Results 31 to 40 of about 7,739 (202)

Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosis [PDF]

open access: yes, 2005
Vertical and horizontal interactions between membrane constituents account for integrity, strength and deformability of the erythrocyte. Disruption of vertical interactions caused by membrane protein deficiencies in hereditary spherocytosis (HS), favor
Agre P   +22 more
core   +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

Erythropoietin levels in the different clinical forms of hereditary spherocytosis [PDF]

open access: yes, 2005
Erythropoietin (EPO), the main growth factor responsible for the regulation of red blood cell production, may be overproduced when blood loss or haemolysis occurs.
Barbot, José   +7 more
core   +1 more source

Cholelitiasis in an adult patient with mild hereditary spherocytosis – a case report [PDF]

open access: yesArchives of the Balkan Medical Union, 2018
Hereditary spherocytosis (HS) is an inherited abnormality of the red blood cell, caused by defects in structural membrane proteins. The condition is dominantly inherited in 75% of people.
Bogdan SOCEA   +10 more
doaj   +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

Is Increased Intracellular Calcium in Red Blood Cells a Common Component in the Molecular Mechanism Causing Anemia?

open access: yesFrontiers in Physiology, 2017
For many hereditary disorders, although the underlying genetic mutation may be known, the molecular mechanism leading to hemolytic anemia is still unclear and needs further investigation.
Laura Hertz   +14 more
doaj   +1 more source

Reactive Thrombocytosis after Splenectomy in Hereditary Spherocytosis: Case Report and Literature Review

open access: yesEuropean Journal of Case Reports in Internal Medicine, 2021
Reactive thrombocytosis after splenectomy is a feared cause of thrombosis throughout the arterial and venous system. There are many causes of splenomegaly, ranging from cirrhosis to lymphoma to hereditary spherocytosis.
Chidinma Ejikeme   +5 more
doaj   +1 more source

Severe autoimmune hemolytic anemia complicating hereditary spherocytosis treated successfully with glucocorticoids and cyclosporine: a case report

open access: yesHematology, 2023
Background Severe autoimmune hemolytic anemia complicating hereditary spherocytosis is life threatening and has not been described in a case report. Here, we report a case in which this intractable disease was treated successfully with glucocorticoids ...
Na Wang   +4 more
doaj   +1 more source

Clinical outcomes of splenectomy in children: Report of the splenectomy in congenital hemolytic anemia registry [PDF]

open access: yes, 2015
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/110704/1/ajh23888 ...
Al-Salem   +35 more
core   +1 more source

Spinal Cord Infarction in a Patient with Hereditary Spherocytosis: A Case Report and Discussion

open access: yesCase Reports in Neurological Medicine, 2016
The etiology of spinal cord infarcts (SCIs), besides being related to aortic perioperative events, in large subset of SCIs, remains cryptogenic.
Waqar Waheed   +5 more
doaj   +1 more source

Home - About - Disclaimer - Privacy