Results 191 to 200 of about 1,010,620 (323)
Khyber Medical University Journal, 2018 OBJECTIVE: To determine the frequency of beta thalassemia trait in pregnant anemic patients attending Khyber Teaching Hospital, Peshawar, Pakistan. METHODS: This descriptive cross sectional study was conducted in Gynecology and Obstetrics Department of ...
Maimoona Qadir, Sohail Amir
doaj
Know your blood: Addressing barriers to preconceptual screening for sickle cell disease
HemaSphere, Volume 9, Issue 8, August 2025.
Ernel Boadi +2 more
wiley +1 more source
Enhancing Rare Disease Awareness and Education Among Medical Professionals and Students in Türkiye
Journal of Evaluation in Clinical Practice, Volume 31, Issue 5, August 2025.ABSTRACT Purpose Rare diseases (RDs), which are often chronic, degenerative, and life‐threatening conditions, pose significant challenges due to their complexity and limited awareness among healthcare professionals. This study assessed the knowledge, awareness, and educational needs related to RDs among 5th‐ and 6th‐year medical students at Atatürk ...
Öznur Karagöz +8 more
wiley +1 more source
Third-degree heart block in thalassemia major: A case report [PDF]
, 2012 Background: First and second-degree heart blocks are partly common rhythm disorders in thalassemic patients but complete heart block is a very rare complication of iron overload cardiomyopathy.
Hosseini, S.M., Maleki, A.R., Nikyar, B.
core +1 more source
Molecular basis and prenatal diagnosis of beta-thalassemia [PDF]
, 1988 HH Jr Kazazian, C D Boehm
openalex +1 more source
Renal tubular dysfunction with nephrocalcinosis in a patient with beta thalassemia minor
Saudi Journal of Kidney Diseases and Transplantation, 2008 Thalassemia is a hereditary anemia resulting from defect in hemoglobin production. Beta thalassemia is due to impaired production of beta globin chains, leading to a relative excess of alpha globin chains.
Prabahar Murugesan +4 more
doaj
Demonstration of non-functional beta-globin mRNA in homozygous beta (0) thalassemia.
, 1975 Y Kan +3 more
openalex +1 more source
Erythrocyte membrane skeleton abnormalities in severe beta-thalassemia [PDF]
, 1987 Eilat Shinar +3 more
openalex +1 more source
Journal of Tehran University Heart Center, 2015 Background: Heart disease is the main cause of mortality and morbidity in patients with beta thalassemia, rendering its early diagnosis vital. We studied and compared echocardiographic findings in patients with beta thalassemia major, patients with beta ...
Noormohammad Noori +5 more
doaj
A distant gene deletion affects beta-globin gene function in an atypical gamma delta beta-thalassemia. [PDF]
, 1985 Peter Curtin +5 more
openalex +1 more source