Phenotypes, genotypes, and the management of paroxysmal movement disorders-Reference-Cited by-全球学者库

Phenotypes, genotypes, and the management of paroxysmal movement disorders

Published:2018-03-30 Issue:6 Volume:60 Page:559-565
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:Dev Med Child Neurol

Author:

Silveira-Moriyama Laura¹²^ORCID,Kovac Stjepana³⁴,Kurian Manju A⁵⁶,Houlden Henry⁷,Lees Andrew J¹,Walker Matthew C³,Roze Emmanuel⁸⁹,Paciorkowski Alex R¹⁰¹¹¹²¹³,Mink Jonathan W¹⁰¹¹,Warner Thomas T¹

Affiliation:

1. Department of Molecular Neuroscience; Reta Lila Weston Institute of Neurological Studies; UCL Institute of Neurology; London UK

2. Postgraduate Program in Medicine; Universidade Nove de Julho, Uninove; São Paulo Brazil

3. Department of Clinical and Experimental Epilepsy; UCL Institute of Neurology; London UK

4. Department of Neurology; University of Münster; Münster Germany

5. Developmental Neurosciences; UCL Great Ormond Street Institute of Child Health; London UK

6. Department of Neurology; Great Ormond Street Hospital; London UK

7. Department of Molecular Neuroscience; MRC Centre for Neuromuscular Diseases and Neurogenetics Laboratory; UCL Institute of Neurology; London UK

8. Brain and Spine Institute; Sorbonne University Group; UPMC University Paris; Paris

9. Department of Neurology; Pitié-Salpêtriere Hospital; Paris France

10. Department of Neurology, Neuroscience; University of Rochester Medical Center; Rochester NY USA

11. Department of Pediatrics; University of Rochester Medical Center; Rochester NY USA

12. Department of Biomedical Genetics; University of Rochester Medical Center; Rochester NY USA

13. Center for Neurotherapeutics Discovery; University of Rochester Medical Center; Rochester NY USA

Funder

Fundo de Apoio ao Ensino, à Pesquisa e Extensão, Universidade Estadual de Campinas

Reta Lila Weston Trust For Medical Research

Muscular Dystrophy Association

Medical Research Council

Wellcome Trust

Publisher

Wiley

Subject

Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/dmcn.13744/fullpdf

Reference29 articles.

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2. Paroxysmal kinesigenic choreoathetosis: from first discovery in 1892 to genetic linkage with benign familial infantile convulsions;Kato;Epilepsy Res,2006

3. Familial paroxysmal choreoathetosis: preliminary report on a hitherto undescribed clinical syndrome;Mount;Arch Neurol Psychiatry,1940

4. Paroxysmal kinesigenic choreoathetosis. An entity within the paroxysmal choreoathetosis syndrome. Description of 10 cases, including 1 autopsied;Kertesz;Neurology,1967

5. Paroxysmal dyskinesias: clinical features and classification;Demirkiran;Ann Neurol,1995

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