(Q58293551)

6

object named as

Julie van der Zee

0 references

author name string

Catarina Chester

1

0 references

Gabriel Miltenberger

3

0 references

Sónia Pereira

4

0 references

Lubina Dillen

5

0 references

Christine van Broeckhoven

7

0 references

Alexandre de Mendonça

Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

8

0 references

publication date

29 June 2012

0 references

published in

0 references

volume

14

0 references

issue

1

0 references

page(s)

70-72

0 references

cites work

Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia.

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2012.690418

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2-21.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2012.690418

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/10.3109%2F17482968.2012.690418

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/10.3109%2F17482968.2012.690418

A C9orf72 promoter repeat expansion in a Flanders-Belgian cohort with disorders of the frontotemporal lobar degeneration-amyotrophic lateral sclerosis spectrum: a gene identification study.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2012.690418

Electrodiagnostic criteria for diagnosis of ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2012.690418

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2012.690418

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2012.690418

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2012.690418

Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2012.690418

A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F17482968.2012.690418