SOD1 mutations associated with amyotrophic lateral sclerosis analysis of variant severity
Berdyński, Mariusz, Miszta, Przemysław, Safranow, Krzysztof, Andersen, Peter M., Morita, Mitsuya, Filipek, Sławomir, Żekanowski, Cezary, Kuźma-Kozakiewicz, Magdalena
Published in Scientific reports (07.01.2022)
Published in Scientific reports (07.01.2022)
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Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis
Weydt, Patrick, Oeckl, Patrick, Huss, André, Müller, Kathrin, Volk, Alexander E., Kuhle, Jens, Knehr, Antje, Andersen, Peter M., Prudlo, Johannes, Steinacker, Petra, Weishaupt, Jochen H., Ludolph, Albert C., Otto, Markus
Published in Annals of neurology (01.01.2016)
Published in Annals of neurology (01.01.2016)
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Neurofilaments in pre-symptomatic ALS and the impact of genotype
Benatar, Michael, Wuu, Joanne, Lombardi, Vittoria, Jeromin, Andreas, Bowser, Robert, Andersen, Peter M., Malaspina, Andrea
Published in Amyotrophic lateral sclerosis and frontotemporal degeneration (02.10.2019)
Published in Amyotrophic lateral sclerosis and frontotemporal degeneration (02.10.2019)
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Neurofilaments in the diagnosis of motoneuron diseases: a prospective study on 455 patients
Steinacker, Petra, Feneberg, Emily, Weishaupt, Jochen, Brettschneider, Johannes, Tumani, Hayrettin, Andersen, Peter M, von Arnim, Christine A F, Böhm, Sarah, Kassubek, Jan, Kubisch, Christian, Lulé, Dorothée, Müller, Hans-Peter, Muche, Rainer, Pinkhardt, Elmar, Oeckl, Patrick, Rosenbohm, Angela, Anderl-Straub, Sarah, Volk, Alexander E, Weydt, Patrick, Ludolph, Albert C, Otto, Markus
Published in Journal of neurology, neurosurgery and psychiatry (01.01.2016)
Published in Journal of neurology, neurosurgery and psychiatry (01.01.2016)
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EFNS guidelines on the Clinical Management of Amyotrophic Lateral Sclerosis (MALS) - revised report of an EFNS task force
Andersen, Peter M., Abrahams, Sharon, Borasio, Gian D., de Carvalho, Mamede, Chio, Adriano, Van Damme, Philip, Hardiman, Orla, Kollewe, Katja, Morrison, Karen E., Petri, Susanne, Pradat, Pierre-Francois, Silani, Vincenzo, Tomik, Barbara, Wasner, Maria, Weber, Markus
Published in European journal of neurology (01.03.2012)
Published in European journal of neurology (01.03.2012)
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Adolescents' challenging and grief-filled transitions when living with a parent with ALS: A qualitative interpretive study
Malmström, Nina, Öhlén, Joakim, Jakobsson Larsson, Birgitta, Nilsson, Stefan, Nygren, Ingela, M. Andersen, Peter, Ozanne, Anneli
Published in Social science & medicine (1982) (01.08.2024)
Published in Social science & medicine (1982) (01.08.2024)
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An observational study on quality of life and preferences to sustain life in locked-in state
Kuzma-Kozakiewicz, Magdalena, Andersen, Peter M, Ciecwierska, Katarzyna, Vázquez, Cynthia, Helczyk, Olga, Loose, Markus, Uttner, Ingo, Ludolph, Albert C, Lulé, Dorothée
Published in Neurology (03.09.2019)
Published in Neurology (03.09.2019)
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Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis
Paré, Bastien, Lehmann, Manuela, Beaudin, Marie, Nordström, Ulrika, Saikali, Stephan, Julien, Jean-Pierre, Gilthorpe, Jonathan D., Marklund, Stefan L., Cashman, Neil R., Andersen, Peter M., Forsberg, Karin, Dupré, Nicolas, Gould, Peter, Brännström, Thomas, Gros-Louis, François
Published in Scientific reports (21.09.2018)
Published in Scientific reports (21.09.2018)
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Journal Article
Increased functional connectivity common to symptomatic amyotrophic lateral sclerosis and those at genetic risk
Menke, Ricarda A L, Proudfoot, Malcolm, Wuu, Joanne, Andersen, Peter M, Talbot, Kevin, Benatar, Michael, Turner, Martin R
Published in Journal of neurology, neurosurgery and psychiatry (01.06.2016)
Published in Journal of neurology, neurosurgery and psychiatry (01.06.2016)
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Two superoxide dismutase prion strains transmit amyotrophic lateral sclerosis-like disease
Bidhendi, Elaheh Ekhtiari, Bergh, Johan, Zetterström, Per, Andersen, Peter M, Marklund, Stefan L, Brännström, Thomas
Published in The Journal of clinical investigation (01.06.2016)
Published in The Journal of clinical investigation (01.06.2016)
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Comprehensive analysis of the mutation spectrum in 301 German ALS families
Müller, Kathrin, Brenner, David, Weydt, Patrick, Meyer, Thomas, Grehl, Torsten, Petri, Susanne, Grosskreutz, Julian, Schuster, Joachim, Volk, Alexander E, Borck, Guntram, Kubisch, Christian, Klopstock, Thomas, Zeller, Daniel, Jablonka, Sibylle, Sendtner, Michael, Klebe, Stephan, Knehr, Antje, Günther, Kornelia, Weis, Joachim, Claeys, Kristl G, Schrank, Berthold, Sperfeld, Anne-Dorte, Hübers, Annemarie, Otto, Markus, Dorst, Johannes, Meitinger, Thomas, Strom, Tim M, Andersen, Peter M, Ludolph, Albert C, Weishaupt, Jochen H
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2018)
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2018)
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Specific analysis of SOD1 enzymatic activity in CSF from ALS patients with and without SOD1 mutations
Leykam, Laura, Forsberg, Karin M.E., Nordström, Ulrika, Hjertkvist, Karin, Öberg, Agneta, Jonsson, Eva, Andersen, Peter M., Marklund, Stefan L., Zetterström, Per
Published in Neurobiology of disease (01.11.2024)
Published in Neurobiology of disease (01.11.2024)
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EPHA4 is a disease modifier of amyotrophic lateral sclerosis in animal models and in humans
Van Hoecke, Annelies, Schoonaert, Lies, Lemmens, Robin, Timmers, Mieke, Staats, Kim A, Laird, Angela S, Peeters, Elke, Philips, Thomas, Goris, An, Dubois, Bénédicte, Andersen, Peter M, Al-Chalabi, Ammar, Thijs, Vincent, Turnley, Ann M, van Vught, Paul W, Veldink, Jan H, Hardiman, Orla, Van Den Bosch, Ludo, Gonzalez-Perez, Paloma, Van Damme, Philip, Brown, Robert H, van den Berg, Leonard H, Robberecht, Wim
Published in Nature medicine (01.09.2012)
Published in Nature medicine (01.09.2012)
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Novel antibodies reveal inclusions containing non-native SOD1 in sporadic ALS patients
Forsberg, Karin, Jonsson, P Andreas, Andersen, Peter M, Bergemalm, Daniel, Graffmo, Karin S, Hultdin, Magnus, Jacobsson, Johan, Rosquist, Roland, Marklund, Stefan L, Brännström, Thomas
Published in PloS one (14.07.2010)
Published in PloS one (14.07.2010)
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Multi-platform mass spectrometry analysis of the CSF and plasma metabolomes of rigorously matched amyotrophic lateral sclerosis, Parkinson's disease and control subjects
Wuolikainen, Anna, Jonsson, Pär, Ahnlund, Maria, Antti, Henrik, Marklund, Stefan L, Moritz, Thomas, Forsgren, Lars, Andersen, Peter M, Trupp, Miles
Published in Molecular bioSystems (01.01.2016)
Published in Molecular bioSystems (01.01.2016)
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The C9ORF72 expansion mutation is a common cause of ALS+/-FTD in Europe and has a single founder
Smith, Bradley N, Newhouse, Stephen, Shatunov, Aleksey, Vance, Caroline, Topp, Simon, Johnson, Lauren, Miller, Jack, Lee, Younbok, Troakes, Claire, Scott, Kirsten M, Jones, Ashley, Gray, Ian, Wright, Jamie, Hortobágyi, Tibor, Al-Sarraj, Safa, Rogelj, Boris, Powell, John, Lupton, Michelle, Lovestone, Simon, Sapp, Peter C, Weber, Markus, Nestor, Peter J, Schelhaas, Helenius J, Asbroek, Anneloor Alm Ten, Silani, Vincenzo, Gellera, Cinzia, Taroni, Franco, Ticozzi, Nicola, Van den Berg, Leonard, Veldink, Jan, Van Damme, Phillip, Robberecht, Wim, Shaw, Pamela J, Kirby, Janine, Pall, Hardev, Morrison, Karen E, Morris, Alex, de Belleroche, Jacqueline, Vianney de Jong, J M B, Baas, Frank, Andersen, Peter M, Landers, John, Brown, Jr, Robert H, Weale, Michael E, Al-Chalabi, Ammar, Shaw, Christopher E
Published in European journal of human genetics : EJHG (01.01.2013)
Published in European journal of human genetics : EJHG (01.01.2013)
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Structural and kinetic analysis of protein-aggregate strains in vivo using binary epitope mapping
Bergh, Johan, Zetterström, Per, Andersen, Peter M., Brännström, Thomas, Graffmo, Karin S., Jonsson, P. Andreas, Lang, Lisa, Danielsson, Jens, Oliveberg, Mikael, Marklund, Stefan L.
Published in Proceedings of the National Academy of Sciences - PNAS (07.04.2015)
Published in Proceedings of the National Academy of Sciences - PNAS (07.04.2015)
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