Hereditary spherocytosis

Known as: Hereditary Spherocytoses, Congenital spherocytic hemolytic anemia, Minkowski Chauffard syndrome 
A group of familial congenital hemolytic anemias characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The… (More)
National Institutes of Health

Papers overview

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Review
2013
Review
2013
Hereditary spherocytosis and elliptocytosis are the two most common inherited red cell membrane disorders resulting from… (More)
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Highly Cited
2012
Highly Cited
2012
Guidelines on hereditary spherocytosis (HS) published in 2004 (Bolton-Maggs et al, 2004) are here replaced to reflect changes in… (More)
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Highly Cited
2008
Highly Cited
2008
Hereditary spherocytosis is a common inherited disorder that is characterised by anaemia, jaundice, and splenomegaly. It is… (More)
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Review
2004
Review
2004
Hereditary spherocytosis (HS) is a heterogeneous group of disorders with regard to clinical severity, protein defects and mode of… (More)
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Review
2004
Review
2004
The molecular causes of hereditary spherocytosis (HS) have been unraveled in the past decade. No frequent defect is found, and… (More)
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Highly Cited
2001
Highly Cited
2001
Clinical manifestations of hereditary spherocytosis (HS) can be abrogated by splenectomy. However, concerns exist regarding… (More)
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Highly Cited
1999
Highly Cited
1999
The precocious formation of bilirubinate gallstones is the most common complication of hereditary spherocytosis (HS), and the… (More)
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Highly Cited
1996
Highly Cited
1996
Hereditary spherocytosis (HS) is the most common inherited haemolytic anaemia in Northern Europeans. The primary molecular… (More)
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Highly Cited
1990
Highly Cited
1990
HEREDITARY spherocytosis (HS) is one of the most common hereditary haemolytic anaemias1. HS red cells from both autosound… (More)
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Highly Cited
1985
Highly Cited
1985
Hereditary spherocytosis (HS) is a common, clinically heterogeneous haemolytic anaemia1,2 in which the primary erythrocyte defect… (More)
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