Results 111 to 120 of about 25,718 (237)

Comparative efficacy of deferiprone, deferoxamine and combination of deferiprone and deferoxamine on serum ferritin value in Beta-Thalassemia patients [PDF]

open access: yes, 2015
Background: Iron overload is a predictable and life-threatening complication in patients with thalassemia. Effective and convenient iron chelation remains one of the main targets of clinical management of thalassemia major.
Amlashi, H.M.   +3 more
core   +1 more source

Late Onset Telomere Biology Disorder Presenting With Pancytopenia, Immune Dysregulation, Interstitial Lung Disease and Alopecia

open access: yes
American Journal of Hematology, Volume 101, Issue 6, Page 1196-1200, June 2026.
Bo A. Wan   +7 more
wiley   +1 more source

BUSM Dean's report [PDF]

open access: yes, 1999
Reports from the Office of the Dean, Boston University School of ...
Office of the Dean, Boston University School of Medicine
core  

IMPORTANCE OF IMPLEMENTING PROGRAM SCREENING NEONATAL HEMOGLOBINOPATHIES IN CAPE VERDE

open access: yesNational Journal of Medical Research, 2015
Hemoglobinopathies are hereditary blood diseases, the most frequent sickle cell anemia. To date not have curative treatment, unless bone marrow transplant, which has yet been carried out experimentally.
Leonel Barbosa Gonçalves
doaj  

A study of hemoglobinopathies and hemoglobin variants by high-performance liquid chromatography and correlation with red blood cell indices in antenatal mothers

open access: yesAsian Journal of Medical Sciences
Background: Hemoglobinopathies are the most commonly inherited red cell disorder around the world. In India, hemoglobinopathies show wide variation of prevalence in different regions and different populations.
Arnab Sinha   +2 more
doaj   +1 more source

Predictors of anemia in preschool children: Biomarkers Reflecting Inflammation and Nutritional Determinants of Anemia (BRINDA) project. [PDF]

open access: yes, 2017
Background: A lack of information on the etiology of anemia has hampered the design and monitoring of anemia-control efforts.Objective: We aimed to evaluate predictors of anemia in preschool children (PSC) (age range: 6-59 mo) by country and infection ...
Aaron, Grant J   +13 more
core  

Erythrocytapheresis as a novel treatment option for adult patients with pyruvate kinase deficiency

open access: yesHaematologica, 2020
Rawia F.G. Jensen   +4 more
doaj   +1 more source

Splenectomy in β‐thalassemia patients: Practices and risks in a nationwide study

open access: yes
HemaSphere, Volume 10, Issue 5, May 2026.
Audrey Benoit   +194 more
wiley   +1 more source

Is Hemoglobin Variant Analysis Helpful in the Diagnostic Work-up of Patients Revealing Microcytic Erythrocytosis on Complete Blood Count? [PDF]

open access: yes, 2015
Introduction: Microcytic erythrocytosis is an abnormal CBC (complete blood count) finding that is under-recognized, poorly understood, and consequently under-utilized in patient care. It is characterized by decreased MCV and increased RBC count.
Dulau-Florea, Alina   +3 more
core   +1 more source

Bases moleculares de hemoglobinopatias na Argentina [PDF]

open access: yes, 2017
Durante el desarrollo de un individuo se expresan distintas cadenas de globina de tipo α y no-α, que se combinan en tetrámeros para formar hemoglobina. Los genes que las codifican se organizan en familias.
Scheps, Karen, Varela, Viviana
core  

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