Inge A Meijer

Inge A Meijer

UNVERIFIED PROFILE

Are you Inge A Meijer?   Register this Author

Register author
Inge A Meijer

Inge A Meijer

Publications by authors named "Inge A Meijer"

Are you Inge A Meijer?   Register this Author

17Publications

387Reads

9Profile Views

The Twists of Pediatric Dystonia: Phenomenology, Classification, and Genetics.

Semin Pediatr Neurol 2018 04 8;25:65-74. Epub 2018 Feb 8.

Department of Neurology, Washington University School of Medicine, Saint Louis, MO. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.spen.2018.02.001DOI Listing
April 2018

Finger extension weakness and downbeat nystagmus motor neuron disease syndrome: A novel motor neuron disorder?

Muscle Nerve 2017 Dec 15;56(6):1164-1168. Epub 2017 May 15.

Department of Neurology, University Hospitals Leuven, Campus Gasthuisberg, Herestraat 49, 3000, Leuven, Belgium.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/mus.25669DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5656559PMC
December 2017

Deep Brain Stimulation in an Additional Patient With ADCY5-Related Movement Disorder.

J Child Neurol 2017 03 5;32(4):438-439. Epub 2016 Dec 5.

Mirken Department of Neurology, Mount Sinai Beth Israel, New York, NY, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1177/0883073816681353DOI Listing
March 2017

The genetic landscape of infantile spasms.

Hum Mol Genet 2014 Sep 29;23(18):4846-58. Epub 2014 Apr 29.

Department of Pediatrics and Department of Neurosciences, Université de Montréal, Montréal, QC, Canada, CHU Ste-Justine Research Center, Montréal, QC, Canada,

View Article

Download full-text PDF

Source
https://academic.oup.com/hmg/article-lookup/doi/10.1093/hmg/
Publisher Site
http://dx.doi.org/10.1093/hmg/ddu199DOI Listing
September 2014

VAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland families.

Am J Hum Genet 2012 Sep;91(3):548-52

The Centre of Excellence in Neurosciences, Centre Hospitalier de l'Université de Montréal Research Center, Université de Montréal, Montréal, QC H2L 2W5, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ajhg.2012.07.018DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3511983PMC
September 2012

A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy.

Arch Neurol 2008 Nov;65(11):1496-501

Centre of Excellence in Neuromics, Centre Hospitalier de l'Université de Montreal and Ste-Justine Hospital, Montreal, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneur.65.11.1496DOI Listing
November 2008

A stop codon mutation in SCN9A causes lack of pain sensation.

Hum Mol Genet 2007 Sep 27;16(17):2114-21. Epub 2007 Jun 27.

Department of Molecular Sciences, AstraZeneca R&D Montréal, Ville-St-Laurent, Quebec, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddm160DOI Listing
September 2007

Characterization of a novel SPG3A deletion in a French-Canadian family.

Ann Neurol 2007 Jun;61(6):599-603

Center for the Study of Brain Diseases, Centre Hospitalier de l'Université de Montréal Research Center-Notre-Dame Hospital, University of Montreal, Québec, Canada.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ana.21114
Publisher Site
http://dx.doi.org/10.1002/ana.21114DOI Listing
June 2007

SPG4 founder effect in French Canadians with hereditary spastic paraplegia.

Can J Neurol Sci 2007 May;34(2):211-4

Center for the Study of Brain Diseases, CHUM Research Center, Notre-Dame Hospital, Montreal, QC, Canada.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1017/s0317167100006065DOI Listing
May 2007

A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1-10q24.1.

Ann Neurol 2004 Oct;56(4):579-82

Centre for Research in Neuroscience and McGill University Health Centre Research Institute, Montreal, Quebec, Canada.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ana.20239
Publisher Site
http://dx.doi.org/10.1002/ana.20239DOI Listing
October 2004

Spectrum of SPG4 mutations in a large collection of North American families with hereditary spastic paraplegia.

Arch Neurol 2002 Feb;59(2):281-6

Centre for Research in Neuroscience, The Montreal General Hospital Research Institute, 1650 Cedar Ave, Room L7-224, Montreal, Quebec, Canada H3G 1A4.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1001/archneur.59.2.281DOI Listing
February 2002