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Results by year

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

Year Number of Results
1976 2
1977 1
1979 1
1980 1
1981 2
1982 4
1983 3
1984 2
1985 2
1986 4
1988 3
1989 5
1990 3
1991 6
1992 7
1993 4
1994 9
1995 7
1996 5
1997 8
1998 8
1999 10
2000 4
2001 7
2002 6
2003 5
2004 4
2005 7
2006 5
2007 4
2008 6
2009 9
2010 6
2011 8
2012 10
2013 8
2014 14
2015 8
2016 13
2017 6
2018 6
2019 3
2020 8
2021 8
2022 7
2023 3
2024 2

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250 results

Results by year

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Page 1
Spinal muscular atrophy.
Arnold ES, Fischbeck KH. Arnold ES, et al. Among authors: fischbeck kh. Handb Clin Neurol. 2018;148:591-601. doi: 10.1016/B978-0-444-64076-5.00038-7. Handb Clin Neurol. 2018. PMID: 29478602 Review.
Oligonucleotide Treatment for Huntington's Disease.
Fischbeck KH, Wexler NS. Fischbeck KH, et al. N Engl J Med. 2019 Jun 13;380(24):2373-2374. doi: 10.1056/NEJMe1904861. Epub 2019 May 6. N Engl J Med. 2019. PMID: 31059640 No abstract available.
Nucleic acid therapeutics in neurodevelopmental disease.
Winkelsas AM, Fischbeck KH. Winkelsas AM, et al. Among authors: fischbeck kh. Curr Opin Genet Dev. 2020 Dec;65:112-116. doi: 10.1016/j.gde.2020.05.022. Epub 2020 Jul 2. Curr Opin Genet Dev. 2020. PMID: 32623324 Free article. Review.
Kennedy disease.
Fischbeck KH. Fischbeck KH. J Inherit Metab Dis. 1997 Jun;20(2):152-8. doi: 10.1023/a:1005344403603. J Inherit Metab Dis. 1997. PMID: 9211187 Review.
Spinal and Bulbar Muscular Atrophy Overview.
Fischbeck KH. Fischbeck KH. J Mol Neurosci. 2016 Mar;58(3):317-20. doi: 10.1007/s12031-015-0674-7. Epub 2015 Nov 7. J Mol Neurosci. 2016. PMID: 26547319 Free PMC article. Review.
Variants in ATP6V0A1 cause progressive myoclonus epilepsy and developmental and epileptic encephalopathy.
Bott LC, Forouhan M, Lieto M, Sala AJ, Ellerington R, Johnson JO, Speciale AA, Criscuolo C, Filla A, Chitayat D, Alkhunaizi E, Shannon P, Nemeth AH; Italian Undiagnosed Diseases Network; Angelucci F, Lim WF, Striano P, Zara F, Helbig I, Muona M, Courage C, Lehesjoki AE, Berkovic SF; ATPase Consortium; Fischbeck KH, Brancati F, Morimoto RI, Wood MJA, Rinaldi C. Bott LC, et al. Among authors: fischbeck kh. Brain Commun. 2021 Oct 18;3(4):fcab245. doi: 10.1093/braincomms/fcab245. eCollection 2021. Brain Commun. 2021. PMID: 34909687 Free PMC article.
The mechanism of myotonic dystrophy.
Fischbeck KH. Fischbeck KH. Ann Neurol. 1994 Mar;35(3):255-6. doi: 10.1002/ana.410350302. Ann Neurol. 1994. PMID: 8122876 No abstract available.
Spinal and Bulbar Muscular Atrophy.
Grunseich C, Fischbeck KH. Grunseich C, et al. Among authors: fischbeck kh. Neurol Clin. 2015 Nov;33(4):847-54. doi: 10.1016/j.ncl.2015.07.002. Epub 2015 Sep 8. Neurol Clin. 2015. PMID: 26515625 Free PMC article. Review.
Trinucleotide repeats in neurogenetic disorders.
Paulson HL, Fischbeck KH. Paulson HL, et al. Among authors: fischbeck kh. Annu Rev Neurosci. 1996;19:79-107. doi: 10.1146/annurev.ne.19.030196.000455. Annu Rev Neurosci. 1996. PMID: 8833437 Review.
250 results