Results 271 to 280 of about 86,962 (305)

Myo-MOVES: a custom electrical stimulation system for functional studies of 3D bioengineered muscle.

open access: yesLab Chip
Ruiz-Gutiérrez M   +4 more
europepmc   +1 more source

Genetic and Clinical Landscape of Duchenne Muscular Dystrophy in Guatemala: Insights from a National Study

open access: yes
Orozco M   +6 more
europepmc   +1 more source

The dystrophy of Duchenne

The Lancet, 2001
Duchenne muscular dystrophy While the eponym, Duchenne muscular dystrophy (DMD), is applied to the most common and most severe muscular dystrophy of childhood, Duchenne was not the first to describe the condition. 10 years before Duchenne reported his first case of Duchenne dystrophy, the London physician Meryon had described the condition.
Jiri Vajsar, Venita Jay
openaire   +3 more sources

Female Duchenne

European Journal of Paediatric Neurology, 2017
Objective: Duchenne muscular dystrophy (DMD) is a X-linked recessive disease caused by mutations in dystrophin gene and is characterized by progressive muscle degeneration and weakness resulting in poor disease outcome. The disease primarily affects boys. Females are usually only asymptomatic carriers of mutations.
Sekelj Fureš, Jadranka   +1 more
openaire   +2 more sources

Duchenne muscular dystrophy

Current Opinion in Genetics & Development, 1991
Progress in understanding the role of dystrophin raises promising hopes for a treatment for Duchenne muscular dystrophy. In addition, great improvements have been made in the ability to diagnose this disease using simple molecular methods.
J. Wicki, J.T. Seto, J.S. Chamberlain
openaire   +3 more sources

Duchenne muscular dystrophy

Neurology India, 2008
AbstractDuchenne muscular dystrophy, an X‐linked disorder, has an incidence of one in 5000 boys and presents in early childhood with proximal muscle weakness. Untreated boys become wheelchair bound by the age of 12 years and die of cardiorespiratory complications in their late teens to early 20s.
Eppie M. Yiu   +2 more
openaire   +5 more sources

DUCHENNE'S MUSCULAR DYSTROPHY

Medical Journal of Australia, 1968
G. B. A. Duchenne's description of pseudohypertrophic muscular paralysis contains not only the first clear account of this disease, but also the first report of a practical instrument of muscle biopsy. Duchenne (1806-1875) was a French neurologist who was led to a careful study of neuromuscular diseases through his interest in the effects of ...
Irwin A. Brody, Robert H. Wilkins
openaire   +6 more sources

Perceptions of Duchenne and non-Duchenne smiles: A meta-analysis

Cognition and Emotion, 2015
A meta-analysis was conducted to compare perceptions of Duchenne smiles, smiles that include activation of the cheek raiser muscle that creates crow's feet around the eyes, with perceptions of non-Duchenne smiles, smiles without cheek raiser activation.
Sarah D. Gunnery, Mollie A. Ruben
openaire   +3 more sources

Facial and emotional reactions to Duchenne and non-Duchenne smiles

International Journal of Psychophysiology, 1998
The purpose of the study was to investigate facial and emotional reactions while viewing two different types of smiles and the relation of emotional empathy to these reactions. Facial EMG was recorded from the orbicularis oculi and zygomaticus major muscle regions while subjects individually watched two blocks of stimuli.
Veikko Surakka, Jari K. Hietanen
openaire   +3 more sources

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