Results 261 to 270 of about 37,969 (302)
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PROGRESSIVE NEURITIC MUSCULAR ATROPHY
Archives of Neurology And Psychiatry, 1927Although the problems concerning muscular dystrophies, particularly the neural ones, are for the moment being ignored, this chapter of neurology is not yet closed either symptomatologically or—and this cannot be emphasized too strongly—in the sense of its pathogenesis. In several recent articles, authors (Pette1) assert that, besides hereditary factors
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Progressive spinal muscular atrophies.
Journal of child neurology, 2000Spinal muscular atrophy is the most common autosomal-recessive genetic disorder lethal to infants. It was first described in the 1890s. Since then our understanding of the disorder has progressed significantly. Progression of the disease is due to loss of anterior horn cells, thought to be caused by apoptosis.
J B, Strober, G I, Tennekoon
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Progressive Muscular Atrophy in an Infant
The American Journal of Nursing, 1963D ON IS A TWO-MONTH-OLD boy with the infantile form of progressive muscular atrophy who was admitted to the pediatric service of a U.S. Air Force Hospital in England. In infants the condition is known as Werdnig-Hoffmann disease. This is primarily a disease of the anterior horn cells of the spinal cord, resulting in degeneration of the peripheral motor
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The Journal of Nervous and Mental Disease, 1926
null Souques, null Alajouanine
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null Souques, null Alajouanine
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Therapeutic approaches for Duchenne muscular dystrophy
Nature Reviews Drug Discovery, 2023Thomas C Roberts, Kay E Davies
exaly