Similar articles for PMID: 29577824

Year	Number of Results
2001	1
2004	1
2009	1
2010	2
2011	1
2012	2
2014	4
2015	3
2016	12
2017	12
2018	20
2019	20
2020	17
2021	14
2022	9
2023	2
2024	0

1

Cavitating Leukoencephalopathy With Posterior Predominance Caused by a Deletion in the APOPT1 Gene in an Indian Boy.

Sharma S, Singh P, Fernandez-Vizarra E, Zeviani M, Van der Knaap MS, Saran RK. Sharma S, et al. J Child Neurol. 2018 May;33(6):428-431. doi: 10.1177/0883073818760875. Epub 2018 Mar 26. J Child Neurol. 2018. PMID: 29577824

2

Mutations in APOPT1, encoding a mitochondrial protein, cause cavitating leukoencephalopathy with cytochrome c oxidase deficiency.

Melchionda L, Haack TB, Hardy S, Abbink TE, Fernandez-Vizarra E, Lamantea E, Marchet S, Morandi L, Moggio M, Carrozzo R, Torraco A, Diodato D, Strom TM, Meitinger T, Tekturk P, Yapici Z, Al-Murshedi F, Stevens R, Rodenburg RJ, Lamperti C, Ardissone A, Moroni I, Uziel G, Prokisch H, Taylor RW, Bertini E, van der Knaap MS, Ghezzi D, Zeviani M. Melchionda L, et al. Am J Hum Genet. 2014 Sep 4;95(3):315-25. doi: 10.1016/j.ajhg.2014.08.003. Epub 2014 Aug 28. Am J Hum Genet. 2014. PMID: 25175347 Free PMC article.

3

Genotypic Spectrum and Natural History of Cavitating Leukoencephalopathies in Childhood.

Zhang J, Liu M, Zhang Z, Zhou L, Kong W, Jiang Y, Wang J, Xiao J, Wu Y. Zhang J, et al. Pediatr Neurol. 2019 May;94:38-47. doi: 10.1016/j.pediatrneurol.2019.01.002. Epub 2019 Jan 8. Pediatr Neurol. 2019. PMID: 30770271

4

Multifocal cavitating leukodystrophy-A distinct image in mitochondrial LYRM7 mutations.

Cherian A, Divya KP, Jose J, Thomas B. Cherian A, et al. Mult Scler Relat Disord. 2021 Jan;47:102615. doi: 10.1016/j.msard.2020.102615. Epub 2020 Nov 5. Mult Scler Relat Disord. 2021. PMID: 33189022

5

Early-Onset Mild Type Leukoencephalopathy Caused by a Homozygous EARS2 Mutation.

Taskin BD, Karalok ZS, Gurkas E, Aydin K, Aydogmus U, Ceylaner S, Karaer K, Yilmaz C, Pearl PL. Taskin BD, et al. J Child Neurol. 2016 Jun;31(7):938-41. doi: 10.1177/0883073816630087. Epub 2016 Feb 18. J Child Neurol. 2016. PMID: 26893310 Free PMC article.

6

Expanding the genotype-phenotype spectrum of ISCA2-related multiple mitochondrial dysfunction syndrome-cavitating leukoencephalopathy and prolonged survival.

Hartman TG, Yosovich K, Michaeli HG, Blumkin L, Ben-Sira L, Lev D, Lerman-Sagie T, Zerem A. Hartman TG, et al. Neurogenetics. 2020 Oct;21(4):243-249. doi: 10.1007/s10048-020-00611-8. Epub 2020 May 18. Neurogenetics. 2020. PMID: 32424628

7

LYRM7-associated mitochondrial complex III deficiency with non-cavitating leukoencephalopathy and stroke-like episodes.

Alfattal R, Alfarhan M, Algaith AM, Albash B, Elshafie RM, Alshammari A, Alahmad A, Dashti F, Alsafi R, Alsharhan H. Alfattal R, et al. Am J Med Genet A. 2023 May;191(5):1401-1411. doi: 10.1002/ajmg.a.63143. Epub 2023 Feb 9. Am J Med Genet A. 2023. PMID: 36757047

8

A novel homozygous mutation of CLCN2 in a patient with characteristic brain MRI images - A first case of CLCN2-related leukoencephalopathy in Japan.

Hoshi M, Koshimizu E, Miyatake S, Matsumoto N, Imamura A. Hoshi M, et al. Brain Dev. 2019 Jan;41(1):101-105. doi: 10.1016/j.braindev.2018.07.011. Epub 2018 Aug 1. Brain Dev. 2019. PMID: 30077506

9

LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance.

Dallabona C, Abbink TE, Carrozzo R, Torraco A, Legati A, van Berkel CG, Niceta M, Langella T, Verrigni D, Rizza T, Diodato D, Piemonte F, Lamantea E, Fang M, Zhang J, Martinelli D, Bevivino E, Dionisi-Vici C, Vanderver A, Philip SG, Kurian MA, Verma IC, Bijarnia-Mahay S, Jacinto S, Furtado F, Accorsi P, Ardissone A, Moroni I, Ferrero I, Tartaglia M, Goffrini P, Ghezzi D, van der Knaap MS, Bertini E. Dallabona C, et al. Brain. 2016 Mar;139(Pt 3):782-94. doi: 10.1093/brain/awv392. Epub 2016 Jan 29. Brain. 2016. PMID: 26912632 Free article.

10

A first CLN6 variant case of late infantile neuronal ceroid lipofuscinosis caused by a homozygous mutation in a boy from China: a case report.

Sun G, Yao F, Tian Z, Ma T, Yang Z. Sun G, et al. BMC Med Genet. 2018 Oct 1;19(1):177. doi: 10.1186/s12881-018-0690-x. BMC Med Genet. 2018. PMID: 30285654 Free PMC article.

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