stomatocytic anemia

Known as: Stomatocytosis 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1967-2017
05101519672017

Papers overview

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2015
2015
Piezo1 ion channels are mediators of mechanotransduction in several cell types including the vascular endothelium, renal tubular… (More)
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Highly Cited
2013
Highly Cited
2013
Dehydrated hereditary stomatocytosis is a genetic condition with defective red blood cell membrane properties that causes an… (More)
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Highly Cited
2013
Highly Cited
2013
Autosomal dominant dehydrated hereditary stomatocytosis (DHSt) usually presents as a compensated hemolytic anemia with… (More)
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2005
2005
Phytosterolaemia (sitosterolaemia) is a recessively inherited metabolic condition in which the absorption of both cholesterol and… (More)
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1999
Highly Cited
1999
425 0968 – 0004/99/$ – See front matter © 1999, Elsevier Science Ltd. All rights reserved. PII: S0968-0004(99)01467-X Stomatin… (More)
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1999
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… (More)
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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… (More)
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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… (More)
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1975
1975
A defect in the protein kinase-mediated phosphorylation of erythrocyte membrane proteins, previously unrecognized in… (More)
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