Skip to search formSkip to main contentSkip to account menu

stomatocytic anemia

Known as: Stomatocytosis 
National Institutes of Health

Related topics

Related topics

2 relations

Broader (1)

Anemia, Hemolytic
Anemia, Hemolytic, Congenital

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2003
Highly Cited
2003
The "stomatin" gene and protein in overhydrated hereditary stomatocytosis.
In overhydrated hereditary stomatocytosis (OHSt), Coomassie- and silver-stained polyacrylamide gels show an apparently complete… 
Highly Cited
2000
Highly Cited
2000
Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24.
Dehydrated hereditary stomatocytosis (DHS) is a rare genetic disorder of red cell permeability to cations, leading to a well… 
1999
1999
A variant of hereditary stomatocytosis with marked pseudohyperkalaemia
A family with an unusual form of hereditary stomatocytosis is described. The affected members showed a mild, dominantly‐inherited… 
1999
1999
Two British families with variants of the ‘cryohydrocytosis’ form of hereditary stomatocytosis
We describe two British families with similar, dominantly‐inherited, temperature‐related variants of hereditary stomatocytosis… 
1998
1998
Rhnull Disease: The Amorph Type Results From a Novel Double Mutation in RhCe Gene on D-Negative Background
Rhnull disease, which includes the amorph and regulator types, is a rare genetic disorder characterized by stomatocytosis and… 
Highly Cited
1994
Highly Cited
1994
Requirement for phosphatidylinositol 4,5-bisphosphate in the Ca(2+)-induced phospholipid redistribution in the human erythrocyte membrane.
Highly Cited
1992
Highly Cited
1992
Mechanisms of amphipath-induced stomatocytosis in human erythrocytes
We studied stomatocytosis induced in human red blood cells (RBC) by vinblastine and chlorpromazine, monitoring the movements of… 
1989
1989
Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency
Summary. We studied the RBC membrane proteins of four patients, including a mother and daughter, with hereditary stomatocytosis… 
Highly Cited
1977
Highly Cited
1977
Calcium ion-dependent diacylglycerol accumulation in erythrocytes is associated with microvesiculation but not with efflux of potassium ions.
Erythrocytes from several different species were exposed to Ca2+ and the bivalent-cation ionophore A23187. The lipid composition… 
Highly Cited
1975
Highly Cited
1975
Characteristics of the membrane defect in the hereditary stomatocytosis syndrome.
Cation permeability and lipid composition have been studied in the red cells of five patients with various features of the… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)