Results 71 to 80 of about 2,098 (173)

Pure Red Cell Aplasia with Adult Onset Still’s Disease

Case Reports in Medicine, 2013
Adult Onset Still’s Disease (AOSD) is a rare inflammatory syndrome mostly seen in young adults. Known for its wide range of clinical manifestations, AOSD often presents with nonremitting systemic signs and symptoms.
Nicholas Robillard, Paul Van Nguyen, Robert Wistaff, Mikhael Laskine   +3 more
doaj   +1 more source

A Conceptual Formalization of Crosscutting in AOSD

, 2005
We propose a formalization of crosscutting based on a conceptual framework for AOSD. Crosscutting is clearly distinguished from the related concepts scattering and tangling. The definitions of these concepts are formalized and visualized with matrices and matrix operations. This allows more precise reasoning about crosscutting.
van den Berg, Klaas Gerrit, Conejero, José María   +1 more
openaire   +1 more source

Connector for Dynamic Composition of Aspects Based on AOSD

The KIPS Transactions:PartD, 2006
Aspect-Oriented Software Development is new software development method. It has many advantages related to software performance, maintenance and repair. Also it offers modularization method to a existing programming language for secondary function such as security and fault tolerance.
Tae-Woong Kim, Tae-Gong Kim
openaire   +2 more sources

Bidirectional Mendelian randomization exploring the causal relationship between immune cell dynamics and adult-onset Still’s disease [PDF]

Exploration of Medicine
Aim: Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disorder marked by fever, rash, joint pain, and hyperferritinemia. While immune dysregulation is implicated in AOSD, the exact causal mechanisms remain unclear.
Jing-Lei Xie, Chu-Qi Wang, He-Yi Zhang, Xiao-Jing Jiang, Meng-Xia Liu, Jing-Fang Zhang, Rui Zhao, Fang Li, Sheng-Xiao Zhang   +8 more
doaj   +1 more source

Increased serum caspase-1 in adult-onset Still's disease.

PLoS ONE
BackgroundCaspase-1 is a crucial component in the inflammasome activation cascade. This study evaluated the potential of serum caspase-1 level as an inflammatory biomarker in patients with adult-onset Still's disease (AOSD).MethodsThe study included 51 ...
Haruki Matsumoto, Shuhei Yoshida, Tomohiro Koga, Yuya Fujita, Yuya Sumichika, Kenji Saito, Jumpei Temmoku, Tomoyuki Asano, Shuzo Sato, Masashi Mizokami, Masaya Sugiyama, Kiyoshi Migita   +11 more
doaj   +1 more source

Traceability and AOSD - From Requirements to Aspects [PDF]

, 2006
The traceability question is addressed through the development of a framework to go from requirements to aspects using the Design by Contract methodology. It is demonstrated that by starting at the requirements stage, and specifying an early aspect in the same semi-formal language as the system's existing requirements, we have the basis from which to ...
van der Linden, Janet, Laney, Robin, Thomas, Pete   +2 more
openaire  

Adding colchicine to immunosuppressive treatments; a potential option for biologics-refractory adult-onset Still’s disease

BMC Research Notes, 2018
Background Adult-onset Still’s disease (AOSD) is a rare inflammatory disorder characterized by the classical triad of daily spiking fever, arthritis, and typical salmon-colored rash.
Tomoyuki Asano, Makiko Yashiro Furuya, Shuzo Sato, Hiroko Kobayashi, Hiroshi Watanabe, Eiji Suzuki, Kiyoshi Migita   +6 more
doaj   +1 more source

Adult-onset Still's Disease (AOSD) with Gastrointestinal Lesions

Internal Medicine
A 51-year-old woman with fever was admitted to our hospital. A computed tomography (CT) scan showed thickened colonic walls. Colonoscopy revealed erosion in the ileum and colon. Adult-onset Still's disease (AOSD) was diagnosed due to a subsequent sore throat and skin rash.
Harada, Takahito, Hirata, Yoshikazu, Kawamura, Hayato, Yamamoto, Yuki, Kobayashi, Yuka, Kumai, Daisuke, Adachi, Akihisa, Nagura, Yoshihito, Ikeuchi, Hirokazu, Hayashi, Noriyuki, Takada, Hiroki, Sobue, Satoshi, Yoshida, Megumi   +12 more
openaire   +2 more sources

Adult-onset Still's Disease Complicated With Hemophagocytic Syndrome

Journal of the Formosan Medical Association, 2010
Hemophagocytic syndrome (HS) that occurs in the course of adult-onset Still's disease (AOSD) has been reported only rarely in the literature. HS and AOSD share overlapping clinical and laboratory features, therefore, it is difficult to recognize HS as a ...
Horng-Ming Yeh, Ming-Fei Liu, Kuo-Kuan Chang, Shian-Min Liu, Chang-Hung Chen   +4 more
doaj   +1 more source

Rare Manifestation of a Rare Disease, Acute Liver Failure in Adult Onset Still’s Disease: Dramatic Response to Methylprednisolone Pulse Therapy—A Case Report and Review

Case Reports in Medicine, 2014
Adult onset Still’s disease (AOSD) is a rare systemic inflammatory disorder of unknown etiology. It is characterized by daily fevers, arthralgias or arthritis, typical skin rash, and leukocytosis.
Nalini Valluru, Venkata S. Tammana, Michael Windham, Eyasu Mekonen, Rehana Begum, Andrew Sanderson   +5 more
doaj   +1 more source