Results 41 to 50 of about 4,398 (288)

Persistent pruritic papules and plaques: a characteristic histopathologic presentation seen in a subset of patients with adult-onset and juvenile Still's disease [PDF]

, 2010
Background: ‘Persistent pruritic papules and plaques' of Still's disease represents a recently described eruption seen in a subset of patients. Most cases reported in the literature to date have been associated with adult-onset Still's disease.
Affleck, Bywaters, Fautrel, Lee, Lűbbe, Mehrpoor, Prendiville, Ravelli, Suzuki, Wolgamot   +9 more
core   +1 more source

Cutaneous manifestations and histologic findings in the hyperimmunoglobulinemia D syndrome [PDF]

, 1994
Contains fulltext : 4767.pdf (publisher's version ) (Open ...
Boom, B.W., Drenth, J.P.H., Meer, J.W.M. van der, Toonstra, J.   +3 more
core   +2 more sources

Germinal center kinase-like kinase (GLK/MAP4K3) expression is increased in adult-onset Still's disease and may act as an activity marker

BMC Medicine, 2012
Background Germinal center kinase-like kinase (GLK, also termed MAP4K3), a member of the MAP4K family, may regulate gene transcription, apoptosis and immune inflammation in response to extracellular signals.
Chen Der-Yuan, Chuang Huai-Chia, Lan Joung-Liang, Chen Yi-Ming, Hung Wei-Ting, Lai Kuo-Lung, Tan Tse-Hua   +6 more
doaj   +1 more source

An interferon-inducible neutrophil-driven blood transcriptional signature in human tuberculosis [PDF]

, 2010
Tuberculosis (TB), caused by infection with Mycobacterium tuberculosis (M. tuberculosis), is a major cause of morbidity and mortality worldwide and efforts to control TB are hampered by difficulties with diagnosis, prevention and treatment 1,2.
A Falk, AM Cooper, AM Cooper, Anne O’Garra, Asuncion Mejias, C Auffray, C Dye, C Manca, C Manca, C Telesca, CE Barry III, Charles Quinn, Christine M. Graham, D Chaussabel, D Ordway, D Salisbury, Damien Chaussabel, DB Young, Derek Blankenship, EB Eruslanov, EC Baechler, F Allantaz, Finlay W. McNab, Jacques Banchereau, Jason Skinner, JL Casanova, JL Flynn, John J. Cush, JS Beck, Katalin A. Wilkinson, L Bennett, M Jacobsen, Matthew P. R. Berry, MI Ardura, O Ramilo, Octavio Ramilo, Onn M. Kon, R Mistry, R Pankla, Ranju Dhawan, Robert J. Wilkinson, Romain Banchereau, SH Kaufmann, Susannah A. A. Bloch, SY Eum, T Decker, Tolu Oni, V Pascual, Virginia Pascual, Zhaohui Xu   +49 more
core   +1 more source

Pneumonitis in Adult Onset Still’s Disease: Uncommon or Under Diagnosed?

Acta Médica Portuguesa, 2017
The adult onset Still’s Disease is an uncommon entity characterized by multiple clinical manifestations. Pneumonitis, less often considered, deserves particular emphasis given the need for differential diagnosis and because it can progress to severe ...
Silvia Fernandes, Margarida Almeida, José Alberto Pereira da Silva, José Carlos Romeu   +3 more
doaj   +1 more source

Adult-onset Still's disease: Evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers [PDF]

, 2016
Background: Adult-onset Still's disease (AOSD) is rare inflammatory disease of unknown etiology that usually affects young adults. The more common clinical manifestations are spiking fevers, arthritis, evanescent rash, elevated liver enzymes ...
Berardicurti O., Carubbi F., Ciccia F., Cipriani P., Di Benedetto P., Giacomelli R., Guggino G., Iacono D., Liakouli V., Masedu F., Ruscitti P., Triolo G., Valenti M., Valentini G.   +13 more
core   +1 more source

Derivation and validation of four patient clusters in Still's disease, results from GIRRCS AOSD-study group and AIDA Network Still Disease Registry [PDF]

, 2023
Background Different patient clusters were preliminarily suggested to dissect the clinical heterogeneity in Still's disease. Thus, we aimed at deriving and validating disease clusters in a multicentre, observational, prospective study to stratify these ...
Alibaz-Oner F., Almaghlouth I. A., Antonelli I. P. D. B., Asfina K., Atzeni F., Bartoloni E., Berardicurti O., Bugatti S., Caggiano V., Cantarini L., Carubbi F., Caso F., Ciccia F., Cipriani P., Costa L., Dagna L., De Stefano L., Del Giudice E., Di Cola I., Di Muzio C., Direskeneli H., Emmi G., Erten S., Fabiani C., Fotis L., Frediani B., Giacomelli R., Giardini H., Gidaro A., Govoni M., Guggino G., Hernandez-Rodriguez J., Hinojosa-Azaola A., Iacono D., Iagnocco A., La Torre F., Lo Gullo A., Lopalco G., Maggio M. C., Maier A., Makowska J., Martin-Nares E., Masedu F., Mauro D., Montecucco C., Monti S., Navarini L., Ogunjimi B., Pantano I., Perosa F., Prete M., Ragab G., Rossi S., Ruscitti P., Sevik G., Sfikakis P. P., Sfriso P., Simonini G., Tharwat S., Torres-Ruiz J., Tufan A., Valenti M., Vitale A.   +62 more
core   +1 more source

Feasibility and Preliminary Efficacy of Integrative Neuromuscular Training for Childhood Cancer Survivors: A Pilot Study

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Survivors of childhood acute lymphoblastic leukemia (ALL) often exhibit early deficits in muscle and movement competence, which can compromise long‐term health. Integrative neuromuscular training (INT), a multifaceted approach combining fundamental movement activities with strength exercises, may help address these deficits during ...
Anna Maria Markarian, Robert U. Newton, Dennis R. Taaffe, Nicholas G. Gottardo, Santosh Valvi, Carolyn J. Peddle‐McIntyre, Jodie Cochrane Wilkie, Daniel A. Galvão   +7 more
wiley   +1 more source

Association between adult-onset still’s disease and COVID-19: A report of two cases and brief review

SAGE Open Medical Case Reports
Adult-onset still’s disease is a rare multisystemic autoinflammatory disorder with an estimated annual incidence of 0.16–0.62 per 100,000 individuals worldwide. It is typically considered a diagnosis of exclusion.
Sarah Fet-He, Gabriel Ibarra Lecompte, Alejandro José Quiroz Alfaro   +2 more
doaj   +1 more source

Adult Onset Still's Disease - current state of knowledge

Journal of Education, Health and Sport
Introduction: Adult-onset Still’s disease (AOSD) is a rare systemic inflammatory disorder of unknown etiology. AOSD lies at the crossroads of innate and adaptive immunity, highlighting the complexity of its pathogenesis.
Anna Centkowska, Natalia Katarzyna Wagner-Bieleń, Martyna Zwierzchowska, Agata Antoniak, Anna Maria Jocz, Joanna Karina Banaśkiewicz, Aleksandra Maria Żyta, Gabriela Helena Dąbrowska, Maria Anna Żmijewska, Jakub Ziółkowski   +9 more
doaj   +1 more source