Results 51 to 60 of about 140,652 (287)

Feasibility of and barriers to thalassemia screening in migrant populations: a cross-sectional study of Myanmar and Cambodian migrants in Thailand

open access: yesBMC Public Health, 2021
Background Thalassemia, an inherited hemoglobin disorder, has become a global public health problem due to population migration. Evidence-based strategies for thalassemia prevention in migrants are lacking.
Julia Z. Xu   +6 more
doaj   +1 more source

Molecular Analysis of Common Types ofホア-Thalassemia Associated with(ホイ-Thalassemia in Northern Thailand [PDF]

open access: yes, 1998
We applied PCR strategies to detect the common types of ホア- thalassemia determinants which were associated with ホイ- thalassemia in northern Thailand. Two types of deletions in the ホア-globin gene locus;the 18 kb deletion of Southeast Asian type(-ホアSEA)and
Asato, Tsuyoshi   +6 more
core  

Depression in mothers of children with thalassemia or blood malignancies: a study from Iran [PDF]

open access: yes
Background Several studies have found that parents of children with chronic diseases or disabilities have higher depression scores than control parents. Mothers usually take on the considerable part of the extra care and support that these children need
AliReza Farrokhi   +9 more
core   +1 more source

Genetic and Clinical Characteristics of Thalassemia Trait and Construction of LASSO‐Based Model for Its Differentiating From Iron Deficiency Anemia in Northern China

open access: yesJournal of Clinical Laboratory Analysis, EarlyView.
This study revealed a β‐thalassemia‐trait‐dominated genetic spectrum in Northern‐Chinese patients with microcytic hypochromic anemia, with _αSEA/αα, HBB:c.316_197C>T and HBB:c.124_127delTTCT being the most prevalent α‐ and β‐globin genotypes. Using LASSO regression, we constructed a nomogram based on four routine complete‐blood‐count parameters (RBC ...
Wen‐jie Yu   +6 more
wiley   +1 more source

Time to Do Something for Vitamin D Deficiency; A Review

open access: yesJournal 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

Impact of pre‐examination video education in Gd‐EOB‐DTPA‐enhanced liver MRI: A comparative study

open access: yesJournal of Medical Radiation Sciences, Volume 72, Issue 1, Page 34-41, March 2025.
This study evaluates the effects of pre‐examination video education on patient anxiety, satisfaction and image quality in Gd‐EOB‐DTPA‐enhanced liver MRI. We found that video education significantly reduced anxiety, increased patient satisfaction and improved image quality compared to standard pre‐MRI guidance, highlighting the potential of video ...
Hongfang Huang   +3 more
wiley   +1 more source

Co-existence of Phenylketonuria (PKU) and beta-Thalassemia Major in a 16 Years Old Girl: A Case Report

open access: yesInternational Journal of Hematology-Oncology and Stem Cell Research, 2012
While thalassemia major (TM) used to be a prevalent genetic disease in the past, however, Phenylketonuria (PKU) is quite rare in spite of consanquiness marriage rate of about 40% in the region. Preventive efforts for TM started >20 years ago but neonatal
Hossein Karami   +5 more
doaj  

Treatment Status of Patients with Β-Thalassemia Major in Northern Iran: Thalassemia Registry System

open access: yesIranian 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

MOESM2 of A validated cellular biobank for β-thalassemia

open access: yes, 2016
Additional file 2: Table S2.
Nicoletta Bianchi (328431)   +15 more
core   +1 more source

Plummer–Vinson syndrome in a 10‐year‐old boy from Côte d'Ivoire: An exceptional paediatric case with African context

open access: yesJPGN Reports, EarlyView.
Abstract Plummer–Vinson syndrome (PVS) is characterised by the triad of dysphagia, iron‐deficiency anaemia, and proximal oesophageal webs. While well described in adults, paediatric cases remain exceptionally rare, particularly in sub‐Saharan Africa.
Paul Mike Tayou Mbobda   +2 more
wiley   +1 more source

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