PubMed for id: 57462

Year	Number of Results
1999	1
2002	1
2009	2
2011	1
2012	1
2015	1
2017	2
2018	5
2019	6
2020	3
2021	2
2022	2
2023	2
2024	0

1

Fahr's disease linked to a novel mutation in MYORG variants manifesting as paroxysmal limb stiffness and dysarthria: Case report and literature review.

Zhao T, Xu S, Liu S, Xu J, Zhang X, Zhan Y. Zhao T, et al. Mol Genet Genomic Med. 2023 Dec;11(12):e2276. doi: 10.1002/mgg3.2276. Epub 2023 Sep 7. Mol Genet Genomic Med. 2023. PMID: 37680026 Free PMC article. Review.

2

Paroxysmal Kinesigenic Dyskinesia Secondary to Brain Calcification with a Homozygous MYORG Mutation.

Du J, Zhu X, Liu J, Tan Y. Du J, et al. Mov Disord. 2021 Nov;36(11):2699-2701. doi: 10.1002/mds.28720. Epub 2021 Aug 3. Mov Disord. 2021. PMID: 34346093 No abstract available.

3

MYORG gene disease-causing variants in a family with primary familial brain calcification presenting with stroke-like episodes.

Malaquias MJ, Martins RC, Oliveira J, Freixo JP, Magalhães M. Malaquias MJ, et al. Clin Genet. 2020 Nov;98(5):517-519. doi: 10.1111/cge.13836. Epub 2020 Sep 8. Clin Genet. 2020. PMID: 32896900 No abstract available.

4

MYORG Mutation Heterozygosity Is Associated With Brain Calcification.

Chen Y, Cen Z, Chen X, Wang H, Chen S, Yang D, Fu F, Wang L, Liu P, Wu H, Zheng X, Xie F, Ouyang Z, Zhang Y, Zhou Y, Huang X, Wang F, Huang G, An H, Liang Y, Hong W, Wang A, Huang S, Chen W, Yin L, Yang Y, Huang H, Zeng R, Zhao N, Jiang B, Zhang B, Luo W; Chinese PFBC Study Group. Chen Y, et al. Mov Disord. 2020 Apr;35(4):679-686. doi: 10.1002/mds.27973. Epub 2020 Jan 17. Mov Disord. 2020. PMID: 31951047

5

Primary familial brain calcification caused by MYORG mutations in an Italian family.

Taglia I, Kuipers DJS, Breedveld GJ, Mignarri A, Dotti MT, Federico A, Bonifati V. Taglia I, et al. Parkinsonism Relat Disord. 2019 Oct;67:24-26. doi: 10.1016/j.parkreldis.2019.09.021. Epub 2019 Sep 17. Parkinsonism Relat Disord. 2019. PMID: 31621601 No abstract available.

6

Biallelic MYORG mutation carriers exhibit primary brain calcification with a distinct phenotype.

Grangeon L, Wallon D, Charbonnier C, Quenez O, Richard AC, Rousseau S, Budowski C, Lebouvier T, Corbille AG, Vidailhet M, Méneret A, Roze E, Anheim M, Tranchant C, Favrole P, Antoine JC, Defebvre L, Ayrignac X, Labauge P, Pariente J, Clanet M, Maltête D, Rovelet-Lecrux A, Boland A, Deleuze JF; French PFBC study group; Frebourg T, Hannequin D, Campion D, Nicolas G. Grangeon L, et al. Brain. 2019 Jun 1;142(6):1573-1586. doi: 10.1093/brain/awz095. Brain. 2019. PMID: 31009047

7

Primary familial brain calcification caused by a novel homozygous MYORG mutation in a consanguineous Italian family.

Ramos EM, Roca A, Chumchim N, Dokuru DR, Van Berlo V, De Michele G, Lieto M, Tedeschi E, De Michele G, Coppola G. Ramos EM, et al. Neurogenetics. 2019 May;20(2):99-102. doi: 10.1007/s10048-019-00571-8. Epub 2019 Mar 21. Neurogenetics. 2019. PMID: 30895394

8

MYORG is associated with recessive primary familial brain calcification.

Arkadir D, Lossos A, Rahat D, Abu Snineh M, Schueler-Furman O, Nitschke S, Minassian BA, Sadaka Y, Lerer I, Tabach Y, Meiner V. Arkadir D, et al. Ann Clin Transl Neurol. 2018 Nov 15;6(1):106-113. doi: 10.1002/acn3.684. eCollection 2019 Jan. Ann Clin Transl Neurol. 2018. PMID: 30656188 Free PMC article.

9

A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification.

Forouhideh Y, Müller K, Ruf W, Assi M, Seker T, Tunca C, Knehr A, Strom TM, Gorges M, Schradt F, Meitinger T, Ludolph AC, Pinkhardt EH, Basak AN, Kassubek J, Uttner I, Weishaupt JH. Forouhideh Y, et al. Brain. 2019 Feb 1;142(2):e4. doi: 10.1093/brain/awy343. Brain. 2019. PMID: 30649222 No abstract available.

10

Evaluation of MYORG mutations as a novel cause of primary familial brain calcification.

Chen Y, Fu F, Chen S, Cen Z, Tang H, Huang J, Xie F, Zheng X, Yang D, Wang H, Huang X, Zhang Y, Zhou Y, Liu JY, Luo W. Chen Y, et al. Mov Disord. 2019 Feb;34(2):291-297. doi: 10.1002/mds.27582. Epub 2018 Dec 27. Mov Disord. 2019. PMID: 30589467

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