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Medicine (United States), ISSN 0025-7974, 08/2017, Volume 96, Issue 31
Journal Article
Internal Medicine, ISSN 0918-2918, 2019
A diagnosis of hereditary angioedema is usually made with recurrent episodes of swelling of the subcutaneous tissue with a family history. We herein report a... 
C1-inhibitor | hereditary angioedema | hypocomplementemia | submucosal edema | acute abdomen
Journal Article
by Xu, W and Pan, B and Zhu, H and Wang, L and Fan, L and Li, J
Hematological Oncology, ISSN 0278-0232, 06/2019, Volume 37, Issue S2, pp. 416 - 418
Journal Article
Reumatologia Clinica, ISSN 1699-258X, 2018
We report the case of a 47-year-old man with a 9-year history of psoriatic arthritis (PsA) in whom we detected renal involvement, hypocomplementemia,... 
Glomerulonephritis | Hypocomplementemia | Cryoglobulinemic vasculitis | Psoriatic arthritis
Journal Article
Journal Article
by X. Wang and Z. Wu and Y. Liang and F. Cheng and R. Feng and X. Fang and S. Yang and B. Gong and J. Tang
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2018, Volume 77, p. 1465
Background Primary Sjögren's syndrome (pSS) is a commono systemic autoimmune disease, characterised by lymphocytic infiltration of the secretory glands and... 
Thrombocytopenia | Sjogren's syndrome | Leukopenia | Hematology | Anemia | Glands | Transaminase | E.S.R | Sedimentation | Patients | Risk factors | Hypocomplementemia | Diagnosis | Neutropenia
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2018, Volume 77, Issue Suppl 2, p. 1434
BackgroundIn patients with primary Sjogren Syndrome (pSS), haematological involvement – autoimmune cytopenia, might be present at the time of the diagnosis or... 
Sjogren's syndrome | Cornea | Hypocomplementemia | Statistical analysis | Hematology | Classification | Rheumatic diseases | Biomarkers | Data processing | Diagnosis | Medical diagnosis
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2018, Volume 77, Issue Suppl 2, p. 1429
BackgroundSystemic lupus erythematosus (SLE), as the prototype of systemic autoimmune diseases, has a wide array of clinical manifestations. An association... 
Lupus | Edema | Anticoagulants | Cryoglobulinemia | Kidneys | Serositis | Cryoglobulins | Hypocomplementemia | Vasculitis | Systemic lupus erythematosus | Immunology | Remission | Autoimmune diseases
Journal Article
Actas Dermo-Sifiliograficas, ISSN 0001-7310, 09/2013, Volume 104, Issue 7, pp. 579 - 585
Introduction: Urticarial vasculitis is a subtype of vasculitis characterized clinically by urticarial lesions and histologically by necrotizing vasculitis.... 
Hypocomplementemia | Autoimmune disease | Urticarial vasculitis
Journal Article
The New England Journal of Medicine, ISSN 0028-4793, 02/2017, Volume 376, Issue 8, pp. 775 - 786
A 57-year-old woman presented with fatigue, night sweats, weight loss, headache, abdominal pain, and skin lesions. Laboratory testing revealed... 
Headache | Immunoglobulins | Hypocomplementemia | Pain | Hypergammaglobulinemia | Skin diseases | Fatigue | Medical diagnosis | Inflammatory diseases | Skin tests
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2018, Volume 77, Issue Suppl 2, p. 1435
BackgroundInfections continue to be an important source of morbidity and mortality in systemic lupus erythematosus (SLE).1 Susceptibility to infections is... 
Lupus | Nephritis | Mycophenolic acid | Infections | Prednisone | Methylprednisolone | Morbidity | Immunosuppressive agents | Cyclophosphamide | Hypocomplementemia | Immunosuppression | Systemic lupus erythematosus | Diagnosis | Drug dosages
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2018, Volume 77, Issue Suppl 2, p. 1465
BackgroundHypocomplementemia (HC) represents a significant clinical finding in Systemic Lupus Erythematosus (SLE) as it suggests complement activation by... 
Lupus | Osteoporosis | Hypocomplementemia | Complement activation | Systemic lupus erythematosus | Complement component C4 | Complement component C3 | Anti-DNA antibodies | Arthritis
Journal Article
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, ISSN 1555-9041, 09/2011, Volume 6, Issue 9, pp. 2165 - 2174
Background and objectives Glomerular deposition of monoclonal Ig has been exceptionally described as the cause of membranoproliferative glomerulonephritis,... 
COMPLEMENT FACTOR-H | HYPOCOMPLEMENTEMIA | HEMOLYTIC-UREMIC SYNDROME | PROLIFERATIVE GLOMERULONEPHRITIS | DISEASE | UNDETERMINED SIGNIFICANCE | UROLOGY & NEPHROLOGY | CHRONIC LYMPHOCYTIC-LEUKEMIA | MEMBRANOPROLIFERATIVE GLOMERULONEPHRITIS | MEMBRANE COFACTOR PROTEIN | IGG DEPOSITS
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2017, Volume 76, Issue Suppl 2, p. 313
ObjectivesTo evaluate BLyS as biomarker in disease activity in urinary sample and renal biopsy from patients with LN.MethodsRetrospective study. Between June... 
Glomerulonephritis | Nephritis | Lupus nephritis | Gene expression | Atrophy | Hypocomplementemia | Lymphocytes B | Biopsy | BLyS protein | Classification | Renal failure | Biomarkers | Remission | Proteinuria
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2017, Volume 76, Issue Suppl 2, p. 874
BackgroundSystemic lupus erythrematosus (SLE) is an autoimmune disease with a myriad of manifestations, that could vary among different ethnic and racial... 
Lupus | Synovitis | Photosensitivity | Nephritis | Leukopenia | Exanthema | Fetuses | Medical records | Sex differences | Antiphospholipid antibodies | Males | Hypocomplementemia | Vasculitis | Alopecia | Thromboembolism | Seizures
Journal Article
Annals of the Rheumatic Diseases, ISSN 0003-4967, 06/2017, Volume 76, Issue Suppl 2, p. 425
BackgroundIgG4-related kidney disease (IgG4-RKD) is a comprehensive term for renal lesions associated with IgG4-related disease [1]. IgG4-RKD is frequently... 
Serum levels | Creatinine | Interleukin 2 receptors | Nephritis | Hypocomplementemia | Kidneys | Immunoglobulin G | Immunoglobulin E | Diagnosis | Kidney diseases | Prednisolone | Glucosaminidase
Journal Article
Lupus, ISSN 0961-2033, 11/2019, Volume 28, Issue 13, pp. 1503 - 1509
Prognosis of pregnancies in women with antiphospholipid syndrome has dramatically improved over the past two decades using conventional treatment with low... 
Pregnancy | Aspirin | Hypocomplementemia | Complement component C4 | Complement component C3 | Pregnancy complications | Heparin | Thrombosis | Risk factors | Morbidity | Molecular weight | Antiphospholipid syndrome
Journal Article
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