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Martin N Rossor

Showing results (41-50 of 177) with videos related to

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Acta Neuropathologica|August 18, 2011
Transportin1: a marker of FTLD-FUSJack Brelstaff, Tammaryn Lashley, Janice L Holton, et al.
Journal of the Neurological Sciences|July 3, 2013
A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroidsRebekah Ahmed, Rita Guerreiro, Jonathan D Rohrer, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2025
Public HealthYun-Hee Jeon, Clare Shaw, Stephen Hall, et al.
The Lancet. Neurology|January 24, 2012
Posterior cortical atrophySebastian J Crutch, Manja Lehmann, Jonathan M Schott, et al.
Trends in Neurosciences|July 24, 2013
Molecular nexopathies: a new paradigm of neurodegenerative diseaseJason D Warren, Jonathan D Rohrer, Jonathan M Schott, et al.
Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Genetic evidence for serum amyloid P component as a drug target for treatment of neurodegenerative disordersA Floriaan Schmidt, Chris Finan, Sandesh Chopade, et al.
The Lancet. Neurology|September 22, 2006
Tracking atrophy progression in familial Alzheimer's disease: a serial MRI studyBasil H Ridha, Josephine Barnes, Jonathan W Bartlett, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 3, 2011
Structural neuroanatomy of tinnitus and hyperacusis in semantic dementiaColin J Mahoney, Jonathan D Rohrer, Johanna C Goll, et al.
JAMA Neurology|December 4, 2018
Aphasic Binary Reversals in Patients With Neurological Disease as a Barrier to Clinical Decision MakingHarri Sivasathiaseelan, Charles R Marshall, Chris J D Hardy, et al.
Dementia and Geriatric Cognitive Disorders|August 10, 2005
A volumetric magnetic resonance imaging study of the amygdala in frontotemporal lobar degeneration and Alzheimer's diseaseJennifer L Whitwell, Elizabeth L Sampson, Hilary C Watt, et al.
Pageof 18

Showing results (41-50 of 177) with videos related to

Sort By:
Pageof 18
Acta Neuropathologica|August 18, 2011
Transportin1: a marker of FTLD-FUSJack Brelstaff, Tammaryn Lashley, Janice L Holton, et al.
Journal of the Neurological Sciences|July 3, 2013
A novel A781V mutation in the CSF1R gene causes hereditary diffuse leucoencephalopathy with axonal spheroidsRebekah Ahmed, Rita Guerreiro, Jonathan D Rohrer, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 23, 2025
Public HealthYun-Hee Jeon, Clare Shaw, Stephen Hall, et al.
The Lancet. Neurology|January 24, 2012
Posterior cortical atrophySebastian J Crutch, Manja Lehmann, Jonathan M Schott, et al.
Trends in Neurosciences|July 24, 2013
Molecular nexopathies: a new paradigm of neurodegenerative diseaseJason D Warren, Jonathan D Rohrer, Jonathan M Schott, et al.
Medrxiv : the Preprint Server for Health Sciences|August 30, 2023
Genetic evidence for serum amyloid P component as a drug target for treatment of neurodegenerative disordersA Floriaan Schmidt, Chris Finan, Sandesh Chopade, et al.
The Lancet. Neurology|September 22, 2006
Tracking atrophy progression in familial Alzheimer's disease: a serial MRI studyBasil H Ridha, Josephine Barnes, Jonathan W Bartlett, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 3, 2011
Structural neuroanatomy of tinnitus and hyperacusis in semantic dementiaColin J Mahoney, Jonathan D Rohrer, Johanna C Goll, et al.
JAMA Neurology|December 4, 2018
Aphasic Binary Reversals in Patients With Neurological Disease as a Barrier to Clinical Decision MakingHarri Sivasathiaseelan, Charles R Marshall, Chris J D Hardy, et al.
Dementia and Geriatric Cognitive Disorders|August 10, 2005
A volumetric magnetic resonance imaging study of the amygdala in frontotemporal lobar degeneration and Alzheimer's diseaseJennifer L Whitwell, Elizabeth L Sampson, Hilary C Watt, et al.
Pageof 18