Search Results - Johanna Krüger
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Genetics of Paroxysmal Dyskinesia: Novel Variants Corroborate the Role of KCNA1 in Paroxysmal Dyskinesia and Highlight the Diverse Phenotypic Spectrum of KCNA1- and SLC2A1-Related... by Josua Kegele, Johanna Krüger, Mahmoud Koko, Lara Lange, Ana Victoria Marco Hernandez, Francisco Martinez, Francisco Martinez, Alexander Münchau, Holger Lerche, Stephan Lauxmann
Published 2021-07-01
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Cognitive Performance at Time of AD Diagnosis: A Clinically Augmented Register-Based Study by Minna Alenius, Minna Alenius, Laura Hokkanen, Sanna Koskinen, Ilona Hallikainen, Tuomo Hänninen, Tuomo Hänninen, Mira Karrasch, Minna M. Raivio, Minna M. Raivio, Marja-Liisa Laakkonen, Marja-Liisa Laakkonen, Marja-Liisa Laakkonen, Johanna Krüger, Johanna Krüger, Noora-Maria Suhonen, Miia Kivipelto, Miia Kivipelto, Miia Kivipelto, Miia Kivipelto, Tiia Ngandu, Tiia Ngandu
Published 2022-07-01
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Modifiable potential risk factors in familial and sporadic frontotemporal dementia by Helmi Soppela, Kasper Katisko, Yasmine Gadola, Johanna Krüger, Päivi Hartikainen, Antonella Alberici, Alberto Benussi, Anne Koivisto, Annakaisa Haapasalo, Anne M Remes, Barbara Borroni, Eino Solje
Published 2022-08-01
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The variability of functional MRI brain signal increases in Alzheimer's disease at cardiorespiratory frequencies by Timo Tuovinen, Janne Kananen, Zalan Rajna, Johannes Lieslehto, Vesa Korhonen, Riikka Rytty, Heli Mattila, Niko Huotari, Lauri Raitamaa, Heta Helakari, Ahmed Abou Elseoud, Johanna Krüger, Pierre LeVan, Osmo Tervonen, Juergen Hennig, Anne M. Remes, Maiken Nedergaard, Vesa Kiviniemi
Published 2020-12-01
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Serum total TDP-43 levels are decreased in frontotemporal dementia patients with C9orf72 repeat expansion or concomitant motoneuron disease phenotype by Kasper Katisko, Nadine Huber, Tarja Kokkola, Päivi Hartikainen, Johanna Krüger, Anna-Leena Heikkinen, Veera Paananen, Ville Leinonen, Ville E. Korhonen, Seppo Helisalmi, Sanna-Kaisa Herukka, Valentina Cantoni, Yasmine Gadola, Silvana Archetti, Anne M. Remes, Annakaisa Haapasalo, Barbara Borroni, Eino Solje
Published 2022-10-01
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Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies by Johanna Krüger, Julian Schubert, Josua Kegele, Audrey Labalme, Miaomiao Mao, Jacqueline Heighway, Guiscard Seebohm, Pu Yan, Mahmoud Koko, Kezban Aslan-Kara, Hande Caglayan, Bernhard J. Steinhoff, Yvonne G. Weber, Pascale Keo-Kosal, Samuel F. Berkovic, Michael S. Hildebrand, Steven Petrou, Roland Krause, Patrick May, Gaetan Lesca, Snezana Maljevic, Holger Lerche
Published 2022-10-01
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