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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.
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 …
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.
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