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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1966 1
1967 1
1968 1
1969 2
1977 1
1979 1
1981 2
1986 1
1987 1
1990 2
1991 1
1992 1
1993 2
1995 5
1996 1
1997 1
1998 2
1999 2
2000 4
2001 10
2002 5
2003 4
2005 2
2006 1
2007 1
2008 2
2009 1
2010 1
2011 8
2012 11
2013 15
2014 3
2015 6
2016 8
2017 8
2018 11
2019 3
2020 3
2021 6
2022 7
2023 4
2024 0

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139 results

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Page 1
Neurodegeneration with brain iron accumulation.
Hayflick SJ, Kurian MA, Hogarth P. Hayflick SJ, et al. Handb Clin Neurol. 2018;147:293-305. doi: 10.1016/B978-0-444-63233-3.00019-1. Handb Clin Neurol. 2018. PMID: 29325618 Free PMC article. Review.
Cerebral Iron Deposition in Neurodegeneration.
Dusek P, Hofer T, Alexander J, Roos PM, Aaseth JO. Dusek P, et al. Biomolecules. 2022 May 17;12(5):714. doi: 10.3390/biom12050714. Biomolecules. 2022. PMID: 35625641 Free PMC article. Review.
Infantile neuroaxonal dystrophy and PLA2G6-associated neurodegeneration: An update for the diagnosis.
Iodice A, Spagnoli C, Salerno GG, Frattini D, Bertani G, Bergonzini P, Pisani F, Fusco C. Iodice A, et al. Brain Dev. 2017 Feb;39(2):93-100. doi: 10.1016/j.braindev.2016.08.012. Epub 2016 Nov 21. Brain Dev. 2017. PMID: 27884548 Review.
Infantile neuroaxonal dystrophy is a rare neurodegenerative disorder characterized by infantile onset of rapid motor and cognitive regression and hypotonia evolving into spasticity. Recessively inherited mutations of the PLA2G6 gene are causative of
Infantile neuroaxonal dystrophy is a rare neurodegenerative disorder characterized by infantile onset of rapid m
Axonal dystrophies.
Nardocci N, Zorzi G. Nardocci N, et al. Handb Clin Neurol. 2013;113:1919-24. doi: 10.1016/B978-0-444-59565-2.00062-9. Handb Clin Neurol. 2013. PMID: 23622415 Review.
The Neuroaxonal Dystrophies (NADs) are a group of clinically and genetically heterogeneous neurodegenerative conditions. ...NADs comprise two main diseases: pantothenate-kinase associated neurodegeneration (PKAN) and infantile neuroaxonal dystrophy
The Neuroaxonal Dystrophies (NADs) are a group of clinically and genetically heterogeneous neurodegenerative conditions. ...NA …
PKAN pathogenesis and treatment.
Hayflick SJ, Jeong SY, Sibon OCM. Hayflick SJ, et al. Mol Genet Metab. 2022 Nov;137(3):283-291. doi: 10.1016/j.ymgme.2022.09.011. Epub 2022 Oct 5. Mol Genet Metab. 2022. PMID: 36240582 Free PMC article. Review.
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.
The role of the PLA2G6 gene in neurodegenerative diseases.
Deng X, Yuan L, Jankovic J, Deng H. Deng X, et al. Ageing Res Rev. 2023 Aug;89:101957. doi: 10.1016/j.arr.2023.101957. Epub 2023 May 24. Ageing Res Rev. 2023. PMID: 37236368 Review.
Usually, it encompasses three autosomal recessive diseases, including infantile neuroaxonal dystrophy or neurodegeneration with brain iron accumulation (NBIA) 2A, atypical neuronal dystrophy with childhood-onset or NBIA2B, and adult-onset dystonia-park …
Usually, it encompasses three autosomal recessive diseases, including infantile neuroaxonal dystrophy or neurodegenerat …
Neuroferritinopathy.
Keogh MJ, Morris CM, Chinnery PF. Keogh MJ, et al. Int Rev Neurobiol. 2013;110:91-123. doi: 10.1016/B978-0-12-410502-7.00006-5. Int Rev Neurobiol. 2013. PMID: 24209436 Review.
PLA2G6-associated neurodegeneration in four different populations-case series and literature review.
Hanna Al-Shaikh R, Milanowski LM, Holla VV, Kurihara K, Yadav R, Kamble N, Muthusamy B, Bellad A, Koziorowski D, Szlufik S, Hoffman-Zacharska D, Fujioka S, Tsuboi Y, Ross OA, Wierenga K, Uitti RJ, Wszolek Z, Pal PK. Hanna Al-Shaikh R, et al. Parkinsonism Relat Disord. 2022 Aug;101:66-74. doi: 10.1016/j.parkreldis.2022.06.016. Epub 2022 Jun 30. Parkinsonism Relat Disord. 2022. PMID: 35803092 Review.
BACKGROUND: PLA2G6-Associated Neurodegeneration, PLAN, is subdivided into: Infantile neuroaxonal dystrophy, atypical neuroaxonal dystrophy, and adult-onset dystonia parkinsonism [1]. ...Phenotypic characteristics were heterogenous and resembled …
BACKGROUND: PLA2G6-Associated Neurodegeneration, PLAN, is subdivided into: Infantile neuroaxonal dystrophy, atypical …
Pathogenic mechanism and modeling of neuroferritinopathy.
Cozzi A, Santambrogio P, Ripamonti M, Rovida E, Levi S. Cozzi A, et al. Cell Mol Life Sci. 2021 Apr;78(7):3355-3367. doi: 10.1007/s00018-020-03747-w. Epub 2021 Jan 13. Cell Mol Life Sci. 2021. PMID: 33439270 Review.
139 results