Astroglial tracer BU99008 detects multiple binding sites in Alzheimer’s disease brain von Kumar, Amit, Koistinen, Niina A., Malarte, Mona-Lisa, Nennesmo, Inger, Ingelsson, Martin, Ghetti, Bernardino, Lemoine, Laetitia, Nordberg, Agneta

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Amyloid, tau, and astrocyte pathology in autosomal-dominant Alzheimer’s disease variants: AβPParc and PSEN1DE9 von Lemoine, Laetitia, Gillberg, Per-Göran, Bogdanovic, Nenad, Nennesmo, Inger, Saint-Aubert, Laure, Viitanen, Matti, Graff, Caroline, Ingelsson, Martin, Nordberg, Agneta

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Resolution of inflammation is altered in Alzheimer's disease von Wang, Xiuzhe, Zhu, Mingqin, Hjorth, Erik, Cortés-Toro, Veronica, Eyjolfsdottir, Helga, Graff, Caroline, Nennesmo, Inger, Palmblad, Jan, Eriksdotter, Maria, Sambamurti, Kumar, Fitzgerald, Jonathan M, Serhan, Charles N, Granholm, Ann-Charlotte, Schultzberg, Marianne

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TBK1 haploinsufficiency results in changes in the K63-ubiquitination profiles in brain and fibroblasts from affected and presymptomatic mutation carriers von Khoshnood, Behzad, Ullgren, Abbe, Laffita-Mesa, Jose, Öijerstedt, Linn, Patra, Kalicharan, Nennesmo, Inger, Graff, Caroline

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Lack of fibrillar amyloid plaques but hypometabolism and astrogliosis in autosomal dominant variant AßPParc Alzheimer’s disease von Lemoine, Laetitia, Gillberg, Per-Göran, Bogdanovic, Nenad, Nennesmo, Inger, Saint-Aubert, Laure, Viitanen, Matti, Graff, Caroline, Ingelsson, Martin, Nordberg, Agneta

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Screening for Anti-HMGCR Antibodies in a Large Single Myositis Center Reveals Infrequent Exposure to Statins and Diversiform Presentation of the Disease von Szczesny, Piotr, Barsotti, Simone, Nennesmo, Inger, Danielsson, Olof, Dastmalchi, Maryam

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Single-cell profiling of muscle-infiltrating T cells in idiopathic inflammatory myopathies von Argyriou, Alexandra, Horuluoglu, Begum, Galindo-Feria, Angeles Shunashy, Diaz-Boada, Juan Sebastian, Sijbranda, Merel, Notarnicola, Antonella, Dani, Lara, van Vollenhoven, Annika, Ramsköld, Daniel, Nennesmo, Inger, Dastmalchi, Maryam, Lundberg, Ingrid E, Diaz-Gallo, Lina-Marcela, Chemin, Karine

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Intra-mitochondrial Methylation Deficiency Due to Mutations in SLC25A26 von Kishita, Yoshihito, Pajak, Aleksandra, Bolar, Nikhita Ajit, Marobbio, Carlo M.T., Maffezzini, Camilla, Miniero, Daniela V., Monné, Magnus, Kohda, Masakazu, Stranneheim, Henrik, Murayama, Kei, Naess, Karin, Lesko, Nicole, Bruhn, Helene, Mourier, Arnaud, Wibom, Rolf, Nennesmo, Inger, Jespers, Ann, Govaert, Paul, Ohtake, Akira, Van Laer, Lut, Loeys, Bart L., Freyer, Christoph, Palmieri, Ferdinando, Wredenberg, Anna, Okazaki, Yasushi, Wedell, Anna

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Pathological Study of a FMR1 Premutation Carrier With Progressive Supranuclear Palsy von Paucar, Martin, Nennesmo, Inger, Svenningsson, Per

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Variability in Skeletal Muscle Protein Synthesis Rates in Critically Ill Patients von Tjäder, Inga, Klaude, Maria, Hssain, Ali Ait, Guillet, Christelle, Nennesmo, Inger, Wernerman, Jan, Rooyackers, Olav

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Development of autoantibodies against muscle-specific FHL1 in severe inflammatory myopathies von Albrecht, Inka, Wick, Cecilia, Hallgren, Åsa, Tjärnlund, Anna, Nagaraju, Kanneboyina, Andrade, Felipe, Thompson, Kathryn, Coley, William, Phadke, Aditi, Diaz-Gallo, Lina-Marcela, Bottai, Matteo, Nennesmo, Inger, Chemin, Karine, Herrath, Jessica, Johansson, Karin, Wikberg, Anders, Ytterberg, A Jimmy, Zubarev, Roman A, Danielsson, Olof, Krystufkova, Olga, Vencovsky, Jiri, Landegren, Nils, Wahren-Herlenius, Marie, Padyukov, Leonid, Kämpe, Olle, Lundberg, Ingrid E

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Amyloid tracers binding sites in autosomal dominant and sporadic Alzheimer's disease von Ni, Ruiqing, Gillberg, Per-Göran, Bogdanovic, Nenad, Viitanen, Matti, Myllykangas, Liisa, Nennesmo, Inger, Långström, Bengt, Nordberg, Agneta

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Vascular endothelial growth factor prolongs survival in a transgenic mouse model of ALS von Zheng, Chengyun, Nennesmo, Inger, Fadeel, Bengt, Henter, Jan-Inge

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A multi-systemic mitochondrial disorder due to a dominant p.Y955H disease variant in DNA polymerase gamma von Siibak, Triinu, Clemente, Paula, Bratic, Ana, Bruhn, Helene, Kauppila, Timo E S, Macao, Bertil, Schober, Florian A, Lesko, Nicole, Wibom, Rolf, Naess, Karin, Nennesmo, Inger, Wedell, Anna, Peter, Bradley, Freyer, Christoph, Falkenberg, Maria, Wredenberg, Anna

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No common founder for C9orf72 expansion mutation in Sweden von Chiang, Huei-Hsin, Forsell, Charlotte, Lindström, Anna-Karin, Lilius, Lena, Thonberg, Håkan, Nennesmo, Inger, Graff, Caroline

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Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disord... von Ek, Marlene, Nilsson, Daniel, Engvall, Martin, Malmgren, Helena, Thonberg, Håkan, Pettersson, Maria, Anderlid, Britt-Marie, Hammarsjö, Anna, Helgadottir, Hafdis T, Arnardottir, Snjolaug, Naess, Karin, Nennesmo, Inger, Paucar, Martin, Hjartarson, Helgi Thor, Press, Rayomand, Solders, Göran, Sejersen, Thomas, Lindstrand, Anna, Kvarnung, Malin

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Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model von Tegelberg, Saara, Tomašić, Nikica, Kallijärvi, Jukka, Purhonen, Janne, Elmér, Eskil, Lindberg, Eva, Nord, David Gisselsson, Soller, Maria, Lesko, Nicole, Wedell, Anna, Bruhn, Helene, Freyer, Christoph, Stranneheim, Henrik, Wibom, Rolf, Nennesmo, Inger, Wredenberg, Anna, Eklund, Erik A, Fellman, Vineta

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PARKIN is not required to sustain OXPHOS function in adult mammalian tissues von Filograna, Roberta, Gerlach, Jule, Choi, Hae-Na, Rigoni, Giovanni, Barbaro, Michela, Oscarson, Mikael, Lee, Seungmin, Tiklova, Katarina, Ringnér, Markus, Koolmeister, Camilla, Wibom, Rolf, Riggare, Sara, Nennesmo, Inger, Perlmann, Thomas, Wredenberg, Anna, Wedell, Anna, Motori, Elisa, Svenningsson, Per, Larsson, Nils-Göran

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Neuropathological characterization of two siblings carrying the MAPT S305S mutation demonstrates features resembling argyrophilic grain disease von Rönnbäck, Annica, Nennesmo, Inger, Tuominen, Hannu, Grueninger, Fiona, Viitanen, Matti, Graff, Caroline

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Neurogenic vs. Myogenic Origin of Acquired Muscle Paralysis in Intensive Care Unit (ICU) Patients: Evaluation of Different Diagnostic Methods von Marrero, Humberto D. J. Gonzalez, Stalberg, Erik V., Cooray, Gerald, Corpeno Kalamgi, Rebeca, Hedstrom, Yvette, Bellander, Bo-Michael, Nennesmo, Inger, Larsson, Lars

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