Results 101 to 110 of about 267,960 (152)

Recurrence of juvenile dermatomyositis 8 years after remission

open access: yesJAAD Case Reports, 2017
Ken Muramatsu, MD   +8 more
doaj   +1 more source

Juvenile Dermatomyositis

open access: yesNishi Nihon Hifuka, 1997
KUBOTA, Yumiko   +2 more
openaire   +1 more source

Panniculitis in Juvenile Dermatomyositis: Report of a Case and Review of the Published Work

open access: yesJournal of Dermatology, 2016
We report a 15-year-old girl who presented with indurated, subcutaneous nodules in addition to classical findings of juvenile dermatomyositis. Histopathological examination confirmed the diagnosis of panniculitis associated with juvenile dermatomyositis.
Özgür Kasapçopur   +2 more
exaly   +3 more sources

Treatment Approaches to Juvenile Dermatomyositis

open access: yesExpert Opinion on Pharmacotherapy, 2004
Juvenile dermatomyositis (JDM) is a rare disease of childhood with significant morbidity. Although the mortality and morbidity has improved over recent decades, it is still a chronic disease for a significant proportion of children with JDM.
Athimalaipet V Ramanan
exaly   +2 more sources
Some of the next articles are maybe not open access.

Related searches:

Juvenile dermatomyositis

The Indian Journal of Pediatrics, 1996
The clinical profile of 7 children and their follow-up is described. There was female preponderance with mate to female ratio of 1:6. The median age of onset was 6 years. All the patients had skin rash, muscle weakness and abnormal enzyme profile. Muscle biopsy was performed in 6 and was abnormal in all of them.
V, Seth   +3 more
openaire   +4 more sources

Juvenile Dermatomyositis

Pediatric Annals, 2002
Juvenile dermatomyositis (JDM) is a multisystem disease characterized by acute and chronic lymphocytic inflammation of the skeletal muscle and skin. The disease is marked early in its course by the presence of a vasculopathy or vasculitis, and later by the development of calcinosis.
Ann M, Reed, Maricarmen, Lopez
  +7 more sources

Cyclosporin in Juvenile Dermatomyositis.

Lancet, The, 1989
Juvenile dermatomyositis in fourteen children who had not responded fully to steroids and other immunosuppressants and who had had chronic active disease for an average of 3 years was successfully treated with cyclosporin. Twelve patients had serious complications of the disease or of previous treatment. The response to cyclosporin included recovery of
Geraldine Cambridge   +2 more
exaly   +3 more sources

Juvenile Dermatomyositis

Zeitschrift für Rheumatologie, 2006
Juvenile dermatomyositis (JDM) is an inflammatory multi-system disease of unknown etiology with classic involvement of the skin and striated muscles. Following a prodromal period, patients develop a progressive proximal muscle weakness. Typical skin involvement includes heliotrope rash, facial erythema, Gottron's sign and nailfold capillary ...
F, Dressler, H-I, Huppertz
openaire   +2 more sources

Juvenile dermatomyositis

2013
Juvenile dermatomyositis (JDM) is a systemic, inflammatory, idiopathic disease, mainly affecting the skin and the muscles, starting before the age of 16, with an incidence around one case per 1 million children. Some patients display typical features of JDM without skin involvement, or even without muscle involvement; however, both tissues are affected
Pierre, Quartier, Romain K, Gherardi
openaire   +2 more sources

Home - About - Disclaimer - Privacy