Results 101 to 110 of about 48,747 (238)
Non-invasive prenatal diagnosis of beta-thalassemia disease using digital PCR
Frontiers in MedicineIntroductionTo evaluate the performance of digital polymerase chain reaction (dPCR) as a non-invasive prenatal test (NIPT) for assessing the risk of the fetus being affected by beta-thalassemia major and beta-thalassemia/Hb E disease.MethodsThis cross ...
Chalit Tangwerapornpong +7 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 5, May 2026.Acute infarcts and microvascular ischemic changes in the brain of a young patient with Sickle‐Cell Disease despite High Fetal Hemoglobin. ABSTRACT Sickle‐cell disease (SCD) is characterized by abnormal hemoglobin (Hb) polymerization, leading to erythrocyte sickling and microvascular obstruction.
Yi Hui Luo +5 more
wiley +1 more source
The levels of nitric oxide in beta-thalassemia minor
Turkish Journal of Hematology, 2008 OBJECTIVE: The aim of this study was to investigate the relationship between NO (nitric oxide) and beta-thalassemia minor. METHODS: A total of 60 patients with beta-thalassemia minor (30 M, 30 F) were included in the study. The control group consisted of
Yalçın Başaran +3 more
doaj
Validity of naked eye single tube red cell osmotic fragility test (NESTROFT) in screening of beta-thalassemia trait [PDF]
, 2011 زمینه و هدف: تالاسمی متداولترین اختلال تک ژنی است که رهایی از آن از طریق درمان قطعی ممکن نبوده و مستلزم پیشگیری از طریق به کارگیری یک روش قابل اعتماد و کم هزینه برای غربالگری ناقلین و در مرحله بعد ارایه آموزش، مشاوره ژنتیک، تشخیص قبل از تولد و خاتمه ...
Amini, S.A. +3 more
core
Deteksi Mutasi Langka, Delesi 619 Bp, Pada Gen Beta-Globin Dari Etnis Melayu Mahasiswa Fakultas Kedokteran Universitas YARSI [PDF]
, 2015 Beta-thalassemia merupakan gangguan hematologis autosomal yang secara genetis mengakibatkan berkurangnya sintesis beta-globin di hemoglobin. Beta-talasemia sebagian besar disebabkan oleh mutasi titik, insersi atau delesi dalam gen beta-globin yang ...
Kenconoviyati, K. (Kenconoviyati) +4 more
core
Health Science Reports, Volume 9, Issue 5, May 2026.ABSTRACT Background and Aims Xerostomia, or dry mouth, significantly impairs quality of life and oral health, particularly in patients subjected to radiation therapy or suffering from systemic disorders. This narrative review summarizes the current evidence on the efficacy and safety of gene therapy interventions for xerostomia, exploring innovative ...
Muhammad Usman Bilal +6 more
wiley +1 more source
Anemia, 2012 Beta thalassemia major is an inherited disease resulting from reduction or total lack of beta globin chains. Patients with this disease need repeated blood transfusion for survival.
Q. Shazia +3 more
doaj +1 more source
A kataláz enzim génje polimorfizmusának hatása az enzim expressziójára = Association of catalase gene and catalase protein expression [PDF]
, 2012 1. Kataláz gén exon 9 C111T polimorfizmus kismértékű vér kataláz csökkenéssel jár vitiligos nők esetében (CEMED 2011) 2. Csökkent vér kataláz aktivitás volt mérhető magyar beta-thalassemia trait betegeknél.
Góth, László +5 more
core
Health Science Reports, Volume 9, Issue 5, May 2026.ABSTRACT Background Maternal mental health influences the key psychological process of maternal–fetal attachment (MFA) during pregnancy. Women with a history of miscarriage are at increased risk of prenatal anxiety and depression, which may affect their emotional bond with the fetus.
Iqra Javaid +5 more
wiley +1 more source
Liver Fibrosis: Molecular Pathogenesis and Therapeutic Interventions
MedComm, Volume 7, Issue 5, May 2026.We systematically summarized the etiologies, diagnostic approaches, and pathogenic mechanisms of liver fibrosis. Also, the therapeutic interventions for liver fibrosis were systematically classified into two main categories: etiological treatment and mechanism‐based antifibrotic therapies.
Jiaorong Qu +8 more
wiley +1 more source