CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME

Known as: Congenital familial hypertrophic synovitis, Arthropathy camptodactyly syndrome, CACP 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1985-2016
024619852016

Papers overview

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2014
2014
Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome is a rare autosomal recessive congenital disorder that includes… (More)
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2013
2013
Camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome is an inherited disorder characterized by congenital or early… (More)
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2013
2013
Familial arthropathy associated with congenital camptodactyly has been previously recognized as a definite clinical entity in the… (More)
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2012
2012
BACKGROUND Camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is a clinically heterogenous congenital disorder… (More)
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2011
2011
BACKGROUND AND AIMS Camptodactyly-arthropathy-coxa-vara-pericarditis (CACP) syndrome is an autosomal recessive condition that… (More)
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Highly Cited
2005
Highly Cited
2005
The long-term integrity of an articulating joint is dependent upon the nourishment of its cartilage component and the protection… (More)
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2004
2004
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is characterized by congenital or early-onset camptodactyly… (More)
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2003
2003
OBJECTIVE To highlight the clinical, radiological, and pathological presentations of 10 Egyptian patients with camptodactyly… (More)
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2000
2000
The camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) is an autosomal recessive condition characterized by the… (More)
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Highly Cited
1999
Highly Cited
1999
Altered growth and function of synoviocytes, the intimal cells which line joint cavities and tendon sheaths, occur in a number of… (More)
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