Similar articles for PMID: 32381541

Year	Number of Results
1990	1
1991	1
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1998	1
2000	2
2001	1
2002	2
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2006	1
2007	2
2008	2
2009	3
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2011	9
2012	2
2013	4
2014	5
2015	5
2016	14
2017	10
2018	12
2019	9
2020	12
2021	5
2022	2

1

The Perirolandic Sign: A Unique Imaging Finding Observed in Association with Polymerase γ-Related Disorders.

Gonçalves FG, Hill B, Guo Y, Muraresku CC, McCormick E, Alves CAPF, Teixeira SR, Martin-Saavedra JS, Zolkipli-Cunningham Z, Falk MJ, Vossough A, Goldstein A, Zuccoli G. Gonçalves FG, et al. AJNR Am J Neuroradiol. 2020 May;41(5):917-922. doi: 10.3174/ajnr.A6514. Epub 2020 May 7. AJNR Am J Neuroradiol. 2020. PMID: 32381541 Free PMC article.

2

Diagnostic algorithm for children presenting with epilepsia partialis continua.

Surana S, Rossor T, Hassell J, Boyd S, D'Arco F, Aylett S, Bhate S, Carr L, Das K, DeVile C, Eltze C, Hemingway C, Kaliakatsos M, O'Callaghan F, Prabhakar P, Robinson R, Varadkar S, Helen Cross J, Hacohen Y. Surana S, et al. Epilepsia. 2020 Oct;61(10):2224-2233. doi: 10.1111/epi.16650. Epub 2020 Sep 2. Epilepsia. 2020. PMID: 32875551

3

Clinico-pathological and Molecular Spectrum of Mitochondrial Polymerase γ Mutations in a Cohort from India.

Deepha S, Govindaraj P, Sankaran BP, Chiplunkar S, Kashinkunti C, Nunia V, Nagappa M, Sinha S, Khanna T, Thangaraj K, Taly AB, Gayathri N. Deepha S, et al. J Mol Neurosci. 2021 Nov;71(11):2219-2228. doi: 10.1007/s12031-020-01765-8. Epub 2021 Jan 19. J Mol Neurosci. 2021. PMID: 33469851

4

Prospective study of POLG mutations presenting in children with intractable epilepsy: prevalence and clinical features.

Uusimaa J, Gowda V, McShane A, Smith C, Evans J, Shrier A, Narasimhan M, O'Rourke A, Rajabally Y, Hedderly T, Cowan F, Fratter C, Poulton J. Uusimaa J, et al. Epilepsia. 2013 Jun;54(6):1002-11. doi: 10.1111/epi.12115. Epub 2013 Feb 28. Epilepsia. 2013. PMID: 23448099 Free PMC article.

5

The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations.

Hikmat O, Tzoulis C, Chong WK, Chentouf L, Klingenberg C, Fratter C, Carr LJ, Prabhakar P, Kumaraguru N, Gissen P, Cross JH, Jacques TS, Taanman JW, Bindoff LA, Rahman S. Hikmat O, et al. Genet Med. 2017 Nov;19(11):1217-1225. doi: 10.1038/gim.2017.35. Epub 2017 Apr 27. Genet Med. 2017. PMID: 28471437 Free article.

6

Decreased Subcortical T2 FLAIR Signal Associated with Seizures.

Nicholson P, Abdulla S, Alshafai L, Mandell DM, Krings T. Nicholson P, et al. AJNR Am J Neuroradiol. 2020 Jan;41(1):111-114. doi: 10.3174/ajnr.A6328. Epub 2019 Dec 5. AJNR Am J Neuroradiol. 2020. PMID: 31806597 Free PMC article.

7

[Clinical and genetic characteristics of 62 children with mitochondrial epilepsy].

Han XD, Fang F, Li H, Liu ZM, Shi YQ, Wang JL, Ren XT, Ding CH, Chen CH, Li JW, Zhang WH, Deng J. Han XD, et al. Zhonghua Er Ke Za Zhi. 2019 Nov 2;57(11):844-851. doi: 10.3760/cma.j.issn.0578-1310.2019.11.006. Zhonghua Er Ke Za Zhi. 2019. PMID: 31665838 Chinese.

8

Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review.

Anagnostou ME, Ng YS, Taylor RW, McFarland R. Anagnostou ME, et al. Epilepsia. 2016 Oct;57(10):1531-1545. doi: 10.1111/epi.13508. Epub 2016 Aug 24. Epilepsia. 2016. PMID: 27554452 Free article. Review.

9

Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases.

Hikmat O, Naess K, Engvall M, Klingenberg C, Rasmussen M, Tallaksen CM, Brodtkorb E, Ostergaard E, de Coo IFM, Pias-Peleteiro L, Isohanni P, Uusimaa J, Darin N, Rahman S, Bindoff LA. Hikmat O, et al. J Inherit Metab Dis. 2020 Jul;43(4):726-736. doi: 10.1002/jimd.12211. Epub 2020 Jan 23. J Inherit Metab Dis. 2020. PMID: 32391929

10

POLG-associated ataxias can represent a substantial part of recessive and sporadic ataxias in adults.

Nuzhnyi E, Seliverstov Y, Klyushnikov S, Krylova T, Tsygankova P, Bychkov I, Zakharova E, Konovalov R, Fedin P, Abramycheva N, Illarioshkin S. Nuzhnyi E, et al. Clin Neurol Neurosurg. 2021 Feb;201:106462. doi: 10.1016/j.clineuro.2020.106462. Epub 2021 Jan 7. Clin Neurol Neurosurg. 2021. PMID: 33434755

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