelator In 4 Cities Of Guangdong Province
155. The Genotypes And Clinical Characteristics Of 44 Hospitalized Patients With Thalassemia
156. Changes Of TF And TFPI In Thalassemia Before And After Splenectomy
157. Research On The Mutation Of ~Aγ-196 Câ†'T Causing Nondeletional Hereditary Persistence Of Fetal Hemoglobin
158. Hepcidin,GDF15 Concentration And Iron Metabolism In Patients With Thalassemia Major And Intermedia
159. Value And Strategy Research Of Hearing Monitoring On The Early Treatment During Thalassemia Patients
160. Effect Of Interruption Of γâ†'β Globin Switch By Using Peptide Nucleic Acid On γ-globin Gene Expression
  <<First  <Prev  Next>  Last>>  Jump to