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Danielle Andrade
Danielle Andrade
Professor of Neurology, University of Toronto
Email verificata su uhn.ca
Titolo
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Anno
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
6062013
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
2742006
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
2612017
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
2272015
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
2142015
Tonic seizures: a diagnostic clue of anti-LGI1 encephalitis?
DM Andrade, P Tai, J Dalmau, R Wennberg
Neurology 76 (15), 1355-1357, 2011
1532011
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
1312008
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
1242019
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
1162015
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
902016
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
832003
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
742014
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
702014
Genetic basis in epilepsies caused by malformations of cortical development and in those with structurally normal brain
DM Andrade
Human genetics 126 (1), 173-193, 2009
692009
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
672012
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
662017
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
662014
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
622017
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
622014
Laforin is a cell membrane and endoplasmic reticulum–associated protein tyrosine phosphatase
BA Minassian, DM Andrade, L Ianzano, EJ Young, E Chan, CA Ackerley, ...
Annals of Neurology: Official Journal of the American Neurological …, 2001
622001
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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