(Q57770190)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21404291%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

title

Rippling is not always electrically silent in rippling muscle disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21404291%20AND%20SRC:MED&resulttype=core&format=json

Erratum: Rippling is not always electrically silent in rippling muscle disease

25 January 2020

main subject

rippling muscle disease

1 reference

based on heuristic

inferred from title

corrigendum / erratum

0 references

Erratum: Rippling is not always electrically silent in rippling muscle disease

0 references

author

Riki Matsumoto

2

1 reference

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25 January 2020

Ichizo Nishino

7

1 reference

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25 January 2020

Akio Ikeda

8

1 reference

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25 January 2020

4

Takayuki Kondo

1 reference

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25 January 2020

author name string

Takakuni Maki

1

1 reference

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25 January 2020

Nobuo Kohara

3

1 reference

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25 January 2020

Insuk Son

5

1 reference

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25 January 2020

Takahiro Mezaki

6

1 reference

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25 January 2020

Ryosuke Takahashi

9

1 reference

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25 January 2020

publication date

1 April 2011

1 reference

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25 January 2020

1 reference

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25 January 2020

volume

43

1 reference

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25 January 2020

issue

4

1 reference

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25 January 2020

page(s)

601-605

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21404291%20AND%20SRC:MED&resulttype=core&format=json

A family with dominant hereditary myotonia, muscular hypertrophy, and increased muscular irritability, distinct from myotonia congenita thomsen

25 January 2020

cites work

1 reference

Caveolin-3 is associated with the T-tubules of mature skeletal muscle fibers

21 January 2018

1 reference

Concentration of caveolin-3 at the neuromuscular junction in young and old rat skeletal muscle fibers

21 January 2018

1 reference

Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease

21 January 2018

1 reference

Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy

21 January 2018

1 reference

Benign familial disease with muscle mounding and rippling

21 January 2018

1 reference

A CAV3 microdeletion differentially affects skeletal muscle and myocardium

21 January 2018

1 reference

21 January 2018

Rippling muscle disease

1 reference

Acquired rippling muscle disease with myasthenia gravis

21 January 2018

1 reference

Rippling muscle disease may be caused by "silent" action potentials in the tubular system of skeletal muscle fibers

21 January 2018

1 reference

Phenotypic variability associated with Arg26Gln mutation in caveolin3.

21 January 2018

1 reference

Phenotypic behavior of caveolin-3 R26Q, a mutant associated with hyperCKemia, distal myopathy, and rippling muscle disease

21 January 2018

1 reference

Phenotypic behavior of caveolin-3 mutations that cause autosomal dominant limb girdle muscular dystrophy (LGMD-1C). Retention of LGMD-1C caveolin-3 mutants within the golgi complex

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MUS.21947

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21404291%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

1 reference