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

Year Number of Results
1946 3
1947 3
1948 6
1949 3
1950 13
1951 9
1952 5
1953 15
1954 10
1955 9
1956 13
1957 6
1958 7
1959 8
1960 8
1961 18
1962 12
1963 29
1964 44
1965 23
1966 17
1967 18
1968 21
1969 27
1970 20
1971 24
1972 22
1973 31
1974 18
1975 17
1976 35
1977 15
1978 53
1979 47
1980 55
1981 41
1982 51
1983 29
1984 53
1985 27
1986 33
1987 34
1988 30
1989 18
1990 26
1991 21
1992 25
1993 27
1994 19
1995 29
1996 33
1997 52
1998 48
1999 67
2000 77
2001 69
2002 72
2003 51
2004 68
2005 62
2006 56
2007 72
2008 74
2009 80
2010 92
2011 87
2012 121
2013 121
2014 109
2015 96
2016 101
2017 92
2018 96
2019 102
2020 116
2021 106
2022 97
2023 107
2024 47

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3,238 results

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Page 1
Ataxia.
Kuo SH. Kuo SH. Continuum (Minneap Minn). 2019 Aug;25(4):1036-1054. doi: 10.1212/CON.0000000000000753. Continuum (Minneap Minn). 2019. PMID: 31356292 Free PMC article. Review.
When these molecular pathways become dysfunctional, patients develop cerebellar ataxia. In addition, several ongoing clinical trials for Friedreich ataxia and spinocerebellar ataxia will likely result in novel symptomatic and disease-modifying therapies for ataxia. …
When these molecular pathways become dysfunctional, patients develop cerebellar ataxia. In addition, several ongoing clinical trials for …
Friedreich ataxia: clinical features and new developments.
Keita M, McIntyre K, Rodden LN, Schadt K, Lynch DR. Keita M, et al. Neurodegener Dis Manag. 2022 Oct;12(5):267-283. doi: 10.2217/nmt-2022-0011. Epub 2022 Jun 29. Neurodegener Dis Manag. 2022. PMID: 35766110 Free PMC article. Review.
The inherited cerebellar ataxias: an update.
Coarelli G, Wirth T, Tranchant C, Koenig M, Durr A, Anheim M. Coarelli G, et al. J Neurol. 2023 Jan;270(1):208-222. doi: 10.1007/s00415-022-11383-6. Epub 2022 Sep 24. J Neurol. 2023. PMID: 36152050 Free PMC article. Review.
We also report on key clinical points for the diagnosis of the main ICAs, including Friedreich ataxia, CANVAS, polyglutamine spinocerebellar ataxias, Fragile X-associated tremor/ataxia syndrome. ...Lastly, we describe new therapeutic leads: antisense oligonucleotide …
We also report on key clinical points for the diagnosis of the main ICAs, including Friedreich ataxia, CANVAS, polyglutamine s …
Friedreich ataxia- pathogenesis and implications for therapies.
Delatycki MB, Bidichandani SI. Delatycki MB, et al. Neurobiol Dis. 2019 Dec;132:104606. doi: 10.1016/j.nbd.2019.104606. Epub 2019 Sep 5. Neurobiol Dis. 2019. PMID: 31494282 Free article. Review.
Friedreich ataxia is the most common of the hereditary ataxias. It is due to homozygous/compound heterozygous mutations in FXN. ...In about 96% of affected individuals there is homozygosity for a GAA repeat expansion in intron 1 of the FXN gene. Studies of people wi …
Friedreich ataxia is the most common of the hereditary ataxias. It is due to homozygous/compound heterozygous mutations in FXN …
Omaveloxolone: an activator of Nrf2 for the treatment of Friedreich ataxia.
Profeta V, McIntyre K, Wells M, Park C, Lynch DR. Profeta V, et al. Expert Opin Investig Drugs. 2023 Jan;32(1):5-16. doi: 10.1080/13543784.2023.2173063. Epub 2023 Feb 8. Expert Opin Investig Drugs. 2023. PMID: 36708320
INTRODUCTION: Friedreich ataxia (FRDA) is a rare autosomal recessive degenerative disorder characterized by ataxia, dysarthria, diabetes, cardiomyopathy, scoliosis, and occasionally vision loss in late-stage disease. ...
INTRODUCTION: Friedreich ataxia (FRDA) is a rare autosomal recessive degenerative disorder characterized by ataxia, dysarthria …
Friedreich's ataxia.
Alper G, Narayanan V. Alper G, et al. Pediatr Neurol. 2003 May;28(5):335-41. doi: 10.1016/s0887-8994(03)00004-3. Pediatr Neurol. 2003. PMID: 12878293 Review.
Friedreich's ataxia: new insights.
Krasilnikova MM, Humphries CL, Shinsky EM. Krasilnikova MM, et al. Emerg Top Life Sci. 2023 Dec 14;7(3):313-323. doi: 10.1042/ETLS20230017. Emerg Top Life Sci. 2023. PMID: 37698160 Review.
Friedreich ataxia (FRDA) is an inherited disease that is typically caused by GAA repeat expansion within the first intron of the FXN gene coding for frataxin. ...
Friedreich ataxia (FRDA) is an inherited disease that is typically caused by GAA repeat expansion within the first intron of t …
Friedreich ataxia: an overview.
Delatycki MB, Williamson R, Forrest SM. Delatycki MB, et al. J Med Genet. 2000 Jan;37(1):1-8. doi: 10.1136/jmg.37.1.1. J Med Genet. 2000. PMID: 10633128 Free PMC article. Review.
Friedreich ataxia, an autosomal recessive neurodegenerative disease, is the most common of the inherited ataxias. The recent discovery of the gene that is mutated in this condition, FRDA, has led to rapid advances in the understanding of the pathogenesis of Fried …
Friedreich ataxia, an autosomal recessive neurodegenerative disease, is the most common of the inherited ataxias. The recent d …
Friedreich's ataxia.
Pilch J, Jamroz E, Marszał E. Pilch J, et al. J Child Neurol. 2002 May;17(5):315-9. doi: 10.1177/088307380201700501. J Child Neurol. 2002. PMID: 12150575 Review.
3,238 results