Results 201 to 210 of about 3,081 (242)

Mucocutaneous Disease Activity and Damage Accrual in Systemic Lupus Erythematosus: Analyses From the Asia‐Pacific Lupus Collaboration Longitudinal Cohort Study

Arthritis Care &Research, EarlyView.
Objective This research article aims to describe the prevalence, associations, and health‐related quality of life (HRQoL) impact of mucocutaneous features of systemic lupus erythematosus (SLE). Methods Data from the Asia‐Pacific Lupus Collaboration cohort were analyzed (2013–2021).
Amanda M. Saracino, Yanjie Hao, Dylan Hansen, Yi‐Hsing Chen, Alberta Hoi, Vera Golder, Jiacai Cho, Aisha Lateef, Worawit Louthrenoo, Laniyati Hamijoyo, Shue Fen Luo, Yeong‐Jian Jan Wu, Sandra Navarra, Leonid Zamora, Chak Sing Lau, Shirley Chan, Zhanguo Li, Hai‐hong Yao, Sargunan Sockalingam, B. M. D. B. Basnayake, Yasuhiro Katsumata, Masayoshi Harigai, Zhuoli Zhang, Jun Kikuchi, Yuko Kaneko, Tsutomu Takeuchi, Madelynn Chan, Sang‐Cheol Bae, Fiona Goldblatt, Sean O'Neill, Geraldine Hassett, Kristine Ng, Nicola Tugnet, Mark Sapsford, Yih Jia Poh, Michael Tee, Cherica Tee, Naoaki Ohkubo, Yoshiya Tanaka, Rangi Kandane‐Rathnayake, Eric Morand, Shereen Oon, Mandana Nikpour   +42 more
wiley   +1 more source

Shock in Adult-Onset Still's Disease Complicated by Macrophage Activation Syndrome: Clinical Characteristics and Prognosis of 14 Patients. [PDF]

Int J Hepatol
Li D, Cheng L, Zhang Y, Qian L.
europepmc   +1 more source

Distinct immune activation patterns in adult-onset Still's disease with fungal infections. [PDF]

Front Immunol
Wu T, Yu Y, Liu X, Chen X, Gu L, Lu L, Guo R.   +6 more
europepmc   +1 more source

Application of machine learning techniques to explore the occurrence of macrophage activation syndrome in Still's disease: results from the GIRRCS AOSD Study Group and the AIDA Network Still's Disease Registry. [PDF]

Front Immunol
Ruscitti P, Masedu F, Vitale A, Caggiano V, Di Cola I, Atzeni F, Sbalchiero J, Lopalco G, Iannone F, Morrone M, Iacono D, Riccio F, Visconti M, Gaggiano C, Caso F, Emmi G, Hinojosa-Azaola A, Torres-Ruiz J, Martín-Nares E, Guggino G, La Barbera L, Batu ED, Ozen S, Sfikakis PP, Navarini L, Costa L, Tufan A, Cakir IY, Perosa F, Hernández-Rodríguez J, Prete M, Dagna L, Campochiaro C, Ursini F, Sfriso P, Bindoli S, Giardini HAM, Fotis L, Kourtesi K, Ragab G, Ghanema M, Saad MA, Direskeneli H, Karamanakos A, Conforti A, La Torre F, Frassi M, Govoni M, Parronchi P, Sarzi-Puttini P, Maggio MC, Bugatti S, De Stefano L, Pelizza J, Bartoloni E, Rigante D, Iagnocco A, Viapiana O, Wiesik-Szewczyk E, Makowska J, Gündüz ÖS, Erten Ş, Ogunjimi B, Sebastiani GD, Del Giudice E, Biancalana E, Conti G, AlMaghlouth IA, Breda L, Gidaro A, Barone P, Olivieri AN, Carubbi F, De Paulis A, Chimenti MS, Lo Gullo A, Tharwat S, Thabet M, Moshrif A, Alessio M, Mauro A, Suzon B, Pucino V, Boyarchuk O, Kovalchuk T, Bes C, Deniz R, Al-Mayouf SM, Cipriani P, Valenti M, Balistreri A, Fabiani C, Ciccia F, Montecucco C, Giacomelli R, Frediani B, Cantarini L.   +96 more
europepmc   +1 more source

Diagnostic Complexity in Systemic Inflammation: Adult-Onset Still's Disease. [PDF]

Cureus
Rivera K, Kesari C.
europepmc   +1 more source

Facilitating Expedited Drug Approval—the Past, Present, and Future of Clinical Trials for Pediatric Rheumatic Disease

Arthritis Care &Research, EarlyView.
Pamela F. Weiss, Hermine I. Brunner
wiley   +1 more source

Pathogenic and genetic landscape of Still's disease across ages, with new insights into age-related IL-18 patterns. [PDF]

Arthritis Res Ther
Rogani G, Kessler H, Mehta B, Baker E, Leavis H, Vastert S, Schulert G.   +6 more
europepmc   +1 more source

Diagnostic Dilemma: Adult Onset Still's Disease Mimicking Lymphoma-A Case Report and Literature Review. [PDF]

Case Reports Immunol
AbuHaweeleh MN, Albaloshi AJ, Al-Hor M, Al-Theyab M, Almaslamani A, Elsayed B, Moursi MO, Hamad A.   +7 more
europepmc   +1 more source

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Adult Still's disease

The American Journal of Medicine, 1980
The clinical and laboratory features in six patients with adult Still's disease are presented and compared with those in 52 other cases gathered from the literature. Although there is no pathognomonic abnormality, the condition can be readily recognized by the striking constellation of clinical and laboratory abnormalities.
J M, Esdaile, H, Tannenbaum, D, Hawkins
openaire   +3 more sources

Adult Still's disease

British Journal of Dermatology, 1994
Adult Still's disease (ASD) is a rare disorder of unknown aetiology, characterized by an evanescent, erythematous, maculopapular rash, fever, arthralgia, and a variety of systemic features. We report a case which illustrates the typical features of ASD, and manifests the hitherto unreported complication of diffuse cutaneous mucinosis.
W G, Phillips, R, Weller, S E, Handfield-Jones, A, Kobza-Black   +3 more
openaire   +2 more sources