Danielle M Andrade

Danielle M Andrade

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Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability.

Epilepsia 2019 Aug 5;60(8):1661-1669. Epub 2019 Jul 5.

Research Institute of the McGill University Health Centre, Montreal, Québec, Canada.

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http://dx.doi.org/10.1111/epi.16273DOI Listing
August 2019

Cerebral Corticoarterial Malformations : A Case Series of Unilateral Polymicrogyria and Ipsilateral Arterial Dysplasia.

Clin Neuroradiol 2019 Aug 8. Epub 2019 Aug 8.

Department of Medical Imaging, University of Toronto, 263 McCaul Street, 4th floor, M5T 1W7, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1007/s00062-019-00824-xDOI Listing
August 2019

STXBP1 encephalopathy is associated with awake bruxism.

Epilepsy Behav 2019 Mar 14;92:121-124. Epub 2019 Jan 14.

Krembil Neurosciences Epilepsy Genetics Program, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada; Division of Neurology, Department of Medicine, Toronto Western Hospital, Krembil Neuroscience Centre, University of Toronto, Toronto, Ontario, Canada. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S15255050183095
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http://dx.doi.org/10.1016/j.yebeh.2018.12.018DOI Listing
March 2019

Schizophrenia is a later-onset feature of PCDH19 Girls Clustering Epilepsy.

Epilepsia 2019 Mar 3;60(3):429-440. Epub 2019 Mar 3.

Division of Neurology, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.

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http://doi.wiley.com/10.1111/epi.14678
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http://dx.doi.org/10.1111/epi.14678DOI Listing
March 2019

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

Ann Clin Transl Neurol 2018 Nov 23;5(11):1314-1322. Epub 2018 Sep 23.

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

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http://doi.wiley.com/10.1002/acn3.641
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http://dx.doi.org/10.1002/acn3.641DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6243376PMC
November 2018

Unilateral abdominal clonic seizures of parietal lobe origin: EEG findings.

Epileptic Disord 2018 Apr;20(2):158-163

Division of Neurology, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1684/epd.2018.0966DOI Listing
April 2018

Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.

JAMA Neurol 2017 11;74(11):1301-1311

Epilepsy Genetics Program, Toronto Western Hospital, Krembil Neuroscience Centre, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1001/jamaneurol.2017.1775DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5710585PMC
November 2017

High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

Authors:
Fadi F Hamdan Candace T Myers Patrick Cossette Philippe Lemay Dan Spiegelman Alexandre Dionne Laporte Christina Nassif Ousmane Diallo Jean Monlong Maxime Cadieux-Dion Sylvia Dobrzeniecka Caroline Meloche Kyle Retterer Megan T Cho Jill A Rosenfeld Weimin Bi Christine Massicotte Marguerite Miguet Ledia Brunga Brigid M Regan Kelly Mo Cory Tam Amy Schneider Georgie Hollingsworth David R FitzPatrick Alan Donaldson Natalie Canham Edward Blair Bronwyn Kerr Andrew E Fry Rhys H Thomas Joss Shelagh Jane A Hurst Helen Brittain Moira Blyth Robert Roger Lebel Erica H Gerkes Laura Davis-Keppen Quinn Stein Wendy K Chung Sara J Dorison Paul J Benke Emily Fassi Nicole Corsten-Janssen Erik-Jan Kamsteeg Frederic T Mau-Them Ange-Line Bruel Alain Verloes Katrin Õunap Monica H Wojcik Dara V F Albert Sunita Venkateswaran Tyson Ware Dean Jones Yu-Chi Liu Shekeeb S Mohammad Peyman Bizargity Carlos A Bacino Vincenzo Leuzzi Simone Martinelli Bruno Dallapiccola Marco Tartaglia Lubov Blumkin Klaas J Wierenga Gabriela Purcarin James J O'Byrne Sylvia Stockler Anna Lehman Boris Keren Marie-Christine Nougues Cyril Mignot Stéphane Auvin Caroline Nava Susan M Hiatt Martina Bebin Yunru Shao Fernando Scaglia Seema R Lalani Richard E Frye Imad T Jarjour Stéphanie Jacques Renee-Myriam Boucher Emilie Riou Myriam Srour Lionel Carmant Anne Lortie Philippe Major Paola Diadori François Dubeau Guy D'Anjou Guillaume Bourque Samuel F Berkovic Lynette G Sadleir Philippe M Campeau Zoha Kibar Ronald G Lafrenière Simon L Girard Saadet Mercimek-Mahmutoglu Cyrus Boelman Guy A Rouleau Ingrid E Scheffer Heather C Mefford Danielle M Andrade Elsa Rossignol Berge A Minassian Jacques L Michaud

Am J Hum Genet 2017 Nov;101(5):664-685

Centre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, QC H3T1C5, Canada; Department of Neurosciences, Université de Montréal, Montreal, QC H3T1J4, Canada; Department of Pediatrics, Université de Montréal, Montreal, QC H3T1C5, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2017.09.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5673604PMC
November 2017

22q11.2 deletion syndrome lowers seizure threshold in adult patients without epilepsy.

Epilepsia 2017 06 27;58(6):1095-1101. Epub 2017 Apr 27.

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

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http://dx.doi.org/10.1111/epi.13748DOI Listing
June 2017

Genetic generalized epilepsy in three siblings with 8q21.13-q22.2 duplication.

Seizure 2017 May 11;48:57-61. Epub 2017 Apr 11.

Division of Neurology, Epilepsy Genetics Program, Krembil Neuroscience Centre, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.seizure.2017.04.004DOI Listing
May 2017

Treatment issues for children with epilepsy transitioning to adult care.

Epilepsy Behav 2017 04 8;69:153-160. Epub 2017 Feb 8.

Dalhousie University & IWK Health Center, Dalhousie University, Halifax, NS, Canada.

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http://dx.doi.org/10.1016/j.yebeh.2016.11.008DOI Listing
April 2017

Adult motor phenotype differentiates Dravet syndrome from Lennox-Gastaut syndrome and links SCN1A to early onset parkinsonian features.

Epilepsia 2017 03 10;58(3):e44-e48. Epub 2017 Feb 10.

Division of Neurology, Krembil Neuroscience Centre, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1111/epi.13692DOI Listing
March 2017

Myoclonus epilepsy and ataxia due to potassium channel mutation (MEAK) is caused by heterozygous KCNC1 mutations.

Epileptic Disord 2016 Sep;18(S2):135-138

Division of Neurology, Department of Medicine, University of Toronto Adult Epilepsy Genetics Program, University of Toronto, Toronto Western Hospital, Toronto, Canada.

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http://dx.doi.org/10.1684/epd.2016.0859DOI Listing
September 2016

Progressive myoclonus epilepsy associated with SACS gene mutations.

Neurol Genet 2016 Aug 23;2(4):e83. Epub 2016 Jun 23.

Division of Neurology (F.A.N., D.M.A.), Epilepsy Genetics Program, Krembil Neuroscience Centre, Toronto Western Hospital, University of Toronto, Ontario, Canada; Department of Neurophysiopathology (L.C., S.F.), Epilepsy Center, C. Besta Neurological Institute IRCCS Foundation, Milan, Italy; Department of Neurology (D.A.), King Fahad Hospital of University, University of Dammam, Saudi Arabia; Folkhälsan Institute of Genetics (M.M., A.-E.L.), Helsinki, Finland; Research Programs Unit (M.M., A.-E.L.), Molecular Neurology and Neuroscience Center, Institute for Molecular Medicine Finland (M.M.), University of Helsinki, Finland; and Epilepsy Research Center (S.F.B.), Department of Medicine, University of Melbourne, Heidelberg, Victoria, Australia.

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http://dx.doi.org/10.1212/NXG.0000000000000083DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4936476PMC
August 2016

Epilepsy Transition: Let's start planting the seed.

Eur J Paediatr Neurol 2016 07 19;20(4):684-5. Epub 2016 Apr 19.

Division of Neurology, Epilepsy Genetics Program, Toronto Western Hospital & Division of Neurology, Hospital for Sick Children (SickKids), University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1016/j.ejpn.2016.04.006DOI Listing
July 2016

Anterior Nucleus Deep Brain Stimulation for Refractory Epilepsy: Insights Into Patterns of Seizure Control and Efficacious Target.

Neurosurgery 2016 Jun;78(6):802-11

‡Division of Neurosurgery, ¶Department of Neurology, University of Toronto, Toronto Western Hospital, Toronto, Ontario, Canada; §Department of Neurosurgery, Tel Aviv Medical Center, Tel Aviv University, Tel Aviv, Israel.

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http://dx.doi.org/10.1227/NEU.0000000000001197DOI Listing
June 2016

Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability.

Psychiatr Genet 2016 Apr;26(2):66-73

aMolecular Neuropsychiatry and Development Lab, The Centre for Addiction & Mental Health (CAMH), The Campbell Family Brain Research Institute bDepartment of Pediatrics, Division of Clinical and Metabolic Genetics, The Hospital for Sick Children cDepartment of Medicine, Division of Neurology dDepartment of Psychiatry eInstitute of Medical Science, University of Toronto fKrembil Neuroscience Centre, Toronto Western Research Institute, Toronto gDepartment of Psychiatry, Division of Developmental Disabilities, Queen's University, Kingston, Ontario, Canada hAtta-ur-Rehman School of Applied Biosciences (ASAB), National University of Sciences and Technology (NUST), Islamabad, Pakistan.

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http://dx.doi.org/10.1097/YPG.0000000000000114DOI Listing
April 2016

Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation.

Neurol Genet 2015 Dec 15;1(4):e28. Epub 2015 Oct 15.

Division of Neurology (F.A.N., F.B., D.M.A.), Epilepsy Genetics Program, Krembil Neuroscience Centre, Toronto Western Hospital, University of Toronto, Ontario, Canada; CHUM Research Center (P.C.), University of Montreal, Quebec, Canada; and Division of Neurology (B.A.M., D.M.A.), Program in Genetics and Genome Biology, The Hospital for Sick Children, University of Toronto, Ontario, Canada.

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http://dx.doi.org/10.1212/NXG.0000000000000028DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4811380PMC
December 2015

GRIN1 polymorphisms do not affect susceptibility or phenotype in NMDA receptor encephalitis.

Neurol Neuroimmunol Neuroinflamm 2015 Oct 24;2(5):e153. Epub 2015 Sep 24.

Department of Medicine (G.S.D., D.M.A.), Division of Neurology, and Dalla Lana School of Public Health (A.D.P.), University of Toronto, Ontario, Canada; Department of Neurology, Charité-Universitätsmedizin Berlin, and German Center for Neurodegenerative Diseases (DZNE) (H.P.), Berlin, Germany; Department of Rheumatology, Alberta Children's Hospital, and Research Institute (S.M.B.), University of Calgary, Alberta, Canada; The Centre for Applied Genomics (T.A.P., A.D.P.), The Hospital for Sick Children, Toronto, Ontario, Canada; and University Health Network (D.M.A.), Toronto Western Hospital, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1212/NXI.0000000000000153DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4582904PMC
October 2015

Whole-Genome Sequencing Suggests Schizophrenia Risk Mechanisms in Humans with 22q11.2 Deletion Syndrome.

G3 (Bethesda) 2015 Sep 16;5(11):2453-61. Epub 2015 Sep 16.

Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada Department of Psychiatry University of Toronto, Ontario, M5T 1R8 Canada, University of Toronto, Toronto, Ontario, Canada Department of Psychiatry, and Toronto General Research Institute, University Health Network, Toronto, Ontario, Canada Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, M5S 2S1 Canada The Dalglish Family Hearts and Minds Clinic for 22q11.2 Deletion Syndrome, Toronto General Hospital, University Health Network, Toronto, Ontario, M5G 2C4 Canada

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http://dx.doi.org/10.1534/g3.115.021345DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632064PMC
September 2015

Practical guidelines for managing adults with 22q11.2 deletion syndrome.

Genet Med 2015 Aug 8;17(8):599-609. Epub 2015 Jan 8.

1] The Dalglish Family Hearts and Minds Clinic for 22q11.2 Deletion Syndrome, Toronto General Hospital, University Health Network, Toronto, Ontario, Canada [2] Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada [3] Department of Psychiatry and Toronto General Research Institute, University Health Network, Toronto, Ontario, Canada [4] Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada [5] Institute of Medical Science, University of Toronto, Toronto, Ontario, Canada [6] Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada [7] Division of Cardiology, Department of Medicine, University Health Network, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1038/gim.2014.175DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4526275PMC
August 2015

Response to clozapine in a clinically identifiable subtype of schizophrenia.

Br J Psychiatry 2015 Jun 5;206(6):484-91. Epub 2015 Mar 5.

Nancy J. Butcher, MSc, Clinical Genetics Research Program, Centre for Addiction and Mental Health and Institute of Medical Science, University of Toronto, Toronto; Wai Lun Alan Fung, MD, ScD, FRCPC, Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto General Research Institute, University Health Network, Toronto, The Dalglish Family Hearts and Minds Clinic for Adults with 22q11.2 Deletion Syndrome and Department of Psychiatry, University Health Network and Department of Psychiatry, University of Toronto, Toronto; Laura Fitzpatrick, Alina Guna, BSc, Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto; Danielle M. Andrade, MD, MSc, FRCPC, Division of Neurology, Department of Medicine, University of Toronto, Toronto; Anthony E. Lang, MD, FRCPC, Institute of Medical Science, University of Toronto, Division of Neurology, Department of Medicine, University of Toronto, Tanz Centre for Research in Neurodegenerative Diseases, Department of Medicine, University of Toronto, Toronto Western Hospital Research Institute, University Health Network and Edmond J. Safra Program in Parkinson's Disease, Toronto Western Hospital, Toronto; Eva W. C. Chow, MD, MPH, FRCPC, Clinical Genetics Research Program, Centre for Addiction and Mental Health and Department of Psychiatry, University of Toronto, Toronto; Anne S. Bassett, MD, FRCPC, Clinical Genetics Research Program, Centre for Addiction and Mental Health, Institute of Medical Science, University of Toronto, Toronto General Research Institute, University Health Network, The Dalglish Family Hearts and Minds Clinic for Adults with 22q11.2 Deletion Syndrome, Department of Medicine and Department of Psychiatry, University Health Network, Department of Psychiatry, University of Toronto, Ontario, Canada.

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http://dx.doi.org/10.1192/bjp.bp.114.151837DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459828PMC
June 2015

Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome.

Am J Med Genet A 2015 Mar 13;167A(3):639-45. Epub 2015 Feb 13.

The Dalglish Family Hearts and Minds Clinic for Adults with 22q11.2 Deletion Syndrome, Toronto, Ontario, Canada; Department of Nuclear Medicine, Academic Medical Centre, Amsterdam, The Netherlands; Department of Psychiatry, University Health Network, Toronto, Ontario, Canada; Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1002/ajmg.a.36928DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459830PMC
March 2015

Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature.

Genet Med 2015 Feb 31;17(2):149-57. Epub 2014 Jul 31.

1] Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada [2] Institute of Medical Science, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada [3] Division of Cardiology, Department of Medicine, University Health Network, Toronto, Ontario, Canada [4] Department of Psychiatry, University of Toronto and University Health Network, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1038/gim.2014.83DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4464824PMC
February 2015

Dravet syndrome, lamotrigine, and personalized medicine.

Dev Med Child Neurol 2015 Feb 8;57(2):118-9. Epub 2014 Dec 8.

Toronto Western Hospital, Krembil Neuroscience Centre, Epilepsy Genetics Program, University of Toronto, Toronto, ON, Canada.

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http://dx.doi.org/10.1111/dmcn.12627DOI Listing
February 2015

A pilot double-blind trial using verapamil as adjuvant therapy for refractory seizures.

Epilepsy Res 2014 Nov 30;108(9):1642-51. Epub 2014 Aug 30.

Division of Neurology, Toronto Western Hospital, Krembil Neurosciences Center, University of Toronto, Toronto, Ontario, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.eplepsyres.2014.08.009DOI Listing
November 2014

Epilepsy transition: challenges of caring for adults with childhood-onset seizures.

Epilepsia 2014 Oct 28;55(10):1659-66. Epub 2014 Aug 28.

Division of Neurology, Epilepsy Genetics Program, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada; Division of Neurology, Hospital for Sick Children (SickKids), University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1111/epi.12752DOI Listing
October 2014

Hemimegalencephaly: what happens when children get older?

Dev Med Child Neurol 2014 Sep 5;56(9):905-9. Epub 2014 Feb 5.

Division of Neurology, Epilepsy Genetics Program, Toronto Western Hospital, Krembil Neuroscience Centre, University of Toronto, Toronto, ON, Canada.

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http://dx.doi.org/10.1111/dmcn.12390DOI Listing
September 2014

Prevalence of hypocalcaemia and its associated features in 22q11·2 deletion syndrome.

Clin Endocrinol (Oxf) 2014 Aug 27;81(2):190-6. Epub 2014 May 27.

Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, ON, Canada.

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http://doi.wiley.com/10.1111/cen.12466
Publisher Site
http://dx.doi.org/10.1111/cen.12466DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4231257PMC
August 2014

Reply from the authors.

Pediatr Neurol 2014 Aug 29;51(2):e5-6. Epub 2014 May 29.

Division of Neurology, Department of Medicine, University of Toronto, Toronto Western Hospital, Toronto, Canada.

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http://dx.doi.org/10.1016/j.pediatrneurol.2014.05.024DOI Listing
August 2014

Antecollis and levodopa-responsive parkinsonism are late features of Dravet syndrome.

Neurology 2014 Jun 21;82(24):2250-1. Epub 2014 May 21.

From Toronto Western Hospital (A.F., F.B., A.E.L., D.M.A.), University of Toronto; The Edmond J. Safra Program in Parkinson's Disease (A.F., A.E.L.), Toronto; and The Hospital for Sick Children (F.B., D.M.A.), University of Toronto, Canada.

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http://dx.doi.org/10.1212/WNL.0000000000000521DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113465PMC
June 2014

Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) may respond to adjunctive ketogenic diet.

Pediatr Neurol 2014 May 7;50(5):498-502. Epub 2014 Jan 7.

Division of Neurology, Department of Medicine, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1016/j.pediatrneurol.2014.01.009DOI Listing
May 2014

Deep brain stimulation for the management of seizures in MECP2 duplication syndrome.

Seizure 2014 May 2;23(5):405-7. Epub 2014 Feb 2.

Division of Neurology, University of Toronto, Toronto, Canada; Epilepsy Genetics Program, University of Toronto, Toronto, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.seizure.2014.01.021DOI Listing
May 2014

Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11.2 deletion syndrome.

Genet Med 2014 Jan 13;16(1):40-4. Epub 2013 Jun 13.

1] Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada [2] Dalglish Family Hearts and Minds Clinic, University Health Network, Toronto, Ontario, Canada [3] Division of Neurology, Krembil Neuroscience Centre, Epilepsy Genetics Program, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada [4] Department of Psychiatry, University of Toronto, Toronto, Ontario, Canada [5] Division of Cardiology, Department of Medicine, University Health Network, Toronto, Ontario, Canada [6] Toronto Congenital Cardiac Centre for Adults, Toronto General Hospital, Toronto, Ontario, Canada [7] Obstetric Medicine, Mount Sinai Hospital, Toronto, Ontario, Canada [8] Department of Psychiatry, University Health Network, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1038/gim.2013.71DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4459858PMC
January 2014

The multiple faces of Dravet syndrome.

Dev Med Child Neurol 2014 Jan;56(1):10-1

Division of Neurology, Toronto Western Hospital, Krembil Neurosciences Program, Lepilepsy Genetics Program, University of Toronto, Toronto, ON, Canada.

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http://dx.doi.org/10.1111/dmcn.12332DOI Listing
January 2014

Nonlesional focal epilepsy: a challenge from genes to surgery.

Can J Neurol Sci 2013 Mar;40(2):137-8

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http://dx.doi.org/10.1017/s0317167100013639DOI Listing
March 2013

A comparison of antiepileptic drug therapy in patients with severe intellectual disability and patients with normal intellect.

Epilepsy Behav 2012 Oct 30;25(2):196-9. Epub 2012 Sep 30.

Department of Medicine, University of Toronto, Canada.

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http://dx.doi.org/10.1016/j.yebeh.2012.07.029DOI Listing
October 2012

Mutation of the CLN6 gene in teenage-onset progressive myoclonus epilepsy.

Pediatr Neurol 2012 Sep;47(3):205-8

Division of Neurology, Krembil Neuroscience Centre, University of Toronto, Toronto Western Hospital, 399 Bathurst Street, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1016/j.pediatrneurol.2012.05.004DOI Listing
September 2012

Dravet syndrome: seizure control and gait in adults with different SCN1A mutations.

Epilepsia 2012 Aug 10;53(8):1421-8. Epub 2012 Jul 10.

Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.

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http://dravet.ca/wp-content/uploads/Andrade-presentation.pdf
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http://doi.wiley.com/10.1111/j.1528-1167.2012.03583.x
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http://dx.doi.org/10.1111/j.1528-1167.2012.03583.xDOI Listing
August 2012

Chromosome 1p36 in migraine with aura: association study of the 5HT(1D) locus.

Neuroreport 2012 Jan;23(1):45-8

Department of Laboratory Medicine and Pathobiology, London Health Sciences Centre, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1097/WNR.0b013e32834e5af3DOI Listing
January 2012

Tonic seizures: a diagnostic clue of anti-LGI1 encephalitis?

Neurology 2011 Apr;76(15):1355-7

Division of Neurology, Toronto Western Hospital, University of Toronto, Toronto, Canada.

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http://dx.doi.org/10.1212/WNL.0b013e3182152808DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090064PMC
April 2011

Dravet syndrome and deep brain stimulation: seizure control after 10 years of treatment.

Epilepsia 2010 Jul 16;51(7):1314-6. Epub 2009 Nov 16.

Division of Neurology, Toronto Western Hospital, Krembil Neuroscience Centre, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1111/j.1528-1167.2009.02408.xDOI Listing
July 2010

Patient awareness of seizures as documented in the epilepsy monitoring unit.

Can J Neurosci Nurs 2009 ;31(4):22-3

University of Toronto, Toronto, Ontario.

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February 2010

Seizure recurrence 29 years after hemispherectomy for Sturge Weber syndrome.

Can J Neurol Sci 2010 Jan;37(1):141-4

Division of Neurology, University of Toronto, Krembil Neuroscience Centre, Toronto Western Hospital, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1017/s0317167100009835DOI Listing
January 2010

Treatment options for epileptic myoclonus and epilepsy syndromes associated with myoclonus.

Expert Opin Pharmacother 2009 Jul;10(10):1549-60

Division of Neurology, Krembil Neuroscience Centre, University of Toronto, Toronto Western Hospital, Toronto, Canada.

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http://dx.doi.org/10.1517/14656560903025189DOI Listing
July 2009

Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain.

Hum Genet 2009 Jul 18;126(1):173-93. Epub 2009 Jun 18.

Division of Neurology, Toronto Western Hospital, Krembil Neuroscience Centre, University of Toronto, 5W-445, 399 Bathurst St., Toronto M5T 2S8, Canada.

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http://dx.doi.org/10.1007/s00439-009-0702-1DOI Listing
July 2009

Deep brain stimulation of the anterior nucleus of the thalamus: effects of electrical stimulation on pilocarpine-induced seizures and status epilepticus.

Epilepsy Res 2008 Feb 20;78(2-3):117-23. Epub 2007 Dec 20.

Division of Neurosurgery, Toronto Western Hospital and University Health Network, University of Toronto, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1016/j.eplepsyres.2007.09.010DOI Listing
February 2008

Genetics of epilepsies.

Expert Rev Neurother 2007 Jun;7(6):727-34

University of Toronto, Division of Neurology, Krembil Neuroscience Centre, Toronto Western Hospital, Toronto, Canada.

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June 2007

Protein therapy for Unverricht-Lundborg disease using cystatin B transduction by TAT-PTD. Is it that simple?

Epilepsy Res 2006 Nov 22;72(1):75-9. Epub 2006 Aug 22.

Department of Molecular and Medical Genetics, University of Toronto, Canada.

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http://dx.doi.org/10.1016/j.eplepsyres.2006.07.009DOI Listing
November 2006

Parietal lobe source localization and sensitivity to hyperventilation in a patient with subclinical rhythmic electrographic discharges of adults (SREDA).

Clin Neurophysiol 2006 Oct 23;117(10):2257-63. Epub 2006 Aug 23.

Division of Neurology, Krembil Neuroscience Centre, University of Toronto, Toronto Western Hospital, 399 Bathurst St., Toronto, Ont., Canada M5T 2S8.

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http://dx.doi.org/10.1016/j.clinph.2006.07.137DOI Listing
October 2006

Source localization of small sharp spikes: low resolution electromagnetic tomography (LORETA) reveals two distinct cortical sources.

Clin Neurophysiol 2006 Jun 27;117(6):1380-7. Epub 2006 Apr 27.

Neurology Department, Krembil Neuroscience Centre, Toronto Western Hospital, University of Toronto, 399 Bathurst Street, Toronto Ont., Canada M5T 2S8.

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June 2006

Clinical aspects of temporal/limbic epilepsy and their relationships to intractability.

Adv Neurol 2006 ;97:39-44

Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

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February 2006

Clinical electrophysiology factors indicative of intractability in patients with temporal lobe epilepsy.

Adv Neurol 2006 ;97:45-62

Department of Medicine, University of Toronto, Toronto, Ontario, Canada.

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February 2006

Atypical absences and recurrent absence status in an adult with Angelman syndrome due to the UBE3A mutation.

Epileptic Disord 2005 Sep;7(3):227-30

Department of Neurology, The Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.

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September 2005

Progressive myoclonus epilepsies: EPM1, EPM2A, EPM2B.

Adv Neurol 2005 ;95:47-57

Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Canada.

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December 2004