Cognitive impairment in neuromuscular disorders. (Q36424108)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16544320 AND SRC:MED&resulttype=core&format=json

18 January 2020

review article

1 reference

title

Cognitive impairment in neuromuscular disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16544320 AND SRC:MED&resulttype=core&format=json

18 January 2020

main subject

cognitive dysfunction

1 reference

based on heuristic

inferred from title

author

Maria Grazia D'Angelo

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16544320 AND SRC:MED&resulttype=core&format=json

18 January 2020

Nereo Bresolin

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16544320 AND SRC:MED&resulttype=core&format=json

18 January 2020

author name string

Maria Grazia D'Angelo

series ordinal

1

1 reference

14 August 2017

publication date

1 July 2006

1 reference

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18 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16544320 AND SRC:MED&resulttype=core&format=json

18 January 2020

volume

34

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18 January 2020

issue

1

1 reference

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18 January 2020

page(s)

16-33

1 reference

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Disturbed personality and psychosocial adjustment in myotonic dystrophy: relationship to intellectual/cognitive function and underlying affective disorder (depression).

18 January 2020

cites work

1 reference

Respiratory function in cybrid cell lines carrying European mtDNA haplogroups: implications for Leber's hereditary optic neuropathy

21 January 2018

1 reference

Cerebral abnormalities in myotonic dystrophy. Cerebral blood flow, magnetic resonance imaging, and neuropsychological tests

21 January 2018

1 reference

Decreased cerebral glucose utilization in myotonic dystrophy

21 January 2018

1 reference

Epilepsy and mental retardation in a subset of early onset 4q35-facioscapulohumeral muscular dystrophy

21 January 2018

1 reference

Elevated levels of the Kearns–Sayre syndrome mitochondrial DNA deletion in temporal cortex of Alzheimer's patients

21 January 2018

1 reference

Poor verbal working memory across intellectual level in boys with Duchenne dystrophy

21 January 2018

1 reference

Heterogeneous phenotypes of mitochondrial encephalomyopathy in a single kindred

21 January 2018

1 reference

The Neuropsychological Features of Mitochondrial Myopathies and Encephalomyopathies

21 January 2018

1 reference

Polyglucosan body disease simulating amyotrophic lateral sclerosis

21 January 2018

1 reference

Reduced cerebral blood flow and impaired visual-spatial function in proximal myotonic myopathy

21 January 2018

1 reference

Collagen VI involvement in Ullrich syndrome: a clinical, genetic, and immunohistochemical study

21 January 2018

1 reference

Cognitive dysfunction as the major presenting feature of Becker's muscular dystrophy

21 January 2018

1 reference

Neuropsychological aspects of dementia of motor neuron disease: a report of two cases

21 January 2018

1 reference

Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.

21 January 2018

1 reference

Myotonic dystrophy. The role of large triplet repeat length in the development of mental retardation.

21 January 2018

1 reference

Specific tau variants in the brains of patients with myotonic dystrophy

21 January 2018

1 reference

Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy

21 January 2018

1 reference

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

21 January 2018

1 reference

5 October 2024

https://opencitations.net/index/api/v1/citations/10.1016/0140-6736(90)92148-B

Identifiers

DOI

10.1002/MUS.20535

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16544320 AND SRC:MED&resulttype=core&format=json

18 January 2020

1 reference