Lista de obras -

18F-florbetapir PET in patients with frontotemporal dementia and Alzheimer disease.

artículo científico publicado en 2015

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

artículo científico publicado en 2011

Analysis of optineurin in frontotemporal lobar degeneration.

artículo científico publicado en 2010

Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease

artículo científico publicado en 2012

Apolipoprotein E epsilon4 allele frequency and age at onset of Alzheimer's disease

artículo científico publicado en 2006

Behavior in Huntington's disease: dissociating cognition-based and mood-based changes

artículo científico publicado en 2002

Behaviour in amyotrophic lateral sclerosis

artículo científico publicado en 2008

CHMP2B mutations are not a common cause of frontotemporal lobar degeneration

artículo científico publicado en 2006

Classification and pathology of primary progressive aphasia

artículo científico

Clinical aspects of hereditary frontotemporal dementia

artículo científico publicado en 2008

Co-Occurrence of Language and Behavioural Change in Frontotemporal Lobar Degeneration

scientific article published on May 2016

Cognitive phenotypes in Alzheimer's disease and genetic risk

artículo científico publicado en 2007

Cognitive phenotypes in Alzheimer's disease and genetic variants in ACE and IDE.

artículo científico publicado en 2011

Cognitive-behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia

artículo científico publicado en 2015

Dementia lacking distinctive histology (DLDH) revisited

scientific article published on 10 August 2006

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

artículo científico publicado en 2012

Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations

artículo científico

Distinct memory profiles in Alzheimer's disease

artículo científico publicado en 2007

Distinct patterns of olfactory impairment in Alzheimer's disease, semantic dementia, frontotemporal dementia, and corticobasal degeneration

artículo científico

Do NIA-AA criteria distinguish Alzheimer's disease from frontotemporal dementia?

artículo científico publicado en 2014

Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation

artículo científico publicado en 2004

Examining the language and behavioural profile in FTD and ALS-FTD.

artículo científico publicado en 2017

Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease

artículo científico publicado en 2014

Famous people knowledge and the right and left temporal lobes.

artículo científico publicado en 2012

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

artículo científico

Frontal lobe dementia, motor neuron disease, and clinical and neuropathological criteria

artículo científico publicado en 2013

Frontotemporal dementia

artículo científico publicado en 2005

Frontotemporal dementia

artículo científico publicado en 2002

Frontotemporal dementia with amyotrophic lateral sclerosis: a clinical comparison of patients with and without repeat expansions in C9orf72.

artículo científico publicado en 2013

Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis

artículo científico publicado en 2011

Frontotemporal lobar degeneration: clinical and pathological relationships

artículo científico publicado en 2007

Glucocerebrosidase mutations in diffuse Lewy body disease

artículo científico publicado en 2011

Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer's disease pathology and is independent of tau, Aβ and TDP-43 pathology

artículo científico publicado en 2011

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

artículo científico publicado en 2006

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation

artículo científico

History of a suspected delirium is more common in dementia with Lewy bodies than Alzheimer's disease: a retrospective study.

artículo científico publicado en 2013

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

artículo científico publicado en 2006

Pathological correlates of frontotemporal lobar degeneration in the elderly

artículo científico publicado en 2010

Personal experience and arithmetic meaning in semantic dementia

artículo científico

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.

artículo científico publicado en 2007

Plasma levels of progranulin and interleukin-6 in frontotemporal lobar degeneration

artículo científico publicado en 2014

Progressive anomia revisited: focal degeneration associated with progranulin gene mutation

artículo científico publicado en 2007

Progressive anomia with preserved oral spelling and automatic speech

artículo científico publicado en 2003

Progressive aphasia presenting with deep dyslexia and dysgraphia

artículo científico publicado en 2012

Psychosis associated with expansions in the C9orf72 gene: the influence of a 10 base pair gene deletion

artículo científico publicado en 2015

Psychosis, C9ORF72 and dementia with Lewy bodies

artículo científico publicado en 2012

Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degeneration.

artículo científico publicado en 2009

Relearning of verbal labels in semantic dementia

artículo científico

Semantic Corticobasal Dementia: Challenging Nosology in Frontotemporal Lobe Degeneration

artículo científico

Semantic dementia and the left and right temporal lobes

artículo científico publicado en 2017

Semantic dementia, progressive non-fluent aphasia and their association with amyotrophic lateral sclerosis

artículo científico publicado en 2017

Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia

artículo científico publicado en 2013

TDP-43 gene analysis in frontotemporal lobar degeneration

article

TDP-43 in ubiquitinated inclusions in the inferior olives in frontotemporal lobar degeneration and in other neurodegenerative diseases: a degenerative process distinct from normal ageing

artículo científico publicado en 2009

TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: association with age, hippocampal sclerosis and clinical phenotype

artículo científico publicado en 2011

TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer's disease and frontotemporal lobar degeneration

artículo científico publicado en 2008

The Effect of tau genotype on clinical features in FTDP-17

article

The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships.

artículo científico

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

artículo científico

Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration

artículo científico publicado en 2009

Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.

artículo científico publicado en 2007

Understanding quantity in semantic dementia

artículo científico publicado en 2010

Variability in cognitive presentation of Alzheimer's disease.

artículo científico publicado en 2007

Working memory, attention, and executive function in Alzheimer's disease and frontotemporal dementia

artículo científico publicado en 2010

p62/SQSTM1 analysis in frontotemporal lobar degeneration

artículo científico publicado en 2014

Lista de obras de

18F-florbetapir PET in patients with frontotemporal dementia and Alzheimer disease.

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

Analysis of optineurin in frontotemporal lobar degeneration.

Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease

Apolipoprotein E epsilon4 allele frequency and age at onset of Alzheimer's disease

Behavior in Huntington's disease: dissociating cognition-based and mood-based changes

Behaviour in amyotrophic lateral sclerosis

CHMP2B mutations are not a common cause of frontotemporal lobar degeneration

Classification and pathology of primary progressive aphasia

Clinical aspects of hereditary frontotemporal dementia

Co-Occurrence of Language and Behavioural Change in Frontotemporal Lobar Degeneration

Cognitive phenotypes in Alzheimer's disease and genetic risk

Cognitive phenotypes in Alzheimer's disease and genetic variants in ACE and IDE.

Cognitive-behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia

Dementia lacking distinctive histology (DLDH) revisited

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations

Distinct memory profiles in Alzheimer's disease

Distinct patterns of olfactory impairment in Alzheimer's disease, semantic dementia, frontotemporal dementia, and corticobasal degeneration

Do NIA-AA criteria distinguish Alzheimer's disease from frontotemporal dementia?

Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation

Examining the language and behavioural profile in FTD and ALS-FTD.

Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease

Famous people knowledge and the right and left temporal lobes.

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

Frontal lobe dementia, motor neuron disease, and clinical and neuropathological criteria

Frontotemporal dementia

Frontotemporal dementia

Frontotemporal dementia with amyotrophic lateral sclerosis: a clinical comparison of patients with and without repeat expansions in C9orf72.

Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis

Frontotemporal lobar degeneration: clinical and pathological relationships

Glucocerebrosidase mutations in diffuse Lewy body disease

Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer's disease pathology and is independent of tau, Aβ and TDP-43 pathology

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation

History of a suspected delirium is more common in dementia with Lewy bodies than Alzheimer's disease: a retrospective study.

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Pathological correlates of frontotemporal lobar degeneration in the elderly

Personal experience and arithmetic meaning in semantic dementia

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.

Plasma levels of progranulin and interleukin-6 in frontotemporal lobar degeneration

Progressive anomia revisited: focal degeneration associated with progranulin gene mutation

Progressive anomia with preserved oral spelling and automatic speech

Progressive aphasia presenting with deep dyslexia and dysgraphia

Psychosis associated with expansions in the C9orf72 gene: the influence of a 10 base pair gene deletion

Psychosis, C9ORF72 and dementia with Lewy bodies

Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degeneration.

Relearning of verbal labels in semantic dementia

Semantic Corticobasal Dementia: Challenging Nosology in Frontotemporal Lobe Degeneration

Semantic dementia and the left and right temporal lobes

Semantic dementia, progressive non-fluent aphasia and their association with amyotrophic lateral sclerosis

Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia

TDP-43 gene analysis in frontotemporal lobar degeneration

TDP-43 in ubiquitinated inclusions in the inferior olives in frontotemporal lobar degeneration and in other neurodegenerative diseases: a degenerative process distinct from normal ageing

TDP-43 pathological changes in early onset familial and sporadic Alzheimer's disease, late onset Alzheimer's disease and Down's syndrome: association with age, hippocampal sclerosis and clinical phenotype

TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer's disease and frontotemporal lobar degeneration

The Effect of tau genotype on clinical features in FTDP-17

The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships.

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

Ubiquitin associated protein 1 is a risk factor for frontotemporal lobar degeneration

Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.

Understanding quantity in semantic dementia

Variability in cognitive presentation of Alzheimer's disease.

Working memory, attention, and executive function in Alzheimer's disease and frontotemporal dementia

p62/SQSTM1 analysis in frontotemporal lobar degeneration