(Q50559968)

15 March 2018

title

Hereditary spastic paraplegia is not associated with C9ORF72 repeat expansions in a Danish cohort. (English)

1 reference

15 March 2018

hereditary spastic paraplegia

main subject

1 reference

T T Nielsen

1

1 reference

15 March 2018

K Svenstrup

series ordinal

2

1 reference

15 March 2018

M Duno

series ordinal

3

1 reference

15 March 2018

J E Nielsen

series ordinal

4

1 reference

15 March 2018

publication date

15 October 2013

1 reference

15 March 2018

published in

Spinal Cord

1 reference

15 March 2018

volume

52

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15 March 2018

issue

1

1 reference

15 March 2018

page(s)

77-79

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15 March 2018

https://scigraph.springernature.com/pub.10.1038/sc.2013.116

exact match

0 references

cites work

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Hereditary spastic paraplegia: clinico-pathologic features and emerging molecular mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis: protein misfolding diseases without amyloidosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

TDP-43 pathology in a case of hereditary spastic paraplegia with a NIPA1/SPG6 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Reduced regional cerebral blood flow in SPG4-linked hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Dystrophic neurites express C9orf72 in Alzheimer's disease brains.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Repeat expansion in C9ORF72 in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Ataxin-2 intermediate-length polyglutamine expansions are associated with increased risk for ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

ATXN2 with intermediate-length CAG/CAA repeats does not seem to be a risk factor in hereditary spastic paraplegia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Misregulated RNA processing in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Parkinson disease is not associated with C9ORF72 repeat expansions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

Hereditary spastic paraplegias: membrane traffic and the motor pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSC.2013.116

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SC.2013.116

1 reference

15 March 2018

Dimensions Publication ID

1027493725

0 references

1 reference

15 March 2018