Search Results - Seppänen, Mikko

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  1. 1
    Myiasis During Adventure Sports Race

    Myiasis During Adventure Sports Race by Seppänen, Mikko, Virolainen-Julkunen, Anni, Kakko, Iiro, Vilkamaa, Pekka, Meri, Seppo

    Published 2004
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  2. 2
    Clinical Challenges: Identification of Patients with Novel Primary Immunodeficiency Syndromes

    Clinical Challenges: Identification of Patients with Novel Primary Immunodeficiency Syndromes by Buchbinder, David, Seppanen, Mikko, Rao, V. Koneti, Uzel, Gulbu, Nugent, Diane

    Published 2018
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  3. 3
    Copy Number Analysis of Complement C4A, C4B and C4A Silencing Mutation by Real-Time Quantitative Polymerase Chain Reaction

    Copy Number Analysis of Complement C4A, C4B and C4A Silencing Mutation by Real-Time Quantitative Polymerase Chain Reaction by Paakkanen, Riitta, Vauhkonen, Hanna, Eronen, Katja T., Järvinen, Asko, Seppänen, Mikko, Lokki, Marja-Liisa

    Published 2012
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  4. 4
    Correction: Copy Number Analysis of Complement C4A, C4B and C4A Silencing Mutation by Real-Time Quantitative Polymerase Chain Reaction

    Correction: Copy Number Analysis of Complement C4A, C4B and C4A Silencing Mutation by Real-Time Quantitative Polymerase Chain Reaction by Paakkanen, Riitta, Vauhkonen, Hanna, Eronen, Katja T., Järvinen, Asko, Seppänen, Mikko, Lokki, Marja-Liisa

    Published 2012
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  5. 5
    Inhibition of rubella virus replication by the broad-spectrum drug nitazoxanide in cell culture and in a patient with a primary immune deficiency

    Inhibition of rubella virus replication by the broad-spectrum drug nitazoxanide in cell culture and in a patient with a primary immune deficiency by Perelygina, Ludmila, Hautala, Timo, Seppänen, Mikko, Adebayo, Adebola, Sullivan, Kathleen E., Icenogle, Joseph

    Published 2017
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  6. 6
    A High Prevalence of Gastrointestinal Manifestations in Common Variable Immunodeficiency

    A High Prevalence of Gastrointestinal Manifestations in Common Variable Immunodeficiency by Pikkarainen, Sampsa, Martelius, Timi, Ristimäki, Ari, Siitonen, Sanna, Seppänen, Mikko R.J., Färkkilä, Martti

    Published 2019
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  7. 7
    Pulmonary Follow-Up Imaging in Cartilage-Hair Hypoplasia: a Prospective Cohort Study

    Pulmonary Follow-Up Imaging in Cartilage-Hair Hypoplasia: a Prospective Cohort Study by Vakkilainen, Svetlana, Klemetti, Paula, Martelius, Timi, Seppänen, Mikko JR, Mäkitie, Outi, Toiviainen-Salo, Sanna

    Published 2021
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  8. 8
    Diversity of Extended HLA-DRB1 Haplotypes in the Finnish Population

    Diversity of Extended HLA-DRB1 Haplotypes in the Finnish Population by Wennerström, Annika, Vlachopoulou, Efthymia, Lahtela, L. Elisa, Paakkanen, Riitta, Eronen, Katja T., Seppänen, Mikko, Lokki, Marja-Liisa

    Published 2013
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  9. 9
    Analysis of clinical and immunologic phenotype in a large cohort of children and adults with cartilage-hair hypoplasia

    Analysis of clinical and immunologic phenotype in a large cohort of children and adults with cartilage-hair hypoplasia by Kostjukovits, Svetlana, Klemetti, Paula, Valta, Helena, Martelius, Timi, Notarangelo, Luigi D., Seppänen, Mikko, Taskinen, Mervi, Mäkitie, Outi

    Published 2017
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  10. 10
    Recurrent Lymphocytic Meningitis Positive for Herpes Simplex Virus Type 2

    Recurrent Lymphocytic Meningitis Positive for Herpes Simplex Virus Type 2 by Kallio-Laine, Katariina, Seppänen, Mikko, Kautiainen, Hannu, Lokki, Marja-Liisa, Lappalainen, Maija, Valtonen, Ville, Färkkilä, Markus, Kalso, Eija

    Published 2009
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  11. 11
    IRF2BP2 Mutation Is Associated with Increased STAT1 and STAT5 Activation in Two Family Members with Inflammatory Conditions and Lymphopenia

    IRF2BP2 Mutation Is Associated with Increased STAT1 and STAT5 Activation in Two Family Members with Inflammatory Conditions and Lymphopenia by Palmroth, Maaria, Viskari, Hanna, Seppänen, Mikko R. J., Keskitalo, Salla, Virtanen, Anniina, Varjosalo, Markku, Silvennoinen, Olli, Isomäki, Pia

    Published 2021
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  12. 12
    Association of Chlamydia pneumoniae Infection with HLA-B*35 in Patients with Coronary Artery Disease

    Association of Chlamydia pneumoniae Infection with HLA-B*35 in Patients with Coronary Artery Disease by Palikhe, Anil, Lokki, Marja-Liisa, Saikku, Pekka, Leinonen, Maija, Paldanius, Mika, Seppänen, Mikko, Valtonen, Ville, Nieminen, Markku S., Sinisalo, Juha

    Published 2008
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  13. 13
    Complement C4 Deficiency – A Plausible Risk Factor for Non-Tuberculous Mycobacteria (NTM) Infection in Apparently Immunocompetent Patients

    Complement C4 Deficiency – A Plausible Risk Factor for Non-Tuberculous Mycobacteria (NTM) Infection in Apparently Immunocompetent Patients by Kotilainen, Hannele, Lokki, Marja-Liisa, Paakkanen, Riitta, Seppänen, Mikko, Tukiainen, Pentti, Meri, Seppo, Poussa, Tuija, Eskola, Jussi, Valtonen, Ville, Järvinen, Asko

    Published 2014
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  14. 14
    European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management

    European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guide... by Brodszki, Nicholas, Frazer-Abel, Ashley, Grumach, Anete S., Kirschfink, Michael, Litzman, Jiri, Perez, Elena, Seppänen, Mikko R. J., Sullivan, Kathleen E., Jolles, Stephen

    Published 2020
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  15. 15
    Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland

    Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland by Trotta, Luca, Hautala, Timo, Hämäläinen, Sari, Syrjänen, Jaana, Viskari, Hanna, Almusa, Henrikki, Lepisto, Maija, Kaustio, Meri, Porkka, Kimmo, Palotie, Aarno, Seppänen, Mikko, Saarela, Janna

    Published 2016
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  16. 16
    Tonsillar granuloma associated with hypogammaglobulinemia

    Tonsillar granuloma associated with hypogammaglobulinemia by Laajala, Aleksi, Kuismin, Outi, Tastula, Mikko, Tiitto, Leena, Kauppila, Saila, Salo, Anna, Åström, Pirjo, Nissinen, Antti, Glumoff, Virpi, Seppänen, Mikko R. J., Hautala, Timo

    Published 2020
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  17. 17
    Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders

    Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders by Trotta, Luca, Norberg, Anna, Taskinen, Mervi, Béziat, Vivien, Degerman, Sofie, Wartiovaara-Kautto, Ulla, Välimaa, Hannamari, Jahnukainen, Kirsi, Casanova, Jean-Laurent, Seppänen, Mikko, Saarela, Janna, Koskenvuo, Minna, Martelius, Timi

    Published 2018
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  18. 18
    Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland

    Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland by Selenius, Jannica S., Martelius, Timi, Pikkarainen, Sampsa, Siitonen, Sanna, Mattila, Eero, Pietikäinen, Risto, Suomalainen, Pekka, Aalto, Arja H., Saarela, Janna, Einarsdottir, Elisabet, Järvinen, Asko, Färkkilä, Martti, Kere, Juha, Seppänen, Mikko

    Published 2017
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  19. 19
    Inborn Errors of Immunity on the Island of Ireland — a Cross-Jurisdictional UKPID/ESID Registry Report

    Inborn Errors of Immunity on the Island of Ireland — a Cross-Jurisdictional UKPID/ESID Registry Report by Ryan, Paul, Redenbaugh, Vyanka, McGucken, Jayne, Kindle, Gerhard, Devlin, Lisa A., Coulter, Tanya, Buckland, Matthew S., Seppänen, Mikko R. J., Conlon, Niall P., Feighery, Conleth, Edgar, J. David M.

    Published 2022
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  20. 20
    Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease

    Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease by Keskitalo, Salla, Haapaniemi, Emma M., Glumoff, Virpi, Liu, Xiaonan, Lehtinen, Ville, Fogarty, Christopher, Rajala, Hanna, Chiang, Samuel C., Mustjoki, Satu, Kovanen, Panu, Lohi, Jouko, Bryceson, Yenan T., Seppänen, Mikko, Kere, Juha, Heiskanen, Kaarina, Varjosalo, Markku

    Published 2019
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