(Q84711235)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22857851%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

title

Clinical spectrum of disease associated with ATP1A3 mutations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22857851%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

author name string

Laurie J Ozelius

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22857851%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

publication date

2 August 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22857851%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22857851%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

volume

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22857851%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22857851%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

page(s)

741-743

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22857851%20AND%20SRC:MED&resulttype=core&format=json

Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study.

9 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970185-0

7 January 2021

Alternating hemiplegia of childhood: early characteristics and evolution of a neurodevelopmental syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970185-0

7 January 2021

Evidence of a non-progressive course of alternating hemiplegia of childhood: study of a large cohort of children and adults

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970185-0

7 January 2021

The treatment and management of alternating hemiplegia of childhood

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970185-0

7 January 2021

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970185-0

7 January 2021

Milestones in dystonia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970185-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970185-0

7 January 2021

New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970185-0

7 January 2021

Na+, K+-ATPase: functions in the nervous system and involvement in neurologic disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2812%2970185-0

7 January 2021

10.1016/S1474-4422(12)70185-0

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22857851%20AND%20SRC:MED&resulttype=core&format=json

9 February 2020

1 reference