Results 121 to 130 of about 107,712 (298)

Hemoglobin D Los Angeles in Two Caucasian Families: Hemoglobin SD Disease and Hemoglobin D Thalassemia [PDF]

, 1968
Rose G. Schneider, Satoshi Ueda, Jack B. Alperin, William C. Levin, Richard T. Jones, Bernadine Brimhall   +5 more
openalex   +1 more source

Extensive extramedullary haematopoiesis in a patient with non‐transfusion‐dependent beta‐thalassaemia

British Journal of Haematology, EarlyView.
Laura Distelmaier, Wolfgang G. Kunz, Sebastian Theurich   +2 more
wiley   +1 more source

Common Hematologic Emergencies—Acute Promyelocytic Leukemia and Microangiopathic Hemolytic Anemias—A Pivotal Role of Clinical Laboratory

International Journal of Laboratory Hematology, EarlyView.
ABSTRACT Hematologic emergencies are urgent health conditions which result in significant mortality and morbidity unless timely therapeutic measures are taken. Therapeutic success depends on their timely and accurate recognition by hematology laboratory services.
Ganna Shestakova, Nicolas Ulrich Edgar, Anton V. Rets   +2 more
wiley   +1 more source

The Metabolism of the Individual C14-labeled Hemoglobins in Patients with H-Thalassemia, with Observations on Radiochromate Binding to the Hemoglobins during Red Cell Survival* [PDF]

, 1965
Thomas G. Gabuzda, David G. Nathan, Frank H. Gardner   +2 more
openalex   +1 more source

Low rates of endothelial cell dysfunction and transplant‐related mortality in 537 children receiving fludarabine–treosulfan conditioning for all transplant indications: A retrospective multicentre study on behalf of the UK Paediatric BMT group

British Journal of Haematology, EarlyView.
Thomas Altmann, Kanchan Rao, Ramya Hanasoge‐Nataraj, Katharine Patrick, Ben Carpenter, Rachael Hough, Anna‐Maria Ewins, Sanjay Tewari, Oana Mirci‐Danicar, Mary Slatter, Robert Wynn, Su Han Lum   +11 more
wiley   +1 more source

Economic burden of sickle cell disease in Australia

Internal Medicine Journal, EarlyView.
Abstract Background Sickle cell disease (SCD) is an inherited condition that impairs red blood cell function, posing a substantial health burden on patients. As the prevalence of SCD in Australia rises due to migration, discussions surrounding treatment and management strategies are becoming more prominent. Aims Australia lacks a dedicated study on the
Steve Nwokeocha, Helen E. Haysom, Cameron Wellard, Tracy Roberts, Mwayi Kachapila, Melissa Chee, Dennis Petrie, Zoe K. McQuilten, Neil Waters, Anthea Greenway, Kylie Mason, Anna Nelson, Zane Kaplan, P. Joy Ho, Erica M. Wood, Adam Irving, on behalf of the Australian Haemoglobinopathy Registry   +16 more
wiley   +1 more source

Inclusions of Hemoglobin in Erythroblasts and Erythrocytes of Thalassemia [PDF]

, 1963
Phaedon Fessas
openalex   +1 more source

Secrets and Their Consequences in Heathcare: A Scoping Review of Worker Experiences

Journal of Advanced Nursing, EarlyView.
ABSTRACT Aims To explore current knowledge of the nature of secrets healthcare consumers reveal to healthcare workers and the impact on the healthcare worker experience resulting from these private disclosures. Design Scoping review. Data Sources Eight electronic databases were searched for studies published between 1980 and 2025 that met the inclusion
Kiriaki Stewart, David Evans, Qunyan Xu, Nicholas Procter   +3 more
wiley   +1 more source

Case report: Rethinking NGS analysis in diagnosing Diamond-Blackfan anemia syndrome

Frontiers in Genetics
Diamond-Blackfan anemia syndrome (DBAS) is a rare inherited bone marrow failure (BMF) syndrome characterized by erythroid aplasia, congenital malformations, and cancer predisposition.
Panayiota L. Papasavva, Konstantinos Kaouranis, Stefania Byrou, Constantina G. Constantinou, Iacovou Efrosini, Marina Kleanthous, Carsten W. Lederer, Thessalia Papasavva   +7 more
doaj   +1 more source

Endocrine Function in Thalassemia Major [PDF]

, 1968
Braden Kuo, Edward C. Zaino, Martin S. Roginsky   +2 more
openalex   +1 more source