Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

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

Year Number of Results
1987 1
1991 1
1993 1
1994 2
1995 1
1996 1
1999 1
2000 2
2001 2
2002 2
2003 2
2004 4
2005 1
2006 1
2007 2
2008 2
2009 3
2011 1
2012 3
2013 3
2014 1
2015 2
2016 2
2017 2
2019 1
2020 5
2021 0
Text availability
Article attribute
Article type
Publication date

PubMed Links for id: 127833

43 results
Results by year
Filters applied: . Clear all
Page 1
Biallelic loss of function variants in SYT2 cause a treatable congenital onset presynaptic myasthenic syndrome.
Donkervoort S, Mohassel P, Laugwitz L, Zaki MS, Kamsteeg EJ, Maroofian R, Chao KR, Verschuuren-Bemelmans CC, Horber V, Fock AJM, McCarty RM, Jain MS, Biancavilla V, McMacken G, Nalls M, Voermans NC, Elbendary HM, Snyder M, Cai C, Lehky TJ, Stanley V, Iannaccone ST, Foley AR, Lochmüller H, Gleeson J, Houlden H, Haack TB, Horvath R, Bönnemann CG. Donkervoort S, et al. Am J Med Genet A. 2020 Oct;182(10):2272-2283. doi: 10.1002/ajmg.a.61765. Epub 2020 Aug 10. Am J Med Genet A. 2020. PMID: 32776697 Free PMC article.
Evaluation of common variants in 16 genes involved in the regulation of neurotransmitter release in ADHD.
Sánchez-Mora C, Cormand B, Ramos-Quiroga JA, Hervás A, Bosch R, Palomar G, Nogueira M, Gómez-Barros N, Richarte V, Corrales M, Garcia-Martinez I, Corominas R, Guijarro S, Bigorra A, Bayés M, Casas M, Ribasés M. Sánchez-Mora C, et al. Eur Neuropsychopharmacol. 2013 Jun;23(6):426-35. doi: 10.1016/j.euroneuro.2012.07.014. Epub 2012 Aug 30. Eur Neuropsychopharmacol. 2013. PMID: 22939005
43 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page