Results 61 to 70 of about 4,278 (194)

Acute liver transplantation in a 41-year-old male patient presenting symptoms of adult-onset Still's disease [PDF]

, 2011
L
Andrès E., Bywaters E.G., Coffernils M., Cush J.J., Fautrel B., Ishikawa M., Kadar J., Linde B., Mehrpoor G., Mert A., Motoo Y., Nemes B., Nemes B., Nemes B., Ogata A., Singh S., Still G.F., Taccone F.S., Takami A., Teran A., Yamaguchi M., Zhu G.   +21 more
core   +2 more sources

Autoimmune meningitis and encephalitis in adult-onset still disease – Case report [PDF]

, 1970
Introduction Adult-onset Still disease (AOSD) is a rare systemic inflammatory disease of unknown cause. Its symptoms usually include persistent fever, fugitive salmon-colored rash, arthritis, sore throat (not specific), but it may also lead to internal ...
Bożek, Milena, Konopko, Magdalena, Makowicz, Grzegorz, Sienkiewicz-Jarosz, Halina, Wierzba-Bobrowicz, Teresa, Witkowski, Grzegorz   +5 more
core   +2 more sources

Clarithromicin in adult-onset Still'disease a study of 6 cases [PDF]

, 2010
Adult-onset Still's disease (AOSD) is a rare rheumatological condition characterized by an acute systemic involvement. There are no treatment guidelines.
Abdi-Ali, L, Baiardi, P, Benucci, M, Bucci, M, Cirino, G, Manfredi, M, Saviola, G   +6 more
core   +1 more source

The progression of initial symptoms and its relationship with the clinical course in adult-onset Still’s disease: from the KEIO-AOSD cohort

EULAR Rheumatology Open
: Objectives: Adult-onset Still’s disease presents with nonspecific and heterogeneous features. This study aims to elucidate the development of initial symptoms and their relationship with the disease course in adult-onset Still’s disease.
Hiroya Tamai, Jun Kikuchi, Tsutomu Takeuchi, Yuko Kaneko   +3 more
doaj   +1 more source

Anakinra for the treatment of adult-onset Still's disease [PDF]

, 2018
: Introduction: Adult onset Still's disease (AOSD) is an uncommon systemic inflammatory disease on the clinical spectrum of autoinflammatory disorders.
Atienza Mateo, Belén, Castañeda Sanz, Santos, González-Gay Mantecón, Miguel Ángel, Martín Varillas, José Luis, Serra López-Matencio, José María   +4 more
core   +2 more sources

Adult Onset Still's Disease

Faridpur Medical College Journal, 2017
Adult Still's disease is rare disease presented with high spiking fever, joint pain, rash, organomegaly and serositis. It is difficult to diagnose as it closely mimics with many systemic diseases, so it can be diagnosed after exclusion of them. There are lots of diagnostic criteria, of them Yamaguchi's criteria is well established.
MM Shahin Ul Islam, Mst Naznin Sarker, Md Iqbal Hossain, Mohammad Iqbal Hossain, Muhammad Kamruzzaman   +4 more
openaire   +2 more sources

Tocilizumab for the treatment of adult-onset Still's disease [PDF]

, 2019
Adult-onset Still´s disease (AOSD) is a systemic inflammatory condition that affects mainly young people. The clinical course consists of two distinctive patterns: one with a predominance of systemic symptoms and another manifested by progressive chronic
Atienza Mateo, Belén, Castañeda, Santos, García-Castañeda, Noelia, González-Gay Mantecón, Miguel Ángel, Martín Varillas, José Luis, Martínez-Quintanilla, Dolores   +5 more
core   +2 more sources

Atypical Adult-onset Still's disease with flagellate morphology in a patient with skin of color

JAAD Case Reports, 2023
Paayal Vora, BS, Elaine Kunzler, MD, Arturo R. Dominguez, MD, Travis Vandergriff, MD, Tamia Harris-Tryon, MD, PhD   +4 more
doaj   +1 more source

Interleukin-18 as a diagnostic marker of adult-onset Still’s disease in older patients: a case report and review of the literature

Journal of Medical Case Reports, 2018
Background Adult onset Still’s disease is a systemic auto-inflammatory condition of unknown etiology characterized by intermittent spiking high fever, an evanescent salmon-pink or erythematous maculopapular skin rash, arthralgia or arthritis, and ...
Daisuke Usuda, Yoshiki Furumura, Kento Takeshima, Ryusho Sangen, Yasuhiro Kawai, Yuji Kasamaki, Yoshitsugu Iinuma, Tsugiyasu Kanda   +7 more
doaj   +1 more source

Macrophage Activation Syndrome Associated with Adult-Onset Still’s Disease Successfully Treated with Anakinra

Case Reports in Rheumatology, 2016
Macrophage activation syndrome (MAS) is a potentially fatal complication of Adult-Onset Still’s disease (Still’s disease). Whereas an increasing body of evidence supports interleukin-1 (IL-1) blockade as a promising treatment for Still’s disease, whether
Aswini Kumar, Hiroshi Kato
doaj   +1 more source