Neurology Medical News about Rippling muscle disease

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Rippling muscle disease: Variable phenotype in a family with five afflicted members
Muscle & Nerve, 08/31/09

Jacobi C et al. – The authors report a family with rippling muscle disease (RMD) who had an autosomal dominant mode of inheritance. The father, mother, and one daughter proved to be heterozygous, and two sons were homozygous for the A92T mutation of the caveolin–3 gene.

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Association of Muscle Strength With the Risk of Alzheimer Disease and the Rate of Cognitive Decline in Community-Dwelling Older Persons
Archives of Neurology, 11/13/09 Relevance Score: 67%

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Cochrane Reviews, 10/09/09 Relevance Score: 67%

Can Autoimmunity Against Calsequestrin Explain the Eye and Eyelid Muscle Inflammation of Thyroid Eye Disease?
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Histopathological analysis of skeletal muscle in patients with Parkinson's disease and ‘dropped head’/‘bent spine’ syndrome
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