Publications by authors named "Inge Meijer"

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Surgical Complications of Deep Brain Stimulation in Children Across Targets and Indications: Multicenter Analysis of the CHILD-DBS Registry.
Arjun Balachandar, Leonard H Verhey, Karim Mithani, Hrishikesh Suresh, Elizabeth N Kerr, Inge A Meijer

Neurology· November 2025

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Paroxysmal Dyskinesia with a Novel Variant in the Histone 3 Family 3B (H3-3B) Gene.
Gianluca D'Onofrio, Sebastien Perreault, Grant Mitchell, Inge A Meijer

Mov Disord Clin Pract· July 2025

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Clinical course, imaging, and pathological features of 45 adult and pediatric cases of myelin oligodendrocyte glycoprotein antibody-associated disease.
Hayet Boudjani, Giulia Fadda, Gabrielle Dufort, Jack Antel, Paul Giacomini, Inge Meijer

Mult Scler Relat Disord· August 2023

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Transcriptome-wide association study reveals increased neuronal FLT3 expression is associated with Tourette's syndrome.
Calwing Liao, Veikko Vuokila, Hélène Catoire, Fulya Akçimen, Jay P Ross, Inge A Meijer

Commun Biol· March 2022

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Association of Essential Tremor With Novel Risk Loci: A Genome-Wide Association Study and Meta-analysis.
Calwing Liao, Charles-Etienne Castonguay, Karl Heilbron, Veikko Vuokila, Miranda Medeiros, Inge A Meijer

JAMA Neurol· February 2022

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EIF2AK2 Missense Variants Associated with Early Onset Generalized Dystonia.
Demy J S Kuipers, Wim Mandemakers, Chin-Song Lu, Simone Olgiati, Guido J Breedveld, Inge A Meijer

Ann Neurol· March 2021

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Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.
Calwing Liao, Fulya Akçimen, Monica Diez-Fairen, Gabrielle Houle, Jay P Ross, Inge A Meijer

Brain· December 2020

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TBC1D24-TLDc-related epilepsy exercise-induced dystonia: rescue by antioxidants in a disease model.
Kevin Lüthy, Davide Mei, Baptiste Fischer, Maurizio De Fusco, Jef Swerts, Inge A Meijer

Brain· August 2019

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18F-Flurodeoxyglucose positron emission tomography with computed tomography (FDG PET/CT) findings in children with encephalitis and comparison to conventional imaging.
Sophie Turpin, Patrick Martineau, Marc-André Levasseur, Inge Meijer, Jean-Claude Décarie

Eur J Nucl Med Mol Imaging· June 2019

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Recessive mutations in VPS13D cause childhood onset movement disorders.
Julie Gauthier, Inge A Meijer, Davor Lessel, Niccolò E Mencacci, Dimitri Krainc

Ann Neurol· June 2018

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The Twists of Pediatric Dystonia: Phenomenology, Classification, and Genetics.
Inge A Meijer, Toni S Pearson

Semin Pediatr Neurol· April 2018

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Finger extension weakness and downbeat nystagmus motor neuron disease syndrome: A novel motor neuron disorder?
Aline Delva, Nimish Thakore, Erik P Pioro, Koen Poesen, Rachel Saunders-Pullman, Inge A Meijer

Muscle Nerve· December 2017

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Deep Brain Stimulation in an Additional Patient With ADCY5-Related Movement Disorder.
Inge A Meijer, Joan Miravite, Brian H Kopell, Naomi Lubarr

J Child Neurol· March 2017

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The genetic landscape of infantile spasms.
Jacques L Michaud, Mathieu Lachance, Fadi F Hamdan, Lionel Carmant, Anne Lortie, Inge A Meijer

Hum Mol Genet· September 2014

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An atypical case of SCN9A mutation presenting with global motor delay and a severe pain disorder.
Inge Anita Meijer, Michel Vanasse, Sonia Nizard, Yves Robitaille, Elsa Rossignol

Muscle Nerve· January 2014

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Analysis of LMNB1 duplications in autosomal dominant leukodystrophy provides insights into duplication mechanisms and allele-specific expression.
Elisa Giorgio, Harshvardhan Rolyan, Laura Kropp, Anish Baswanth Chakka, Svetlana Yatsenko, Inge Meijer

Hum Mutat· August 2013

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VAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland families.
Cynthia V Bourassa, Inge A Meijer, Nancy D Merner, Kanwal K Grewal, Mark G Stefanelli

Am J Hum Genet· September 2012

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A novel duplication confirms the involvement of 5q23.2 in autosomal dominant leukodystrophy.
Inge A Meijer, Ana A Simoes-Lopes, Sandra Laurent, Tanya Katz, Judith St-Onge

Arch Neurol· November 2008

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CSCI/RCPSC Henry Friesen lecture: the past and the future of neurogenetics.
Guy Rouleau, Inge Meijer

Clin Invest Med· February 2008

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A stop codon mutation in SCN9A causes lack of pain sensation.
Sultan Ahmad, Leif Dahllund, Anders B Eriksson, Dennis Hellgren, Urban Karlsson, Inge A Meijer

Hum Mol Genet· September 2007

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Linkage to a known gene but no mutation identified: comprehensive reanalysis of SPG4 HSP pedigrees reveals large deletions as the sole cause.
Christian Beetz, Stephan Zuchner, Allison Ashley-Koch, Michaela Auer-Grumbach, Paula Byrne, Inge A Meijer

Hum Mutat· July 2007

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Characterization of a novel SPG3A deletion in a French-Canadian family.
Inge A Meijer, Patrick Dion, Sandra Laurent, Nicolas Dupré, Bernard Brais

Ann Neurol· June 2007

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SPG4 founder effect in French Canadians with hereditary spastic paraplegia.
Inge A Meijer, Nicolas Dupré, Bernard Brais, Patrick Cossette, Judith St-Onge

Can J Neurol Sci· May 2007

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