Jeremy Brown

发表

Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations

C. van Broeckhoven, J. Collinge, P. Johannsen, 2010, Human molecular genetics.

FUS pathology deﬁnes the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

P. Deyn, J. Trojanowski, M. Rossor, 2010 .

Frontotemporal Dementia, Chromosome 3-Linked

P. Johannsen, A. Isaacs, I. Holm, 2012 .

A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies

P. Lantos, M. Rossor, M. Goedert, 2000, Annals of neurology.

Familial dementia with swollen achromatic neurons and corticobasal inclusion bodies: a clinical and pathological study

P. Lantos, M. Rossor, P. Roques, 1996, Journal of the Neurological Sciences.

Tau Protein in Frontotemporal Dementia Linked to Chromosome 3 (FTD‐3)

R. Crowther, M. Spillantini, D. Yancopoulou, 2003, Journal of neuropathology and experimental neurology.

Test Your Memory (TYM) and Test Your Memory for Mild Cognitive Impairment (TYM-MCI): A Review and Update Including Results of Using the TYM Test in a General Neurology Clinic and Using a Telephone Version of the TYM Test

J. Rowe, T. Rittman, J. Wiggins, 2019, Diagnostics.

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

R. Petersen, J. Trojanowski, M. Rossor, 2010, Acta Neuropathologica.

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

Holger Hummerich, Elizabeth MC Fisher, Sebastian Brandner, 2005, Nature Genetics.

Test Your Memory (TYM test): diagnostic evaluation of patients with non-Alzheimer dementias

J. Rowe, T. Rittman, J. Wiggins, 2019, Journal of Neurology.

Self administered cognitive screening test (TYM) for detection of Alzheimer’s disease: cross sectional study

George Pengas, Philip Clatworthy, G. Pengas, 2009, BMJ : British Medical Journal.

Genetic characterization of a familial non-specific dementia originating in Jutland, Denmark

M. Palmer, J. Hardy, M. Rossor, 1993, Journal of the Neurological Sciences.

Molecular Genetic Characterisation of Frontotemporal Dementia on Chromosome 3

A. Brun, J. Collinge, E. Englund, 1999, Dementia and Geriatric Cognitive Disorders.

Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.

Nick C Fox, Colin J. Mahoney, J. Hardy, 2013, American journal of human genetics.

The use and misuse of short cognitive tests in the diagnosis of dementia

Jeremy Brown, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Familial dementia lacking specific pathological features presenting with clinical features of corticobasal degeneration

P. Lantos, M. Rossor, Jeremy Brown, 1998, Journal of neurology, neurosurgery, and psychiatry.

The Test Your Memory for Mild Cognitive Impairment (TYM-MCI)

J. Rowe, J. Wiggins, K. Dawson, 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

Genetic Characterization of a Novel Familial Dementia

J. Hardy, A. Goate, A. Brun, 1991, Annals of the New York Academy of Sciences.

TMEM106B and ApoE polymorphisms in CHMP2B-mediated frontotemporal dementia (FTD-3)

E. Budtz-Jørgensen, A. Gade, J. Collinge, 2017, Neurobiology of Aging.

Six generations of CHMP2B‐mediated Frontotemporal Dementia: Clinical features, predictive testing, progression, and survival

E. Budtz-Jørgensen, J. Collinge, P. Johannsen, 2022, Acta neurologica Scandinavica.

Changes in appetite, food preference, and eating habits in frontotemporal dementia and Alzheimer’s disease

J R Hodges, J. Hodges, A. Holland, 2002, Journal of neurology, neurosurgery, and psychiatry.

Validation of the Test Your Memory (F-TYM Test) in a French Memory Clinic Population

J. Ménard, F. Pasquier, O. Hanon, 2014, The Clinical neuropsychologist.

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

T. Crow, J. Hardy, R. Ridley, 1992, Brain : a journal of neurology.

Chromosome 3 linked frontotemporal dementia (FTD-3)

S Gydesen, J M Brown, A Brun, 2002, Neurology.

Large C9orf72 hexanucleotide repeat expansions are seen in multiple neurodegenerative syndromes and are more frequent than expected in the UK population.

Nick C Fox, Colin J. Mahoney, J. Hodges, 2013, American journal of human genetics.