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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.
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 …
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
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.
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 …
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.
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.
α-Synucleinopathy phenotypes.
McCann H, Stevens CH, Cartwright H, Halliday GM. McCann H, et al. Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S62-7. doi: 10.1016/S1353-8020(13)70017-8. Parkinsonism Relat Disord. 2014. PMID: 24262191 Review.
There are three main types of alpha-synucleinopathy, Parkinson's disease (PD), dementia with Lewy bodies (DLB), and multiple system atrophy (MSA), with other rare disorders also having alpha-synuclein pathologies, such as various neuroaxonal dystrophies. Multiple cl …
There are three main types of alpha-synucleinopathy, Parkinson's disease (PD), dementia with Lewy bodies (DLB), and multiple system atrophy …
Hallervorden-Spatz syndrome.
Swaiman KF. Swaiman KF. Pediatr Neurol. 2001 Aug;25(2):102-8. doi: 10.1016/s0887-8994(01)00253-3. Pediatr Neurol. 2001. PMID: 11551740 Review.
139 results