Results 121 to 130 of about 13,011 (272)
Deferasirox in mucormycosis: hopefully, not defeated [PDF]
R. Soman +3 more
openalex +1 more source
Chronic blood transfusions are responsible to cause iron overload, which leads to several complications to end organs and osteoporosis. Iron chelation is needed to remove iron excess and to contain bone-mass loss. Deferasirox is the most recent oral iron
Francesca Punzo +5 more
doaj +1 more source
R2 imaging of ferritin iron in thalassaemia patients off and on iron-chelation therapy [PDF]
Myocardial Tissue Characterization: Fat, Hemorrhage & Edema - Poster presentationAccurate assessment of iron burden is crucial for the management of iron-chelation therapy.
Brittenham, GM +6 more
core
A synopsis of current care of thalassaemia major patients in Hong Kong [PDF]
OBJECTIVE: To provide a synopsis of current thalassaemia major patient care in Hong Kong. DESIGN: Retrospective study. SETTING: All haematology units of the Hospital Authority in Hong Kong.
Au, WY +18 more
core
Anna W Chalmers, Jamile M Shammo Department of Internal Medicine, Division of Hematology/Oncology, Rush University Medical Center, Chicago, IL, USA Abstract: Transfusion-dependent anemia is a common feature in a wide array of hematological disorders ...
Chalmers AW, Shammo JM
doaj
Long-term safety and efficacy of deferasirox in patients with myelodysplastic syndrome, aplastic anemia and other rare anemia in Taiwan [PDF]
Bor‐Sheng Ko +10 more
openalex +1 more source
Iron overload as a consequence of red blood cell transfusions in patients with hematological diseases [PDF]
Preopterećenje željezom česta je i ozbiljna komplikacija višestrukih transfuzija deplazmatiziranih eritrocita koja pridonosi oštećenju organa te utječe na preživljenje bolesnika s hematološkim bolestima.
Antica Načinović-Duletić +3 more
core +3 more sources
Hubungan Derajat Klinis dengan Kadar Feritin Penyandang Thalassemia Β di RSUD Arifin Achmad [PDF]
Thalassemia is a genetic disorder which there is interference with the synthesis of hemoglobin that causes a decreased of synthesis of α or β chain, If the abnormalities are β chain called β thalassemia.
Ridar, E. (Elmi) +2 more
core
Early Kidney Damage Markers after Deferasirox Treatment in Patients with Thalassemia Major: A Case-Control Study [PDF]
Hamidreza Badeli +9 more
openalex +1 more source

