Results 101 to 110 of about 30,419 (262)
Journal of Genetic Counseling, Volume 34, Issue 3, June 2025.Abstract Although guidelines have historically recommended deferring decisions about learning genomic information for conditions not actionable in childhood until adulthood, youth have increasing access to personal genomic information through research, clinical, and direct‐to‐consumer testing. However, little is known about young people's reactions to,
Haley N. Grimes +5 more
wiley +1 more source
The compound state: Hb S/beta-thalassemia
Revista Brasileira de Hematologia e Hemoterapia, 2015 The polymerization of deoxygenated Hb S (sickling) is theprimary event in the molecular pathogenesis of SCD. How-ever, this event is highly dependent on the intracellular Hbcomposition; in other words, it is dependent on the concen-tration of Hb S, and type and concentration of the other typesof Hb.
openaire +4 more sources
Plastic bronchitis in beta thalassemia minor
Lung India, 2013 Plastic bronchitis is a rare pulmonary disorder associated with various conditions like cystic fibrosis, asthma, pulmonary infection and characterized by formation and expectoration of cast which assumes the shape of the bronchial tree. We report a case of a 33-year-old woman with beta thalassemia minor who developed plastic bronchitis.
Jyotsna M Joshi +2 more
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Factors Influencing Beta-Thalassemia Awareness in Western India
National Journal of Community Medicine, 2016 Context: Beta-thalassemia is highly prevalent in western India. Our organization runs a screening and prevention program to create awareness and reduce the incidence of homozygous beta-thalassemia cases.
Ashwin P Patel +4 more
doaj
Sickle Cell Disease in Africa: SickleInAfrica Registry in Ghana, Nigeria and Tanzania
eJHaem, Volume 6, Issue 3, June 2025.ABSTRACT Introduction Sickle cell disease (SCD) is most prevalent in Sub‐Saharan Africa (SSA), where incomplete patient profiles and limited management strategies hinder research and healthcare standards. Methods We describe the first large‐scale and multinational assessment of 13,403 SCD patients enrolled from 2017–2021 across 31 facilities in Ghana ...
Jack Morrice +23 more
wiley +1 more source
eJHaem, Volume 6, Issue 3, June 2025.Abstract Introduction The Danish national haemoglobinopathy screening programme offers screening to at‐risk pregnant women. Despite efforts to increase awareness of the screening programme, most women in the target population remain unscreened. In contrast, > 90% of pregnant women in Denmark attend a screening for chromosomal abnormalities by combined ...
Esther Agnethe Ejskjær Gravholt +6 more
wiley +1 more source
International Journal of Laboratory Hematology, Volume 47, Issue 3, Page 373-375, June 2025.
Sara Sacchetti +4 more
wiley +1 more source
Link Your Large Health Data Sets to the Area Deprivation Index, the ezADI Way
Research in Nursing &Health, Volume 48, Issue 3, Page 406-412, June 2025.ABSTRACT Increasing attention has been paid to investigations on how social determinants of health (SDOH; e.g., income, employment, education, housing, etc.) impact health outcomes. However, these variables are often not collected in routine clinical practice.
Sunnie Reagan +5 more
wiley +1 more source
The First Observation of Homozygous Hemoglobin S-Alpha Thalassemia Disease and Two Types of Sickle Cell Thalassemia Disease: (a) Sickle Cell-Alpha Thalassemia Disease, (b) Sickle Cell-Beta Thalassemia Disease [PDF]
, 1963 Muzaffer Aksoy
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Lupus eritematosus sistemik pada anak dengan thalassemia beta trait. Laporan kasus [PDF]
, 2004 Ninik Sukartini, Lyana Setiawan, Farida Oesman, Riadi Wirawan, Zakiudin Munasir â Systemic lupus erythematosus in a 9-year-old patient with beta-thalassemia trait.
Ninik Sukartini, Lyana Setiawan,Farida Oesman, Riadi Wirawan, Zakiudin Munasir
core +1 more source