نتایج جستجو برای: onset stills disease
تعداد نتایج: 1614380 فیلتر نتایج به سال:
Adult-onset Still's disease (AOSD) is an inflammatory disorder characterized by recurrent fevers, arthralgia, leukocytosis, and a salmon-colored rash. Diagnosis is made based on the Yamaguchi criteria. Various cardiac and pulmonary manifestations have been described in association with AOSD, including acute respiratory distress syndrome (ARDS) and pulmonary arterial hypertension (PAH). We descr...
summary: adult-onset still’s disease (aosd) is a rare systemic inflammatory disorder of unknown etiology. it is characterized by high grade fever, skin rash, arthritis, leukocytosis, increased esr, crp and liver enzyme levels and high levels of ferritin. the treatment of aosd includes nsaids, steroids, and disease-modifying antirheumatic drugs (dmards). recently biologic agents have been used f...
adult-onset still’s disease (aosd) is a rare systemic inflammatory disorder of unknown etiology. there is not currently any specific serological markers for aosd , and diagnosis still relying on the exclusion of other likely diagnoses. yamaguchi’s criteria are used as a diagnostic criterion which contains negative serologic markers for other collagen vascular diseases including systemic lupus ...
behcet's disease (bd) is a multisystemic inflammatory disease that occurs most often between the second and fourth decade of life. patients have been reported during the first months of life and after 70 years. our objective was to determine the clinical, paraclinical and genetic characteristics of bd in patients aged < 20 and > 40 years. we conducted a comparative retrospective study including...
background : alzheimer's disease (ad) is one of the most common problems for old peoples. etiology of ad is not clear, but genetic factors play a major role in determining a person's risk to develop ad. twin and family studies con-firm that ad has a genetic basis.ad genetics has been split into two broad categories: early-onset and late-onset. eo-ad cases are inherited in an autosomal dominant ...
abstract: there is always a need to increase a distillate output of solar still. if plates will be used inside solar still then distillate output of solar still are expected to increase. hence, an experimental study is conducted to improve distillate output of basin solar stills by increasing the effective surface area with the help of different plates. for the purpose of experiment, three sola...
Adult Still's disease is a rare systemic disorder of unknown etiology. Its course often complicated by interstitial pneumonia and fulminant hepatitis. Published data have indicated some common mechanisms inflammation in patients with autoimmune disorders SARS-COV-19. We present clinical case 74-year old female patient long standing, slowly progressive Stills disease, who developed honeycomb lun...
Parallax Photography: Creating 3D Motions from Stills
how to cite this article: ashrafi mr, tavasoli ar. infantile-onset pompe disease. iran j child neurol autumn 2012; 6:4(suppl. 1):7-9. pls see pdf. refe r ences: 1. kishnani ps, steiner rd. pompe disease diagnosis and management guidelines. american j med genetic. 2006 .vol; 8; no5. 2. case se, beckemyer aa. infantile pompe disease on ert-updateonclinicalpresentation,musculoskeletal management...
The article describes the clinical onset of Takayasu's arteritis (non-specific aortoarteritis) which occurred after coronavirus disease in a young woman with Still's her medical history. primarily affects women, most commonly Asian race. Clinical manifestations can be conditionally divided into two groups: non-specific symptoms, indicating systemic inflammatory response, and specific symptoms a...
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