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Hemoglobin
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October 20, 2025
Utility of Molecular Sequencing and Hematologic Parameters for Diagnosis of α-Thalassemia: A Perspective of the National Reference Laboratory
Ryan Shean, Nicole Deshmukh, Michael Palmer, et al.
Hemoglobin
|
October 5, 2025
Hemoglobin Dieppe (<i>HBB:c. 383A > G</i>): A Rare Dominant β-Thalassemia in an Iraqi Kurdish Family
Tara Jamel Osman, Ashna H Karim, Rozhgar A Khailany, et al.
Hemoglobin
|
July 7, 2025
<i>HBA2</i>: C.4delG: A Novel Frameshift Mutation Causing α<sup>+</sup>-Thalassemia Found in a Chinese Family
Wei Li, Guixi Wei, Shan Ren, et al.
Hemoglobin
|
December 21, 2025
Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child
Ai- Yang, Ti-Long Huang, Chun-Yan Song, et al.
Hemoglobin
|
April 14, 2025
Death from <i>S. pneumoniae</i> in HbSC Disease: Was Expanded Pneumococcal Vaccination Too Late?
Charles A Coomer, Rebecca A Levin, Caitlin M Neri
Hemoglobin
|
April 15, 2025
Estradiol is Pro-Nociceptive and Associated with a Small-Fiber Neuropathy Among Premenopausal Women with Sickle Cell Disease
Zachary Ramsay, Deva Sharma, Margaret Wisdom-Phipps, et al.
Hemoglobin
|
April 25, 2025
Dynamic Viscosity of Hemoglobin Solutions Determined by Transverse Proton Magnetic Relaxation
Néstor Juan Rodríguez de la Cruz, Yulianela Mengana Torres, Juan Carlos García Naranjo, et al.
Hemoglobin
|
October 29, 2025
Pituitary Versus Hepatic Iron Assessment in Transfusion-Dependent Thalassemia: Is Signal Intensity Ratio a Reliable Tool?
Sultan Okur Acar, Müge Gürçinar, Sezer Acar, et al.
Hemoglobin
|
November 7, 2025
Genetically Confirmed Dual Hematologic Disorder: A Case of β-Thalassemia with Frameshift Mutation and Type 3 von Willebrand Disease in a Pediatric Patient
Muhammad Tariq Masood Khan, Ihtisham Ul Haq, Aamir Ali, et al.
Hemoglobin
|
October 31, 2025
Influence of Alpha Thalassaemia on Hematological and Clinical Presentations in Patients of Sickle Cell-β-Thalassaemia with IVS I-5 (G→C) Mutation (<i>HBB</i>: C.20A > T/<i>HBB</i>: C.92 + 5G > C)
Snehadhini Dehury, Pradeep Kumar Mohanty, Kishalaya Das, et al.
Page
of 322
Search research articles
Search
Showing results (521-530 of 3,216) with videos related to
Sort By:
Page
of 322
Hemoglobin
|
October 20, 2025
Utility of Molecular Sequencing and Hematologic Parameters for Diagnosis of α-Thalassemia: A Perspective of the National Reference Laboratory
Ryan Shean, Nicole Deshmukh, Michael Palmer, et al.
Hemoglobin
|
October 5, 2025
Hemoglobin Dieppe (<i>HBB:c. 383A > G</i>): A Rare Dominant β-Thalassemia in an Iraqi Kurdish Family
Tara Jamel Osman, Ashna H Karim, Rozhgar A Khailany, et al.
Hemoglobin
|
July 7, 2025
<i>HBA2</i>: C.4delG: A Novel Frameshift Mutation Causing α<sup>+</sup>-Thalassemia Found in a Chinese Family
Wei Li, Guixi Wei, Shan Ren, et al.
Hemoglobin
|
December 21, 2025
Nonsense Variant in the β-Spectrin Gene Causing Hereditary Spherocytosis Identified by Whole-Exome Sequencing in a Child
Ai- Yang, Ti-Long Huang, Chun-Yan Song, et al.
Hemoglobin
|
April 14, 2025
Death from <i>S. pneumoniae</i> in HbSC Disease: Was Expanded Pneumococcal Vaccination Too Late?
Charles A Coomer, Rebecca A Levin, Caitlin M Neri
Hemoglobin
|
April 15, 2025
Estradiol is Pro-Nociceptive and Associated with a Small-Fiber Neuropathy Among Premenopausal Women with Sickle Cell Disease
Zachary Ramsay, Deva Sharma, Margaret Wisdom-Phipps, et al.
Hemoglobin
|
April 25, 2025
Dynamic Viscosity of Hemoglobin Solutions Determined by Transverse Proton Magnetic Relaxation
Néstor Juan Rodríguez de la Cruz, Yulianela Mengana Torres, Juan Carlos García Naranjo, et al.
Hemoglobin
|
October 29, 2025
Pituitary Versus Hepatic Iron Assessment in Transfusion-Dependent Thalassemia: Is Signal Intensity Ratio a Reliable Tool?
Sultan Okur Acar, Müge Gürçinar, Sezer Acar, et al.
Hemoglobin
|
November 7, 2025
Genetically Confirmed Dual Hematologic Disorder: A Case of β-Thalassemia with Frameshift Mutation and Type 3 von Willebrand Disease in a Pediatric Patient
Muhammad Tariq Masood Khan, Ihtisham Ul Haq, Aamir Ali, et al.
Hemoglobin
|
October 31, 2025
Influence of Alpha Thalassaemia on Hematological and Clinical Presentations in Patients of Sickle Cell-β-Thalassaemia with IVS I-5 (G→C) Mutation (<i>HBB</i>: C.20A > T/<i>HBB</i>: C.92 + 5G > C)
Snehadhini Dehury, Pradeep Kumar Mohanty, Kishalaya Das, et al.
Page
of 322