(Q73851194)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

title

Central core disease and congenital neuromuscular disease with uniform type 1 fibers in one family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

main subject

neuromuscular disease

1 reference

M Tojo

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

M Ozawa

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

I Nonaka

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

publication date

1 June 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

published in

Brain and Development

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

volume

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

page(s)

262-264

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

CONGENITAL NONPROGRESSIVE MYOPATHY. CENTRAL CORE DISEASE AND NEMALINE MYOPATHY IN ONE FAMILY

7 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900108-X

7 January 2021

Nonprogressive Congenital Neuromuscular Disease With Uniform Type 1 Fiber

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900108-X

7 January 2021

A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900108-X

7 January 2021

A mutation in the human ryanodine receptor gene associated with central core disease

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900108-X

7 January 2021

Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900108-X

7 January 2021

Central core disease or not? Observations on a family with a non-progressive myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900108-X

7 January 2021

Familial non-progressive myopathy with muscle cramps after exercise. A new disease associated with cores in the muscle fibres.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2800%2900108-X

7 January 2021

10.1016/S0387-7604(00)00108-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10838116%20AND%20SRC:MED&resulttype=core&format=json

7 November 2019

1 reference