Evaluating the prevalence of polyglutamine repeat expansions in amyotrophic lateral sclerosis. (Q35034856)

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31 January 2020

title

Evaluating the prevalence of polyglutamine repeat expansions in amyotrophic lateral sclerosis (English)

1 reference

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amyotrophic lateral sclerosis

31 January 2020

main subject

0 references

author

Yun Rose Li

2

1 reference

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31 January 2020

author name string

T Lee

1

1 reference

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31 January 2020

A Chesi

3

1 reference

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31 January 2020

M P Hart

4

1 reference

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31 January 2020

D Ramos

5

1 reference

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31 January 2020

N Jethava

6

1 reference

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31 January 2020

D Hosangadi

7

1 reference

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31 January 2020

J Epstein

8

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31 January 2020

B Hodges

9

1 reference

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31 January 2020

N M Bonini

10

1 reference

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31 January 2020

A D Gitler

11

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31 January 2020

language of work or name

English

0 references

publication date

11 May 2011

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31 January 2020

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31 January 2020

volume

76

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31 January 2020

issue

24

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page(s)

2062-2065

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

31 January 2020

cites work

1 reference

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Adapting proteostasis for disease intervention

8 July 2018

1 reference

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Progressive disruption of cellular protein folding in models of polyglutamine diseases.

8 July 2018

1 reference

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Diseases of unstable repeat expansion: mechanisms and common principles

8 July 2018

1 reference

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From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS

8 July 2018

1 reference

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A case of spinocerebellar ataxia accompanied by severe involvement of the motor neuron system

8 July 2018

1 reference

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Glutamine repeats and neurodegeneration

8 July 2018

1 reference

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A case of severe involvement of the motor neuron system accompanied with cerebellar ataxia

8 July 2018

1 reference

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Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

8 July 2018

1 reference

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Spinocerebellar ataxia type 6 with motor neuron loss: a follow-up autopsy report

8 July 2018

1 reference

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Motor neuron loss in a patient with spinocerebellar ataxia type 6: chance co-occurrence or causally related?

25 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21562248

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Androgen receptor gene polymorphisms in amyotrophic lateral sclerosis

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21562248

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Two cases of spinocerebellar ataxia accompanied by involvement of the skeletal motor neuron system and bulbar palsy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21562248

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1212/WNL.0B013E31821F4447

1 reference

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31 January 2020

1 reference

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31 January 2020

PubMed publication ID

21562248

1 reference