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Hemoglobin|June 8, 2021
Elevated Hb A<sub>2</sub> is Not Always Indicative of β-ThalassemiaLi-Ping Luo, Li Ma, Shao-Bin Lin, et al.
Hemoglobin|June 10, 2021
Prolonged QTc Interval in Nigerian Children with Sickle Cell AnemiaMaxwell U Anah, Anthony C Nlemadim, Chigozie I Uzomba, et al.
Hemoglobin|March 17, 2020
Hb S/<b>β</b>-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular CharacteristicsAndré R Belisário, Anna B Carneiro-Proietti, Ester Cerdeira Sabino, et al.
Hemoglobin|January 7, 2020
Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional StudyAhmad Shoujaa, Faten Moasses, Yasser Mukhalalaty, et al.
Hemoglobin|September 14, 2020
Fifteen Cases of Hb J-Meerut: The Rare Association with Hb E and/or <i>HBA1</i>: c.-24C>G (or <i>HBA2</i>) VariantsMohamed S M Khalil, Adele T Timbs, Shirley J Henderson, et al.
Hemoglobin|November 30, 2020
Twelve Cases of Hb Manitoba [α102(G9)Ser→Arg]: the Fluctuation in the Variant ExpressionMohamed S M Khalil, Adele T Timbs, Shirley J Henderson, et al.
Hemoglobin|January 12, 2021
Calcium Channel Blockers in Conjunction with Standard Iron-Chelating Agents for β-Thalassemia Major: Systematic Literature SearchMohammed A Alali, Khalid M A Alanazi, Sarah N Alsayil, et al.
Hemoglobin|October 23, 2020
Prenatal Diagnosis and Screening of Thalassemia Mutations in Bangladesh: Presence of Rare MutationsMd Abdul Aziz, Waqar A Khan, Bilquis Banu, et al.
Hemoglobin|September 8, 2022
Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell DiseasePrashant P Warang, Nikhil S Shinde, Vinod D Umare, et al.
Hemoglobin|January 19, 2021
The Prevention of Thalassemia Revisited: A Historical and Ethical Perspective by the Thalassemia International FederationMichael Angastiniotis, Mary Petrou, Dimitrios Loukopoulos, et al.
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