Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration-Reference-Cited by-同舟云学术

Periventricular nodular heterotopia in 22q11.2 deletion and frontal lobe migration

Published:2018-09-23 Issue:11 Volume:5 Page:1314-1322
ISSN:2328-9503
Container-title:Annals of Clinical and Translational Neurology
language:en
Short-container-title:Ann Clin Transl Neurol

Author:

Rezazadeh Arezoo¹,Bercovici Eduard¹,Kiehl Tim-Rasmus²,Chow Eva W.³,Krings Timo⁴,Bassett Anne S.³⁵,Andrade Danielle M.¹⁶

Affiliation:

1. Division of Neurology; Department of Medicine; Krembil Neuroscience Centre; Toronto Western Hospital; University of Toronto; Toronto Ontario Canada

2. Department of Pathology; University Health Network; University of Toronto; Toronto Ontario Canada

3. Clinical Genetics Research Program; Centre for Addiction and Mental Health and Department of Psychiatry; Toronto Ontario Canada

4. Division of Neuroradiology; Joint Department of Medical Imaging; Toronto Western Hospital; University Health Network; University of Toronto; Toronto Canada

5. Dalglish Family 22q Clinic; Toronto General Research Institute and Department of Psychiatry; Campbell Family Mental Health Research Institute; University Health Network; Centre for Addiction and Mental Health; Toronto Ontario Canada

6. Krembil Neurosciences Epilepsy Genetics Program; Toronto Western Hospital; University of Toronto; Toronto Ontario Canada

Funder

Ontario Brain Institute

Publisher

Wiley

Subject

Neurology (clinical),General Neuroscience

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/acn3.641/fullpdf

Reference44 articles.

1. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population;Botto;Pediatrics,2003

2. Practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;J Pediatr,2011