Results 41 to 50 of about 23,651 (244)
Cryoglobulinaemic vasculitis: classification and clinical and therapeutic aspects [PDF]
, 2007 Cryoglobulinaemia may cause cutaneous vasculitis and glomerulonephritis, potentially leading to end stage renal failure. An important proportion of cryoglobulinaemias are secondary to hepatitis C virus infection.
Braun, Gerald S. +4 more
core +2 more sources
Urinary proteomics using capillary electrophoresis coupled to mass spectrometry for diagnosis and prognosis in kidney diseases [PDF]
, 2016 Purpose of review: Urine is the most useful of body fluids for biomarker research. Therefore, we have focused on urinary proteomics, using capillary electrophoresis coupled to mass spectrometry, to investigate kidney diseases in recent years.
Magalhães, Pedro +2 more
core +1 more source
Association of Vasculitis and Familial Mediterranean Fever
Frontiers in Immunology, 2019 Certain types of vasculitis occur more frequently and present differently in patients with familial Mediterranean fever (FMF). We assessed the characteristics of patients with FMF and systemic vasculitis through a systematic review of the literature ...
Salam Abbara +4 more
doaj +1 more source
IgA Vasculitis and IgA Nephropathy: Same Disease? [PDF]
Journal of Clinical Medicine, 2021 Many authors suggested that IgA Vasculitis (IgAV) and IgA Nephropathy (IgAN) would be two clinical manifestations of the same disease; in particular, that IgAV would be the systemic form of the IgAN. A limited number of studies have included sufficient children or adults with IgAN or IgAV (with or without nephropathy) and followed long enough to ...
openaire +3 more sources
Renal biopsy in children with IgA vasculitis [PDF]
Brazilian Journal of Nephrology, 2022 Abstract Introduction Henoch-Schönlein purpura nephritis (HSN) is defined as Henoch-Schönlein purpura with kidney involvement, including hematuria and/or proteinuria. The aim of this study was to evaluate the data of HSN patients who underwent renal biopsy, and compare the main clinical and laboratory parameters that may affect renal biopsy findings ...
Mehtap Akbalik Kara +3 more
openaire +6 more sources
Rheumatology & Autoimmunity, 2022 Objective: To explore a possible association between systemic immunoglobulin A (IgA) vasculitis and RS3PE syndrome and to investigate specific treatment regimens for adults who present with IgA vasculitis with renal involvement.
Shawn Mathew +3 more
doaj +1 more source
Intravenous γ Globulin for Intractable Abdominal Pain due to IgA Vasculitis
Case Reports in Pediatrics, 2020 IgA vasculitis (formerly known as Henoch–Schönlein purpura or anaphylactoid purpura) is a usually benign vasculitis that affects children of school age. The disease is characterized by the tetrad of palpable purpura, arthralgia/arthritis, abdominal pain,
George Naifa +4 more
doaj +1 more source
Fasciitis as a Complication of IgA Vasculitis. [PDF]
CureusImmunoglobulin A vasculitis (IgAV) is a systemic small-vessel vasculitis caused by the deposition of IgA-based immune complexes, with myalgia being a rare complication. This study reports a pediatric case of IgAV with fasciitis. A five-year-old boy with no previous medical history was admitted to the hospital with abdominal pain and repeated bilious ...
Nii K +4 more
europepmc +3 more sources
Immunoglobulin A vasculitis induced by atypical pneumonia infection with Chlamydophila pneumonia
IDCases, 2022 Infections are a common trigger for IgA vasculitis. Among the bacteria that cause atypical pneumonia, Mycoplasma pneumoniae infection has strongly been associated with IgA vasculitis, with Chlamydophila pneumoniae reported with IgA vasculitis in only one
Seung Ah Kang +2 more
doaj
Scientific Reports, 2022 A nomogram for assessing the risk of IgA vasculitis nephritis (originally termed Henoch–Schönlein purpura nephritis, HSPN) in IgA vasculitis (originally termed Henoch–Schönlein purpura, HSP) pediatric patients can effectively improve early diagnosis and ...
Yuna Bi +10 more
doaj +1 more source