Results 81 to 90 of about 6,718,803 (257)
Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY. [PDF]
, 2010 The unparalleled collection of clinical data and biomaterials within the EHDN's REGISTRY can expedite the search for disease modifiers (genetic and environmental) of age at onset and disease progression that could be harnessed for the development of ...
Handley, Olivia J +59 more
core +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background Factors associated with relapse course and disability in myelin oligodendrocyte glycoprotein antibody‐associated disease (MOGAD) remain incompletely understood. Objectives To identify clinical and modifiable factors associated with relapse and disability in MOGAD. Methods In this ambispective multicentre cohort study using data from
Yingtao Wang +23 more
wiley +1 more source
Cryoglobulinemia vasculitis associated with adult‐onset Still's disease
Clinical Case ReportsKey Clinical Message The present case indicates that cryoglobulinemia vasculitis should be considered in the differential diagnosis of purpura in patients with adult‐onset Still's disease (AOSD).
Noriharu Nakagawa +3 more
doaj +1 more source
Successful treatment of refractory adult onset Still’s disease with rituximab
, 2016 Adult-onset Still’s disease (AOSD) is an uncommon inflammatory condition of unknown origin. In chronic disease, joint involvement is often predominant and erosions are noted in one third of patients. Therapeutic strategies derive from observational data.
T. Ben Salem +7 more
core +1 more source
Predictive Value of Composite Inflammatory Markers for Stroke Prognosis: A Prospective Cohort Study
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background Novel composite inflammatory markers' role in stroke prognosis is understudied, and the best predictor is unclear, requiring further exploration. Objectives This study aimed to systematically evaluate the associations of 6 novel composite inflammatory markers on stroke prognosis.
Bing Wu +7 more
wiley +1 more source
Ritka betegség, atípusos bőrtünetekkel: felnőttkori Still-betegség = Adult Onset Still’s disease with atypical cutaneous manifestations [PDF]
, 2016 A felnőttkori Still-betegség a juvenilis reumatoid artritisz ismeretlen etiológiájú, ritka, felnőttkori variánsa. A szerzők egy 62 éves nőbeteg esetét ismertetik, akit intermittáló magas láz, ízületi fájdalmak, maculo-papulosus bőrtünetek, elesett ...
Kása-Kovács, Adrienn, Vajda, Adrienne
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Современная ревматология, 2016 The paper considers a case of adult-onset Still's disease that occurred as acute pericarditis, two-spike hectic fever, and neutrophilic leukocytosis in a young man.
V. Yu. Myachikova +5 more
doaj +1 more source
Deep Learning Pose Estimation for Phenotyping of Co‐Occurring Hyperkinetic Movement Disorders
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To explore whether routine outpatient video combined with deep learning‐based pose estimation and clinically interpretable kinematic features can support multi‐label phenotyping of co‐occurring hyperkinetic movement disorders (HMDs).
Laura Cif +17 more
wiley +1 more source
The cause of fever and pulmonary infiltrate: a difficult etiological diagnosis
Emergency Care Journal, 2017 Adult-onset Still’s disease is a rare condition that typically presents itself with intermittent fever, arthralgia and salmon colored rash. The involvement of the in lung is less common and very rare.
Bahjat Barakat, Raffaele Pezzilli
doaj +1 more source
Adult onset Still’s disease: a comparison of two clinical cases
, 2013 Still’s disease is a disease of unknown etiology that was identified for the first time in 1897 by George Still who noted the association of fever, arthralgias and cutaneous rash in a group of 22 children.
Sebastiano Pavone +8 more
core +1 more source