Results 21 to 30 of about 118,357 (315)

Landscape of intestinal microbiota in patients with IgA nephropathy, IgA vasculitis and Kawasaki disease

open access: yesFrontiers in Cellular and Infection Microbiology, 2022
ObjectiveTo explore the common differential flora of IgAN, Kawasaki disease and IgA vasculitis by screening and analyzing the differential intestinal flora between the three disease groups of IgAN, Kawasaki disease and IgA vasculitis and their healthy ...
Xueli Hu   +10 more
doaj   +1 more source

Diagnosis of incomplete Kawasaki disease [PDF]

open access: yes, 2012
Several authors suggested that the clinical characteristics of incomplete presentation of Kawasaki disease are similar to those of complete presentation and that the 2 forms of presentation are not separate entities. Based on this suggestion, a diagnosis
Jeong Jin Yu
core   +1 more source

Activin a suppresses peripheral CD8+ T lymphocyte activity in acute-phase Kawasaki disease

open access: yesBMC Immunology, 2021
Background Kawasaki disease is an autoimmune disease characterized by systemic vasculitis of unknown aetiology and most commonly occurs in children under 5 years old.
Qian Wu   +5 more
doaj   +1 more source

Association of Familial History of Diabetes, Hypertension, Dyslipidemia, Stroke, or Myocardial Infarction With Risk of Kawasaki Disease

open access: yesJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2022
Background There are few studies on the association with Kawasaki disease in children and the family’s history of cardiovascular disease (CVD). The aim of this study was to identify the association of increased risks for Kawasaki disease in children with
Ji Hee Kwak   +5 more
doaj   +1 more source

Adult Kawasaki disease in a European patient: a case report and review of the literature [PDF]

open access: yes, 2015
© 2015 Kontopoulou et al.; licensee BioMed Central.Introduction: Kawasaki disease is an acute necrotising vasculitis of the medium- and small-sized vessels, occurring mainly in Japanese and Korean babies and children, aged 6 months to 5 years.
Kontopoulos, DG   +3 more
core   +1 more source

Hemophagocytosis in the Acute Phase of Fatal Kawasaki Disease in a 4 Month-Old Girl

open access: yesBalkan Medical Journal, 2016
Background: Kawasaki disease is a systemic vasculitis predominately affecting coronary arteries. Hemophagocytic lymphohistiocytosis can complicate the course of Kawasaki disease.
Vehbi Doğan   +4 more
doaj   +1 more source

Incomplete, atypical kawasaki disease or evolving systemic juvenile idiopathic arthritis: a case report [PDF]

open access: yes, 2009
Kawasaki disease is an acute febrile condition seen in children. However, it is also well recognized that some Patients do not fulfill the classic diagnostic criteria for the diagnosis of kawasaki disease.
Shakeel Shaikh   +2 more
core   +2 more sources

Calculating the fraction of Kawasaki disease potentially attributable to seasonal pathogens: a time series analysisResearch in context

open access: yesEClinicalMedicine, 2023
Summary: Background: Kawasaki disease is an acute, febrile, systemic vasculitis of children that primarily affects medium-sized blood vessels with a tropism for the coronary arteries. Although the etiological factors remain unknown, infections have been
Zaba Valtuille   +11 more
doaj   +1 more source

Kawasaki disease: clinical experience in a university hospital [PDF]

open access: yes, 2010
OBJETIVO: A doença de Kawasaki é uma vasculite sistêmica aguda de etiologia desconhecida. Seu diagnóstico baseia-se em critérios clínicos. O objetivo deste estudo foi descrever os casos de pacientes com doença de Kawasaki internados no Hospital ...
CARDOSO, Débora Morais   +4 more
core   +2 more sources

Lymphadenitis and Fever: First Presentation of Kawasaki Disease

open access: yesJournal of Pediatric Research, 2017
Kawasaki disease is a vasculitis of infant and childhood period. Diagnosis of Kawasaki disease is based on clinical criteria including cervical lymphadenopathy.
Şule Gökçe   +4 more
doaj   +1 more source

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