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

Year Number of Results
2005 1
2006 1
2014 1
2015 2
2016 3
2017 2
2018 1
2019 2
2020 7
2021 9
2022 6
2023 5
2024 1

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38 results

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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.
Genetic Evaluation of Prelingual Hearing Impairment: Recommendations of an European Network for Genetic Hearing Impairment.
Jonard L, Brotto D, Moreno-Pelayo MA, Del Castillo I, Kremer H, Pennings R, Caria H, Fialho G, Boudewyns A, Van Camp G, Ołdak M, Oziębło D, Deggouj N, De Siati RD, Gasparini P, Girotto G, Verstreken M, Dossena S, Roesch S, Battelino S, Trebušak Podkrajšek K, Warnecke A, Lenarz T, Lesinski-Schiedat A, Mondain M, Roux AF, Denoyelle F, Loundon N, Serey Gaut M, Trevisi P, Rubinato E, Martini A, Marlin S. Jonard L, et al. Among authors: battelino s. Audiol Res. 2023 May 10;13(3):341-346. doi: 10.3390/audiolres13030029. Audiol Res. 2023. PMID: 37218840 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.
Vector-Borne Tularemia: A Re-Emerging Cause of Cervical Lymphadenopathy.
Troha K, Božanić Urbančič N, Korva M, Avšič-Županc T, Battelino S, Vozel D. Troha K, et al. Among authors: battelino s. Trop Med Infect Dis. 2022 Aug 16;7(8):189. doi: 10.3390/tropicalmed7080189. Trop Med Infect Dis. 2022. PMID: 36006281 Free PMC article. Review.
Autologous Platelet and Extracellular Vesicle-Rich Plasma as Therapeutic Fluid: A Review.
Troha K, Vozel D, Arko M, Bedina Zavec A, Dolinar D, Hočevar M, Jan Z, Kisovec M, Kocjančič B, Pađen L, Pajnič M, Penič S, Romolo A, Repar N, Spasovski V, Steiner N, Šuštar V, Iglič A, Drobne D, Kogej K, Battelino S, Kralj-Iglič V. Troha K, et al. Among authors: battelino s. Int J Mol Sci. 2023 Feb 8;24(4):3420. doi: 10.3390/ijms24043420. Int J Mol Sci. 2023. PMID: 36834843 Free PMC article. Review.
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.
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.
38 results