(Q43447667)

23 November 2017

title

Plasma progranulin levels in cortical dementia phenotypes with asymmetric perisylvian atrophy (English)

1 reference

23 November 2017

1 reference

E Gómez-Tortosa

1

1 reference

23 November 2017

R Guerrero-López

2

1 reference

23 November 2017

E Gil-Neciga

3

1 reference

23 November 2017

E Franco

4

1 reference

23 November 2017

T del Ser

5

1 reference

23 November 2017

A Jiménez Escrig

6

1 reference

23 November 2017

J Pérez-Pérez

7

1 reference

23 November 2017

M J Sainz

8

1 reference

23 November 2017

publication date

31 May 2013

1 reference

European Journal of Neurology

23 November 2017

published in

1 reference

23 November 2017

volume

20

1 reference

23 November 2017

issue

9

1 reference

23 November 2017

page(s)

1319-1324

1 reference

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

23 November 2017

cites work

1 reference

Classification of primary progressive aphasia and its variants

21 January 2018

1 reference

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

21 January 2018

1 reference

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

21 January 2018

1 reference

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

21 January 2018

1 reference

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.

21 January 2018

1 reference

Serum biomarker for progranulin-associated frontotemporal lobar degeneration

21 January 2018

1 reference

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

21 January 2018

1 reference

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

21 January 2018

1 reference

Diagnosis and management of dementia with Lewy bodies: third report of the DLB Consortium

21 January 2018

1 reference

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

21 January 2018

1 reference

Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes

21 January 2018

1 reference

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

21 January 2018

1 reference

Novel PSEN1 and PGRN mutations in early-onset familial frontotemporal dementia

21 January 2018

1 reference

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

21 January 2018

1 reference

Pathogenic cysteine mutations affect progranulin function and production of mature granulins

21 January 2018

1 reference

Optimal plasma progranulin cutoff value for predicting null progranulin mutations in neurodegenerative diseases: a multicenter Italian study.

21 January 2018

1 reference

Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/ENE.12211

1 reference

23 November 2017

1 reference