(Q36605219)

15 August 2017

Analysis of the C9orf72 repeat in Parkinson's disease, essential tremor and restless legs syndrome (English)

1 reference

15 August 2017

1 reference

restless legs syndrome

1 reference

1 reference

10

Ryan J Uitti

1 reference

15 August 2017

13

Zbigniew K Wszolek

1 reference

15 August 2017

14

Rosa Rademakers

1 reference

15 August 2017

15

Owen A Ross

1 reference

15 August 2017

Neill R Graff-Radford

8

object named as

Neill Graff-Radford

1 reference

15 August 2017

5

Michael G Heckman

1 reference

Alexandra I Soto-Ortolaza

15 August 2017

3

object named as

Alexandra I Soto-Ortolaza

1 reference

15 August 2017

9

Jay Van Gerpen

1 reference

15 August 2017

7

Audrey Strongosky

1 reference

15 August 2017

6

Sharleen Traynor

1 reference

15 August 2017

2

Sruti Rayaprolu

1 reference

15 August 2017

12

Siong-Chi Lin

1 reference

15 August 2017

Mariely Dejesus-Hernandez

1

1 reference

15 August 2017

Nicola J Rutherford

4

1 reference

15 August 2017

Jerry J Shih

11

1 reference

15 August 2017

18 October 2012

1 reference

Parkinsonism and Related Disorders

15 August 2017

4

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

15 August 2017

19

1 reference

15 August 2017

2

1 reference

15 August 2017

198-201

1 reference

Length of normal alleles of C9ORF72 GGGGCC repeat do not influence disease phenotype

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

Large C9orf72 repeat expansions are not a common cause of Parkinson's disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

Angiogenin variation and Parkinson disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

Repeat expansion in C9ORF72 in Alzheimer's disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

Clinical aspects of familial forms of frontotemporal dementia associated with parkinsonism

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

Ataxin-2 repeat-length variation and neurodegeneration

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

Roles of trinucleotide-repeat RNA in neurological disease and degeneration.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

RNA-mediated neurodegeneration in repeat expansion disorders

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3570692

10.1016/J.PARKRELDIS.2012.09.013

20 September 2018

Identifiers

DOI

1 reference

15 August 2017

1 reference

15 August 2017

PubMed publication ID

23084342

1 reference