Erick Sell
Erick Sell
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YouTube videos as a teaching tool and patient resource for infantile spasms
MJ Lim Fat, A Doja, N Barrowman, E Sell
Journal of Child Neurology 26 (7), 804-809, 2011
DNM1L-related mitochondrial fission defect presenting as refractory epilepsy
JR Vanstone, AM Smith, S McBride, T Naas, M Holcik, G Antoun, ...
European Journal of Human Genetics 24 (7), 1084-1088, 2016
Evidence for clinical, genetic and biochemical variability in spinal muscular atrophy with progressive myoclonic epilepsy
DA Dyment, E Sell, MR Vanstone, AC Smith, D Garandeau, V Garcia, ...
Clinical genetics 86 (6), 558-563, 2014
Lumbar puncture simulation in pediatric residency training: improving procedural competence and decreasing anxiety
HJ McMillan, H Writer, KA Moreau, K Eady, E Sell, AT Lobos, J Grabowski, ...
BMC medical education 16 (1), 1-7, 2016
Autosomal recessive hereditary spastic paraplegia—clinical and genetic characteristics of a well-defined cohort
G Yoon, B Baskin, M Tarnopolsky, KM Boycott, MT Geraghty, E Sell, ...
Neurogenetics 14 (3), 181-188, 2013
Congenital microcephaly: case definition & guidelines for data collection, analysis, and presentation of safety data after maternal immunisation
M DeSilva, FM Munoz, E Sell, H Marshall, AT Kawai, A Kachikis, P Heath, ...
Vaccine 35 (48Part A), 6472, 2017
Case report of novel DYRK1A mutations in 2 individuals with syndromic intellectual disability and a review of the literature
SM Luco, D Pohl, E Sell, JD Wagner, DA Dyment, H Daoud
BMC medical genetics 17 (1), 1-8, 2016
Matchmaking facilitates the diagnosis of an autosomal‐recessive mitochondrial disease caused by biallelic mutation of the tRNA isopentenyltransferase (TRIT1) gene
KD Kernohan, DA Dyment, M Pupavac, Z Cramer, A McBride, G Bernard, ...
Human mutation 38 (5), 511-516, 2017
The impact of electronic consultation on a Canadian tertiary care pediatric specialty referral system: A prospective single-center observational study
L Lai, C Liddy, E Keely, A Afkham, J Kurzawa, N Abdeen, T Audcent, ...
PloS one 13 (1), e0190247, 2018
Public perception of tourette syndrome on YouTube
MJL Fat, E Sell, N Barrowman, A Doja
Journal of Child Neurology 27 (8), 1011-1016, 2012
Broad spectrum of neuropsychiatric phenotypes associated with white matter disease in PTEN hamartoma tumor syndrome
TB Balci, J Davila, D Lewis, A Boafo, E Sell, J Richer, SM Nikkel, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 177 …, 2018
Hashimoto encephalopathy responding to risperidone
Z Bismilla, E Sell, E Donner
Journal of child neurology 22 (7), 855-857, 2007
Central nervous system vasculitis with positive antithyroid antibodies in an adolescent boy
SL Tsai, EC Lewis, E Sell, S Whiting
Pediatric neurology 45 (3), 189-192, 2011
Demystifying vaccination-associated encephalopathy.
E Sell, BA Minassian
The Lancet. Neurology 5 (6), 465-466, 2006
Investigating the necessity of computed tomographic scans in children with headaches: a retrospective review
R Gandhi, EC Lewis, JW Evans, E Sell
Canadian Journal of Emergency Medicine 17 (2), 148-153, 2015
Chiari 1 malformation and holocord syringomyelia presenting as abrupt onset foot drop
HJ McMillan, E Sell, M Nzau, ECG Ventureyra
Child's Nervous System 27 (1), 183-186, 2011
Resonancia magnética funcional
E Sell
Medicina (Buenos Aires) 67 (6), 661-664, 2007
Miller Fisher syndrome in a toddler with influenza A (pH1N1) infection
CT Costiniuk, N Le Saux, E Sell, A Doja, T Karnauchow, P Jacob, C Hui
Journal of child neurology 26 (3), 385-388, 2011
MEG source estimation from mesio‐basal temporal areas in a child with a porencephalic cyst
K Imai, H Otsubo, E Sell, I Mohamed, A Ochi, R RamachandranNair, ...
Acta neurologica scandinavica 116 (4), 263-267, 2007
No cases of PANDAS on follow-up of patients referred to a pediatric movement disorders clinic
S Kilbertus, R Brannan, E Sell, A Doja
Frontiers in pediatrics 2, 104, 2014
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