(Q50645413)

17 March 2018

title

Cognitive profile and MRI findings in limb-girdle muscular dystrophy 2I. (English)

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17 March 2018

limb-girdle muscular dystrophy

main subject

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2

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17 March 2018

Luca Bello

3

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17 March 2018

Giovanni Mento

4

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17 March 2018

Corrado Angelini

8

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17 March 2018

author name string

A Palmieri

1

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17 March 2018

L Lazzarini

5

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17 March 2018

C Borsato

6

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17 March 2018

L Bortolussi

7

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17 March 2018

E Pegoraro

9

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17 March 2018

publication date

4 February 2011

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17 March 2018

published in

Journal of Neurology

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17 March 2018

volume

258

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17 March 2018

issue

7

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17 March 2018

page(s)

1312-1320

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17 March 2018

Brain involvement in muscular dystrophies with defective dystroglycan glycosylation

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cysts

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Spectrum of brain changes in patients with congenital muscular dystrophy and FKRP gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

The phenotype of limb-girdle muscular dystrophy type 2I

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Clinical and molecular characterization of patients with limb-girdle muscular dystrophy type 2I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of alpha-dystroglycan

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Brain MRI abnormalities in muscular dystrophy due to FKRP mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

An Inventory for Measuring Depression

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Dementia: the estimation of premorbid intelligence levels using the New Adult Reading Test

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Construct validity of the Trail Making Test: role of task-switching, working memory, inhibition/interference control, and visuomotor abilities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Twenty years after Spinnler and Tognoni: new instruments in the Italian neuropsychologist's toolbox

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Measurement of the area of the anterior horn of the right lateral ventricle for the diagnosis of brain atrophy by CT. Correlation with several ventricular indices.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

An fMRI study of the Trail Making Test.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Using fMRI to decompose the neural processes underlying the Wisconsin Card Sorting Test

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Wisconsin Card Sorting Test synchronizes the prefrontal, temporal and posterior association cortex in different frequency ranges and extensions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Combined analysis of DTI and fMRI data reveals a joint maturation of white and grey matter in a fronto-parietal network

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-011-5930-3

Visuoconstructional problems in dementia: contribution of executive systems functions.

21 January 2018

1 reference

12 December 2020

Wisconsin Card Sorting revisited: distinct neural circuits participating in different stages of the task identified by event-related functional magnetic resonance imaging.

1 reference

12 December 2020

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C

1 reference

12 December 2020

Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy.

1 reference

12 December 2020

Muscle pathology in dysferlin deficiency

1 reference

12 December 2020

10.1007/S00415-011-5930-3

Identifiers

DOI

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17 March 2018

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17 March 2018