Results 21 to 30 of about 8,777 (197)
Pharmacy, 2022 Sickle-cell disease (SCD) is an inherited hemoglobinopathy, causing lifelong complications such as painful vaso-occlusive episodes, acute chest syndrome, stroke, chronic anemia, and end-organ damage, with negative effects on quality of life and life ...
Michael Migotsky +2 more
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Fetomaternal outcome of pregnancy with hemoglobinopathy [PDF]
New Indian Journal of OBGYNObjectives: The objectives of this study are to determine the obstetric and neonatal outcome in pregnancy with hemoglobinopathy. Methods and materials: A prospective observational study to evaluate maternal and neonatal outcome in pregnant women with ...
Bivarani Goswami +2 more
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Hemoglobinopathy is Associated With Total Hip Arthroplasty Indication Even Beyond Sickle Cell Anemia [PDF]
, 2023 Background: The extent to which hemoglobinopathies other than sickle anemia (HbSS) are associated with hip osteonecrosis is unknown. Sickle cell trait (HbS), hemoglobin SC (HbSC), and sickle/β-thalassemia (HbSβTh) may also predispose to osteonecrosis of ...
Cohen-Rosenblum, Anna +7 more
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Hematology, 2023 We present a family that carries the β-hemoglobin variant Hb Santa Juana (HBB:c.326A>G, β 108(G10) Asn>Ser), also known as Hb Serres, in three generations. All affected family members had an anomal hemoglobin fraction as detected by HPLC but normal blood
N. P. Wildenberg +3 more
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Indian Journal of Public Health, 2023 Hemoglobinopathy is a major concern among the tribal population which constitutes 8.6% of the total population, and West Bengal (WB) is the home to 5.3 million tribes.
Jyoti Shaw +4 more
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HPLC Market Trends Advancements in HbA1C Hemoglobinopathy Testing for USA Point-of-Care
, 2023 HPLC Market Trends Advancements in HbA1C Hemoglobinopathy Testing for USA Point-of ...
Rahul Jagtap (16753542)
core +1 more source
Frontiers in Cardiovascular Medicine, 2022 IntroductionSickle cell disease (SCD) is an inherited hemoglobinopathy disorder. The main consequence is synthesis of hemoglobin S leading to chronic hemolysis associated with morbidity. The aim of this study was to investigate Thrombin Generation Assay (
Guillaume Feugray +8 more
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Hemoglobinopathy screening in primary care in the Netherlands: exploring the problems and needs of patients and general practitioners [PDF]
, 2022 The prevalence of hemoglobinopathies in The Netherlands is increasing due to migration. Hemoglobinopathies are severe hereditary diseases. An informed reproductive choice by at-risk couples, such as pre-implantation diagnosis or termination of affected ...
Harteveld, C.L. +7 more
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Acute Ischemic Stroke in Sickle Cell Disease Challenges for Thrombolysis
Dubai Medical Journal, 2020 Sickle cell disease (SCD) is a hemoglobinopathy disorder that was recognized in 1949. Stroke is one of the most devastating complications of this disorder.
Amal Al Hashmi, Sanjith Aaron
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Review of clinical and hematological profile of hemoglobin D cases in a single centre
Journal of Marine Medical Society, 2023 Introduction: Hemoglobin D Punjab is a common hemoglobin D variant, which is essentially known to cause a mild disease even in homozygous state. Heterozygous state of hemoglobin D Punjab with sickle cell is the only presentation when a severe disease may
Neha Singh, Tulika Seth, Seema Tyagi
doaj +1 more source