Results 31 to 40 of about 23,138 (242)

Cutaneous Manifestations in Inflammatory Bowel Diseases [PDF]

open access: yes, 2015
Inflammatory bowel diseases have a high frequency in Europe. They are chronic disorders that evolve with relapses and remissions. Clinical features include the signs of underlying inflammatory bowel disease and also signs of extraintestinal ...
Benea, Vasile   +6 more
core   +6 more sources

Adult-onset immunoglobulin A vasculitis

open access: yesAPIK Journal of Internal Medicine, 2021
We describe a case of adult-onset immunoglobulin A vasculitis (IgA vasculitis) presenting with cutaneous, renal and gastrointestinal manifestations without any evidence of articular involvement.
Megha Amarapur, Sangram Biradar
doaj   +1 more source

IgA Vasculitis during Atezolizumab Treatment

open access: goldInternal Medicine, 2023
Yoshinao Ono   +3 more
openalex   +4 more sources

Cryoglobulinaemic vasculitis: classification and clinical and therapeutic aspects [PDF]

open access: yes, 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

Association of Vasculitis and Familial Mediterranean Fever

open access: yesFrontiers 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

Intravenous γ Globulin for Intractable Abdominal Pain due to IgA Vasculitis

open access: yesCase 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

IgA vasculitis nephritis (Schönlein-Henoch purpura with nephritis) following COVID-19 vaccination [PDF]

open access: yesJournal of Nephropathology, 2023
IgA vasculitis nephritis (Schönlein-Henoch purpura nephritis) is an autoimmune circumstance characterized by palpable purpura involving the lower limbs, arthralgia, abdominal pain and kidney involvement.
Leila Mahmoodnia   +11 more
doaj   +1 more source

IgA vasculitis with nephritis in children

open access: yesAdvances in Clinical and Experimental Medicine, 2020
Immunoglobulin A vasculitis (IgAV), formerly known as Henoch-Schönlein purpura (HSP), is the most common form of systemic vasculitis in children. Although the first case of IgAV was described more than 200 years ago, its etiology still remains unclear. Nephrological symptoms are observed in 30-50% of children during the course of the disease, and in up
Katarzyna Dyga, Maria Szczepańska
openaire   +2 more sources

Severe IgA vasculitis with features of remitting seronegative symmetrical synovitis with pitting edema (RS3PE) syndrome in a 60‐year‐old male treated with plasmapheresis

open access: yesRheumatology & 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

What is new in the management of rapidly progressive glomerulonephritis? [PDF]

open access: yes, 2015
Rapidly progressive glomerulonephritis (RPGN) results from severe crescentic damage to glomeruli and leads to irreversible kidney failure if not diagnosed and managed in a timely fashion.
Greenhall, GHB, Salama, AD
core   +1 more source

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