Ngā hua rapu - Minna Pöyhönen
- E whakaatu ana i te 1 - 16 hua o te 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... mā Qing Miao, Timo Paloneva, Susanna Tuominen, Minna Pöyhönen, Seppo Tuisku, Matti Viitanen, Hannu Kalimo
I whakaputaina 2004Artigo -
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Insidious Cognitive Decline in CADASIL mā Kaarina Amberla, Minna Wäljas, Susanna Tuominen, Ove Almkvist, Minna Pöyhönen, Seppo Tuisku, Hannu Kalimo, Matti Viitanen
I whakaputaina 2004Artigo -
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Positron Emission Tomography Examination of Cerebral Blood Flow and Glucose Metabolism in Young CADASIL Patients mā Susanna Tuominen, Qing Miao, Timo Kurki, Seppo Tuisku, Minna Pöyhönen, Hannu Kalimo, Matti Viitanen, Hannu Sipilä, Jörgen Bergman, Juha O. Rinne
I whakaputaina 2004Artigo -
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Evidence of Founder Mutations in Finnish BRCA1 and BRCA2 Families mā Pia Huusko, Kati Pääkkönen, Virpi Launonen, Minna Pöyhönen, Guillermo Blanco, Antti Kauppila, Ulla Puistola, Heikki Kiviniemi, Marika Kujala, Jaakko Leisti, Robert Winqvist
I whakaputaina 1998Carta -
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Congruence between NOTCH3 mutations and GOM in 131 CADASIL patients mā Saara Tikka, Kati Mykkänen, Marie‐Magdeleine Ruchoux, Robert Bergholm, Maija Junna, Minna Pöyhönen, Hannele Yki‐Järvinen, Anne Joutel, Matti Viitanen, Marc Baumann, Hannu Kalimo
I whakaputaina 2009Artigo -
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Breast cancer in neurofibromatosis type 1: overrepresentation of unfavourable prognostic factors mā 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
I whakaputaina 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 mā 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
I whakaputaina 2001Artigo -
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Large genomic rearrangements and germline epimutations in Lynch syndrome mā 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
I whakaputaina 2008Artigo -
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Loss of SUFU Function in Familial Multiple Meningioma mā 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
I whakaputaina 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 mā 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
I whakaputaina 2021Artigo -
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Novel TMEM173 Mutation and the Role of Disease Modifying Alleles mā 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
I whakaputaina 2019Artigo -
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Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy mā 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
I whakaputaina 2016Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Medicine
Internal medicine
Pathology
Biology
Disease
Gene
Genetics
Environmental health
Leukoencephalopathy
Population
CADASIL
Mutation
Neurofibromatosis
Dementia
Magnetic resonance imaging
Radiology
Allele
Cancer
Engineering
Incidence (geometry)
Mechanical engineering
Optics
Pediatrics
Physics
Stroke (engine)
White matter
Cancer registry
Cardiology
Cerebral arteries
Cohort