Rezultati - Inger‐Lise Mero

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  1. 1
    Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis

    Oligoclonal bands and age at onset correlate with genetic risk score in multiple sclerosis od Hanne F. Harbo, Noriko Isobe, Pål Berg‐Hansen, Steffan D. Bos, Stacy J. Caillier, Marte W. Gustavsen, Inger-Lise Mero, Elisabeth Gulowsen Celius, Stephen L. Hauser, Jorge R. Oksenberg, Pierre‐Antoine Gourraud

    Izdano 2013
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  2. 2
    Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies

    Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies od Nathan L. Absalom, Vivian W. Y. Liao, Katrine M. Johannesen, Elena Gardella, Julia Jacobs, Gaëtan Lesca, Zeynep Gokce‐Samar, Alexis Arzimanoglou, Shimriet Zeidler, Pasquale Striano, Pierre Meyer, Ira Benkel-Herrenbrueck, Inger‐Lise Mero, Jutta Rummel, Mary Chebib, Rikke S. Møller, Philip K. Ahring

    Izdano 2022
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  3. 3
    Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA

    Assessment of gene–disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA od Nicole Revençu, Astrid Eijkelenboom, Claire Bracquemart, Pia Alhopuro, Judith Armstrong, Eulàlia Baselga, Claudia Cesario, Maria Lisa Dentici, Mélanie Eyries, Sofia Frisk, Helena Gásdal Karstensen, Nagore Gene‐Olaciregui, Sirpa Kivirikko, Cinzia Lavarino, Inger‐Lise Mero, Rodolphe Michiels, Elisa Pisaneschi, Bitten Schönewolf‐Greulich, Ilse Wieland, Martin Zenker, Miikka Vikkula

    Izdano 2024
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  4. 4
    A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis

    A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis od Inger‐Lise Mero, Åslaug Rudjord Lorentzen, Maria Ban, C. Smestad, Elisabeth Gulowsen Celius, Jan Aarseth, Kjell‐Morten Myhr, Jenny Link, Jan Hillert, Tomas Olsson, Ingrid Kockum, Thomas Masterman, Annette Oturai, Helle Bach Søndergaard, Finn Sellebjerg, Janna Saarela, Anu Kemppinen, Irina Elovaara, Anne Spurkland, Frank Dudbridge, Benedicte A. Lie, Hanne F. Harbo

    Izdano 2009
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  5. 5
    Oligoclonal Band Status in Scandinavian Multiple Sclerosis Patients Is Associated with Specific Genetic Risk Alleles

    Oligoclonal Band Status in Scandinavian Multiple Sclerosis Patients Is Associated with Specific Genetic Risk Alleles od Inger‐Lise Mero, Marte W. Gustavsen, Hanne Skarpodde Sæther, Siri T. Flåm, Pål Berg‐Hansen, Helle Bach Søndergaard, Poul Erik Jensen, Tone Berge, Anja Bjølgerud, Aslaug Muggerud, Jan Aarseth, Kjell‐Morten Myhr, Elisabeth Gulowsen Celius, Finn Sellebjerg, Jan Hillert, Lars Alfredsson, Tomas Olsson, Annette Oturai, Ingrid Kockum, Benedicte A. Lie, Bettina Kulle Andreassen, Hanne F. Harbo

    Izdano 2013
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  6. 6
    Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene

    Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene od Eveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, Teppo Varilo, S. Kallio, Anu Kemppinen, Shaun Purcell, Keijo Koivisto, Pentti J. Tienari, Marja‐Liisa Sumelahti, Irina Elovaara, Tuula Pirttilä, Mauri Reunanen, Arpo Aromaa, Annette Oturai, Helle Bach Søndergaard, Hanne F. Harbo, Inger‐Lise Mero, Stacey B. Gabriel, Daniel B. Mirel, Stephen L. Hauser, Ludwig Kappos, Chris H. Polman, Philip L. De Jager, David A. Hafler, Mark J. Daly, Aarno Palotie, Janna Saarela, Leena Peltonen

    Izdano 2010
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