Campbell C - Search Results

1

Twinkle-Associated Mitochondrial DNA Depletion.

Remtulla S, Emilie Nguyen CT, Prasad C, Campbell C. Remtulla S, et al. Among authors: campbell c. Pediatr Neurol. 2019 Jan;90:61-65. doi: 10.1016/j.pediatrneurol.2018.08.007. Epub 2018 Aug 9. Pediatr Neurol. 2019. PMID: 30391088

2

9 year old girl with progressive weakness.

Seemann N, Campbell C, Hammond R, Prasad C. Seemann N, et al. Among authors: campbell c. Brain Pathol. 2010 Jan;20(1):255-6. doi: 10.1111/j.1750-3639.2009.00344.x. Brain Pathol. 2010. PMID: 20438484 Free PMC article.

3

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. Prasad C, et al. Among authors: campbell c. Can J Neurol Sci. 2014 Sep;41(5):626-31. doi: 10.1017/cjn.2014.12. Can J Neurol Sci. 2014. PMID: 25373814

4

Seizures Related to Hypomagnesemia: A Case Series and Review of the Literature.

Chen BB, Prasad C, Kobrzynski M, Campbell C, Filler G. Chen BB, et al. Among authors: campbell c. Child Neurol Open. 2016 Oct 27;3:2329048X16674834. doi: 10.1177/2329048X16674834. eCollection 2016 Jan-Dec. Child Neurol Open. 2016. PMID: 28503619 Free PMC article.

5

Further delineation of TBCK - Infantile hypotonia with psychomotor retardation and characteristic facies type 3.

Zapata-Aldana E, Kim DD, Remtulla S, Prasad C, Nguyen CT, Campbell C. Zapata-Aldana E, et al. Among authors: campbell c. Eur J Med Genet. 2019 Apr;62(4):273-277. doi: 10.1016/j.ejmg.2018.08.004. Epub 2018 Aug 11. Eur J Med Genet. 2019. PMID: 30103036 Review.

6

Clinical and technical assessment of MedExome vs. NGS panels in patients with suspected genetic disorders in Southwestern Ontario.

Aref-Eshghi E, Kerkhof J, Carere DA, Volodarsky M, Bhai P, Colaiacovo S, Saleh M, Caudle M, Karp N, Prasad C, Balci T, Lin H, Campbell C, Siu VM, Sadikovic B. Aref-Eshghi E, et al. Among authors: campbell c. J Hum Genet. 2021 May;66(5):451-464. doi: 10.1038/s10038-020-00860-3. Epub 2020 Oct 23. J Hum Genet. 2021. PMID: 33093641

7

Acute Flaccid Paralysis, Seizures, and Encephalopathy in a Pediatric Patient With Influenza A and Coronavirus Disease 2019 Infection.

Sloof N, Hue CD, Campbell C, Barton MA, Nouri MN. Sloof N, et al. Among authors: campbell c. Pediatr Neurol. 2024 Mar;152:127-129. doi: 10.1016/j.pediatrneurol.2023.12.024. Epub 2024 Jan 1. Pediatr Neurol. 2024. PMID: 38262228 No abstract available.

8

Resting State and Diffusion Neuroimaging Predictors of Clinical Improvements Following Constraint-Induced Movement Therapy in Children With Hemiplegic Cerebral Palsy.

Manning KY, Fehlings D, Mesterman R, Gorter JW, Switzer L, Campbell C, Menon RS. Manning KY, et al. Among authors: campbell c. J Child Neurol. 2015 Oct;30(11):1507-14. doi: 10.1177/0883073815572686. Epub 2015 Mar 11. J Child Neurol. 2015. PMID: 25762587

9

Factors Associated With Health-Related Quality of Life in Children With Duchenne Muscular Dystrophy.

Wei Y, Speechley KN, Zou G, Campbell C. Wei Y, et al. Among authors: campbell c. J Child Neurol. 2016 Jun;31(7):879-86. doi: 10.1177/0883073815627879. Epub 2016 Feb 10. J Child Neurol. 2016. PMID: 26863997

10

Drisapersen associated with elevated serum factor VIII levels in Duchenne muscular dystrophy.

McMillan HJ, Amid A, Gonorazky H, Almobarak S, Campbell C. McMillan HJ, et al. Among authors: campbell c. Neurology. 2020 Mar 24;94(12):538-540. doi: 10.1212/WNL.0000000000009139. Epub 2020 Feb 19. Neurology. 2020. PMID: 32075891 No abstract available.

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