Results 21 to 30 of about 7,830 (207)

Spleen histology in children with sickle cell disease and hereditary spherocytosis: Hints on the disease pathophysiology [PDF]

open access: yes, 2016
open2Hereditary spherocytosis (HS) and sickle cell disease (SCD) are associated with splenomegaly and spleen dysfunction in pediatric patients. Scant data exist on possible correlations between spleen morphology and function in HS and SCD.
Alaggio Rita   +10 more
core   +1 more source

Quality of life and behavioral functioning in Dutch pediatric patients with hereditary spherocytosis [PDF]

open access: yes, 2014
The objective of this study was to evaluate health-related quality of life (HRQoL) and behavioral functioning in pediatric patients with hereditary spherocytosis (HS).
Bronner, M.B. (Madelon)   +5 more
core   +1 more source

Previously undiagnosed hereditary spherocytosis in a patient with jaundice and pyelonephritis: a case report

open access: yesJournal of Medical Case Reports, 2016
Background Hereditary spherocytosis is autosomal dominant inherited extravascular hemolytic disorder and is the commonest cause of inherited hemolysis in northern Europe and the United States.
Yuki Tateno   +2 more
doaj   +1 more source

Positive predictive value of diagnosis coding for hemolytic anemias in the Danish National Patient Register [PDF]

open access: yes, 2016
PURPOSE: The nationwide public health registers in Denmark provide a unique opportunity for evaluation of disease-associated morbidity if the positive predictive values (PPVs) of the primary diagnosis are known.
Frederiksen, Henrik   +3 more
core   +2 more sources

Clinical course of 63 children with hereditary spherocytosis: a retrospective study

open access: yesRevista Brasileira de Hematologia e Hemoterapia, 2012
BACKGROUND: Hereditary spherocytosis (HS) is an inherited hemolytic anemia that is caused by deficiency or dysfunction of erythrocyte cytoskeletal proteins.
Maria Christina Lopes Araujo Oliveira   +5 more
doaj   +1 more source

Artificial neural networks for 3D cell shape recognition from confocal images

open access: yes, 2020
We present a dual-stage neural network architecture for analyzing fine shape details from microscopy recordings in 3D. The system, tested on red blood cells, uses training data from both healthy donors and patients with a congenital blood disease ...
Bianchi, P.   +9 more
core   +2 more sources

An overview about erythrocyte membrane [PDF]

open access: yes, 2010
© 2010 – IOS Press and the authors. All rights reservedIn the sixties and seventies, erythrocytes or red blood cells (RBCs) were extensively studied. Much has been learnt particularly concerning their metabolism and gas transporter function. In the past
Oliveira, Sofia de, Saldanha, Carlota
core   +1 more source

Hereditary spherocytosis: Consequences of delayed diagnosis

open access: yesSAGE Open Medicine, 2014
Objective: To determine whether patients with undiagnosed hereditary spherocytosis hospitalized for transfusions might have avoided hospitalization via earlier diagnosis. Study design: Charts of all (N = 30) patients with hereditary spherocytosis seen in
Sarah C Steward   +2 more
doaj   +1 more source

Intravascular Large B-Cell Lymphoma Presenting as Dementia and Hemolytic Anemia [PDF]

open access: yes, 2010
Background: Intravascular lymphoma (IVL) is an uncommon disease characterized by atypical lymphoid cells growing inside the lumina of small vessels. The diversity of clinical presentation due to possible involvement of multiple organs often complicates ...
Ahle, Guido   +6 more
core   +1 more source

Novel Variant of the SLC4A1 Gene Associated with Hereditary Spherocytosis

open access: yesBiomedicines, 2023
Hereditary spherocytosis (HS) refers to the group of the most frequently occurring non-immune hereditary hemolytic anemia in people of Caucasian central or northern European ancestry.
Dżamila M. Bogusławska   +5 more
doaj   +1 more source

Home - About - Disclaimer - Privacy