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

Year Number of Results
1993 2
2003 2
2004 1
2005 3
2006 2
2007 1
2011 1
2012 1
2013 3
2014 3
2015 2
2017 4
2018 1
2019 5
2020 12
2021 15
2022 5
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53 results
Results by year
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Page 1
Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency.
Vavassori S, Chou J, Faletti LE, Haunerdinger V, Opitz L, Joset P, Fraser CJ, Prader S, Gao X, Schuch LA, Wagner M, Hoefele J, Maccari ME, Zhu Y, Elakis G, Gabbett MT, Forstner M, Omran H, Kaiser T, Kessler C, Olbrich H, Frosk P, Almutairi A, Platt CD, Elkins M, Weeks S, Rubin T, Planas R, Marchetti T, Koovely D, Klämbt V, Soliman NA, von Hardenberg S, Klemann C, Baumann U, Lenz D, Klein-Franke A, Schwemmle M, Huber M, Sturm E, Hartleif S, Häffner K, Gimpel C, Brotschi B, Laube G, Güngör T, Buckley MF, Kottke R, Staufner C, Hildebrandt F, Reu-Hofer S, Moll S, Weber A, Kaur H, Ehl S, Hiller S, Geha R, Roscioli T, Griese M, Pachlopnik Schmid J. Vavassori S, et al. Among authors: kottke r. J Allergy Clin Immunol. 2021 Aug;148(2):381-393. doi: 10.1016/j.jaci.2021.03.045. Epub 2021 Apr 17. J Allergy Clin Immunol. 2021. PMID: 33872655 Free PMC article. Clinical Trial.
[Gastrointestinal stromal tumors].
Kottke R, Ioanoviciu S, Horger M. Kottke R, et al. Rofo. 2006 Feb;178(2):141-4. doi: 10.1055/s-2006-932244. Rofo. 2006. PMID: 16435237 Review. German. No abstract available.
Lissencephaly with Brainstem Hypoplasia and Dysplasia: Think MACF1.
Bölsterli BK, Steindl K, Kottke R, Steinfeld R, Boltshauser E. Bölsterli BK, et al. Among authors: kottke r. Neuropediatrics. 2021 Jun;52(3):227. doi: 10.1055/s-0040-1722690. Epub 2021 Jan 28. Neuropediatrics. 2021. PMID: 33511591 No abstract available.
Genotype-phenotype spectrum in isolated and syndromic nanophthalmos.
Lang E, Koller S, Atac D, Pfäffli OA, Hanson JVM, Feil S, Bähr L, Bahr A, Kottke R, Joset P, Fasler K, Barthelmes D, Steindl K, Konrad D, Wille DA, Berger W, Gerth-Kahlert C. Lang E, et al. Among authors: kottke r. Acta Ophthalmol. 2021 Jun;99(4):e594-e607. doi: 10.1111/aos.14615. Epub 2020 Sep 30. Acta Ophthalmol. 2021. PMID: 32996714
Pontocerebellar Hypoplasia: a Pattern Recognition Approach.
Rüsch CT, Bölsterli BK, Kottke R, Steinfeld R, Boltshauser E. Rüsch CT, et al. Among authors: kottke r. Cerebellum. 2020 Aug;19(4):569-582. doi: 10.1007/s12311-020-01135-5. Cerebellum. 2020. PMID: 32410094
Sinus pericranii with facial involvement-A great mimicker.
Knöpfel N, Theiler M, Nieman E, Gnannt R, Kottke R, Altermatt S, Bayliss SJ, Weibel L. Knöpfel N, et al. Among authors: kottke r. Pediatr Dermatol. 2021 Jul;38(4):899-903. doi: 10.1111/pde.14654. Epub 2021 Jun 21. Pediatr Dermatol. 2021. PMID: 34152030
Heterozygous truncating variants in SUFU cause congenital ocular motor apraxia.
Schröder S, Li Y, Yigit G, Altmüller J, Bader I, Bevot A, Biskup S, Dreha-Kulaczewski S, Christoph Korenke G, Kottke R, Mayr JA, Preisel M, Toelle SP, Wente-Schulz S, Wortmann SB, Hahn H, Boltshauser E, Uhmann A, Wollnik B, Brockmann K. Schröder S, et al. Among authors: kottke r. Genet Med. 2021 Feb;23(2):341-351. doi: 10.1038/s41436-020-00979-w. Epub 2020 Oct 7. Genet Med. 2021. PMID: 33024317 Free PMC article.
Genetic Analysis in a Swiss Cohort of Bilateral Congenital Cataract.
Rechsteiner D, Issler L, Koller S, Lang E, Bähr L, Feil S, Rüegger CM, Kottke R, Toelle SP, Zweifel N, Steindl K, Joset P, Zweier M, Suter AA, Gogoll L, Haas C, Berger W, Gerth-Kahlert C. Rechsteiner D, et al. Among authors: kottke r. JAMA Ophthalmol. 2021 Jul 1;139(7):691-700. doi: 10.1001/jamaophthalmol.2021.0385. JAMA Ophthalmol. 2021. PMID: 34014271 Free PMC article.
Emerging magnetic resonance imaging techniques in open spina bifida in utero.
Jakab A, Payette K, Mazzone L, Schauer S, Muller CO, Kottke R, Ochsenbein-Kölble N, Tuura R, Moehrlen U, Meuli M. Jakab A, et al. Among authors: kottke r. Eur Radiol Exp. 2021 Jun 17;5(1):23. doi: 10.1186/s41747-021-00219-z. Eur Radiol Exp. 2021. PMID: 34136989 Free PMC article. Review.
53 results