McColgan, Peter

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

Hensman Moss, D. J., Poulter, M., Beck, J., Hehir, J., Polke, J. M., Campbell, T., Adamson, G., Mudanohwo, E., McColgan, P., Haworth, A., et al. (2014) · Neurology

Genetic Neurodegenerative DiseasesAmyotrophic Lateral Sclerosis Research

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Cerebrospinal fluid inflammatory biomarkers reflect clinical severity in Huntington's disease

Rodrigues, F. B., Byrne, L. M., McColgan, P., Robertson, N., Tabrizi, S. J., Zetterberg, H., & Wild, E. J. (2016) · PLOS ONE

Genetic Neurodegenerative DiseasesNeuroinflammation and Neurodegeneration Mechanisms

Cited by 79

Longitudinal thalamic white and grey matter changes associated with visual hallucinations in Parkinson’s disease

Zarkali, A., McColgan, P., Leyland, L. A., Lees, A. J., & Weil, R. S. (2022) · Journal of Neurology, Neurosurgery & Psychiatry

Hallucinations in medical conditionsParkinson's Disease Mechanisms and Treatments

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