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

Year Number of Results
2010 1
2011 4
2012 2
2013 2
2014 1
2015 1
2016 2
2017 3
2018 2
2019 1
2020 2
2021 2
2022 1
2024 2

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20 results

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Page 1
Therapeutic Approaches to Type I Interferonopathies.
Bienias M, Brück N, Griep C, Wolf C, Kretschmer S, Kind B, Tüngler V, Berner R, Lee-Kirsch MA. Bienias M, et al. Among authors: tungler v. Curr Rheumatol Rep. 2018 Apr 20;20(6):32. doi: 10.1007/s11926-018-0743-3. Curr Rheumatol Rep. 2018. PMID: 29679241 Review.
[Genetic methods for analysis of autoinflammatory diseases].
Bienias M, König N, Wolf C, Kretschmer S, Rösen-Wolff A, Berner R, Tüngler V, Lee-Kirsch MA. Bienias M, et al. Among authors: tungler v. Z Rheumatol. 2017 May;76(4):295-302. doi: 10.1007/s00393-017-0300-x. Z Rheumatol. 2017. PMID: 28378116 Review. German.
Neurofilament light protein as a biomarker for spinal muscular atrophy: a review and reference ranges.
Bayoumy S, Verberk IMW, Vermunt L, Willemse E, den Dulk B, van der Ploeg AT, Pajkrt D, Nitz E, van den Hout JMP, van der Post J, Wolf NI, Beerepoot S, Groen EJN, Tüngler V, Teunissen CE. Bayoumy S, et al. Among authors: tungler v. Clin Chem Lab Med. 2024 Jan 15. doi: 10.1515/cclm-2023-1311. Online ahead of print. Clin Chem Lab Med. 2024. PMID: 38215341 Free article. Review.
Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome.
Wendel EM, Thonke HS, Bertolini A, Baumann M, Blaschek A, Merkenschlager A, Karenfort M, Kornek B, Lechner C, Pohl D, Pritsch M, Schanda K, Schimmel M, Thiels C, Waltz S, Wiegand G, Anlar B, Barisic N, Blank C, Breu M, Broser P, Della Marina A, Diepold K, Eckenweiler M, Eisenkölbl A, Freilinger M, Gruber-Sedlmayr U, Hackenberg A, Iff T, Knierim E, Koch J, Kutschke G, Leiz S, Lischetzki G, Nosadini M, Pschibul A, Reiter-Fink E, Rohrbach D, Salandin M, Sartori S, Schlump JU, Stoffels J, Strautmanis J, Tibussek D, Tüngler V, Utzig N, Reindl M, Rostásy K; BIOMARKER Study Group. Wendel EM, et al. Among authors: tungler v. Neurol Neuroimmunol Neuroinflamm. 2022 Oct 13;9(6):e200035. doi: 10.1212/NXI.0000000000200035. Print 2022 Nov. Neurol Neuroimmunol Neuroinflamm. 2022. PMID: 36229191 Free PMC article.
Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation.
Tüngler V, Doebler-Neumann M, Salandin M, Kaufmann P, Wolf C, Lucas N, Harmuth F, Reichbauer J, Krägeloh-Mann I, Schüle R, Lee-Kirsch MA. Tüngler V, et al. Neurol Genet. 2019 Dec 19;6(1):e384. doi: 10.1212/NXG.0000000000000384. eCollection 2020 Feb. Neurol Genet. 2019. PMID: 32042913 Free PMC article. No abstract available.
Single-stranded nucleic acids promote SAMHD1 complex formation.
Tüngler V, Staroske W, Kind B, Dobrick M, Kretschmer S, Schmidt F, Krug C, Lorenz M, Chara O, Schwille P, Lee-Kirsch MA. Tüngler V, et al. J Mol Med (Berl). 2013 Jun;91(6):759-70. doi: 10.1007/s00109-013-0995-3. Epub 2013 Jan 31. J Mol Med (Berl). 2013. PMID: 23371319
Defective removal of ribonucleotides from DNA promotes systemic autoimmunity.
Günther C, Kind B, Reijns MA, Berndt N, Martinez-Bueno M, Wolf C, Tüngler V, Chara O, Lee YA, Hübner N, Bicknell L, Blum S, Krug C, Schmidt F, Kretschmer S, Koss S, Astell KR, Ramantani G, Bauerfeind A, Morris DL, Cunninghame Graham DS, Bubeck D, Leitch A, Ralston SH, Blackburn EA, Gahr M, Witte T, Vyse TJ, Melchers I, Mangold E, Nöthen MM, Aringer M, Kuhn A, Lüthke K, Unger L, Bley A, Lorenzi A, Isaacs JD, Alexopoulou D, Conrad K, Dahl A, Roers A, Alarcon-Riquelme ME, Jackson AP, Lee-Kirsch MA. Günther C, et al. Among authors: tungler v. J Clin Invest. 2015 Jan;125(1):413-24. doi: 10.1172/JCI78001. Epub 2014 Dec 15. J Clin Invest. 2015. PMID: 25500883 Free PMC article.
20 results