(Q48922587)

English

A novel presentation of DYT 16: acute onset in infancy and association with MRI abnormalities.

scientific article published on 18 October 2013

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

A novel presentation of DYT 16: acute onset in infancy and association with MRI abnormalities. (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

1 reference

based on heuristic

inferred from title

4

object named as

Ada Hamosh

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

5

object named as

Aylin Tekes

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

author name string

Monica E Lemmon

1

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

Bennett Lavenstein

2

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

Carolyn D Applegate

3

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

Harvey S Singer

6

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

language of work or name

0 references

publication date

18 October 2013

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

Movement Disorders

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

28

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

14

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

1937-1938

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

The monogenic primary dystonias

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25703

21 January 2018

ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25703

21 January 2018

Molecular pathways in dystonia

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25703

21 January 2018

DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25703

21 January 2018

Reversible generalized dystonia and encephalopathy from thiamine transporter 2 deficiency.

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25703

21 January 2018

Identifiers

10.1002/MDS.25703

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/24142417

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