(Q28216315)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11558787%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

review article

1 reference

title

Nemaline myopathy: a clinical study of 143 cases (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11558787%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

1 reference

1

1 reference

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11 November 2019

Nigel G Laing

7

1 reference

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11 November 2019

Alan H. Beggs

8

1 reference

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11 November 2019

Kathryn North

9

1 reference

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11 November 2019

6

S T Iannaccone

1 reference

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11 November 2019

author name string

C Schnell

2

1 reference

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11 November 2019

C D Strickland

3

1 reference

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11 November 2019

L K Shield

4

1 reference

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11 November 2019

G Morgan

5

1 reference

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11 November 2019

language of work or name

English

0 references

publication date

1 September 2001

1 reference

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11 November 2019

1 reference

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11 November 2019

volume

50

1 reference

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11 November 2019

issue

3

1 reference

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11 November 2019

page(s)

312-320

1 reference

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Nemaline myopathy: current concepts. The ENMC International Consortium and Nemaline Myopathy

11 November 2019

cites work

1 reference

Report of the 70th ENMC International Workshop: nemaline myopathy, 11-13 June 1999, Naarden, The Netherlands.

21 January 2018

1 reference

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

21 January 2018

1 reference

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

21 January 2018

1 reference

Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy

21 January 2018

1 reference

A novel nemaline myopathy in the Amish caused by a mutation in troponin T1

21 January 2018

1 reference

Nemaline myopathy. Report of four cases and review of the literature

21 January 2018

1 reference

Nemaline myopathy: histological, histochemical and ultrastructural studies

21 January 2018

1 reference

Respiratory failure in nemaline myopathy.

21 January 2018

1 reference

Neonatal nemaline myopathy presenting with multiple joint contractures

21 January 2018

1 reference

Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy

21 January 2018

1 reference

Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.1080

2 references

Consolidated OpenCitations Corpus – April 2017

2076546

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11558787%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

2076546

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

2076546