Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Jan;31(1):147-8.
doi: 10.1002/mds.26494. Epub 2015 Dec 21.

ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias

Jennifer R Friedman  1 , Aurélie Méneret  2   3 , Dong-Hui Chen  4 , Oriane Trouillard  2 , Marie Vidailhet  2   3 , Wendy H Raskind  5   6 , Emmanuel Roze  2   3
Affiliations

ADCY5 mutation carriers display pleiotropic paroxysmal day and nighttime dyskinesias

Jennifer R Friedman et al. Mov Disord. 2016 Jan.
No abstract available

Keywords: dyskinesia; dystonia; genetics; paroxysmal movement disorders; sleep.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest

None.

References

    1. Roze E, Meneret A, Vidailhet M. Paroxysmal Movement Disorders: Clinical and Genetic Features. In: LeDoux MS, editor. Movement Disorders. 2nd Edition. 2015. pp. 767–778.
    1. Waln O, Jankovic J. Paroxysmal movement disorders. Neurol Clin. 2015;33:137–152. - PubMed
    1. Demirkiran M, Jankovic J. Paroxysmal dyskinesias: clinical features and classification. Ann Neurol. 1995;38:571–579. - PubMed
    1. Chen DH, Méneret A, Friedman JR, et al. ADCY5-related dyskinesia: broader spectrum and genotype/phenotype correlations. Neurology. 2015 in press. - PMC - PubMed
    1. McWilliam CA, Ridout CK, Brown RM, McWilliam RC, Tolmie J, Brown GK. Pyruvate dehydrogenase E2 deficiency: a potentially treatable cause of episodic dystonia. Eur J Paediatr Neurol. 2010;14:349–353. - PubMed

Publication types