Weidenheim, Karen M.

Neuropathology of Cockayne syndrome: Evidence for impaired development, premature aging, and neurodegeneration

Weidenheim, K. M., Dickson, D. W., & Rapin, I. (2009) · Mechanisms of Ageing and Development

DNA Repair MechanismsGenomics and Rare Diseases

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Transgenic overexpression of caveolin-3 in skeletal muscle fibers induces a Duchenne-like muscular dystrophy phenotype

Galbiati, F., Volonté, D., Chu, J. B., Li, M., Fine, S. W., Fu, M., Bermudez, J., Pedemonte, M., Weidenheim, K. M., Pestell, R. G., et al. (2000) · Proceedings of the National Academy of Sciences

Muscle Physiology and DisordersCaveolin-1 and cellular processes

Cited by 155

Cockayne syndrome in adults: Review with clinical and pathologic study of a new case

Rapin, I., Weidenheim, K., Lindenbaum, Y., Rosenbaum, P., Merchant, S. N., Krishna, S., & Dickson, D. W. (2006) · Journal of Child Neurology

Genomics and Rare DiseasesGenetic and rare skin diseases.

Cited by 124

Morphological and Biochemical Correlations of Abnormal Tau Filaments in Progressive Supranuclear Palsy

Takahashi, M., Weidenheim, K. M., Dickson, D. W., & Ksiezak-Reding, H. (2002) · Journal of Neuropathology & Experimental Neurology

Alzheimer's disease research and treatmentsParkinson's Disease Mechanisms and Treatments

Cited by 56