Measures of adult and juvenile dermatomyositis, polymyositis, and inclusion body myositis: physician and patient/parent global activity, manual muscle testing (mmt) …

LG Rider, VP Werth, AM Huber… - Arthritis care & …, 2011 - Wiley Online Library
The idiopathic inflammatory myopathies, including adult and juvenile dermatomyositis (DM),
polymyositis (PM), and inclusion body myositis (IBM), are rare systemic autoimmune …

An overview of polymyositis and dermatomyositis

AR Findlay, NA Goyal, T Mozaffar - Muscle & nerve, 2015 - Wiley Online Library
Polymyositis and dermatomyositis are inflammatory myopathies that differ in their clinical
features, histopathology, response to treatment, and prognosis. Although their clinical …

MRI biomarker assessment of neuromuscular disease progression: a prospective observational cohort study

JM Morrow, CDJ Sinclair, A Fischmann… - The Lancet …, 2016 - thelancet.com
Background A substantial impediment to progress in trials of new therapies in
neuromuscular disorders is the absence of responsive outcome measures that correlate with …

Practical medical applications of quantitative MR relaxometry

HL Margaret Cheng, N Stikov… - Journal of Magnetic …, 2012 - Wiley Online Library
Conventional MR images are qualitative, and their signal intensity is dependent on several
complementary contrast mechanisms that are manipulated by the MR hardware and …

Skeletal muscle quantitative nuclear magnetic resonance imaging and spectroscopy as an outcome measure for clinical trials

PG Carlier, B Marty, O Scheidegger… - Journal of …, 2016 - content.iospress.com
Recent years have seen tremendous progress towards therapy of many previously incurable
neuromuscular diseases. This new context has acted as a driving force for the development …

Juvenile dermatomyositis and other idiopathic inflammatory myopathies of childhood

BM Feldman, LG Rider, AM Reed, LM Pachman - The Lancet, 2008 - thelancet.com
Juvenile dermatomyositis, the most common inflammatory myopathy of childhood, is a rare
systemic autoimmune vasculopathy that is characterised by weakness in proximal muscles …

Idiopathic inflammatory myopathies: clinical approach and management

A Malik, G Hayat, JS Kalia, MA Guzman - Frontiers in neurology, 2016 - frontiersin.org
Idiopathic inflammatory myopathies (IIM) are a group of chronic, autoimmune conditions
affecting primarily the proximal muscles. The most common types are dermatomyositis (DM) …

The Juvenile Dermatomyositis National Registry and Repository (UK and Ireland)—clinical characteristics of children recruited within the first 5 yr

LJ McCann, AD Juggins, SM Maillard… - …, 2006 - academic.oup.com
Objectives. To identify epidemiological, clinical and laboratory characteristics of juvenile
dermatomyositis (JDM) in a national multi-centre cohort of patients, and to review recent …

Idiopathic inflammatory myopathies: current trends in pathogenesis, clinical features, and up-to-date treatment recommendations

FC Ernste, AM Reed - Mayo Clinic Proceedings, 2013 - Elsevier
Recently, there have been important advances in the understanding of the pathophysiologic
features, assessment, and management of patients with a newly diagnosed idiopathic …

Neurological manifestations of chronic graft-versus-host disease after allogeneic haematopoietic stem cell transplantation: report from the Consensus Conference on …

O Grauer, D Wolff, H Bertz, H Greinix, JS Kühl… - Brain, 2010 - academic.oup.com
A major obstacle of allogeneic haematopoietic stem cell transplantation is graft-versus-host
disease, an immune-mediated disorder that affects multiple tissues and organs with varying …