Armstrong, Dawna

Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation

Jiang, Y.-H., Armstrong, D., Albrecht, U., Atkins, C. M., Noebels, J. L., Eichele, G., Sweatt, J. D., & Beaudet, A. L. (1998) · Neuron

Genetic Syndromes and ImprintingGenetics and Neurodevelopmental Disorders

Cited by 852

Mutation of TDP1, encoding a topoisomerase I–dependent DNA damage repair enzyme, in spinocerebellar ataxia with axonal neuropathy

Takashima, H., Boerkoel, C. F., John, J., Saifi, G. M., Salih, M. A. M., Armstrong, D., Mao, Y., Quiocho, F. A., Roa, B. B., Nakagawa, M., et al. (2002) · Nature Genetics

Genetic Neurodegenerative DiseasesDNA Repair Mechanisms

Cited by 522

Selective dendritic alterations in the cortex of Rett syndrome

Armstrong, D., Dunn, J. K., Antalffy, B., & Trivedi, R. (1995) · Journal of Neuropathology and Experimental Neurology

Genetics and Neurodevelopmental DisordersNeuroscience and Neuropharmacology Research

Cited by 378

Neuropathology of Rett syndrome

Jellinger, K., Armstrong, D., Zoghbi, H. Y., & Percy, A. K. (1988) · Acta Neuropathologica

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 204

Malformations of cortical development and epilepsies: neuropathological findings with emphasis on focal cortical dysplasia

Blümcke, I., Vinters, H. V., Armstrong, D., Aronica, E., Thom, M., & Spreafico, R. (2009) · Epileptic Disorders

Epilepsy research and treatmentFetal and Pediatric Neurological Disorders

Cited by 145