Early neuropsychological characteristics of progranulin mutation carriers (Q44334424)

2 December 2017

Early neuropsychological characteristics of progranulin mutation carriers (English)

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2 December 2017

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11

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2 December 2017

Howard H Feldman

12

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Rosa Rademakers

8

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Rosa Rademakers

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2 December 2017

Bradley J Hallam

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2 December 2017

Claudia Jacova

2

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2 December 2017

Ging-Yuek R Hsiung

3

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2 December 2017

Dana Wittenberg

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2 December 2017

Pheth Sengdy

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2 December 2017

Phoenix Bouchard-Kerr

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2 December 2017

Penny Slack

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2 December 2017

Matthew Baker

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2 December 2017

Tiffany W Chow

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2 December 2017

Ian R Mackenzie

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2 December 2017

4 July 2014

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Journal of the International Neuropsychological Society

2 December 2017

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2 December 2017

20

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2 December 2017

7

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2 December 2017

694-703

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The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

2 December 2017

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Mild cognitive impairment as a diagnostic entity

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Distinctive neuropsychological patterns in frontotemporal dementia, semantic dementia, and Alzheimer disease

21 January 2018

2 references

https://api.crossref.org/works/10.1017%2FS1355617714000551

21 January 2018

https://api.crossref.org/works/10.1017%2FS1355617714000551

7 January 2021

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Anterior brain glucose hypometabolism predates dementia in progranulin mutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Frontal asymmetry in behavioral variant frontotemporal dementia: clinicoimaging and pathogenetic correlates

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Classification of primary progressive aphasia and its variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Mutations in progranulin (GRN) within the spectrum of clinical and pathological phenotypes of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Familial aggregation in frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Benton Controlled Oral Word Association Test: reliability and updated norms.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Mapping the progression of progranulin-associated frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Inheritance of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Sensitivity of revised diagnostic criteria for the behavioural variant of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Advanced interpretation of the Neuropsychological Assessment Battery with older adults: base rate analyses, discrepancy scores, and interpreting change.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Advanced clinical interpretation of the WAIS-IV and WMS-IV: prevalence of low scores varies by level of intelligence and years of education.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Brain magnetic resonance imaging structural changes in a pedigree of asymptomatic progranulin mutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

"Frontotemporoparietal" dementia: clinical phenotype associated with the c.709-1G>A PGRN mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Neuropsychological features of asymptomatic c.709-1G>A progranulin mutation carriers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Frontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

The neuroimaging signature of frontotemporal lobar degeneration associated with Granulin mutations: an effective connectivity study

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Mutations in progranulin gene: clinical, pathological, and ribonucleic acid expression findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Heterogeneity within a large kindred with frontotemporal dementia: A novel progranulin mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

Granulin mutation drives brain damage and reorganization from preclinical to symptomatic FTLD

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

7 January 2021

The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

7 January 2021

Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

7 January 2021

Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

7 January 2021

Substantial risk of "Accidental MCI" in healthy older adults: base rates of low memory scores in neuropsychological assessment.

1 reference

https://api.crossref.org/works/10.1017%2FS1355617714000551

7 January 2021

10.1017/S1355617714000551

Identifiers

DOI

1 reference

2 December 2017

1 reference