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
2000 1
2005 2
2006 1
2012 1
2014 1
2015 2
2016 4
2017 2
2018 1
2019 2
2020 7
2021 9
2022 4
Text availability
Article attribute
Article type
Publication date

Search Results

34 results
Results by year
Filters applied: . Clear all
Page 1
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients.
Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, Gherbi S, Testa F, Simonelli F, Banfi S, Fakin A, Glavač D, Jarc-Vidmar M, Zupan A, Battelino S, Martorell Sampol L, Claveria MA, Catala Mora J, Dad S, Møller LB, Rodriguez Jorge J, Hawlina M, Auricchio A, Sahel JA, Marlin S, Zrenner E, Audo I, Petit C. Bonnet C, et al. Among authors: battelino s. Eur J Hum Genet. 2016 Dec;24(12):1730-1738. doi: 10.1038/ejhg.2016.99. Epub 2016 Jul 27. Eur J Hum Genet. 2016. PMID: 27460420 Free PMC article.
Glucagon-like peptide-1, a matter of taste?
Jensterle M, DeVries JH, Battelino T, Battelino S, Yildiz B, Janez A. Jensterle M, et al. Among authors: battelino s. Rev Endocr Metab Disord. 2021 Dec;22(4):763-775. doi: 10.1007/s11154-020-09609-x. Epub 2020 Oct 29. Rev Endocr Metab Disord. 2021. PMID: 33123893 Review.
Dataset on amelogenesis-related genes variants (ENAM and ENAM interacting genes) and on human leukocyte antigen alleles (DQ2 and DQ8) distribution in children with and without molar-incisor hypomineralisation (MIH).
Hočevar L, Kovač J, Podkrajšek KT, Battelino S, Pavlič A. Hočevar L, et al. Among authors: battelino s. Data Brief. 2020 Aug 25;32:106224. doi: 10.1016/j.dib.2020.106224. eCollection 2020 Oct. Data Brief. 2020. PMID: 32944598 Free PMC article.
Review article: Structural brain alterations in prelingually deaf.
Hribar M, Šuput D, Battelino S, Vovk A. Hribar M, et al. Among authors: battelino s. Neuroimage. 2020 Oct 15;220:117042. doi: 10.1016/j.neuroimage.2020.117042. Epub 2020 Jun 10. Neuroimage. 2020. PMID: 32534128 Free article. Review.
Central nystagmus in progressive supranuclear palsy: A neglected clinical feature?
Klarendic M, Hribar M, Urbancic NB, Zupancic N, Kramberger MG, Trost M, Battelino S, Kaski D, Kojovic M. Klarendic M, et al. Among authors: battelino s. Parkinsonism Relat Disord. 2021 Mar;84:15-22. doi: 10.1016/j.parkreldis.2021.01.003. Epub 2021 Jan 12. Parkinsonism Relat Disord. 2021. PMID: 33517029
The Importance of Early Genetic Diagnostics of Hearing Loss in Children.
Božanić Urbančič N, Battelino S, Tesovnik T, Trebušak Podkrajšek K. Božanić Urbančič N, et al. Among authors: battelino s. Medicina (Kaunas). 2020 Sep 14;56(9):471. doi: 10.3390/medicina56090471. Medicina (Kaunas). 2020. PMID: 32937936 Free PMC article. Review.
34 results