Results 1 to 10 of about 112,843 (300)

Tubulointerstitial nephritis without glomerular crescent formation as an underestimated subgroup of renal involvement among microscopic polyangiitis patients: A case report

open access: yesClinical Case Reports, 2021
Although extra‐glomerular involvement of microscopic polyangiitis is not regarded as a characteristic finding of the disease, tubulointerstitial nephritis should be considered as a new subclass of renal involvement.
Se Hee Kim   +3 more
doaj   +1 more source

Freqüência de síndrome metabólica em pacientes com nefrite lúpica Frequency of metabolic syndrome in patients with lupus nephritis

open access: yesRevista Brasileira de Reumatologia, 2008
INTRODUÇÃO: Os pacientes com lúpus eritematoso sistêmico (LES) apresentam morbimortalidade importante por doenças cardiovasculares (DCV). A síndrome metabólica (SM) é um transtorno complexo representado por um conjunto de fatores de risco para DCV ...
Bernardo Matos da Cunha   +6 more
doaj   +1 more source

A Patient with Henoch-Schönlein Purpura with Intussusception and intractable Nephritis [PDF]

open access: yesChildhood Kidney Diseases, 2016
Henoch-Schönlein purpura (HSP) is the most common vasculitis in children, mainly affecting the small vessels of the skin, joints, gastrointestinal tract, and kidneys.
Min Kyoung Seo   +3 more
doaj   +1 more source

Experience of Using Activated Protein C in a Patient With Emphysematous Pyelonephritis Receiving Percutaneous Nephrostomy Drainage

open access: yesInternational Journal of Gerontology, 2010
Drotrecogin alfa, a type of recombinant human activated protein C, has potential to reduce the mortality in severe sepsis, but may simultaneously increase the risk of serious bleeding events.
Yueh-Hung Lin   +5 more
doaj   +1 more source

Prognostic Impact of Genetic Variants of MECP2 and TIRAP on Clinical Outcomes of Systemic Lupus Erythematosus with and without Nephritis

open access: yesBiomolecules, 2021
Systemic lupus erythematosus (SLE) is a chronic autoimmune illness with a growing prevalence in many populations. Few studies have examined genetic predisposition to SLE, so we aimed to examine the clinical impact of the genetic polymorphisms MECP2 ...
Safaa I. Tayel   +7 more
doaj   +1 more source

Molecular mechanisms governing the progression of nephritis in lupus prone mice and human lupus patients

open access: yesFrontiers in Immunology, 2023
IntroductionPathologic inflammation is a major driver of kidney damage in lupus nephritis (LN), but the immune mechanisms of disease progression and risk factors for end organ damage are poorly understood.MethodsTo characterize molecular profiles through
Andrea R. Daamen   +10 more
doaj   +1 more source

Loss of interleukin-1 beta is not protective in the lupus-prone NZM2328 mouse model

open access: yesFrontiers in Immunology, 2023
Aberrant activation of the innate immune system is a known driver of lupus pathogenesis. Inhibition of the inflammasome and its downstream signaling components in murine models of lupus has been shown to reduce the severity of disease. Interleukin-1 beta
Shannon N. Loftus   +11 more
doaj   +1 more source

The Association of Angiotension Converting Enzyme Gene Polimorphism with Prognosis of Henoch-Schönlein Purpura with Renal Involvement in the Children

open access: yesNamık Kemal Tıp Dergisi, 2020
Aim:Henoch-Schönlein purpura (HSP) is a vasculitis rarely progresses to renal failure. The mechanism of renal failure in HSP has been associated with increased angiotensin converting enzyme (ACE) activity and increased local angiotension-II concentration
Sevliya ÖCAL DEMİR, Müferet ERGÜVEN
doaj   +1 more source

Immunoglobulin a vasculitis after a not so innocuous wasp bite

open access: yesIndian Pediatrics Case Reports, 2022
Background: Immunoglobulin A vasculitis (IgAV), previously known as Henoch–Schonlein purpura (HSP), is the most common vasculitis in children. Previous studies have identified various triggers of IgAV, with infections being the most common.
Aditi Sharma   +2 more
doaj   +1 more source

THE CLASSIFICATION OF NEPHRITIS [PDF]

open access: yesArchives of Internal Medicine, 1913
Classifications of the so-called hematogenous inflammations of the kidney, commonly grouped as Bright's disease, have been made from five standpoints: 1. Etiological; 2, pathogenetic or histogenetic; 3, functional or physiological; 4, clinical (according to the symptom complex); 5, descriptive (a) according to the topography or (b) according to the ...
openaire   +2 more sources

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