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UnknownPregnancy outcomes in women with a hemoglobinopathy trait: a multicenter, retrospective study.
Not available
S-EPMC8490217 | biostudies-literature
UnknownMetastatic SMARCB1-Deficient Renal Medullary Carcinoma without Hemoglobinopathy with Durable and Dramatic Response to Pembrolizumab plus Lenvatinib: Case Report.
Not available
S-EPMC11521492 | biostudies-literature
UnknownHemoglobinopathy is Associated With Total Hip Arthroplasty Indication Even Beyond Sickle Cell Anemia.
Not available
S-EPMC9947981 | biostudies-literature
UnknownCan Automated Hematology Analyzers Predict the Presence of a Genetic Hemoglobinopathy? An Analysis of Hematological Biomarkers in Cambodian Women.
Not available
S-EPMC7913495 | biostudies-literature
UnknownHemoglobinopathy screening in primary care in the Netherlands: exploring the problems and needs of patients and general practitioners.
Not available
S-EPMC10133269 | biostudies-literature
UnknownDeep Learning Detection of Sea Fan Neovascularization From Ultra-Widefield Color Fundus Photographs of Patients With Sickle Cell Hemoglobinopathy.
Not available
S-EPMC7774049 | biostudies-literature
ProteomicsA Mass Spectrometry-based Multiplexed Targeted Assay for Detection of Hemoglobinopathies from Dried Blood Spots
Hemoglobinopathies are the most common inherited disorders worldwide. Accurate analysis of hemoglobin variants is critical for diagnosis of hemoglobinopathies. Although high-performance liquid chromatography and capillary zone electrophoresis are widely used as screening tools, they possess inherent...
ORGANISM(S): Homo sapiens (Human) 
2025-08-01 | PXD061996 | Pride
Hemoglobinopathy Srm Thalassemia Screening Stable isotope labeled standard Structural variants Lc-ms/ms 
UnknownMolecular prevalence of HBB-associated hemoglobinopathy among reproductive-age adults and the prenatal diagnosis in Jiangxi Province, southern central China.
Not available
S-EPMC9554255 | biostudies-literature
UnknownThalassemia and hemoglobinopathy prevalence in a community-based sample in Sylhet, Bangladesh.
Not available
S-EPMC10355052 | biostudies-literature
UnknownWhole transcriptome analysis of human erythropoietic cells during ontogenesis suggests a role of VEGFA gene as modulator of fetal hemoglobin and pharmacogenomic biomarker of treatment response to hydroxyurea in β-type hemoglobinopathy patients.
Not available
S-EPMC5654038 | biostudies-literature
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