Publications by authors named "Meyke I Schouten"

7Publications

A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene.

Parkinsonism Relat Disord 2020 Sep 12;80:98-101. Epub 2020 Sep 12.

Department of Neurology, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2020.09.016DOI Listing
September 2020

Predictive genetic testing in Huntington's disease: should a neurologist be involved?

Eur J Hum Genet 2020 Sep 13;28(9):1205-1209. Epub 2020 May 13.

Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.

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http://dx.doi.org/10.1038/s41431-020-0633-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7608370PMC
September 2020

Autosomal dominant GCH1 mutations causing spastic paraplegia at disease onset.

Parkinsonism Relat Disord 2020 05 1;74:12-15. Epub 2020 Apr 1.

Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.parkreldis.2020.03.019DOI Listing
May 2020