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Hereditary angioedema type 1 in a 39-year-old woman with a three-generation pedigree: a case report

open access: yesAllergy Medicine
Background: Hereditary angioedema (HAE) is a rare autosomal dominant genetic disorder, clinically manifested as recurrent localized edema of the skin and mucous membranes, which can involve the gastrointestinal tract and cause severe abdominal pain when ...
Xiaolei Liu, Huali Ren, Xige Liu
doaj   +1 more source

Correlation Between C4/IgG with Macroproteinuria in Chronic Kidney Disease: A Pilot Study

open access: yesImmunoTargets and Therapy
Hao Zhang,1,* Anqi Xu,2,* Xiangxiang Li,3,* Binbin Pan,1 Xin Wan1 1Department of Nephrology, Nanjing First Hospital, Nanjing Medical University, Nanjing, People’s Republic of China; 2Department of Quality Management, Nanjing Red Cross Blood ...
Zhang H, Xu A, Li X, Pan B, Wan X
doaj  

Low complement items play different roles on the classification performance of SLICC-2012, EULAR/ACR-2019, and SLERPI

open access: yesFrontiers in Medicine
ObjectivesThis study aimed to explore the association of low complement items with the performance of the systemic lupus erythematosus (SLE) classification criteria.MethodsThis study included 352 patients with SLE and 385 individuals with positive ...
Shanshan Chen   +5 more
doaj   +1 more source

Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies. [PDF]

open access: yesAnn Rheum Dis, 2023
Zhou D   +38 more
europepmc   +1 more source

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