Danielle Andrade
Danielle Andrade
Professor of Neurology, University of Toronto
Potvrđena adresa e-pošte na
Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1
GL Carvill, SB Heavin, SC Yendle, JM McMahon, BJ O'Roak, J Cook, ...
Nature genetics 45 (7), 825-830, 2013
High rate of recurrent de novo mutations in developmental and epileptic encephalopathies
FF Hamdan, CT Myers, P Cossette, P Lemay, D Spiegelman, AD Laporte, ...
The American Journal of Human Genetics 101 (5), 664-685, 2017
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
M Muona, SF Berkovic, LM Dibbens, KL Oliver, S Maljevic, MA Bayly, ...
Nature genetics 47 (1), 39-46, 2015
Long-term follow-up of patients with thalamic deep brain stimulation for epilepsy
DM Andrade, D Zumsteg, C Hamani, M Hodaie, S Sarkissian, AM Lozano, ...
Neurology 66 (10), 1571-1573, 2006
Practical guidelines for managing adults with 22q11. 2 deletion syndrome
WLA Fung, NJ Butcher, G Costain, DM Andrade, E Boot, EWC Chow, ...
Genetics in Medicine 17 (8), 599-609, 2015
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
ILAE definition of the idiopathic generalized epilepsy syndromes: position statement by the ILAE task force on nosology and definitions
E Hirsch, J French, IE Scheffer, A Bogacz, T Alsaadi, MR Sperling, ...
Epilepsia 63 (6), 1475-1499, 2022
Tonic seizures: a diagnostic clue of anti-LGI1 encephalitis?
DM Andrade, P Tai, J Dalmau, R Wennberg
Neurology 76 (15), 1355-1357, 2011
Deep brain stimulation of the anterior nucleus of the thalamus: effects of electrical stimulation on pilocarpine-induced seizures and status epilepticus
C Hamani, M Hodaie, J Chiang, M del Campo, DM Andrade, D Sherman, ...
Epilepsy research 78 (2-3), 117-123, 2008
Delineating the 15q13. 3 microdeletion phenotype: a case series and comprehensive review of the literature
C Lowther, G Costain, DJ Stavropoulos, R Melvin, CK Silversides, ...
Genetics in Medicine 17 (2), 149-157, 2015
Anterior nucleus deep brain stimulation for refractory epilepsy: insights into patterns of seizure control and efficacious target
V Krishna, NKK King, F Sammartino, I Strauss, DM Andrade, ...
Neurosurgery 78 (6), 802-811, 2016
Neonatal hypocalcemia, neonatal seizures, and intellectual disability in 22q11. 2 deletion syndrome
ENM Cheung, SR George, DM Andrade, EWC Chow, CK Silversides, ...
Genetics in Medicine 16 (1), 40-44, 2014
Epilepsy: transition from pediatric to adult care. Recommendations of the Ontario epilepsy implementation task force
DM Andrade, AS Bassett, E Bercovici, F Borlot, E Bui, P Camfield, ...
Epilepsia 58 (9), 1502-1517, 2017
Prevalence of pathogenic copy number variation in adults with pediatric-onset epilepsy and intellectual disability
F Borlot, BM Regan, AS Bassett, DJ Stavropoulos, DM Andrade
JAMA neurology 74 (11), 1301-1311, 2017
Skin biopsy in Lafora disease: genotype–phenotype correlations and diagnostic pitfalls
DM Andrade, CA Ackerley, TSC Minett, HAG Teive, S Bohlega, ...
Neurology 61 (11), 1611-1614, 2003
Prevalence of hypocalcaemia and its associated features in 22q11· 2 deletion syndrome
ENM Cheung, SR George, GA Costain, DM Andrade, EWC Chow, ...
Clinical endocrinology 81 (2), 190-196, 2014
Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) may respond to adjunctive ketogenic diet
C Steriade, DM Andrade, H Faghfoury, MA Tarnopolsky, P Tai
Pediatric neurology 50 (5), 498-502, 2014
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disability
R Law, T Dixon-Salazar, J Jerber, N Cai, AA Abbasi, MS Zaki, K Mittal, ...
The American Journal of Human Genetics 95 (6), 721-728, 2014
Response to clozapine in a clinically identifiable subtype of schizophrenia
NJ Butcher, WLA Fung, L Fitzpatrick, A Guna, DM Andrade, AE Lang, ...
The British Journal of Psychiatry 206 (6), 484-491, 2015
Dravet syndrome: Seizure control and gait in adults with different SCN1A mutations
JJ Rilstone, FM Coelho, BA Minassian, DM Andrade
Epilepsia 53 (8), 1421-1428, 2012
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