Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
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 3
1982 4
1983 3
1984 2
1985 2
1986 5
1987 4
1988 4
1989 5
1990 3
1991 7
1992 7
1993 4
1994 9
1995 8
1996 5
1997 9
1998 10
1999 10
2000 5
2001 7
2002 6
2003 5
2004 5
2005 8
2006 5
2007 4
2008 7
2009 11
2010 9
2011 8
2012 10
2013 9
2014 14
2015 9
2016 14
2017 6
2018 6
2019 4
2020 8
2021 1
Text availability
Article attribute
Article type
Publication date

Search Results

256 results
Results by year
Filters applied: . Clear all
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.
Senataxin Mutation Reveals How R-Loops Promote Transcription by Blocking DNA Methylation at Gene Promoters.
Grunseich C, Wang IX, Watts JA, Burdick JT, Guber RD, Zhu Z, Bruzel A, Lanman T, Chen K, Schindler AB, Edwards N, Ray-Chaudhury A, Yao J, Lehky T, Piszczek G, Crain B, Fischbeck KH, Cheung VG. Grunseich C, et al. Among authors: fischbeck kh. Mol Cell. 2018 Feb 1;69(3):426-437.e7. doi: 10.1016/j.molcel.2017.12.030. Epub 2018 Jan 27. Mol Cell. 2018. PMID: 29395064 Free PMC article.
Toxic proteins in neurodegenerative disease.
Taylor JP, Hardy J, Fischbeck KH. Taylor JP, et al. Among authors: fischbeck kh. Science. 2002 Jun 14;296(5575):1991-5. doi: 10.1126/science.1067122. Science. 2002. PMID: 12065827 Review.
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation.
Guo L, Bertola DR, Takanohashi A, Saito A, Segawa Y, Yokota T, Ishibashi S, Nishida Y, Yamamoto GL, Franco JFDS, Honjo RS, Kim CA, Musso CM, Timmons M, Pizzino A, Taft RJ, Lajoie B, Knight MA, Fischbeck KH, Singleton AB, Ferreira CR, Wang Z, Yan L, Garbern JY, Simsek-Kiper PO, Ohashi H, Robey PG, Boyde A, Matsumoto N, Miyake N, Spranger J, Schiffmann R, Vanderver A, Nishimura G, Passos-Bueno MRDS, Simons C, Ishikawa K, Ikegawa S. Guo L, et al. Among authors: fischbeck kh. Am J Hum Genet. 2019 May 2;104(5):925-935. doi: 10.1016/j.ajhg.2019.03.004. Epub 2019 Apr 11. Am J Hum Genet. 2019. PMID: 30982609 Free PMC article.
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.
Combinatorial treatment for spinal muscular atrophy: An Editorial for 'Combined treatment with the histone deacetylase inhibitor LBH589 and a splice-switch antisense oligonucleotide enhances SMN2 splicing and SMN expression in Spinal Muscular Atrophy cells' on page 264.
Poletti A, Fischbeck KH. Poletti A, et al. Among authors: fischbeck kh. J Neurochem. 2020 Apr;153(2):146-149. doi: 10.1111/jnc.14974. Epub 2020 Feb 14. J Neurochem. 2020. PMID: 32056234 Free article.
256 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page