Results 21 to 30 of about 7,739 (202)

Intraoperative Cell-Saver Caused More Autologous Salvage Hemolysis in a Hereditary Spherocytosis Patient Than in a Normal Erythrocyte Patient

open access: yesFrontiers in Physiology, 2022
Hereditary spherocytosis is a common red blood cell disease caused by an inherited red blood cell membrane defect, leading to a spherical shape and propensity for hemolysis.
Di Jin   +4 more
doaj   +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

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

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

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

Iron overload in hereditary spherocytosis: Are genetic factors the cause? [PDF]

open access: yesBr J Haematol
Summary Non‐transfusional iron overload (IOL) in hereditary spherocytosis (HS) is poorly documented compared with other red blood cell disorders. We studied 13 HS adults with confirmed IOL to identify potential genetic factors. Using a next‐generation sequencing panel of 46 genes related to HS, anaemia and iron metabolism, we found no association ...
Donaty L   +6 more
europepmc   +2 more sources

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

Analysis of Human Spleen Contamination [PDF]

open access: yes, 2007
Besides carbon, oxygen and nitrogen, numerous other elements and their compounds are significant in the body of humans and other animals. Accumulation of some elements and their compounds is recognized by clinical and biochemical evaluation. The physical-
Jan Jakubovsky   +2 more
core   +2 more sources

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