(Q41885438)

13 October 2017

Sensory and motor neuronopathy in a patient with the A382P TDP-43 mutation (English)

1 reference

13 October 2017

4

Guy A Rouleau

1 reference

13 October 2017

Christelle Créac'h

5

0 references

Philippe Convers

object named as

Philippe Convers

6

0 references

author name string

Jean-Philippe Camdessanché

1

1 reference

13 October 2017

Véronique V Belzil

2

1 reference

13 October 2017

Guillemette Jousserand

3

1 reference

13 October 2017

Jean-Christophe Antoine

7

1 reference

13 October 2017

language of work or name

1 reference

5 February 2011

1 reference

Orphanet Journal of Rare Diseases

13 October 2017

1 reference

13 October 2017

6

1 reference

13 October 2017

4

1 reference

Transgenic rat model of neurodegeneration caused by mutation in the TDP gene.

13 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

A method and server for predicting damaging missense mutations

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

ALS motor phenotype heterogeneity, focality, and spread: deconstructing motor neuron degeneration

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

TDP-43 localizes in mRNA transcription and processing sites in mammalian neurons

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

The pattern and diagnostic criteria of sensory neuronopathy: a case-control study

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

Rethinking ALS: the FUS about TDP-43.

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

Anti-Hu-associated paraneoplastic encephalomyelitis: analysis of 200 patients

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

Predicting deleterious amino acid substitutions

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

Pathology of roots, spinal cord and brainstem in syringomyelia-like syndrome of Tangier disease

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

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

5 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

TDP-43 neuropathology is similar in sporadic amyotrophic lateral sclerosis with or without TDP-43 mutations.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

Facial onset sensory and motor neuronopathy (FOSMN syndrome): a novel syndrome in neurology

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3042904

Clinical and magnetic resonance imaging findings in chronic sensory ganglionopathies

18 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21294910

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Neurophysiological diagnosis of acquired sensory ganglionopathies

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21294910

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21294910

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1750-1172-6-4

1 reference

Dimensions Publication ID

13 October 2017

0 references

1 reference

13 October 2017

PubMed publication ID

21294910

1 reference