(Q37942499)

25 August 2017

1 reference

title

Clinical phenomenology and neuroimaging correlates in ALS-FTD. (English)

1 reference

amyotrophic lateral sclerosis

25 August 2017

0 references

1 reference

inferred from title

author

Catherine Lomen-Hoerth

series ordinal

1

object named as

Catherine Lomen-Hoerth

1 reference

25 August 2017

language of work or name

1 reference

5 October 2011

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Journal of Molecular Neuroscience

25 August 2017

published in

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25 August 2017

volume

45

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25 August 2017

issue

3

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25 August 2017

page(s)

656-662

1 reference

https://scigraph.springernature.com/pub.10.1007/s12031-011-9636-x

25 August 2017

exact match

0 references

cites work

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

A prospective cohort study of neuropsychological test performance in ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

Survival in frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

Survival profiles of patients with frontotemporal dementia and motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

Are amyotrophic lateral sclerosis patients cognitively normal?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

Continuum of frontal lobe impairment in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

Cognitive change in motor neurone disease/amyotrophic lateral sclerosis (MND/ALS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

The effects of executive and behavioral dysfunction on the course of ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

Prevalence and patterns of cognitive impairment in sporadic ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

Frontotemporal dementia progresses to death faster than Alzheimer disease

21 January 2018

1 reference

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Relationship between ALS and the degree of cognitive impairment, markers of neurodegeneration and predictors for poor outcome. A prospective study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS12031-011-9636-X

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

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21971978

12 December 2020

inferred from PubMed ID database lookup

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21971978

12 December 2020

inferred from PubMed ID database lookup

A voxel-based morphometry study of patterns of brain atrophy in ALS and ALS/FTLD.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21971978

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S12031-011-9636-X

1 reference

25 August 2017

1 reference