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

Year Number of Results
1946 12
1947 16
1948 11
1949 10
1950 34
1951 39
1952 55
1953 38
1954 33
1955 21
1956 20
1957 36
1958 26
1959 41
1960 22
1961 27
1962 23
1963 17
1964 7
1965 4
1966 9
1967 7
1968 12
1969 3
1970 5
1971 6
1972 10
1973 8
1974 3
1975 5
1976 1
1977 6
1978 3
1979 6
1980 4
1981 4
1982 1
1983 5
1984 2
1985 5
1986 2
1987 5
1988 9
1989 8
1990 8
1991 5
1992 12
1993 19
1994 8
1995 7
1996 16
1997 12
1998 8
1999 19
2000 19
2001 30
2002 11
2003 28
2004 19
2005 30
2006 22
2007 13
2008 19
2009 22
2010 28
2011 40
2012 50
2013 46
2014 33
2015 45
2016 46
2017 38
2018 41
2019 51
2020 49
2021 39
2022 34
2023 28
2024 13

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1,420 results

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Page 1
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, encoding a phospholipase A2, is mutated in neurodegenerative disorders with high brain iron.
Morgan NV, Westaway SK, Morton JE, Gregory A, Gissen P, Sonek S, Cangul H, Coryell J, Canham N, Nardocci N, Zorzi G, Pasha S, Rodriguez D, Desguerre I, Mubaidin A, Bertini E, Trembath RC, Simonati A, Schanen C, Johnson CA, Levinson B, Woods CG, Wilmot B, Kramer P, Gitschier J, Maher ER, Hayflick SJ. Morgan NV, et al. Nat Genet. 2006 Jul;38(7):752-4. doi: 10.1038/ng1826. Epub 2006 Jun 18. Nat Genet. 2006. PMID: 16783378 Free PMC article.
Neurodegenerative disorders with high brain iron include Parkinson disease, Alzheimer disease and several childhood genetic disorders categorized as neuroaxonal dystrophies. We mapped a locus for infantile neuroaxonal dystrophy (INAD) and neurod …
Neurodegenerative disorders with high brain iron include Parkinson disease, Alzheimer disease and several childhood genetic di …
Ferritinophagy/ferroptosis: Iron-related newcomers in human diseases.
Tang M, Chen Z, Wu D, Chen L. Tang M, et al. J Cell Physiol. 2018 Dec;233(12):9179-9190. doi: 10.1002/jcp.26954. Epub 2018 Aug 4. J Cell Physiol. 2018. PMID: 30076709 Review.
Notably, ferritinophagy also plays a central role in driving some pathological processes, including Parkinson's disease (PD) and urinary tract infections. Some evidence has demonstrated that ferritinophagy is critical to induce ferroptosis. ...Conversely, the activation of …
Notably, ferritinophagy also plays a central role in driving some pathological processes, including Parkinson's disease (PD) and urin …
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.
It leads to iron deposition particularly in the cerebellum, basal ganglia and motor cortex. The disease becomes clinically apparent in adulthood mainly with extrapyramidal signs and progresses slowly over decades. ...Neuroimaging is the most helpful investigation and shows …
It leads to iron deposition particularly in the cerebellum, basal ganglia and motor cortex. The disease becomes clinically apparent i …
Neuroaxonal dystrophy in childhood. Report of two second cousins with Hallerworden-Spatz disease, and a case of Seitelberger's disease.
Malmström-Groth AG, Kristensson K. Malmström-Groth AG, et al. Acta Paediatr Scand. 1982 Nov;71(6):1045-9. doi: 10.1111/j.1651-2227.1982.tb09574.x. Acta Paediatr Scand. 1982. PMID: 7158329
Three late infantile cases of neuroaxonal dystrophy are presented, two of them second cousins with Hallerworden-Spatz disease and one sporadic case with Seitelberger's disease. ...Iron deposits and axonal dystrophy were found in the pallidum. Th …
Three late infantile cases of neuroaxonal dystrophy are presented, two of them second cousins with Hallerworden-Spatz disease …
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. These disorders show the unique pathological feature of neuroaxonal dystrophy (NAD): axonal swelling (spheroids) localized throughout the …
The Neuroaxonal Dystrophies (NADs) are a group of clinically and genetically heterogeneous neurodegenerative conditions. These …
Equine Neuroaxonal Dystrophy and Degenerative Myeloencephalopathy.
Finno CJ, Johnson AL. Finno CJ, et al. Vet Clin North Am Equine Pract. 2022 Aug;38(2):213-224. doi: 10.1016/j.cveq.2022.04.003. Epub 2022 Jul 7. Vet Clin North Am Equine Pract. 2022. PMID: 35811203 Review.
Neuroaxonal degenerative disease in the horse is termed equine neuroaxonal dystrophy (eNAD), when pathologic lesions are localized to the brainstem and equine degenerative myeloencephalopathy (EDM) and degenerative changes extend throughout the spinal cord. B …
Neuroaxonal degenerative disease in the horse is termed equine neuroaxonal dystrophy (eNAD), when pathologic lesions ar …
Exploring therapeutic strategies for infantile neuronal axonal dystrophy (INAD/PARK14).
Lin G, Tepe B, McGrane G, Tipon RC, Croft G, Panwala L, Hope A, Liang AJH, Zuo Z, Byeon SK, Wang L, Pandey A, Bellen HJ. Lin G, et al. Elife. 2023 Jan 16;12:e82555. doi: 10.7554/eLife.82555. Elife. 2023. PMID: 36645408 Free PMC article.
Infantile neuroaxonal dystrophy (INAD) is caused by recessive variants in PLA2G6 and is a lethal pediatric neurodegenerative disorder. ...
Infantile neuroaxonal dystrophy (INAD) is caused by recessive variants in PLA2G6 and is a lethal pediatric neurodegenerative disorder …
Adult onset Hallervorden-Spatz syndrome or Seitelberger's disease with late onset: variants of the same entity? A clinico-pathological study.
Gaytan-Garcia S, Kaufmann JC, Young GB. Gaytan-Garcia S, et al. Clin Neuropathol. 1990 May-Jun;9(3):136-42. Clin Neuropathol. 1990. PMID: 2364593
The clinical and pathological features, including electron microscopy of a sporadic case of neuroaxonal dystrophy with findings of both Hallervorden-Spatz syndrome (HS) and Seitelberger's disease (SD) are presented. ...
The clinical and pathological features, including electron microscopy of a sporadic case of neuroaxonal dystrophy with findings of bo …
1,420 results