检索结果 - Minna Pöyhönen

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  1. 1
    Prevalence of neurofibromatosis type 1 in the Finnish population

    Prevalence of neurofibromatosis type 1 in the Finnish population 由 Roope A. Kallionpää, Elina Uusitalo, Jussi Leppävirta, Minna Pöyhönen, Sirkku Peltonen, Juha Peltonen

    出版 2017
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  2. 2
    Fibrosis and Stenosis of the Long Penetrating Cerebral Arteries: the Cause of the White Matter Pathology in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy

    Fibrosis and Stenosis of the Long Penetrating Cerebral Arteries: the Cause of the White Matter Pathology in Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and L... 由 Qing Miao, Timo Paloneva, Susanna Tuominen, Minna Pöyhönen, Seppo Tuisku, Matti Viitanen, Hannu Kalimo

    出版 2004
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  3. 3
    Insidious Cognitive Decline in CADASIL

    Insidious Cognitive Decline in CADASIL 由 Kaarina Amberla, Minna Wäljas, Susanna Tuominen, Ove Almkvist, Minna Pöyhönen, Seppo Tuisku, Hannu Kalimo, Matti Viitanen

    出版 2004
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  4. 4
    Incidence and Mortality of Neurofibromatosis: A Total Population Study in Finland

    Incidence and Mortality of Neurofibromatosis: A Total Population Study in Finland 由 Elina Uusitalo, Jussi Leppävirta, Anna Koffert, Sakari Suominen, Jussi Vahtera, Tero Vahlberg, Minna Pöyhönen, Juha Peltonen, Sirkku Peltonen

    出版 2014
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  5. 5
    Pediatric malignancies in neurofibromatosis type 1: A population‐based cohort study

    Pediatric malignancies in neurofibromatosis type 1: A population‐based cohort study 由 Sirkku Peltonen, Roope A. Kallionpää, Matti Rantanen, Elina Uusitalo, Päivi M. Lähteenmäki, Minna Pöyhönen, Janne Pitkäniemi, Juha Peltonen

    出版 2019
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  6. 6
    Positron Emission Tomography Examination of Cerebral Blood Flow and Glucose Metabolism in Young CADASIL Patients

    Positron Emission Tomography Examination of Cerebral Blood Flow and Glucose Metabolism in Young CADASIL Patients 由 Susanna Tuominen, Qing Miao, Timo Kurki, Seppo Tuisku, Minna Pöyhönen, Hannu Kalimo, Matti Viitanen, Hannu Sipilä, Jörgen Bergman, Juha O. Rinne

    出版 2004
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  7. 7
    <scp>CADASIL</scp> and <scp>CARASIL</scp>

    <scp>CADASIL</scp> and <scp>CARASIL</scp> 由 Saara Tikka, Marc Baumann, Maija Siitonen, Petra Pasanen, Minna Pöyhönen, Liisa Myllykangas, Matti Viitanen, Toshio Fukutake, Emmanuel Cognat, Anne Joutel, Hannu Kalimo

    出版 2014
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    Revisão
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  8. 8
    Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families

    Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families 由 Pia Huusko, Kati Pääkkönen, Virpi Launonen, Minna Pöyhönen, Guillermo Blanco, Antti Kauppila, Ulla Puistola, Heikki Kiviniemi, Marika Kujala, Jaakko Leisti, Robert Winqvist

    出版 1998
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  9. 9
    Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients

    Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients 由 Saara Tikka, Kati Mykkänen, Marie‐Magdeleine Ruchoux, Robert Bergholm, Maija Junna, Minna Pöyhönen, Hannele Yki‐Järvinen, Anne Joutel, Matti Viitanen, Marc Baumann, Hannu Kalimo

    出版 2009
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  10. 10
    Breast cancer in neurofibromatosis type 1: overrepresentation of unfavourable prognostic factors

    Breast cancer in neurofibromatosis type 1: overrepresentation of unfavourable prognostic factors 由 Elina Uusitalo, Roope A. Kallionpää, Samu Kurki, Matti Rantanen, Janne Pitkäniemi, Pauliina Kronqvist, Pirkko Härkönen, Riikka Huovinen, Olli Carpén, Minna Pöyhönen, Sirkku Peltonen, Juha Peltonen

    出版 2016
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  11. 11
    Phenotype of a Homozygous CADASIL Patient in Comparison to 9 Age-Matched Heterozygous Patients With the Same R133C <b> <i>Notch3</i> </b> Mutation

    Phenotype of a Homozygous CADASIL Patient in Comparison to 9 Age-Matched Heterozygous Patients With the Same R133C <b> <i>Notch3</i> </b> Mutation 由 Susanna Tuominen, Vesa Juvonen, Kaarina Amberla, T. Jolma, Juha O. Rinne, Seppo Tuisku, Timo Kurki, Reijo J. Marttila, Minna Pöyhönen, Marja‐Liisa Savontaus, Matti Viitanen, Hannu Kalimo

    出版 2001
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  12. 12
    Large genomic rearrangements and germline epimutations in Lynch syndrome

    Large genomic rearrangements and germline epimutations in Lynch syndrome 由 Annette Gylling, Maaret Ridanpää, Outi Vierimaa, Kristiina Aittomäki, Kristiina Avela, Helena Kääriäinen, Hannele Laivuori, Minna Pöyhönen, Satu‐Leena Sallinen, Carina Wallgren‐Pettersson, Heikki Järvinen, Jukka‐Pekka Mecklin, Païvi Peltomäki

    出版 2008
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  13. 13
    Loss of SUFU Function in Familial Multiple Meningioma

    Loss of SUFU Function in Familial Multiple Meningioma 由 Mervi Aavikko, Song-Ping Li, Silva Saarinen, Pia Alhopuro, Eevi Kaasinen, Ekaterina Morgunova, Yilong Li, Kari Vesanen, Miriam J. Smith, D. Gareth Evans, Minna Pöyhönen, Anne Kiuru, Anssi Auvinen, Lauri A. Aaltonen, Jussi Taipale, Pia Vahteristo

    出版 2012
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  14. 14
    APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study

    APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study 由 Samu Kurki, Jonas Kantonen, Karri Kaivola, Laura Hokkanen, Mikko I. Mäyränpää, Henri Puttonen, Juha Martola, Minna Pöyhönen, Mia Kero, Jarno Tuimala, Olli Carpén, Anu Kantele, Olli Vapalahti, Marjaana Tiainen, Pentti J. Tienari, Kai Kaila, Johanna Hästbacka, Liisa Myllykangas

    出版 2021
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  15. 15
    Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

    Novel TMEM173 Mutation and the Role of Disease Modifying Alleles 由 Salla Keskitalo, Emma Haapaniemi, Elísabet Einarsdóttir, Kristiina Rajamäki, Hannele Heikkilä, Mette Ilander, Minna Pöyhönen, Ekaterina Morgunova, Kati Hokynar, Sonja Lagström, Sirpa Kivirikko, Satu Mustjoki, Kari K. Eklund, Janna Saarela, Juha Kere, Mikko Seppänen, Annamari Ranki, Katariina Hannula-Jouppi, Markku Varjosalo

    出版 2019
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  16. 16
    Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy

    Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy 由 Mikko Muona, Ryosuke Ishimura, Anni Laari, Yoshinobu Ichimura, Tarja Linnankivi, Riikka Keski‐Filppula, Riitta Herva, Heikki Rantala, Anders Paetau, Minna Pöyhönen, Miki Obata, Takefumi Uemura, Thomas Karhu, Norihisa Bizen, Hirohide Takebayashi, Shane McKee, Michael Parker, Nadia Akawi, Jeremy F. McRae, Matthew E. Hurles, Outi Kuismin, Mitja Kurki, Anna‐Kaisa Anttonen, Keiji Tanaka, Aarno Palotie, Satoshi Waguri, Anna‐Elina Lehesjoki, Masaaki Komatsu

    出版 2016
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