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stomatocytic anemia

Known as: Stomatocytosis 
 
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
Piezo1 ion channels are mediators of mechanotransduction in several cell types including the vascular endothelium, renal tubular… Expand
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2014
2014
Background: Asymmetrical distribution of specific phospholipids between the two leaflets of biological membranes is generated and… Expand
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Highly Cited
2013
Highly Cited
2013
Dehydrated hereditary stomatocytosis (DHS) is a genetic condition with defective red blood cell (RBC) membrane properties that… Expand
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Highly Cited
2013
Highly Cited
2013
Autosomal dominant dehydrated hereditary stomatocytosis (DHSt) usually presents as a compensated hemolytic anemia with… Expand
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Review
2005
Review
2005
Pulmonary hypertension is a common complication of sickle cell disease (SCD). In spite of the mild elevations in pulmonary artery… Expand
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Highly Cited
2005
Highly Cited
2005
Phytosterolaemia (sitosterolaemia) is a recessively inherited metabolic condition in which the absorption of both cholesterol and… Expand
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Highly Cited
1999
Highly Cited
1999
Sequencing of HFE exons 2, 3, 4, and 5, and of portions of introns 2, 4, and 5 revealed novel mutations in four of twenty… Expand
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1999
1999
  • Pierre Wong
  • Journal of theoretical biology
  • 1999
  • Corpus ID: 5726631
A mechanism of erythrocyte shape control has been previously hypothesized in which Band 3, the anion exchange protein, controls… Expand
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Highly Cited
1996
Highly Cited
1996
Nine cases of hereditary stomatocytosis (HSt) are presented which show documented thrombotic complications after splenectomy. In… Expand
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Highly Cited
1985
Highly Cited
1985
Cell morphology changes are used to examine the interaction of exogenous phosphatidylserine and phosphatidylethanolamine with… Expand
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