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Items: 11

1.

Endolysosomal dysfunction in Parkinson's disease: Recent developments and future challenges.

Kett LR, Dauer WT.

Mov Disord. 2016 Oct;31(10):1433-1443. doi: 10.1002/mds.26797. Review.

2.

A diagnostic approach for neurodegeneration with brain iron accumulation: clinical features, genetics and brain imaging.

Salomão RP, Pedroso JL, Gama MT, Dutra LA, Maciel RH, Godeiro-Junior C, Chien HF, Teive HA, Cardoso F, Barsottini OG.

Arq Neuropsiquiatr. 2016 Jul;74(7):587-96. doi: 10.1590/0004-282X20160080. Review.

3.

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

Ács P, Molnár MJ, Klivényi P, Kálmán B.

Ideggyogy Sz. 2016 Mar 30;69(5-6):157-66. Review. Hungarian.

PMID:
27468605
4.

Hereditary Parkinsonism-Associated Genetic Variations in PARK9 Locus Lead to Functional Impairment of ATPase Type 13A2.

Park JS, Sue CM.

Curr Protein Pept Sci. 2017;18(7):725-732. doi: 10.2174/1389203717666160311121534. Review.

PMID:
26965689
5.

Neurodegeneration with Brain Iron Accumulation: Genetic Diversity and Pathophysiological Mechanisms.

Meyer E, Kurian MA, Hayflick SJ.

Annu Rev Genomics Hum Genet. 2015;16:257-79. doi: 10.1146/annurev-genom-090314-025011. Epub 2015 May 8. Review.

PMID:
25973518
6.

The role of ATP13A2 in Parkinson's disease: Clinical phenotypes and molecular mechanisms.

Park JS, Blair NF, Sue CM.

Mov Disord. 2015 May;30(6):770-9. doi: 10.1002/mds.26243. Epub 2015 Apr 21. Review.

PMID:
25900096
7.

Peripheral neuropathy and parkinsonism: a large clinical and pathogenic spectrum.

Vital A, Lepreux S, Vital C.

J Peripher Nerv Syst. 2014 Dec;19(4):333-42. doi: 10.1111/jns.12099. Review.

PMID:
25582874
8.

Mutations in the ATP13A2 gene and Parkinsonism: a preliminary review.

Yang X, Xu Y.

Biomed Res Int. 2014;2014:371256. doi: 10.1155/2014/371256. Epub 2014 Aug 14. Review.

9.

Biomarkers in Parkinson's disease (recent update).

Sharma S, Moon CS, Khogali A, Haidous A, Chabenne A, Ojo C, Jelebinkov M, Kurdi Y, Ebadi M.

Neurochem Int. 2013 Sep;63(3):201-29. doi: 10.1016/j.neuint.2013.06.005. Epub 2013 Jun 19. Review.

PMID:
23791710
10.

PLA2G6 mutations and other rare causes of neurodegeneration with brain iron accumulation.

McNeill A.

Curr Drug Targets. 2012 Aug;13(9):1204-6. Review.

PMID:
22515743
11.

Impact of recent genetic findings in Parkinson's disease.

Klein C, Lohmann-Hedrich K.

Curr Opin Neurol. 2007 Aug;20(4):453-64. Review.

PMID:
17620882

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