Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality (Q43739867)

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English	Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality	scientific article

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scholarly article

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Europe PubMed Central

26 November 2017

Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality (English)

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Europe PubMed Central

26 November 2017

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amyotrophic lateral sclerosis

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Russell McLaughlin

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Europe PubMed Central

26 November 2017

Andrew J. Fagan

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Europe PubMed Central

26 November 2017

Niall P. Pender

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Europe PubMed Central

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Europe PubMed Central

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object named as

Harald Hampel

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Europe PubMed Central

26 November 2017

object named as

Susan Byrne

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object named as

Peter Bede

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Europe PubMed Central

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object named as

Marwa Elamin

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Europe PubMed Central

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object named as

Norah Jordan

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Europe PubMed Central

26 November 2017

Catherine Lynch

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object named as

Catherine Lynch

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Europe PubMed Central

26 November 2017

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object named as

Arun Bokde

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Europe PubMed Central

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author name string

Laura Gallagher

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language of work or name

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publication date

20 October 2012

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26 November 2017

Journal of Neurology, Neurosurgery and Psychiatry

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Europe PubMed Central

26 November 2017

84

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Europe PubMed Central

26 November 2017

766-773

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Europe PubMed Central

26 November 2017

7

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Europe PubMed Central

26 November 2017

The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. BDNF ALS Study Group (Phase III).

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https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Progression in ALS is not linear but is curvilinear.

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https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Progression rate of ALSFRS-R at time of diagnosis predicts survival time in ALS.

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https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

SOMATIC MOTOR AND SENSORY REPRESENTATION IN THE CEREBRAL CORTEX OF MAN AS STUDIED BY ELECTRICAL STIMULATION

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https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Pattern of spread and prognosis in lower limb-onset ALS.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Upper and extra-motoneuron involvement in early motoneuron disease: a diffusion tensor imaging study

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Volumetric analysis reveals corticospinal tract degeneration and extramotor involvement in ALS.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Differential corticospinal tract degeneration in homozygous 'D90A' SOD-1 ALS and sporadic ALS.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Presymptomatic spinal cord neurometabolic findings in SOD1-positive people at risk for familial ALS.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Distinct cerebral lesions in sporadic and 'D90A' SOD1 ALS: studies with [11C]flumazenil PET.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Detection of motor cortex thinning and corticospinal tract involvement by quantitative MRI in amyotrophic lateral sclerosis

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https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Structural MRI reveals cortical thinning in amyotrophic lateral sclerosis

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https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Motor network degeneration in amyotrophic lateral sclerosis: a structural and functional connectivity study

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Global brain atrophy and corticospinal tract alterations in ALS, as investigated by voxel-based morphometry of 3-D MRI.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Voxel-based morphometry study of brain volumetry and diffusivity in amyotrophic lateral sclerosis patients with mild disability.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Widespread sensorimotor and frontal cortical atrophy in Amyotrophic Lateral Sclerosis

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Corpus callosum involvement is a consistent feature of amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Diffusion tensor imaging and voxel based morphometry study in amyotrophic lateral sclerosis: relationships with motor disability

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Frontotemporal white matter changes in amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Impaired action knowledge in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Establishing subtypes of the continuum of frontal lobe impairment in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Epidemiology and clinical features of amyotrophic lateral sclerosis in Ireland between 1995 and 2004.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Frontal lobe dysfunction in amyotrophic lateral sclerosis. A PET study.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Voxel-based morphometry–the methods

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Advances in functional and structural MR image analysis and implementation as FSL

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Nonparametric permutation tests for functional neuroimaging: a primer with examples

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

The diagnostic pathway and prognosis in bulbar-onset amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Cognitive functions and white matter tract damage in amyotrophic lateral sclerosis: a diffusion tensor tractography study.

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Neurodevelopmental and neurodegenerative diseases - is there a pathophysiological link? Attention-deficit/hyperactivity disorder and amyotrophic lateral sclerosis as examples

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Sensorimotor Functional Connectivity Changes in Amyotrophic Lateral Sclerosis

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Excellent inter‐rater, intra‐rater, and telephone‐administered reliability of the ALSFRS‐R in a multicenter clinical trial

1 reference

https://api.crossref.org/works/10.1136%2FJNNP-2012-302674

21 January 2018

Identifiers

10.1136/JNNP-2012-302674

1 reference

Europe PubMed Central

26 November 2017

1 reference

Europe PubMed Central

26 November 2017

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