Gilbert DL - Search Results

1

A Novel Variant of ATP5MC3 Associated with Both Dystonia and Spastic Paraplegia.

Neilson DE, Zech M, Hufnagel RB, Slone J, Wang X, Homan S, Gutzwiller LM, Leslie EJ, Leslie ND, Xiao J, Hedera P, LeDoux MS, Gebelein B, Wilbert F, Eckenweiler M, Winkelmann J, Gilbert DL, Huang T. Neilson DE, et al. Among authors: gilbert dl. Mov Disord. 2022 Feb;37(2):375-383. doi: 10.1002/mds.28821. Epub 2021 Oct 11. Mov Disord. 2022. PMID: 34636445 Free PMC article.

2

An updated review of the long-term neurological effects of galactosemia.

Ridel KR, Leslie ND, Gilbert DL. Ridel KR, et al. Among authors: gilbert dl. Pediatr Neurol. 2005 Sep;33(3):153-61. doi: 10.1016/j.pediatrneurol.2005.02.015. Pediatr Neurol. 2005. PMID: 16087312 Review.

3

A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24-2q31.

Gilbert DL, Leslie EJ, Keddache M, Leslie ND. Gilbert DL, et al. Mov Disord. 2009 Feb 15;24(3):364-70. doi: 10.1002/mds.22363. Mov Disord. 2009. PMID: 19006192

4

Motor tics, stereotypies, and self-flagellation in primrose syndrome.

Dalal P, Leslie ND, Lindor NM, Gilbert DL, Espay AJ. Dalal P, et al. Among authors: gilbert dl. Neurology. 2010 Jul 20;75(3):284-6. doi: 10.1212/WNL.0b013e3181e8e754. Neurology. 2010. PMID: 20644156 Free PMC article. No abstract available.

5

Association of cortical disinhibition with tic, ADHD, and OCD severity in Tourette syndrome.

Gilbert DL, Bansal AS, Sethuraman G, Sallee FR, Zhang J, Lipps T, Wassermann EM. Gilbert DL, et al. Mov Disord. 2004 Apr;19(4):416-25. doi: 10.1002/mds.20044. Mov Disord. 2004. PMID: 15077239

6

Clinical and positron emission tomography findings of chorea associated with primary antiphospholipid antibody syndrome.

Wu SW, Graham B, Gelfand MJ, Gruppo RE, Dinopolous A, Gilbert DL. Wu SW, et al. Among authors: gilbert dl. Mov Disord. 2007 Sep 15;22(12):1813-5. doi: 10.1002/mds.21657. Mov Disord. 2007. PMID: 17659641

7

GNAO1-associated epileptic encephalopathy and movement disorders: c.607G>A variant represents a probable mutation hotspot with a distinct phenotype.

Arya R, Spaeth C, Gilbert DL, Leach JL, Holland KD. Arya R, et al. Among authors: gilbert dl. Epileptic Disord. 2017 Mar 1;19(1):67-75. doi: 10.1684/epd.2017.0888. Epileptic Disord. 2017. PMID: 28202424

8

An Atypical Rett Syndrome Phenotype Due to a Novel Missense Mutation in CACNA1A.

Epperson MV, Haws ME, Standridge SM, Gilbert DL. Epperson MV, et al. Among authors: gilbert dl. J Child Neurol. 2018 Mar;33(4):286-289. doi: 10.1177/0883073818754987. Epub 2018 Jan 25. J Child Neurol. 2018. PMID: 29366381 Free PMC article.

9

Ecopipam, a D1 receptor antagonist, for treatment of tourette syndrome in children: A randomized, placebo-controlled crossover study.

Gilbert DL, Murphy TK, Jankovic J, Budman CL, Black KJ, Kurlan RM, Coffman KA, McCracken JT, Juncos J, Grant JE, Chipkin RE. Gilbert DL, et al. Mov Disord. 2018 Aug;33(8):1272-1280. doi: 10.1002/mds.27457. Epub 2018 Sep 7. Mov Disord. 2018. PMID: 30192018 Clinical Trial.

10

Rapid Onset Functional Tic-Like Behaviors in Young Females During the COVID-19 Pandemic.

Pringsheim T, Ganos C, McGuire JF, Hedderly T, Woods D, Gilbert DL, Piacentini J, Dale RC, Martino D. Pringsheim T, et al. Among authors: gilbert dl. Mov Disord. 2021 Dec;36(12):2707-2713. doi: 10.1002/mds.28778. Epub 2021 Aug 31. Mov Disord. 2021. PMID: 34387394 Free PMC article. No abstract available.

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