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Items: 1 to 20 of 97

1.

Infantile-Onset Multisystem Neurologic, Endocrine, and Pancreatic Disease: Case and Review.

Le C, Prasad AN, Rupar CA, Debicki D, Andrade A, Prasad C.

Can J Neurol Sci. 2019 Jul;46(4):459-463. doi: 10.1017/cjn.2019.35. Epub 2019 May 6.

PMID:
31057140
2.

Small RNA responses of Culex mosquitoes and cell lines during acute and persistent virus infection.

Rückert C, Prasad AN, Garcia-Luna SM, Robison A, Grubaugh ND, Weger-Lucarelli J, Ebel GD.

Insect Biochem Mol Biol. 2019 Jun;109:13-23. doi: 10.1016/j.ibmb.2019.04.008. Epub 2019 Apr 5.

3.

Development of Criteria for Epilepsy Genetic Testing in Ontario, Canada.

Jain P, Andrade D, Donner E, Dyment D, Prasad AN, Goobie S, Boycott K, Lines M, Snead OC.

Can J Neurol Sci. 2019 Jan;46(1):7-13. doi: 10.1017/cjn.2018.341. Epub 2018 Nov 13. Review.

PMID:
30419982
4.

Altered activation and functional asymmetry of exner's area but not the visual word form area in a child with sudden-onset, persistent mirror writing.

Linke A, Roach-Fox E, Vriezen E, Prasad AN, Cusack R.

Neuropsychologia. 2018 Aug;117:322-331. doi: 10.1016/j.neuropsychologia.2018.05.022. Epub 2018 Jun 2.

PMID:
29870776
5.

Magnetic resonance imaging in the diagnosis of white matter signal abnormalities.

Datar R, Prasad AN, Tay KY, Rupar CA, Ohorodnyk P, Miller M, Prasad C.

Neuroradiol J. 2018 Aug;31(4):362-371. doi: 10.1177/1971400918764016. Epub 2018 Mar 8.

6.

Heterozygous De Novo UBTF Gain-of-Function Variant Is Associated with Neurodegeneration in Childhood.

Edvardson S, Nicolae CM, Agrawal PB, Mignot C, Payne K, Prasad AN, Prasad C, Sadler L, Nava C, Mullen TE, Begtrup A, Baskin B, Powis Z, Shaag A, Keren B, Moldovan GL, Elpeleg O.

Am J Hum Genet. 2017 Aug 3;101(2):267-273. doi: 10.1016/j.ajhg.2017.07.002.

7.

Inborn Errors of Metabolism and Epilepsy: Current Understanding, Diagnosis, and Treatment Approaches.

Sharma S, Prasad AN.

Int J Mol Sci. 2017 Jul 2;18(7). pii: E1384. doi: 10.3390/ijms18071384. Review.

8.

Epilepsy, birth weight and academic school readiness in Canadian children: Data from the national longitudinal study of children and youth.

Prasad AN, Corbett B.

Epilepsy Res. 2017 Feb;130:101-106. doi: 10.1016/j.eplepsyres.2017.01.003. Epub 2017 Jan 12.

PMID:
28187363
9.

Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole-exome sequencing.

Balci TB, Hartley T, Xi Y, Dyment DA, Beaulieu CL, Bernier FP, Dupuis L, Horvath GA, Mendoza-Londono R, Prasad C, Richer J, Yang XR, Armour CM, Bareke E, Fernandez BA, McMillan HJ, Lamont RE, Majewski J, Parboosingh JS, Prasad AN, Rupar CA, Schwartzentruber J, Smith AC, Tétreault M; FORGE Canada Consortium; Care4Rare Canada Consortium, Innes AM, Boycott KM.

Clin Genet. 2017 Sep;92(3):281-289. doi: 10.1111/cge.12987. Epub 2017 Mar 13.

PMID:
28170084
10.

Epilepsy and its Impact on psychosocial outcomes in Canadian children: Data from the National Longitudinal Study of Children and Youth (NLSCY).

Prasad AN, Corbett B.

Epilepsy Res. 2016 Dec;128:119-125. doi: 10.1016/j.eplepsyres.2016.10.019. Epub 2016 Nov 3.

PMID:
27835781
11.

Menkes disease: what a multidisciplinary approach can do.

Ojha R, Prasad AN.

J Multidiscip Healthc. 2016 Aug 17;9:371-85. doi: 10.2147/JMDH.S93454. eCollection 2016. Review.

13.

Genetic Drift during Systemic Arbovirus Infection of Mosquito Vectors Leads to Decreased Relative Fitness during Host Switching.

Grubaugh ND, Weger-Lucarelli J, Murrieta RA, Fauver JR, Garcia-Luna SM, Prasad AN, Black WC 4th, Ebel GD.

Cell Host Microbe. 2016 Apr 13;19(4):481-92. doi: 10.1016/j.chom.2016.03.002. Epub 2016 Mar 31.

14.

The expanding phenotype of MELAS caused by the m.3291T > C mutation in the MT-TL1 gene.

Keilland E, Rupar CA, Prasad AN, Tay KY, Downie A, Prasad C.

Mol Genet Metab Rep. 2016 Feb 22;6:64-9. doi: 10.1016/j.ymgmr.2016.02.003. eCollection 2016 Mar.

15.

Old gene, new phenotype: mutations in heparan sulfate synthesis enzyme, EXT2 leads to seizure and developmental disorder, no exostoses.

Farhan SM, Wang J, Robinson JF, Prasad AN, Rupar CA, Siu VM; FORGE Canada Consortium, Hegele RA.

J Med Genet. 2015 Oct;52(10):666-75. doi: 10.1136/jmedgenet-2015-103279. Epub 2015 Aug 5.

PMID:
26246518
16.

Vertebral Artery Dissection Causing Stroke After Trampoline Use.

Casserly CS, Lim RK, Prasad AN.

Pediatr Emerg Care. 2015 Nov;31(11):771-3. doi: 10.1097/PEC.0000000000000388.

PMID:
25875987
17.

Intravenous immunoglobulin in pediatrics: A review.

Prasad AN, Chaudhary S.

Med J Armed Forces India. 2014 Jul;70(3):277-80. doi: 10.1016/j.mjafi.2013.05.011. Epub 2013 Aug 6.

18.

Case of multiple sulfatase deficiency and ocular albinism: a diagnostic odyssey.

Prasad C, Rupar CA, Campbell C, Napier M, Ramsay D, Tay KY, Sharan S, Prasad AN.

Can J Neurol Sci. 2014 Sep;41(5):626-31. doi: 10.1017/cjn.2014.12.

PMID:
25373814
19.

Epilepsy, comorbid conditions in Canadian children: analysis of cross-sectional data from cycle 3 of the National Longitudinal Study of Children and Youth.

Prasad AN, Burneo JG, Corbett B.

Seizure. 2014 Nov;23(10):869-73. doi: 10.1016/j.seizure.2014.07.012. Epub 2014 Jul 25.

20.

Linkage analysis and exome sequencing identify a novel mutation in KCTD7 in patients with progressive myoclonus epilepsy with ataxia.

Farhan SM, Murphy LM, Robinson JF, Wang J, Siu VM, Rupar CA, Prasad AN; FORGE Canada Consortium, Hegele RA.

Epilepsia. 2014 Sep;55(9):e106-11. doi: 10.1111/epi.12730. Epub 2014 Jul 24.

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