Recent advances in the genetics of the ALS-FTLD complex (Q38000119)

26 August 2017

title

Recent advances in the genetics of the ALS-FTLD complex (English)

1 reference

amyotrophic lateral sclerosis

26 August 2017

main subject

1 reference

Huw R Morris

1

1 reference

26 August 2017

Adrian J Waite

2

1 reference

26 August 2017

Nigel M Williams

3

1 reference

26 August 2017

James W Neal

4

1 reference

26 August 2017

Derek J Blake

5

1 reference

26 August 2017

publication date

1 June 2012

1 reference

Current Neurology and Neuroscience Reports

26 August 2017

published in

1 reference

26 August 2017

volume

12

1 reference

26 August 2017

issue

3

1 reference

26 August 2017

page(s)

243-250

1 reference

Presenile dementia with motor neuron disease in Japan. A new entity?

26 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Frontal lobe dementia and motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis. Morphology, distribution, and specificity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

New ubiquitin-positive intraneuronal inclusions in the extra-motor cortices in patients with amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Motor neuron disease and dementia reported among 13 members of a single family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Semantic dementia with ubiquitin-positive tau-negative inclusion bodies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Prevalence and correlates of neuropsychological deficits in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Cognitive impairment in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Prevalence and patterns of cognitive impairment in sporadic ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Recent insights into the molecular genetics of dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Genetic and clinical features of progranulin-associated frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Valosin-containing protein disease: inclusion body myopathy with Paget's disease of the bone and fronto-temporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Exome sequencing reveals VCP mutations as a cause of familial ALS

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Ubiquilin at a crossroads in protein degradation pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Ubiquilin functions in autophagy and is degraded by chaperone-mediated autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

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/10.1007/S11910-012-0268-5

Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Chromosome 9 ALS and FTD locus is probably derived from a single founder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

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/10.1007/S11910-012-0268-5

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/10.1007/S11910-012-0268-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Repeat expansion in C9ORF72 in Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

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/10.1007/S11910-012-0268-5

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

RNA-mediated neurodegeneration in repeat expansion disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007/S11910-012-0268-5

Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis

21 January 2018

1 reference

12 December 2020

Classic amyotrophic lateral sclerosis with dementia

1 reference

12 December 2020

Motor neurone disease-inclusion dementia

1 reference

12 December 2020

An emerging role for Ubiquilin 1 in regulating protein quality control system and in disease pathogenesis

1 reference

12 December 2020

10.1007/S11910-012-0268-5

Identifiers

DOI

1 reference

Dimensions Publication ID

26 August 2017

1005543934

0 references

1 reference