Relapsing encephalopathy with cerebellar ataxia related to an ATP1A3 mutation

Publisher： John Wiley & Sons Inc

E-ISSN： 1469-8749|57|12|1183-1186

ISSN： 0012-1622

Source： DEVELOPMENTAL MEDICINE & CHILD NEUROLOGY, Vol.57, Iss.12, 2015-12, pp. : 1183-1186

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

The multiple faces of the ATP1A3‐related dystonic movement disorder

By  

MOVEMENT DISORDERS, Vol. 28, Iss. 10, 2013-09 ,pp. : 1457-1459

John Wiley & Sons Inc

Access to resources Recommend Favorite

Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 2, 2015-02 ,pp. : 284-286

John Wiley & Sons Inc

Access to resources Recommend Favorite

Treatable causes of cerebellar ataxia

By  

MOVEMENT DISORDERS, Vol. 30, Iss. 5, 2015-04 ,pp. : 614-623

John Wiley & Sons Inc

Access to resources Recommend Favorite

Mutagen sensitivity of human lymphoblastoid cells with a BRCA1 mutation in comparison to ataxia telangiectasia heterozygote cells

By  

Cytogenetic and Genome Research, Vol. 91, Iss. 1-4, 2001-01 ,pp. : 261-266

Karger

Access to resources Recommend Favorite

New ATP‐binding cassette A3 mutation causing surfactant metabolism dysfunction pulmonary type 3

By  

PEDIATRICS INTERNATIONAL, Vol. 57, Iss. 5, 2015-10 ,pp. : 970-974

John Wiley & Sons Inc

Access to resources Recommend Favorite