6-minute walk test as a measure of disease progression and fatigability in a cohort of individuals with RYR1-related myopathies. (Q55498109)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29970108%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

title

6-minute walk test as a measure of disease progression and fatigability in a cohort of individuals with RYR1-related myopathies (English)

1 reference

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4 April 2020

author

Jessica W Witherspoon

1

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4 April 2020

author name string

Ruhi P Vasavada

2

1 reference

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4 April 2020

Melissa R Waite

3

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4 April 2020

Monique Shelton

4

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4 April 2020

Irene C Chrismer

5

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4 April 2020

Paul G Wakim

6

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4 April 2020

Minal S Jain

7

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4 April 2020

Carsten G Bönnemann

8

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4 April 2020

Katherine G Meilleur

9

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4 April 2020

publication date

3 July 2018

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Orphanet Journal of Rare Diseases

4 April 2020

published in

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4 April 2020

volume

13

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4 April 2020

issue

1

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4 April 2020

page(s)

105

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Creative Commons Attribution 4.0 International

4 April 2020

copyright license

start time

3 July 2018

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Decreased variability of the 6-minute walk test by heart rate correction in patients with neuromuscular disease

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Comparison of walking performance over the first 2 minutes and the full 6 minutes of the Six-Minute Walk Test

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Six-minute walk test: reference values and prediction equation in healthy boys aged 5 to 12 years

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The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: reliability, concurrent validity, and minimal clinically important differences from a multicenter study

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Fatigue and fatigability in neurologic illnesses: proposal for a unified taxonomy

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Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy

15 July 2018

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15 July 2018

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Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalization and large areas of myofibrillar disorganization

15 July 2018

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Fatigue in neuromuscular disorders: focus on Guillain-Barré syndrome and Pompe disease

15 July 2018

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15 July 2018

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An autosomal dominant congenital myopathy with cores and rods is associated with a neomutation in the RYR1 gene encoding the skeletal muscle ryanodine receptor

15 July 2018

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Reference equations for the six-minute walk in healthy adults

15 July 2018

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15 July 2018

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Two- and 6-minute walk tests assess walking capability equally in neuromuscular diseases.

12 August 2018

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Ambulatory capacity and disease progression as measured by the 6-minute-walk-distance in Duchenne muscular dystrophy subjects on daily corticosteroids

12 August 2018

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Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

12 August 2018

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12 August 2018

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Reference values for the 6-min walk test in healthy subjects 20-50 years old.

12 August 2018

1 reference

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[The problem of fatigue in neurological disorders]

12 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/29970108

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Prevalence of congenital myopathies in a representative pediatric united states population

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/29970108

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/29970108

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S13023-018-0848-9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29970108%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

4 April 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29970108%20AND%20SRC:MED&resulttype=core&format=json

4 April 2020

PubMed publication ID

29970108

1 reference