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Page 1
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: kivirikko s. 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
Nagashima-type palmoplantar keratosis in Finland caused by a SERPINB7 founder mutation.
Hannula-Jouppi K, Harjama L, Einarsdottir E, Elomaa O, Kettunen K, Saarela J, Soronen M, Bouchard L, Lappalainen K, Heikkilä H, Kivirikko S, Seppänen MRJ, Kere J, Ranki A. Hannula-Jouppi K, et al. Among authors: kivirikko s. J Am Acad Dermatol. 2020 Aug;83(2):643-645. doi: 10.1016/j.jaad.2019.11.004. Epub 2019 Nov 7. J Am Acad Dermatol. 2020. PMID: 31706940 Free article. No abstract available.
Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma.
Harjama L, Kettunen K, Elomaa O, Einarsdottir E, Heikkilä H, Kivirikko S, Lappalainen K, Saarela J, Alby C, Ranki A, Kere J, Hadj-Rabia S, Hannula-Jouppi K. Harjama L, et al. Among authors: kivirikko s. Acta Derm Venereol. 2020 Feb 25;100(4):adv00060. doi: 10.2340/00015555-3404. Acta Derm Venereol. 2020. PMID: 31944258 Free PMC article. No abstract available.
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: kivirikko s. Front Immunol. 2019 Dec 5;10:2770. doi: 10.3389/fimmu.2019.02770. eCollection 2019. Front Immunol. 2019. PMID: 31866997 Free PMC article.
Intrafamily and Interfamilial Phenotype Variation and Immature Immunity in Patients With Netherton Syndrome and Finnish SPINK5 Founder Mutation.
Hannula-Jouppi K, Laasanen SL, Ilander M, Furio L, Tuomiranta M, Marttila R, Jeskanen L, Häyry V, Kanerva M, Kivirikko S, Tuomi ML, Heikkilä H, Mustjoki S, Hovnanian A, Ranki A. Hannula-Jouppi K, et al. Among authors: kivirikko s. JAMA Dermatol. 2016 Apr;152(4):435-42. doi: 10.1001/jamadermatol.2015.5827. JAMA Dermatol. 2016. PMID: 26865388
Recessive MYH3 variants cause "Contractures, pterygia, and variable skeletal fusions syndrome 1B" mimicking Escobar variant multiple pterygium syndrome.
Hakonen AH, Lehtonen J, Kivirikko S, Keski-Filppula R, Moilanen J, Kivisaari R, Almusa H, Jakkula E, Saarela J, Avela K, Aittomäki K. Hakonen AH, et al. Among authors: kivirikko s. Am J Med Genet A. 2020 Nov;182(11):2605-2610. doi: 10.1002/ajmg.a.61836. Epub 2020 Sep 9. Am J Med Genet A. 2020. PMID: 32902138
IgE allergen component-based profiling and atopic manifestations in patients with Netherton syndrome.
Hannula-Jouppi K, Laasanen SL, Heikkilä H, Tuomiranta M, Tuomi ML, Hilvo S, Kluger N, Kivirikko S, Hovnanian A, Mäkinen-Kiljunen S, Ranki A. Hannula-Jouppi K, et al. Among authors: kivirikko s. J Allergy Clin Immunol. 2014 Oct;134(4):985-8. doi: 10.1016/j.jaci.2014.07.008. Epub 2014 Aug 23. J Allergy Clin Immunol. 2014. PMID: 25159469 No abstract available.
The Value of FLG Null Mutations in Predicting Treatment Response in Atopic Dermatitis: An Observational Study in Finnish Patients.
Luukkonen TM, Kiiski V, Ahola M, Mandelin J, Virtanen H, Pöyhönen M, Kivirikko S, Surakka I, Reitamo S, Palotie A, Heliövaara M, Jakkula E, Remitz A. Luukkonen TM, et al. Among authors: kivirikko s. Acta Derm Venereol. 2017 Apr 6;97(4):456-463. doi: 10.2340/00015555-2578. Acta Derm Venereol. 2017. PMID: 27840886 Free article.
38 results