Results 51 to 60 of about 26,664 (228)
Beta thalassemia major new births from 1972 to 2015. [PDF]
, 2019 Beta thalassemia major new births from 1972 to 2015.
K. K. Hemantha (7256006) +29 more
core +1 more source
EVALUATION OF HEARING IN PATIENTS WITH BETA THALASSEMIA MAJOR [PDF]
Basrah Journal of Surgery, 2018 EVALUATION OF HEARING IN PATIENTS WITH BETA THALASSEMIA MAJOR Ahmed Fadhil Hasan*, Husam Haider Salman# & Jaafar Muhsen Khalaf@ *MB, ChB, FICMS, CABS ENT HNS, ENT Senior Surgeon at Al Shafaa General Hospital. #FRCS, DLO. Retired, Department Of Surgery,
Ahmed Fadhil Hasan +2 more
doaj +1 more source
Cerebral Blood Transit in Sickle Cell Anemia
Journal of Magnetic Resonance Imaging, EarlyView.ABSTRACT Background Sickle cell anemia (SCA) patients upregulate cerebral blood flow to compensate for decreased arterial oxygen content. Such hyperemic conditions can manifest as venous hyperintense signal on arterial spin labeling (ASL) MRI, which may reflect faster capillary blood transit, altered oxygen extraction fraction (OEF), and infarct risk ...
Wesley T. Richerson +10 more
wiley +1 more source
Chronic hyperplastic anemia as an independent risk factor for atherosclerotic lesions: a lesson from thalassemia intermedia [PDF]
, 2010 Introduction. Cardiovascular involvement represents a well-known complication and the primary cause of mortality, both in transfusion-dependent beta thalassemia major (β-TM) and in transfusion-independent beta thalassemia intermedia (β-TI ...
Pier Luigi Cocco +7 more
core +1 more source
An Investigation of Group-Based Mobile Learning on Stress, Anxiety, Depression, and Pain Among Beta-Thalassemia Major Patients: A Randomized Control Trial [PDF]
Objective: Beta-thalassemia major (B-TM) is an inherited hematological disease that affects nearly 300 million people worldwide. This study aimed to evaluate the effects of group-based mobile learning on stress, anxiety, depression, and pain among beta ...
Mahsa Imanian +2 more
core +1 more source
Examination and Sampling of Chorionic Villi for the Diagnosis of Beta-Thalassemia Major in the First Trimester of Pregnancy in Southwestern Iran [PDF]
Armaghane Danesh Bimonthly Journal, 2023 Background & aim: Beta thalassemia is one of the most common hereditary diseases in Iran. The birth of a child with thalassemia causes many social and economic problems for parents and the health care system.
E Shams +3 more
doaj
Endocrine Complications in Patients with -thalassemia Major [PDF]
Journal of Tropical Pediatrics, 2002 Thirty-seven patients with thalassemina major (TM) were studied to determine the extent and rate of endocrine complications. Mean haemoglobin and ferritin concentrations were 8.8 +/- 0.6 and 3,597 +/- 1,931, respectively. Provocation tests for growth hormone secretion were applied in patients with standing heights below the third centile and/or growth ...
Aydinok, Y +7 more
openaire +3 more sources
Neuroprotection, EarlyView.Abstract Prime editing, a novel clustered regularly interspaced short palindromic repeats (CRISPR)‐based technology, fuses a reverse transcriptase (RT) to an engineered CRISPR‐associated protein 9 (Cas9) and uses a prime editing guide RNA (pegRNA)‐encoded template.
Tianshan Ji +4 more
wiley +1 more source
Prenatal Diagnosis, EarlyView.ABSTRACT Aim In this article, we present two cases of severe fetal hemolytic anemia based on a beta‐thalassaemia trait inherited from a single parent. Results These cases, presented at 20 and 28 weeks' gestation, necessitated intra‐uterine blood transfusions.
Eva van der Meij +11 more
wiley +1 more source
Epidemiology and treatment of beta thalassemia major in China
Pediatric Investigation, 2019 AbstractThalassemia, classified as the main types α‐ and β‐thalassemia, is a single gene disorder resulting from globin chain synthesis impairment through the mutation or deletion of globin genes. The incidence of thalassemia is high worldwide, with high associated mortality. Therefore, treatment is important to improve patient outcomes.
Xiaoxiao Xu, Xuedong Wu
openaire +3 more sources