Red cell phospholipid defect with hemolysis

Known as: Leaky Red cell syndrome, Phosphatidylcholine Red cell membrane disorder, High red cell phosphatidylcholine hemolytic anemia 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1989-2016
012319892016

Papers overview

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2016
2016
Hereditary xerocytosis (HX) or dehydrated hereditary stomatocytosis (DHS) [OMIM 194380], in which PIEZO1 gene mutation has… (More)
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Review
1996
Review
1996
HPCA is a rare disease among hemolytic anemias. A dominantly transmitted chronic anemia characterized by an increase of… (More)
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1995
1995
We designed a model vascular prosthesis consisting of expanded polytetrafluoroethylene (Gore Tex) loaded with basic fibroblast… (More)
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Review
1993
Review
1993
We have compared characteristics of red cells from patients who were originally diagnosed as having two different disorders, high… (More)
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1990
1990
The clinical features and red cell membrane characteristics of 20 patients with hereditary high red cell membrane… (More)
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1990
1990
Previous descriptions of hereditary high-phosphatidylcholine hemolytic anemia (HPCHA) have highlighted the association of… (More)
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1989
1989
We have studied the erythrocyte membrane phospholipid organization in hereditary high red cell membrane phosphatidylcholine… (More)
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Review
1989
Review
1989
A Japanese family of congenital high red cell membrane phosphatidylcholine hemolytic anemia (HPCHA) is reported. The propositus… (More)
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1989
1989
Clinical and experimental studies on hereditary spherocytosis (HS) and high red cell membrane phosphatidylcholine hemolytic… (More)
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