Results 101 to 110 of about 9,026 (213)

Knowledge, Attitude, and Practice of Sickle Cell Disease Among Sickle Cell Disease Patients in Sudurpashchim Province of Nepal: A Cross‐Sectional Study

Health Science Reports
Background Sickle cell disease (SCD) is a genetic hemoglobinopathy which is responsible for about 3.5% of deaths in
Gauri Datt Joshi, Sher Bahadur Kamar, Pradip Mishra, Hemraj Pandey, Sandesh Rimal, Yogendra Shah, Ravi Mohan Tiwari, Ananda Kumar Mandal, Ankit Kumar Singh, Shyam Prakash Dumre, Kishor Pandey, Eak Dev Khanal, Basu Dev Pandey, Bishnu Prasad Marasini, Pramod Joshi   +14 more
doaj   +1 more source

Markers of coagulation activation in patients with hemoglobinopathy in Western Saudi Arabia

, 2017
Objective: This study aims to examine markers of coagulation activation and their possible clinical associations in sickle cell disease (SCD) and thalassemia.
Soheir Adam, Galila Zaher
core   +1 more source

The Role of Ferroptosis Induced by Iron Overload in Osteoblast and Osteoclast Function

Cell Biology International, Volume 50, Issue 10, October 2026.
ABSTRACT Iron overload disrupts bone homeostasis by suppressing osteoblast survival and mineralization, while promoting osteoclastogenesis. As a programmed cell death driven by iron‐dependent lipid peroxidation and glutathione peroxidase 4 (GPX4) downregulation. This study investigated the role of ferroptosis in bone cells under iron overload. Exposure
Supagarn Sooksawanwit, Kornkamon Lertsuwan, Natnicha Tannop, Ploypapus Lapatkeattisukul, Thanayuth Jenpichitkulchai, Nittiyaporn Sotapong, Jarinthorn Teerapornpuntakit, Tueanjai Khunluck, Siriwan Punvilai, Narattaphol Charoenphandhu   +9 more
wiley   +1 more source

Hemoglobin SD-Punjab with Stroke and Moyamoya Syndrome and Genotype-Phenotype Correlation: A Report of Two Siblings

Indian Pediatrics Case Reports
Background: Hemoglobin (Hb) SD-Punjab is a rare Hb disorder which may present at any age ranging from infancy to adulthood with variable clinical severity. There are very few reports of HbSD-Punjab with stroke, leading to moyamoya syndrome. We report two
Kanika Singh, Meenakshi Bothra, Ranjana Mishra, Seema Kapoor   +3 more
doaj   +1 more source

Current advances in 2025: A critical review of selected topics by the Association for the Advancement of Blood and Biotherapies (AABB) Clinical Transfusion Medicine Committee

Transfusion, EarlyView.
Nabiha H. Saifee, Jennifer Andrews, Mary Berg, Stella T. Chou, Mischa Covington, Elizabeth P. Crowe, Ruchika Goel, Juliana A. Guarente, Tina Ipe, Jeremy W. Jacobs, Jessica Jacobson, Cyril Jacquot, Jenna Khan, Thane A. Kubik, Theodros Mamo, Michael F. Murphy, Kerry O'Brien, Monica B. Pagano, Anil K. Panigrahi, Jacqueline N. Poston, Scott E. Potter, Simon J. Stanworth, Moritz Stolla, Alyssa Ziman, Ryan A. Metcalf   +24 more
wiley   +1 more source

Multisystem Complications in Non‐Transfusion‐Dependent β‐Thalassemia Intermedia: A Case Highlighting the Need for Early Intervention

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT This case highlights that severe complications of non‐transfusion‐dependent β‐thalassemia may be preventable with appropriate monitoring and timely intervention; however, once established, multisystem complications can be challenging to treat.
Oldooz Aloosh, Seyedeh Esmat Hosseini, Mohammad Karimi   +2 more
wiley   +1 more source

Hemoglobinopathy and COVID-19

Hematology, Transfusion and Cell Therapy, 2021
Rujittika Mungmunpuntipantip, Viroj Wiwanitkit   +1 more
doaj   +1 more source

A Novel Homozygous Frameshift Variant in ZNF699 Associated With DEGCAGS Syndrome With Severe Transfusion‐Dependent Anemia in an Indian Child: A Case Report

Clinical Case Reports, Volume 14, Issue 10, October 2026.
ABSTRACT In children with unexplained multisystem involvement—global developmental delay, dysmorphism, skeletal anomalies, and severe transfusion‐dependent anemia—especially from consanguineous families, whole‐exome sequencing should be pursued early to enable timely diagnosis, proactive iron chelation, and genetic counseling.
Arimanda Chaitanya Laasya Reddy, A. Vamshee Priya, Aditya Pachwa, Boilla Abhignya Reddy, Lakshya Nehal Samineni, Lanka Gourav Reddy   +5 more
wiley   +1 more source

Co-Existence of Hereditary Pyrimidine 5'-Nucleotidase Deficiency and Heterozygous α-Thalassemia: A Case Presentation

Turkish Journal of Hematology, 2012
A. Agapidou, S. Theodoridou, K. Tegos, E. Mandala, E. Leukou, O. Karakasidou, B. Aletra, A. Sevastidou, M. Alemayehou, E. Voskaridou   +9 more
doaj   +1 more source

Acute Occlusion of Central Retinal Artery with Sickle Cell Thalassemia Hemoglobinopathy

, 1971
Presenting Symptom: Occluded retinal artery. Pathology: Retinal artery occlusion. Clinical: The patient was a 44-year old male who had had a confirmed sickle cell thalassemia hemoglobinopathy established at age 28 following a splenic infarct.
David G. Cogan, MD (1908-1993)
core