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Felippe Borlot, MD, MSc, CSCN diplomate (EEG)
Felippe Borlot, MD, MSc, CSCN diplomate (EEG)
University of Manitoba & University of Calgary
Verified email at ucalgary.ca - Homepage
Title
Cited by
Cited by
Year
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
972017
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
952017
Epilepsy transition: Challenges of caring for adults with childhood‐onset seizures
F Borlot, JF Tellez‐Zenteno, A Allen, A Ali, OC Snead III, DM Andrade
Epilepsia 55 (10), 1659-1666, 2014
652014
Antecollis and levodopa-responsive parkinsonism are late features of Dravet syndrome
A Fasano, F Borlot, AE Lang, DM Andrade
Neurology 82 (24), 2250-2251, 2014
632014
KCNT1‐related epilepsy: An international multicenter cohort of 27 pediatric cases
F Borlot, A Abushama, N Morrison‐Levy, P Jain, K Puthenveettil Vinayan, ...
Epilepsia 61 (4), 679-692, 2020
552020
Two definite cases of sudden unexpected death in epilepsy in a family with a DEPDC5 mutation
FA Nascimento, F Borlot, P Cossette, BA Minassian, DM Andrade
Neurology: Genetics 1 (4), e28, 2015
532015
Clinical utility of multigene panel testing in adults with epilepsy and intellectual disability
F Borlot, BI de Almeida, SL Combe, DM Andrade, FM Filloux, KA Myers
Epilepsia 60 (8), 1661-1669, 2019
472019
A pilot double-blind trial using verapamil as adjuvant therapy for refractory seizures
F Borlot, RG Wither, A Ali, N Wu, F Verocai, DM Andrade
Epilepsy research 108 (9), 1642-1651, 2014
422014
Multigene panel testing in a large cohort of adults with epilepsy: diagnostic yield and clinically actionable genetic findings
D McKnight, SL Bristow, RM Truty, A Morales, M Stetler, MJ Westbrook, ...
Neurology: Genetics 8 (1), e650, 2021
372021
22q11. 2 deletion syndrome lowers seizure threshold in adult patients without epilepsy
RG Wither, F Borlot, A MacDonald, NJ Butcher, EWC Chow, AS Bassett, ...
Epilepsia 58 (6), 1095-1101, 2017
372017
Which patients with epilepsy are at risk for psychogenic nonepileptic seizures (PNES)? A multicenter case–control study
BD Wissel, AK Dwivedi, TE Gaston, FJ Rodriguez-Porcel, D Aljaafari, ...
Epilepsy & Behavior 61, 180-184, 2016
362016
Genetic testing to inform epilepsy treatment management from an international study of clinical practice
D McKnight, A Morales, KE Hatchell, SL Bristow, JL Bonkowsky, MS Perry, ...
JAMA neurology 79 (12), 1267-1276, 2022
352022
Early-onset developmental and epileptic encephalopathies of infancy: an overview of the genetic basis and clinical features
N Morrison-Levy, F Borlot, P Jain, R Whitney
Pediatric neurology 116, 85-94, 2021
352021
New insights in mucopolysaccharidosis type VI: neurological perspective
F Borlot, PR Arantes, CR Quaio, JF da Silva Franco, CM Lourenço, ...
Brain and Development 36 (7), 585-592, 2014
302014
Clinical and laboratory findings in a series of cases of infective endocarditis
CA Pereira, SC Rocio, MF Ceolin, AP Lima, F Borlot, RS Pereira, ...
J Pediatr (Rio J) 79 (5), 423-428, 2003
26*2003
MEF2C-related epilepsy: Delineating the phenotypic spectrum from a novel mutation and literature review
F Borlot, R Whitney, RD Cohn, SK Weiss
Seizure 67, 86-90, 2019
252019
Mucopolysaccharidosis type IVA: evidence of primary and secondary central nervous system involvement
F Borlot, PR Arantes, CR Quaio, JFS Franco, CM Lourenço, I Gomy, ...
American Journal of Medical Genetics Part A 164 (5), 1162-1169, 2014
222014
Acute hemorrhagic encephalomyelitis in childhood: case report and literature review
F Borlot, JA da Paz, EB Casella, MJ Marques-Dias
Journal of Pediatric Neurosciences 6 (1), 48-51, 2011
222011
PURA-Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum
KM Johannesen, E Gardella, CE Gjerulfsen, A Bayat, RPW Rouhl, ...
Neurology: Genetics 7 (6), e613, 2021
202021
Anti-N-methyl D-aspartate receptor encephalitis in childhood
F Borlot, MLF Santos, M Bandeira, PB Liberalesso, F Kok, A Löhr Jr, ...
Jornal de Pediatria 88, 275-278, 2012
202012
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Articles 1–20