Search Results - Minna Pöyhönen
- Showing 1 - 16 results of 16
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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... by Qing Miao, Timo Paloneva, Susanna Tuominen, Minna Pöyhönen, Seppo Tuisku, Matti Viitanen, Hannu Kalimo
Published 2004Artigo -
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Positron Emission Tomography Examination of Cerebral Blood Flow and Glucose Metabolism in Young CADASIL Patients by Susanna Tuominen, Qing Miao, Timo Kurki, Seppo Tuisku, Minna Pöyhönen, Hannu Kalimo, Matti Viitanen, Hannu Sipilä, Jörgen Bergman, Juha O. Rinne
Published 2004Artigo -
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Breast cancer in neurofibromatosis type 1: overrepresentation of unfavourable prognostic factors by 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
Published 2016Artigo -
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Phenotype of a Homozygous CADASIL Patient in Comparison to 9 Age-Matched Heterozygous Patients With the Same R133C <b> <i>Notch3</i> </b> Mutation by 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
Published 2001Artigo -
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Large genomic rearrangements and germline epimutations in Lynch syndrome by 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
Published 2008Artigo -
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Loss of SUFU Function in Familial Multiple Meningioma by 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
Published 2012Artigo -
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APOE ε4 associates with increased risk of severe COVID-19, cerebral microhaemorrhages and post-COVID mental fatigue: a Finnish biobank, autopsy and clinical study by 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
Published 2021Artigo -
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Novel TMEM173 Mutation and the Role of Disease Modifying Alleles by 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
Published 2019Artigo -
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Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy by 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
Published 2016Artigo
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