The importance of mdx mouse in the pathophysiology of Duchenne’s muscular distrophy. Arq. Neuro-Psiquiatr. [online]. , vol, n.3B, pp Importância do camundongo mdx na fisiopatologia da distrofia muscular de Duchenne. The importance of mdx mouse in the pathophysiology of Duchenne’s . Palavras-chave: Distrofia muscular de Duchenne, retardo mental, atraso do . Ao longo da história, os maiores focos da pesquisa sobre a fisiopatologia da.

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Services on Demand Article. Results of manual resistance exercise on a manifesting carrier of duchenne muscular dystrophy: Leibowitz D, Dubowitz V. Predictive factors of cessation of ambulation in patients with duchenne muscular dystrophy, Am J Phys Med Rehabil.

Duchenne muscular dystrophy, dystrophin, mdx, animal model. Exercise effect on contractile properties of skeletal muscle in mouse muscular dystrophy.

Learn Disabil Res Pract. Muscle damage is not a function of muscle force but active muscle strain.


The molecular and biochemical basis of Duchenne muscular dystrophy. An Introduction to electromyography. Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.

Clinical orthopaedics and related research. Trends Biochem Sci ; Scand J Immunol ; Duchenne, Becker, muscular dystrophy, dystrophin diagnosis.

Distrofia muscular (para Padres)

Hsu J D, Furumasu J. Mcneil P, Khakee R.

Taylor R, Fowler W, Doerr l. Acta Neuropathol Berl ; Acute gastric dilatation in Duchenne muscular dystrophy: Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than Kb Upstream of the nearest known promoter. Rodemann HP, Bayreuther K.

Scandinavian University Books; Evidence for early impairment of verbal intelligence in Duchenne muscular dystrophy. To survey the medical literature directed to the study of cognitive dysfunction in patients with Duchenne muscular dystrophy through description of the milestones of neurological development and psychometric tests for quantifying muscylar.

Deconinck N, Dan B. Mental retardation in association with progressive muscular dystrophy.

Importância do camundongo mdx na fisiopatologia da distrofia muscular de Duchenne

Changes in spirometry over time as a prognostic marker in patients with Duchenne muscular dystrophy. Isokinetic strength training protocols: Despite showing less intense myofibrosis and scarce deposition of fatty tissue, mdx mice are considered an adequate animal model for studies on the pathogenesis of Duchenne-type muscular dystrophy.


The effects of limitation of activity upon the human body. Investigation of poor academic achievement in children with Duchenne muscular dystrophy. Respiratory care of the patient with Duchenne muscular dystrophy: Direct diagnosis of carriers of point mutations in Duchenne muscular dystrophy.

Distrofia muscular

Aerobic walking in slowly progressive neuromuscular Disease: Mental retardation and lifetime events of Duchenne muscular dystrophy in Japan. Epub Nov Verma S, Anziska Y. De acordo com os resultados de Prosser et al.

The neuropsychological profile of Duchenne muscular dystrophy.