(Q28286980)

27 March 2017

2 references

12

A. Munchau

1 reference

Patricia de Carvalho Aguiar

27 March 2017

Patricia de Carvalho Aguiar

P. de Carvalho Aguiar

3

1 reference

27 March 2017

Andrew Green

Andrew Green

A. Green

7

0 references

William B. Dobyns

William B Dobyns

W. B. Dobyns

2

1 reference

27 March 2017

Jacek Zaremba

Jacek Zaremba

J. Zaremba

18

0 references

Rachel Saunders-Pullman

15

R. Saunders-Pullman

Rachel Saunders-Pullman

1 reference

27 March 2017

10

C. Klein

Christine Klein

1 reference

27 March 2017

13

Deborah Raymond

D. Raymond

1 reference

27 March 2017

1

Allison Brashear

A. Brashear

1 reference

27 March 2017

20

Laurie J Ozelius

L. J. Ozelius

1 reference

27 March 2017

19

Susan B Bressman

S. B. Bressman

1 reference

27 March 2017

16

Marina A J Tijssen

0 references

author name string

Michel Borg

4

0 references

C J M Frijns

5

0 references

Seema Gollamudi

6

0 references

João Guimaraes

8

0 references

Bret C Haake

9

0 references

Gurutz Linazasoro

11

0 references

David Riley

14

0 references

David Webb

17

0 references

M. Borg

4

1 reference

27 March 2017

C. J. M. Frijns

5

1 reference

27 March 2017

S. Gollamudi

6

1 reference

27 March 2017

J. Guimaraes

8

1 reference

27 March 2017

B. C. Haake

9

1 reference

27 March 2017

G. Linazasoro

11

1 reference

27 March 2017

D. Riley

14

1 reference

27 March 2017

M. A. J. Tijssen

16

1 reference

27 March 2017

D. Webb

17

1 reference

27 March 2017

language of work or name

English

0 references

publication date

March 2007

0 references

4 February 2007

1 reference

27 March 2017

1 reference

27 March 2017

volume

130

1 reference

27 March 2017

issue

Pt 3

0 references

3

1 reference

27 March 2017

page(s)

828-35

0 references

828-835

1 reference

Cerebrospinal fluid homovanillic acid levels in rapid-onset dystonia-parkinsonism

27 March 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Variable phenotype of rapid-onset dystonia-parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

PET imaging of the pre-synaptic dopamine uptake sites in rapid-onset dystonia-parkinsonism (RDP).

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Update on the genetics of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Increased risk for recurrent major depression in DYT1 dystonia mutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Genetic heterogeneity in rapid onset dystonia-parkinsonism: description of a new family

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Refined linkage to the RDP/DYT12 locus on 19q13.2 and evaluation of GRIK5 as a candidate gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Dystonia: clinical features, genetics, and treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Possible sporadic rapid-onset dystonia-parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Variable clinical expression of mutations in the P/Q-type calcium channel gene in familial hemiplegic migraine. Dutch Migraine Genetics Research Group.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Rare missense variants in ATP1A2 in families with clustering of common forms of migraine

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FBRAIN%2FAWL340

Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions

21 January 2018

1 reference

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Rapid-onset dystonia-parkinsonism: a fourth family consistent with linkage to chromosome 19q13.

21 January 2018

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Rapid-onset dystonia-parkinsonism: A clinical and genetic analysis of a new kindred

21 January 2018

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21 January 2018

Identifiers

DOI

10.1093/BRAIN/AWL340

2 references

27 March 2017

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

17282997

1 reference

Consolidated OpenCitations Corpus – April 2017