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Year Number of Results
2004 1
2006 3
2009 1
2011 2
2012 1
2013 1
2014 1
2015 4
2016 3
2017 4
2018 4
2019 1
2020 1
2021 5
2022 5
2023 4
2024 0

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37 results

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Page 1
Rezidivierende fulminante Myokarditis mit wiederholtem Einsatz der ECMO bei einem Kind.
Vercek G, Markelj G, Mlakar G, Primec ZR, Bertok S, Writzl K, Stefanija MA, Bajic S, Vesel S, Ihan A, Stritar A, Pokorn M, Kovac J, Debeljak M, Vidmar I, Avcin T, Grosek S. Vercek G, et al. Among authors: bertok s. Klin Padiatr. 2019 Mar;231(2):80-86. doi: 10.1055/a-0831-2593. Epub 2019 Mar 14. Klin Padiatr. 2019. PMID: 30870874 German.
Diverse manifestations of a sickle cell crisis.
Hashemzehi T, Bertok S, Figaszewska MJ, Batura D. Hashemzehi T, et al. Among authors: bertok s. BMJ Case Rep. 2021 Jan 28;14(1):e236743. doi: 10.1136/bcr-2020-236743. BMJ Case Rep. 2021. PMID: 33509861 Free PMC article.
Assessment of the Genetic Spectrum of Uncombable Hair Syndrome in a Cohort of 107 Individuals.
Basmanav FB, Cesarato N, Kumar S, Borisov O, Kokordelis P, Ralser DJ, Wehner M, Axt D, Xiong X, Thiele H, Dolgin V, Gossmann Y, Fricker N, Dewenter MK, Weller K, Suri M, Reichenbach H, Oji V, Addor MC, Ramirez K, Stewart H, Garcia Bartels N, Weibel L, Wagner N, George S, Kilic A, Tantcheva-Poor I, Stewart A, Dikow N, Blaumeiser B, Medvecz M, Blume-Peytavi U, Farrant P, Grimalt R, Bertok S, Bradley L, Eskin-Schwartz M, Birk OS, Bygum A, Simon M, Krawitz P, Fischer C, Hamm H, Fritz G, Betz RC. Basmanav FB, et al. Among authors: bertok s. JAMA Dermatol. 2022 Nov 1;158(11):1245-1253. doi: 10.1001/jamadermatol.2022.2319. JAMA Dermatol. 2022. PMID: 36044230 Free PMC article.
Long-Term Follow-Up of Three Family Members with a Novel NNT Pathogenic Variant Causing Primary Adrenal Insufficiency.
Krasovec T, Sikonja J, Zerjav Tansek M, Debeljak M, Ilovar S, Trebusak Podkrajsek K, Bertok S, Tesovnik T, Kovac J, Suput Omladic J, Hartmann MF, Wudy SA, Avbelj Stefanija M, Battelino T, Kotnik P, Groselj U. Krasovec T, et al. Among authors: bertok s. Genes (Basel). 2022 Apr 20;13(5):717. doi: 10.3390/genes13050717. Genes (Basel). 2022. PMID: 35627102 Free PMC article.
Genetic and clinical characteristics including occurrence of testicular adrenal rest tumors in Slovak and Slovenian patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Saho R, Dolzan V, Zerjav Tansek M, Pastorakova A, Petrovic R, Knapkova M, Trebusak Podkrajsek K, Suput Omladic J, Bertok S, Avbelj Stefanija M, Kotnik P, Battelino T, Pribilincova Z, Groselj U. Saho R, et al. Among authors: bertok s. Front Endocrinol (Lausanne). 2023 Mar 17;14:1134133. doi: 10.3389/fendo.2023.1134133. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37008950 Free PMC article.
Clinical and genetic characteristics of a patient with phosphoribosyl pyrophosphate synthetase 1 deficiency and a systematic literature review.
Štajer K, Kovač N, Šikonja J, Mlinarič M, Bertok S, Brecelj J, Debeljak M, Kovač J, Markelj G, Neubauer D, Rus R, Žerjav Tanšek M, Drole Torkar A, Zver A, Battelino T, Jiménez Torres R, Grošelj U. Štajer K, et al. Among authors: bertok s. Mol Genet Metab Rep. 2023 Jun 19;36:100986. doi: 10.1016/j.ymgmr.2023.100986. eCollection 2023 Sep. Mol Genet Metab Rep. 2023. PMID: 37670898 Free PMC article.
37 results