Risultati della ricerca - Seppänen, Mikko

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

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

Testo Testo Testo

Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders di 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

Testo Testo Testo

Unexpectedly High Prevalence of Common Variable Immunodeficiency in Finland di 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

Testo Testo Testo

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

Testo Testo Testo

Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease di 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

Testo Testo Testo