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1دورية أكاديمية
المؤلفون: Samu N. Kurki, Jonas Kantonen, Karri Kaivola, Laura Hokkanen, Mikko I. Mäyränpää, Henri Puttonen, FinnGen, 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
المصدر: Acta Neuropathologica Communications, Vol 9, Iss 1, Pp 1-13 (2021)
مصطلحات موضوعية: APOE4, COVID-19 sequelae, Brain microhaemorrhage, Post-viral fatigue, Neuropathology, SARS-CoV-2, Neurology. Diseases of the nervous system, RC346-429
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2051-5960
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2دورية أكاديمية
المؤلفون: Clemens Messerschmidt, Marco Foddis, Sonja Blumenau, Susanne Müller, Kajetan Bentele, Manuel Holtgrewe, Celia Kun-Rodrigues, Isabel Alonso, Maria do Carmo Macario, Ana Sofia Morgadinho, Ana Graça Velon, Gustavo Santo, Isabel Santana, Saana Mönkäre, Liina Kuuluvainen, Johanna Schleutker, Minna Pöyhönen, Liisa Myllykangas, Assunta Senatore, Daniel Berchtold, Katarzyna Winek, Andreas Meisel, Aleksandra Pavlovic, Vladimir Kostic, Valerija Dobricic, Ebba Lohmann, Hasmet Hanagasi, Gamze Guven, Basar Bilgic, Jose Bras, Rita Guerreiro, Dieter Beule, Ulrich Dirnagl, Celeste Sassi
المصدر: Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2045-2322
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3دورية أكاديمية
المؤلفون: Salla Keskitalo, Emma Haapaniemi, Elisabet Einarsdottir, Kristiina Rajamäki, Hannele Heikkilä, Mette Ilander, Minna Pöyhönen, Ekaterina Morgunova, Kati Hokynar, Sonja Lagström, Sirpa Kivirikko, Satu Mustjoki, Kari Eklund, Janna Saarela, Juha Kere, Mikko R. J. Seppänen, Annamari Ranki, Katariina Hannula-Jouppi, Markku Varjosalo
المصدر: Frontiers in Immunology, Vol 10 (2019)
مصطلحات موضوعية: TMEM173, stimulator of interferon genes, interferon type I, IFIH1, additive effect, protein interactions, Immunologic diseases. Allergy, RC581-607
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Jussi Leppävirta, Roope A. Kallionpää, Elina Uusitalo, Tero Vahlberg, Minna Pöyhönen, Juha Peltonen, Sirkku Peltonen
المصدر: Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-8 (2018)
مصطلحات موضوعية: Neurofibromatosis type 1, Congenital malformation, Birth defect, Rasopathy, Anomaly, Heart, Medicine
وصف الملف: electronic resource
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المساهمون: HUSLAB, Department of Medical and Clinical Genetics, HUS Diagnostic Center, Department of Pathology, Helsinki University Hospital Area, Minna Pöyhönen / Principal Investigator, University of Helsinki
المصدر: Acta Neurologica Scandinavica. 146:643-651
مصطلحات موضوعية: Arthrogryposis, Receptors, Notch, phenotype, MUTATIONS, genotype, Finnish, 3112 Neurosciences, CADASIL, General Medicine, Magnetic Resonance Imaging, 3124 Neurology and psychiatry, PREVALENCE, Neurology, Leukoencephalopathies, NOTCH3, Humans, Neurology (clinical), mutation, Receptor, Notch3, Finland, Retrospective Studies
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المؤلفون: Minttu Kansikas, Laura Vähätalo, Jukka Kantelinen, Mariann Kasela, Jaana Putula, Anni Døhlen, Pauliina Paloviita, Emmi Kärkkäinen, Niklas Lahti, Philippe Arnez, Sami Kilpinen, Beatriz Alcala-Repo, Kirsi Pylvänäinen, Minna Pöyhönen, Päivi Peltomäki, Heikki J. Järvinen, Toni T. Seppälä, Laura Renkonen-Sinisalo, Anna Lepistö, Jukka-Pekka Mecklin, Minna Nyström
المساهمون: Molecular and Integrative Biosciences Research Programme, Faculty of Biological and Environmental Sciences, Department of Medical and Clinical Genetics, HUSLAB, Minna Pöyhönen / Principal Investigator, HUS Abdominal Center, Department of Surgery, ATG - Applied Tumor Genomics, II kirurgian klinikka, Genetics, Minna Nyström / Principal Investigator, Tampere University, Clinical Medicine, Department of Gastroenterology
مصطلحات موضوعية: syöpägeenit, testausmenetelmät, validointi, 3122 Cancers, syöpätaudit, Lynchin oireyhtymä, diagnostiikka
وصف الملف: application/pdf; fulltext
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32e54f361c10c02e70a40a394c6cfa64
http://hdl.handle.net/10138/358562 -
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المؤلفون: Laura M. Tanner, Shinji Kunishima, Elina Lehtinen, Tuukka Helin, Kirsi Volmonen, Riitta Lassila, Minna Pöyhönen
المساهمون: HUSLAB, Department of Medical and Clinical Genetics, Research Program in Systems Oncology, HUS Medical Imaging Center, HUS Comprehensive Cancer Center, Clinicum, Minna Pöyhönen / Principal Investigator
المصدر: American Journal of Medical Genetics Part A. 188:1716-1722
مصطلحات موضوعية: Filamins, 1184 Genetics, developmental biology, physiology, thrombocytopenia, panlobular emphysema, OF-FUNCTION MUTATION, Phenotype, Periventricular Nodular Heterotopia, Pulmonary Emphysema, Mutation, platelet function test, Genetics, Humans, filamin A, HETEROGENEITY, Female, 3111 Biomedicine, Child, Genetics (clinical)
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المؤلفون: Sirpa Arte, Minna Pöyhönen, Emmi Myllymäki, Elisa Ronkainen, David P. Rice, Pekka Nieminen
المصدر: Orthodontics & Craniofacial Research.
مصطلحات موضوعية: Otorhinolaryngology, Surgery, Orthodontics, Oral Surgery
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المؤلفون: Saana Mönkäre, Liina Kuuluvainen, Johanna Schleutker, Jose Bras, Susanna Roine, Minna Pöyhönen, Rita Guerreiro, Liisa Myllykangas
المساهمون: HUSLAB, Department of Medical and Clinical Genetics, HUS Diagnostic Center, Minna Pöyhönen / Principal Investigator, University of Helsinki, Department of Pathology
المصدر: Acta neurologica Scandinavica. 146(1)
مصطلحات موضوعية: RISK, TREX1, Dementia, Vascular, 3112 Neurosciences, cerebrovascular disorders, vascular dementia, ASSOCIATION, General Medicine, High-Temperature Requirement A Serine Peptidase 1, 3124 Neurology and psychiatry, whole exome sequencing, METHYLENETETRAHYDROFOLATE REDUCTASE, Stroke, HTRA1 MUTATIONS, Neurology, Cerebral Small Vessel Diseases, Humans, Cognitive Dysfunction, Neurology (clinical), Genetic Testing, GENOMICS, 3' Untranslated Regions, COPY NUMBER VARIATION
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المؤلفون: Sirkku Peltonen, Roope A. Kallionpää, Juha Peltonen, Hannu Järveläinen, Jussi Leppävirta, Kari Auranen, Minna Pöyhönen
المساهمون: HUSLAB, Department of Medical and Clinical Genetics, Helsinki University Hospital Area, HUS Diagnostic Center, University of Helsinki, Minna Pöyhönen / Principal Investigator
المصدر: Journal of Medical Genetics
مصطلحات موضوعية: 0301 basic medicine, Adult, Male, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Neurofibromatosis 1, genetic association studies, Type 2 diabetes, Haploinsufficiency, Cohort Studies, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, Diabetes mellitus, Genes, Neurofibromatosis 1, Genetics, medicine, Humans, autoimmune diseases, Neurofibromatosis, Child, neoplasms, Genetics (clinical), Proportional Hazards Models, genetic predisposition to disease, Proportional hazards model, business.industry, Genotype-Phenotype Correlations, 1184 Genetics, developmental biology, physiology, Middle Aged, medicine.disease, Obesity, eye diseases, 3. Good health, nervous system diseases, 030104 developmental biology, Diabetes Mellitus, Type 2, 030220 oncology & carcinogenesis, Relative risk, Cohort, diabetes mellitus, Female, 3111 Biomedicine, business
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