Hypocomplementemia

Known as: SERUM COMPLEMENT DECREASED 
 
National Institutes of Health

Papers overview

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2011
2011
Abnormalities of the complement system in Henoch–Schönlein purpura (HSP) have been reported, but how this abnormality in the… (More)
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Highly Cited
2010
Highly Cited
2010
IgG4-related disease is a recently recognized multi-organ disorder characterized by high levels of serum IgG4 and dense… (More)
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2008
2008
BACKGROUND Hypocomplementemia has been detected in about 15% of unselected series of SSc patients. It constitutes one of the 10… (More)
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Highly Cited
2008
Highly Cited
2008
We conducted the current study to characterize the clinical presentation of primary Sjögren syndrome (SS) in a large cohort of… (More)
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Highly Cited
2006
Highly Cited
2006
OBJECTIVE To study 5 type I interferon (IFN)-inducible genes (LY6E, OAS1, OASL, MX1, and ISG15) in patients with systemic lupus… (More)
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2005
2005
BACKGROUND The clinical course and prognosis of Henoch-Schonlein purpura (HSP) associated with hypocomplementemia are not clear… (More)
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Highly Cited
2001
Highly Cited
2001
This study reports the clinicopathologic findings and outcome in 34 patients with renal monoclonal immunoglobulin deposition… (More)
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Highly Cited
1999
Highly Cited
1999
Familial hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP) carry a very poor outcome and have been… (More)
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1991
1991
We investigated the association between serum titers of IgG antibodies against C1q (C1qAb) and clinical and laboratory variables… (More)
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Highly Cited
1971
Highly Cited
1971
Reality: At least ten diagnostic/classifi cation criteria for SjS have been published since the 1960s. The 2002 American… (More)
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