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

Year Number of Results
1956 1
2000 1
2004 2
2005 2
2006 2
2008 1
2010 4
2012 2
2013 3
2014 3
2015 4
2016 5
2017 1
2020 2
2021 1
2024 0

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31 results

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Page 1
AIRE-Deficient Patients Harbor Unique High-Affinity Disease-Ameliorating Autoantibodies.
Meyer S, Woodward M, Hertel C, Vlaicu P, Haque Y, Kärner J, Macagno A, Onuoha SC, Fishman D, Peterson H, Metsküla K, Uibo R, Jäntti K, Hokynar K, Wolff ASB; APECED patient collaborative; Krohn K, Ranki A, Peterson P, Kisand K, Hayday A. Meyer S, et al. Cell. 2016 Jul 28;166(3):582-595. doi: 10.1016/j.cell.2016.06.024. Epub 2016 Jul 14. Cell. 2016. PMID: 27426947 Free PMC article.
IL-6-specific autoantibodies among APECED and thymoma patients.
Kärner J, Pihlap M, Ranki A, Krohn K, Trebusak Podkrajsek K, Bratanic N, Battelino T, Willcox N, Peterson P, Kisand K. Kärner J, et al. Among authors: bratanic n. Immun Inflamm Dis. 2016 May 25;4(2):235-243. doi: 10.1002/iid3.109. eCollection 2016 Jun. Immun Inflamm Dis. 2016. PMID: 27957331 Free PMC article.
Universal Screening for Familial Hypercholesterolemia in Children.
Klančar G, Grošelj U, Kovač J, Bratanič N, Bratina N, Trebušak Podkrajšek K, Battelino T. Klančar G, et al. Among authors: bratanic n. J Am Coll Cardiol. 2015 Sep 15;66(11):1250-1257. doi: 10.1016/j.jacc.2015.07.017. J Am Coll Cardiol. 2015. PMID: 26361156 Free article.
Multifocal gastric adenocarcinoma in a patient with LRBA deficiency.
Bratanič N, Kovač J, Pohar K, Trebušak Podkrajšek K, Ihan A, Battelino T, Avbelj Stefanija M. Bratanič N, et al. Orphanet J Rare Dis. 2017 Jul 18;12(1):131. doi: 10.1186/s13023-017-0682-5. Orphanet J Rare Dis. 2017. PMID: 28720148 Free PMC article.
GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.
Ludvigsson J, Krisky D, Casas R, Battelino T, Castaño L, Greening J, Kordonouri O, Otonkoski T, Pozzilli P, Robert JJ, Veeze HJ, Palmer J, Samuelsson U, Elding Larsson H, Åman J, Kärdell G, Neiderud Helsingborg J, Lundström G, Albinsson E, Carlsson A, Nordvall M, Fors H, Arvidsson CG, Edvardson S, Hanås R, Larsson K, Rathsman B, Forsgren H, Desaix H, Forsander G, Nilsson NÖ, Åkesson CG, Keskinen P, Veijola R, Talvitie T, Raile K, Kapellen T, Burger W, Neu A, Engelsberger I, Heidtmann B, Bechtold S, Leslie D, Chiarelli F, Cicognani A, Chiumello G, Cerutti F, Zuccotti GV, Gomez Gila A, Rica I, Barrio R, Clemente M, López Garcia MJ, Rodriguez M, Gonzalez I, Lopez JP, Oyarzabal M, Reeser HM, Nuboer R, Stouthart P, Bratina N, Bratanic N, de Kerdanet M, Weill J, Ser N, Barat P, Bertrand AM, Carel JC, Reynaud R, Coutant R, Baron S. Ludvigsson J, et al. Among authors: bratanic n. N Engl J Med. 2012 Feb 2;366(5):433-42. doi: 10.1056/NEJMoa1107096. N Engl J Med. 2012. PMID: 22296077 Free article. Clinical Trial.
Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency.
Avbelj Stefanija M, Kotnik P, Bratanič N, Žerjav Tanšek M, Bertok S, Bratina N, Battelino T, Trebušak Podkrajšek K. Avbelj Stefanija M, et al. Among authors: bratanic n. Horm Res Paediatr. 2015;84(3):153-8. doi: 10.1159/000433468. Epub 2015 Jun 24. Horm Res Paediatr. 2015. PMID: 26111865
31 results