Prominent phenotypic variability associated with mutations in Progranulin (Q35188858)

7 August 2017

title

Prominent phenotypic variability associated with mutations in Progranulin (English)

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7 August 2017

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7 August 2017

Stuart Pickering-Brown

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7 August 2017

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7 August 2017

Glenn E Smith

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Rosa Rademakers

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7 August 2017

Ronald C Petersen

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7 August 2017

David S Knopman

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7 August 2017

Bradley F Boeve

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7 August 2017

Neill R Graff-Radford

object named as

Neill R Graff-Radford

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7 August 2017

Keith A Josephs

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7 August 2017

Robert J Ivnik

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7 August 2017

Maria Shiung

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7 August 2017

Joseph E Parisi

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7 August 2017

Karen M Kuntz

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7 August 2017

Matt Baker

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7 August 2017

Brendan J Kelley

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7 August 2017

Wael Haidar

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7 August 2017

Thomas Krefft

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7 August 2017

Andrew R Frank

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7 August 2017

Sotirios A Parashos

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7 August 2017

Mike Hutton

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7 August 2017

Jennifer Adamson

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7 August 2017

publication date

18 October 2007

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7 August 2017

published in

Neurobiology of Aging

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7 August 2017

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7 August 2017

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7 August 2017

page(s)

739-751

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Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations

7 August 2017

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

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Characteristics of frontotemporal dementia patients with a Progranulin mutation

28 July 2018

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

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Granulin precursor gene: a sex steroid-inducible gene involved in sexual differentiation of the rat brain

28 July 2018

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28 July 2018

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Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.

28 July 2018

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Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

28 July 2018

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28 July 2018

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28 July 2018

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28 July 2018

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

28 July 2018

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

28 July 2018

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

27 September 2018

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Clinicopathologic features of frontotemporal dementia with progranulin sequence variation

27 September 2018

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A novel deletion in progranulin gene is associated with FTDP-17 and CBS.

27 September 2018

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

27 September 2018

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Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study

27 September 2018

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Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

27 September 2018

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

27 September 2018

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27 September 2018

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27 September 2018

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Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.

27 September 2018

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Frontotemporal dementia with ubiquitinated neuronal inclusions and visuospatial impairment.

27 September 2018

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Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration.

27 September 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3164546

Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia

27 September 2018

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Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

27 September 2018

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Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

27 September 2018

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Motor neuron disease-inclusion dementia presenting as cortical-basal ganglionic degeneration

27 September 2018

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A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

27 September 2018

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Clinical characteristics of a chromosome 17-linked rapidly progressive familial frontotemporal dementia

27 September 2018

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

27 September 2018

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Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation

15 November 2018

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A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

15 November 2018

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Corticobasal Degeneration and Frontotemporal Dementia Presentations in a Kindred with Nonspecific Histopathology

15 November 2018

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Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions

15 November 2018

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Frontotemporal dementia linked to chromosome 3

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12 December 2020

Frontotemporal lobar degeneration and ubiquitin immunohistochemistry

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12 December 2020

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Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations

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Dementia lacking distinctive histology (DLDH) revisited

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Identifiers

DOI

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7 August 2017

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7 August 2017

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