Results 21 to 30 of about 9,026 (213)
Experiences, Attitudes, and Knowledge within the Hemoglobinopathy Community [PDF]
, 2022 Hemoglobinopathies are highly prevalent conditions, with a global carrier rate of about 7%, and where carriers often present with microcytic anemia. Despite this, a standard of care or treatment is not yet established for cases of hemoglobinopathies ...
Klinder, Anusha Beth
core +1 more source
Time to Do Something for Vitamin D Deficiency; A Review
Journal of Pediatrics Review, 2015 Context: Vitamin D deficiency is a common nutritional disorder in Iran. Vitamin D is an essential health factor from birth onward. This study was conducted to summarize epidemiologic researches regarding vitamin D deficiency in different parts of the ...
Mehrnoush Kosaryan +3 more
doaj +3 more sources
Hemoglobinopathy SD presenting as Hemoglobinopathy SS
Medicina, 2017 This case report shows the interaction of hemoglobin (Hb) S with Hb D. in a child previously diagnosed with sickle cell anemia based on the Hb electrophoretic migration pattern in alkaline pH.
Sonia Maria Lissa +4 more
doaj +1 more source
Bromhexine is a potential drug for COVID-19; From hypothesis to clinical trials
Вопросы вирусологии, 2022 COVID-19 (novel coronavirus disease 2019), caused by the SARS-CoV-2 virus, has various clinical manifestations and several pathogenic pathways. Although several therapeutic options have been used to control COVID-19, none of these medications have been ...
S. Bahadoram +6 more
doaj +1 more source
Early Screening of Hemoglobinopathy in Indonesia Using Erythrocyte Indices [PDF]
, 2017 BACKGROUND: The mutation spectrums of hemoglobinopathy are different among populations that yield a different result of erythrocyte indices. Calculation of erythrocyte indices with some formula has been reported to differentiate between hemoglobinopathy ...
Yenny Surjawan +11 more
core +1 more source
Hematology Reports, 2018 Beta thalassemia dominant results from mutations in the β globin chain gene resulting in the production of elongated, highly unstable beta globin chains.
Alexandra Agapidou +3 more
doaj +1 more source
Treatment Status of Patients with Β-Thalassemia Major in Northern Iran: Thalassemia Registry System
Iranian Journal of Public Health, 2019 Background: Electronic registry system of beta-thalassemia patients was run by Thalassemia Research Center (TRC) in 2017. The aim of the current study was presentation of therapeutic status in these patients at Mazandaran Province, Iran.
Mehrnoush KOSARYAN +5 more
doaj +1 more source
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
core +1 more source
Parasite, 2021 Background: Artemisinin-based treatment in malaria patients with abnormal hemoglobin may be ineffective because of their genetic particularity, which could lead to resistance.
Gbessi Eric A. +10 more
doaj +1 more source
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
doaj +1 more source