Congenital amegakaryocytic thrombocytopenia

Known as: AMEGAKARYOCYTIC THROMBOCYTOPENIA, CONGENITAL, CAMT 
A rare, autosomal recessive inherited disorder caused by mutation in the c-Mpl gene. It is characterized by thrombocytopenia and absence of… (More)
National Institutes of Health

Papers overview

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2013
2013
Congenital amegakaryocytic thrombocytopenia (CAMT) is caused by the loss of thrombopoietin receptor-mediated (MPL-mediated… (More)
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Review
2009
Review
2009
Congenital amegakaryocytic thrombocytopenia (MIM #604498) is an extremely rare inherited bone marrow failure syndrome, usually… (More)
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Review
2009
Review
2009
Thrombocytopenia is a relatively common clinical problem in hospitalized neonates, and it is critical to distinguish infants who… (More)
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2007
2007
BACKGROUND AND OBJECTIVES Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare, autosomal recessive disorder induced by… (More)
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2005
2005
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare bone marrow failure syndrome characterised by isolated… (More)
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2004
2004
Summary:Five patients with confirmed congenital amegakaryocytic thrombocytopenia (CAT) underwent stem cell transplantation (SCT… (More)
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Highly Cited
2001
Highly Cited
2001
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare disease presenting with isolated thrombocytopenia in infancy and… (More)
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Highly Cited
1999
Highly Cited
1999
Congenital amegakaryocytic thrombocytopenia (CAMT) is a rare disorder expressed in infancy and characterized by isolated… (More)
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1995
1995
Two thrombocytopenic infants with essentially normal initial bone marrow morphology were believed to have idiopathic… (More)
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1990
1990
Serial studies of bone marrow (BM) hematopoiesis using clonogenic assays were performed in an infant with congenital… (More)
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