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

Year Number of Results
2003 2
2004 1
2005 2
2006 1
2008 3
2009 3
2010 1
2011 1
2012 1
2013 4
2014 2
2015 1
2016 2
2017 1
2018 2
2019 4
2020 2
2021 5
2022 3
2023 2
2024 1

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35 results

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Page 1
Skin Microbiota and Clinical Associations in Netherton Syndrome.
Sillanpää V, Soratto TAT, Eränkö E, Barrientos-Somarribas M, Hannula-Jouppi K, Andersson B, Ranki A. Sillanpää V, et al. Among authors: hannula jouppi k. JID Innov. 2021 Mar 5;1(2):100008. doi: 10.1016/j.xjidi.2021.100008. eCollection 2021 Jun. JID Innov. 2021. PMID: 34909712 Free PMC article.
Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis.
Sliz E, Huilaja L, Pasanen A, Laisk T, Reimann E, Mägi R; FinnGen; Estonian Biobank Research Team; Hannula-Jouppi K, Peltonen S, Salmi T, Koulu L, Tasanen K, Kettunen J. Sliz E, et al. Among authors: hannula jouppi k. J Allergy Clin Immunol. 2022 Mar;149(3):1105-1112.e9. doi: 10.1016/j.jaci.2021.07.043. Epub 2021 Aug 27. J Allergy Clin Immunol. 2022. PMID: 34454985 Free article.
Genetic susceptibility to non-necrotizing erysipelas/cellulitis.
Hannula-Jouppi K, Massinen S, Siljander T, Mäkelä S, Kivinen K, Leinonen R, Jiao H, Aitos P, Karppelin M, Vuopio J, Syrjänen J, Kere J. Hannula-Jouppi K, et al. PLoS One. 2013;8(2):e56225. doi: 10.1371/journal.pone.0056225. Epub 2013 Feb 20. PLoS One. 2013. PMID: 23437094 Free PMC article.
Cyclosporine treatment in severe gestational pemphigoid.
Huilaja L, Mäkikallio K, Hannula-Jouppi K, Väkevä L, Höök-Nikanne J, Tasanen K. Huilaja L, et al. Among authors: hannula jouppi k. Acta Derm Venereol. 2015 May;95(5):593-5. doi: 10.2340/00015555-2032. Acta Derm Venereol. 2015. PMID: 25519774 Free article.
Novel DSP Spectrin 6 Region Variant Causes Neonatal Erythroderma, Failure to Thrive, Severe Herpes Simplex Infections and Brain Lesions.
Vakkilainen S, Puhakka L, Klemetti P, Heiskanen K, Seppänen M, Muona M, Posseme C, Duffy D, Väisänen T, Elomaa O, Palomäki M, Saxén H, Ranki A, Hannula-Jouppi K. Vakkilainen S, et al. Among authors: hannula jouppi k. Acta Derm Venereol. 2019 Jul 1;99(9):789-796. doi: 10.2340/00015555-3203. Acta Derm Venereol. 2019. PMID: 31037311 Free article. Review.
Immune cell phenotype and functional defects in Netherton syndrome.
Eränkö E, Ilander M, Tuomiranta M, Mäkitie A, Lassila T, Kreutzman A, Klemetti P, Mustjoki S, Hannula-Jouppi K, Ranki A. Eränkö E, et al. Among authors: hannula jouppi k. Orphanet J Rare Dis. 2018 Nov 26;13(1):213. doi: 10.1186/s13023-018-0956-6. Orphanet J Rare Dis. 2018. PMID: 30477583 Free PMC article.
Hereditary palmoplantar keratoderma - phenotypes and mutations in 64 patients.
Harjama L, Karvonen V, Kettunen K, Elomaa O, Einarsdottir E, Heikkilä H, Kivirikko S, Ellonen P, Saarela J, Ranki A, Kere J, Hannula-Jouppi K. Harjama L, et al. Among authors: hannula jouppi k. J Eur Acad Dermatol Venereol. 2021 Sep;35(9):1874-1880. doi: 10.1111/jdv.17314. Epub 2021 May 21. J Eur Acad Dermatol Venereol. 2021. PMID: 33914963
Novel TMEM173 Mutation and the Role of Disease Modifying Alleles.
Keskitalo S, Haapaniemi E, Einarsdottir E, Rajamäki K, Heikkilä H, Ilander M, Pöyhönen M, Morgunova E, Hokynar K, Lagström S, Kivirikko S, Mustjoki S, Eklund K, Saarela J, Kere J, Seppänen MRJ, Ranki A, Hannula-Jouppi K, Varjosalo M. Keskitalo S, et al. Among authors: hannula jouppi k. Front Immunol. 2019 Dec 5;10:2770. doi: 10.3389/fimmu.2019.02770. eCollection 2019. Front Immunol. 2019. PMID: 31866997 Free PMC article.
DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma.
Heliö K, Brandt E, Vaara S, Weckström S, Harjama L, Kandolin R, Järviö J, Hannula-Jouppi K, Heliö T, Holmström M, Koskenvuo JW. Heliö K, et al. Among authors: hannula jouppi k. Front Cardiovasc Med. 2023 Mar 15;10:1130903. doi: 10.3389/fcvm.2023.1130903. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37008330 Free PMC article.
35 results