Wisniewski, Krystyna E.

Adult fragile X syndrome: Clinico-neuropathologic findings

Rudelli, R. D., Brown, W. T., Wisniewski, K., Jenkins, E. C., Laure-Kamionowska, M., Connell, F., & Wisniewski, H. M. (1985) · Acta Neuropathologica

Genetics and Neurodevelopmental DisordersDown syndrome and intellectual disability research

Cited by 362

The fra(X) syndrome: Neurological, electrophysiological, and neuropathological abnormalities

Wisniewski, K. E., Segan, S. M., Miezejeski, C. M., Sersen, E. A., & Rudelli, R. D. (1991) · American Journal of Medical Genetics

Genetics and Neurodevelopmental DisordersDown syndrome and intellectual disability research

Cited by 261

Intraneuronal Aβ42 accumulation in Down syndrome brain: Original Articles

Mori, C., Spooner, E. T., Wisniewski, K. E., Wisniewski, T. M., Yamaguchi, H., Saido, T. C., Tolan, D. R., Selkoe, D. J., & Lemere, C. A. (2002) · Amyloid

Alzheimer's disease research and treatmentsDown syndrome and intellectual disability research

Cited by 255

Temporal Accrual of Complement Proteins in Amyloid Plaques in Down's Syndrome with Alzheimer's Disease

Stoltzner, S. E., Grenfell, T. J., Mori, C., Wisniewski, K. E., Wisniewski, T. M., Selkoe, D. J., & Lemere, C. A. (2000) · The American Journal of Pathology

Alzheimer's disease research and treatmentsComplement system in diseases

Cited by 187

Normal ageing in adults with Down's syndrome: a longitudinal study

Devenny, D. A., Silverman, W. P., Hill, A. L., Jenkins, E., Sersen, E. A., & Wisniewski, K. E. (1996) · Journal of Intellectual Disability Research

Down syndrome and intellectual disability researchDementia and Cognitive Impairment Research

Cited by 171

Deposition of apolipoproteins E and J in senile plaques is topographically determined in both Alzheimer's disease and Down's syndrome brain

Kida, E., Choi-Miura, N.-H., & Wisniewski, K. E. (1995) · Brain Research

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 79

Molecular screening of Batten disease: identification of a missense mutation (E295K) in the CLN3 gene

Zhong, N., Wisniewski, K. E., Kaczmarski, A. L., Ju, W., Xu, W. M., Xu, W. W., Mclendon, L., Liu, B., Kaczmarski, W., Brooks, S. S., et al. (1998) · Human Genetics

Lysosomal Storage Disorders ResearchMetabolism and Genetic Disorders

Cited by 34