Autosomal recessive axonal neuropathy with neuromyotonia: a rare entity. (Q54747569)

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English	Autosomal recessive axonal neuropathy with neuromyotonia: a rare entity.	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

title

Autosomal recessive axonal neuropathy with neuromyotonia: a rare entity. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

main subject

axonal neuropathy

1 reference

based on heuristic

inferred from title

neuromyotonia

1 reference

based on heuristic

inferred from title

author name string

Joana Serra Caetano

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

Carmen Costa

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

Jonathan Baets

series ordinal

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

Madgalena Zimon Phd

series ordinal

4

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

Margarida Venâncio Phd

series ordinal

5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

Jorge Saraiva Phd

series ordinal

6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

Luís Negrão

series ordinal

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

Isabel Fineza

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

publication date

13 October 2013

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stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

published in

Pediatric Neurology

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stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

volume

50

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stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

issue

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

page(s)

104-107

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

Identifiers

DOI

10.1016/J.PEDIATRNEUROL.2013.08.028

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

PubMed publication ID

24131582

1 reference

stated in

Europe PubMed Central

PubMed publication ID

24131582

retrieved

3 June 2018

reference URL

http://europepmc.org/abstract/MED/24131582

ResearchGate publication ID

257888332

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