Similar articles for PMID: 27021474

Year	Number of Results
1957	1
1961	1
1999	2
2001	2
2005	1
2007	1
2008	2
2009	1
2010	2
2011	2
2012	6
2013	13
2014	8
2015	7
2016	13
2017	10
2018	7
2019	7
2020	1
2021	1
2022	2
2024	0

1

Mutational analysis of COASY in an Italian patient with NBIA.

Annesi G, Gagliardi M, Iannello G, Quattrone A, Iannello G, Quattrone A. Annesi G, et al. Parkinsonism Relat Disord. 2016 Jul;28:150-1. doi: 10.1016/j.parkreldis.2016.03.011. Epub 2016 Mar 18. Parkinsonism Relat Disord. 2016. PMID: 27021474 No abstract available.

2

Neurodegeneration with brain iron accumulation: Insights into the mitochondria dysregulation.

Wang ZB, Liu JY, Xu XJ, Mao XY, Zhang W, Zhou HH, Liu ZQ. Wang ZB, et al. Biomed Pharmacother. 2019 Oct;118:109068. doi: 10.1016/j.biopha.2019.109068. Epub 2019 Aug 9. Biomed Pharmacother. 2019. PMID: 31404774 Free article. Review.

3

A new NBIA patient from Turkey with homozygous C19ORF12 mutation.

Kasapkara ÇS, Tümer L, Gregory A, Ezgü F, İnci A, Derinkuyu BE, Fox R, Rogers C, Hayflick S. Kasapkara ÇS, et al. Acta Neurol Belg. 2019 Dec;119(4):623-625. doi: 10.1007/s13760-018-1026-5. Epub 2018 Oct 8. Acta Neurol Belg. 2019. PMID: 30298423 Free PMC article. No abstract available.

4

[GENETICALLY DETERMINED DISEASES ASSOCIATED WITH PATHOLOGICAL BRAIN IRON ACCUMULATION AND NEURODEGENERATION].

Ács P, Molnár MJ, Klivényi P, Kálmán B. Ács P, et al. Ideggyogy Sz. 2016 Mar 30;69(5-6):157-66. doi: 10.18071/isz.69.0157. Ideggyogy Sz. 2016. PMID: 27468605 Free article. Review. Hungarian.

5

Transcranial sonography in mitochondrial membrane protein-associated neurodegeneration.

Skowronska M, Walter U, Kmiec T, Czlonkowska A. Skowronska M, et al. Parkinsonism Relat Disord. 2013 Nov;19(11):1061-3. doi: 10.1016/j.parkreldis.2013.06.020. Epub 2013 Jul 17. Parkinsonism Relat Disord. 2013. PMID: 23871464 No abstract available.

6

Novel case of neurodegeneration with brain iron accumulation 4 (NBIA4) caused by a pathogenic variant affecting splicing.

Sparber P, Marakhonov A, Filatova A, Sharkova I, Skoblov M. Sparber P, et al. Neurogenetics. 2018 Dec;19(4):257-260. doi: 10.1007/s10048-018-0558-4. Epub 2018 Nov 3. Neurogenetics. 2018. PMID: 30392167

7

A novel FTL mutation responsible for neuroferritinopathy with asymmetric clinical features and brain anomalies.

Moutton S, Fergelot P, Trocello JM, Plante-Bordeneuve V, Houcinat N, Wenisch E, Larue V, Brugières P, Clot F, Lacombe D, Arveiler B, Goizet C. Moutton S, et al. Parkinsonism Relat Disord. 2014 Aug;20(8):935-7. doi: 10.1016/j.parkreldis.2014.04.026. Epub 2014 May 9. Parkinsonism Relat Disord. 2014. PMID: 24907184 No abstract available.

8

C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation.

Panteghini C, Zorzi G, Venco P, Dusi S, Reale C, Brunetti D, Chiapparini L, Zibordi F, Siegel B, Garavaglia B, Simonati A, Bertini E, Nardocci N, Tiranti V. Panteghini C, et al. Semin Pediatr Neurol. 2012 Jun;19(2):75-81. doi: 10.1016/j.spen.2012.03.006. Semin Pediatr Neurol. 2012. PMID: 22704260

9

Neuroferritinopathy.

Lehn A, Boyle R, Brown H, Airey C, Mellick G. Lehn A, et al. Parkinsonism Relat Disord. 2012 Sep;18(8):909-15. doi: 10.1016/j.parkreldis.2012.06.021. Epub 2012 Jul 17. Parkinsonism Relat Disord. 2012. PMID: 22818529 Review.

10

Classification and molecular pathogenesis of NBIA syndromes.

Di Meo I, Tiranti V. Di Meo I, et al. Eur J Paediatr Neurol. 2018 Mar;22(2):272-284. doi: 10.1016/j.ejpn.2018.01.008. Epub 2018 Jan 17. Eur J Paediatr Neurol. 2018. PMID: 29409688 Review.

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