Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Camille K. Hunt"'
Autor:
Matthew A. White, Ziqiang Lin, Eugene Kim, Christopher M. Henstridge, Emiliano Pena Altamira, Camille K. Hunt, Ella Burchill, Isobel Callaghan, Andrea Loreto, Heledd Brown-Wright, Richard Mead, Camilla Simmons, Diana Cash, Michael P. Coleman, Jemeen Sreedharan
Publikováno v:
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-16 (2019)
Abstract Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative condition that primarily affects the motor system and shares many features with frontotemporal dementia (FTD). Evidence suggests that ALS is a ‘dying-back’ disease, with pe
Externí odkaz:
https://doaj.org/article/b35f0addc8214d21bfcb06a8a00887df
Autor:
Ahmad Al Khleifat, Joerg Ederle, Jemeen Sreedharan, Ammar Al-Chalabi, Ella Burchill, Camille K. Hunt
Publikováno v:
Hunt, C K, Al Khleifat, A, burchill, E, Ederle, J, Al-Chalabi, A & Sreedharan, J 2021, ' Does genetic anticipation occur in familial Alexander disease? ', NEUROGENETICS, vol. 22, no. 3, pp. 215-219 . https://doi.org/10.1007/s10048-021-00642-9
Neurogenetics
Neurogenetics
Alexander Disease (AxD) is a rare leukodystrophy caused by missense mutations of glial fibrillary acidic protein (GFAP). Primarily seen in infants and juveniles, it can present in adulthood. We report a family with inherited AxD in which the mother p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9789135ca5921e1a281d2c4f41dba877
https://kclpure.kcl.ac.uk/en/publications/c3a04e77-77be-4107-aaab-a7e862fc17d6
https://kclpure.kcl.ac.uk/en/publications/c3a04e77-77be-4107-aaab-a7e862fc17d6
Autor:
Ella Burchill, Diana Cash, Jemeen Sreedharan, Isobel Callaghan, Camilla Simmons, Matthew White, Heledd Brown-Wright, Andrea Loreto, Emiliano Pena Altamira, Richard J. Mead, Michael P. Coleman, Eugene Kim, Christopher M. Henstridge, Camille K. Hunt, Ziqiang Lin
Publikováno v:
Acta Neuropathologica Communications
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-16 (2019)
White, M A, Lin, Z, Kim, E, Henstridge, C M, Pena Altamira, E, Hunt, C K, Burchill, E, Callaghan, I, Loreto, A, Brown-Wright, H, Mead, R, Simmons, C, Cash, D, Coleman, M P & Sreedharan, J 2019, ' Sarm1 deletion suppresses TDP-43-linked motor neuron degeneration and cortical spine loss ', Acta Neuropathologica Communications, vol. 7, no. 1, 166, pp. 1-16 . https://doi.org/10.1186/s40478-019-0800-9
Acta Neuropathologica Communications, Vol 7, Iss 1, Pp 1-16 (2019)
White, M A, Lin, Z, Kim, E, Henstridge, C M, Pena Altamira, E, Hunt, C K, Burchill, E, Callaghan, I, Loreto, A, Brown-Wright, H, Mead, R, Simmons, C, Cash, D, Coleman, M P & Sreedharan, J 2019, ' Sarm1 deletion suppresses TDP-43-linked motor neuron degeneration and cortical spine loss ', Acta Neuropathologica Communications, vol. 7, no. 1, 166, pp. 1-16 . https://doi.org/10.1186/s40478-019-0800-9
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative condition that primarily affects the motor system and shares many features with frontotemporal dementia (FTD). Evidence suggests that ALS is a ‘dying-back’ disease, with peripheral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1b57ee5c0ca7a0b513a8510f3a29653
https://eprints.whiterose.ac.uk/153342/1/s40478-019-0800-9.pdf
https://eprints.whiterose.ac.uk/153342/1/s40478-019-0800-9.pdf