Results 111 to 120 of about 8,109 (242)
Sickle cell hemoglobinopathy genotypes and retinal manifestations in patients of a university hospital [PDF]
, 2000 Objetivo: Identificar as alterações retinianas em pacientes com hemoglobinopatia falciforme e comparar sua prevalência nos diferentes genótipos da doença em uma população de pacientes de hospital universitário de Porto Alegre – Brasil.
Bisol, Tiago +3 more
core
, 2017 The pregnant patient with sickle hemoglobinopathy (SH) and mitral stenosis (MS) presenting for emergency lower (uterine) segment cesarean section (LSCS) represents a challenge to the anesthesiologist. In such a case, the choice of anesthesia is dependent
Vasundhara V Dhale +2 more
core +1 more source
Clinical Case Reports, Volume 14, Issue 6, June 2026.ABSTRACT Hereditary hemochromatosis (HH) is an inherited disorder of iron metabolism characterized by progressive iron accumulation in multiple organs. While most cases are associated with HFE mutations, non‐HFE variants such as mutations in the transferrin receptor‐2 (TFR2) gene represent rare causes of iron overload.
Omar M. Raslan, Dana S. Alamoudi
wiley +1 more source
Hemoglobinas anormales en la población neonatal de Costa Rica
Revista de Biología Tropical, 2008 Se han analizado un total de 70 943 muestras de sangre total en papel filtro S&S 903 de neonatos de Costa Rica (octubre 2005 a Octubre 2006) con el fin de detectar variantes de hemoglobina mediante la técnica de isoelectroenfoque. Se detectaron 891 casos
Gabriela Abarca +4 more
doaj
Complex karyotype in myelodysplastic syndromes: Diagnostic procedure and prognostic susceptibility
Oncology Reviews, 2019 Complex karyotype (CK) is a poor prognosis factor in hematological malignancies. Studies have shown that the presence of CK in myelodysplastic syndrome (MDS) can be associated with MDS progression to acute myeloid leukemia. The goal of this review was to
Mohammad Shahjahani +4 more
doaj +1 more source
Immunotherapy 3.0: Breakthroughs Steering the Next Generation of Cancer Control
Cancer Reports, Volume 9, Issue 6, June 2026.ABSTRACT Background Hematologic disorders, including sickle cell disease, anemias, hemoglobinopathies, leukemias, lymphomas, and bleeding disorders, constitute a substantial and growing burden of morbidity and mortality across Africa. Structural health system constraints—limited diagnostic capacity, shortages of trained hematology specialists ...
Emmanuel Ifeanyi Obeagu
wiley +1 more source
Tissue oxygenation in patients with hemoglobinopathy H
, 1997 To evaluate the degree of tissue hypoxia in patients with hemoglobinopathy H disease, whole blood oxygen affinity was estimated and analyzed in 33 patients.
Kanavakis, E +3 more
core
Clinical and Experimental Dental Research, Volume 12, Issue 3, June 2026.ABSTRACT Objective To investigate the development of oral premalignant and malignant lesions as a major long‐term complication following hematopoietic stem cell transplantation. Methods This single‐center retrospective study identified 17 patients who developed 26 pathology‐confirmed oral premalignant and malignant lesions after hematopoietic stem cell
Pei Hsuan Lu +3 more
wiley +1 more source
Microalbuminuria in hemoglobinopathy patients who are taking Deferasirox
, 2015 Background: Chelation therapy which is needed to prevent or reverse iron overload may also affect renal function in patients with hemoglobinopathy. The early indicator as well as predictor of nephropathy and glomerular damage among patients with sickle ...
Asaad A Khalaf +2 more
core
Information Shocks, Legal Liability and Physician Decisions
Health Economics, Volume 35, Issue 6, Page 896-909, June 2026.ABSTRACT Physician adoption of new information about a medical procedure can affect patient outcomes. Medical malpractice law may influence physician use of such information. We analyze how physician reactions to information shocks regarding vaginal births after cesarean sections (VBACs) in the 1990s were mediated by tort reform and the standard used ...
David Mushinski, Sammy Zahran
wiley +1 more source