Prediction of survival in amyotrophic lateral sclerosis: a nationwide, Danish cohort study von Kjældgaard, Anne-Lene, Pilely, Katrine, Olsen, Karsten Skovgaard, Jessen, Anders Hedegaard, Lauritsen, Anne Øberg, Pedersen, Stephen Wørlich, Svenstrup, Kirsten, Karlsborg, Merete, Thagesen, Helle, Blaabjerg, Morten, Theódórsdóttir, Ásta, Elmo, Elisabeth Gundtoft, Møller, Anette Torvin, Bonefeld, Lone, Berg, Mia, Garred, Peter, Møller, Kirsten

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Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience von Effraimidis, Grigoris, Rasmussen, Åse Krogh, Dunoe, Morten, Hasholt, Lis F, Wibrand, Flemming, Sorensen, Soren S, Lund, Allan M, Kober, Lars, Bundgaard, Henning, Yazdanfard, Puriya D W, Oturai, Peter, Larsen, Vibeke A, Fraga de Abreu, Vitor Hugo, Enevoldsen, Lotte Hahn, Kristensen, Tatiana, Svenstrup, Kirsten, Bille, Margrethe Bastholm, Arif, Farah, Mogensen, Mette, Klokker, Mads, Backer, Vibeke, Kistorp, Caroline, Feldt-Rasmussen, Ulla

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Correction: Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience von Effraimidis, Grigoris, Rasmussen, Åse Krogh, Dunoe, Morten, Hasholt, Lis F, Wibrand, Flemming, Sorensen, Soren S, Lund, Allan M, Kober, Lars, Bundgaard, Henning, Yazdanfard, Puriya D W, Oturai, Peter, Larsen, Vibeke A, de Abreu, Victor Hugo Fraga, Enevoldsen, Lotte Hahn, Kristensen, Tatiana, Svenstrup, Kirsten, Bille, Margrethe Bastholm, Arif, Farah, Mogensen, Mette, Klokker, Mads, Backer, Vibeke, Kistorp, Caroline, Feldt-Rasmussen, Ulla

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Novel Homozygous Truncating Variant Widens the Spectrum of Early-Onset Multisystemic SYNE1 Ataxia von Karlsson, William Kristian, Højgaard, Joan Lilja Sunnleyg, Vilhelmsen, Anna, Crone, Clarissa, Andersen, Birgit, Law, Ian, Møller, Lisbeth Birk, Nielsen, Troels Tolstrup, Nielsen, Emilie Neerup, Krag, Thomas, Svenstrup, Kirsten, Nielsen, Jørgen Erik

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Genetic analysis of Charcot-Marie-Tooth disease in Denmark and the implementation of a next generation sequencing platform von Vaeth, Signe, Christensen, Rikke, Dunø, Morten, Lildballe, Dorte Launholt, Thorsen, Kasper, Vissing, John, Svenstrup, Kirsten, Hertz, Jens Michael, Andersen, Henning, Jensen, Uffe Birk

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High incidence of amyotrophic lateral sclerosis in the Faroe Islands 2010–2020 von Johansen, Malan, Svenstrup, Kirsten, Joensen, Poul, Steig, Bjarni á, Andorsdóttir, Guðrið, Hansen, Torben, Petersen, Maria Skaalum

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A Unique Constellation of Multiple Cranial Neuropathies in a Patient with Preeclampsia von Zarifkar, Pardis, Hansen, Klaus, Crone, Clarissa, Svenstrup, Kirsten, Larsen, Vibeke Andrée, Karlsson, William Kristian

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Clinical and molecular characterization of limb-girdle muscular dystrophy due to LAMA2 mutations von Gavassini, Bruno F., Carboni, Nicola, Nielsen, Jørgen E., Danielsen, Else R., Thomsen, Carsten, Svenstrup, Kirsten, Bello, Luca, Maioli, Maria Antonietta, Marrosu, Giovanni, Ticca, Anna Filomena, Mura, Marco, Marrosu, Maria Giovanna, Soraru, Gianni, Angelini, Corrado, Vissing, John, Pegoraro, Elena

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Intravenous immunoglobulin treatment in a patient with adrenomyeloneuropathy von Jønch, Aia Elise, Danielsen, Else Rubæk, Thomsen, Carsten, Meden, Per, Svenstrup, Kirsten, Nielsen, Jørgen Erik

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Precisionsmedicinsk genterapi har bromsat utveckling av ALS: SOD1 gene therapy delays ALS disease progression von Forsberg, Karin, Karlsborg, Merete, Salvesen, Lisette, Svenstrup, Kirsten, Winroth, Ivar, Berntsson, Henrik, Andersen, Peter M.

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Peripheral neuropathy in hereditary spastic paraplegia caused by REEP1 variants von Toft, Anders, Birk, Steffen, Ballegaard, Martin, Dunø, Morten, Hjermind, Lena E., Nielsen, Jørgen E., Svenstrup, Kirsten

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Improved Glucose Tolerance and Acinar Dysmorphogenesis by Targeted Expression of Transcription Factor PDX-1 to the Exocrine Pancreas von HELLER, R. Scott, STOFFERS, Doris A, BOCK, Troels, SVENSTRUP, Kirsten, JENSEN, Jan, HORN, Thomas, MILLER, Christopher P, HABENER, Joel F, MADSEN, Ole D, SERUP, Palle

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Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment von Roux, Thomas, Barbier, Mathieu, Papin, Mélanie, Davoine, Claire-Sophie, Sayah, Sabrina, Coarelli, Giulia, Charles, Perrine, Marelli, Cecilia, Parodi, Livia, Tranchant, Christine, Goizet, Cyril, Klebe, Stephan, Lohmann, Ebba, Van Maldergem, Lionel, van Broeckhoven, Christine, Coutelier, Marie, Tesson, Christelle, Stevanin, Giovanni, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra

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SOD1 gene therapy delays ALS disease progression von Forsberg, Karin, Karlsborg, Merete, Salvesen, Lisette, Svenstrup, Kirsten, Winroth, Ivar, Berntsson, Henrik, M Andersen, Peter

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TDP-43–specific Autoantibody Decline in Patients With Amyotrophic Lateral Sclerosis von Nielsen, Anne Kallehauge, Folke, Jonas, Owczarek, Sylwia, Svenstrup, Kirsten, Winge, Kristian, Pakkenberg, Bente, Aznar, Susana, Brudek, Tomasz

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Complement Profiles in Patients with Amyotrophic Lateral Sclerosis: A Prospective Observational Cohort Study von Kjældgaard, Anne-Lene, Pilely, Katrine, Olsen, Karsten Skovgaard, Øberg Lauritsen, Anne, Wørlich Pedersen, Stephen, Svenstrup, Kirsten, Karlsborg, Merete, Thagesen, Helle, Blaabjerg, Morten, Theódórsdóttir, Ásta, Gundtoft Elmo, Elisabeth, Torvin Møller, Anette, Pedersen, Niels Anker, Kirkegaard, Niels, Møller, Kirsten, Garred, Peter

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Correction: Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment von Roux, Thomas, Barbier, Mathieu, Papin, Mélanie, Davoine, Claire-Sophie, Sayah, Sabrina, Coarelli, Giulia, Charles, Perrine, Marelli, Cecilia, Parodi, Livia, Tranchant, Christine, Goizet, Cyril, Klebe, Stephan, Lohmann, Ebba, Van Maldergem, Lionel, van Broeckhoven, Christine, Coutelier, Marie, Tesson, Christelle, Stevanin, Giovanni, Duyckaerts, Charles, Brice, Alexis, Durr, Alexandra, Durr, Alexandra, Stevanin, Giovanni, Brice, Alexis, Darios, Frédéric, Forlani, Sylvie, Site, Pitié-Salpêtrière, Banneau, Guillaume, Cazeneuve, Cécile, Charles, Perrine, Duyckaerts, Charles, Fontaine, Bertrand, Azulay, Jean-Philippe, Boesfplug-Tanguy, Odile, Goizet, Cyril, Hannequin, Didier, Hazan, Jamilé, Burgo, Andrea, Verny, Christophe, Koenig, Michel, Labauge, Pierre, Marelli, Cecilia, N’guyen, Karine, Rodriguez, Diana, Belarbi, Soraya, Hamri, Abdelmadjid, Tazir, Meriem, Boesch, Sylvia, Pandolfo, Massimo, Laura, Jardim, Guergueltcheva, Velina, Tournev, Ivalo, Pedraza Linarès, Olga Lucia, Nielsen, Jørgen E., Svenstrup, Kirsten, Zaki, Maha, Bauer, Peter, Schöls, Lüdger, Schüle, Rebecca, Lossos, Alexander, Bassi, Maria-Teresa, Basso, Manuela, Bertini, Enrico, Brusco, Alfredo, Casali, Carlo, Casari, Giorgio, Criscuolo, Chiara, Filla, Alessandro, Orsi, Laura, Santorelli, Filippo M., Valente, Enza Maria, Vavla, Marinela, Vazza, Giovanni, Megarbane, André, Benomar, Ali, Kremer, Berry, Van Roon-Mom, Willeke, Roxburgh, Richard, Erichsen, Anne Kjersti, Tallaksen, Chantal, Alonso, Isabel, Coutinho, Paula, Loureiro, José Léal, Sequeiros, Jorge, Salih, Mustapha, Kostic, Vladimir S, Rouco Axpe, Idoia, Elsayed, Liena, Paucar, Martin Arce, Roumani, Samir, Bing-Wen, Soong, Reid, Evan, Suran, Nethisinghe, Warner, Thomas, Wood, Nicholas

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July 2017 ENCALS statement on edaravone von Al-Chalabi, Ammar, Andersen, Peter M., Chandran, Siddharthan, Chio, Adriano, Corcia, Philippe, Couratier, Philippe, Danielsson, Olof, de Carvalho, Mamede, Desnuelle, Claude, Grehl, Torsten, Grosskreutz, Julian, Holmøy, Trygve, Ingre, Caroline, Karlsborg, Merete, Kleveland, Grethe, Christoph Koch, Jan, Koritnik, Blaz, KuzmaKozakiewicz, Magdalena, Laaksovirta, Hannu, Ludolph, Albert, McDermott, Christopher, Meyer, Thomas, Ropero, Bernardo Mitre, Pardina, Jesus Mora, Nygren, Ingela, Petri, Susanne, Povedano Panades, Mónica, Salachas, Francois, Shaw, Pamela, Silani, Vincenzo, Staaf, Gert, Svenstrup, Kirsten, Talbot, Kevin, Tysnes, Ole-Bjørn, Van Damme, Philip, van der Kooi, Anneke, Weber, Markus, Weydt, Patrick, Wolf, Joachim, Hardiman, Orla, van den Berg, Leonard H.

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SCA28: Novel Mutation in the AFG3L2 Proteolytic Domain Causes a Mild Cerebellar Syndrome with Selective Type-1 Muscle Fiber Atrophy von Svenstrup, Kirsten, Nielsen, Troels Tolstrup, Aidt, Frederik, Rostgaard, Nina, Duno, Morten, Wibrand, Flemming, Vinther-Jensen, Tua, Law, Ian, Vissing, John, Roos, Peter, Hjermind, Lena Elisabeth, Nielsen, Jørgen Erik

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Clinical trials in pediatric ALS: a TRICALS feasibility study von Kliest, Tessa, Van Eijk, Ruben P.A, Al-Chalabi, Ammar, Albanese, Alberto, Andersen, Peter M, Amador, Maria Del Mar, BrAthen, Geir, Brunaud-Danel, Veronique, Brylev, Lev, Camu, William, De Carvalho, Mamede, Cereda, Cristina, Cetin, Hakan, Chaverri, Delia, Chio, Adriano, Corcia, Philippe, Couratier, Philippe, De Marchi, Fabiola, Desnuelle, Claude, Van Es, Michael A, Esteban, JesUs, Filosto, Massimiliano, Redondo, Alberto GarcIa, Grosskreutz, Julian, Hanemann, Clemens O, Holmoy, Trygve, Hoyer, Helle, Ingre, Caroline, Koritnik, Blaz, Kuzma-Kozakiewicz, Magdalena, Lambert, Thomas, Leigh, Peter N, Lunetta, Christian, Mandrioli, Jessica, Mcdermott, Christopher J, Meyer, Thomas, Mora, Jesus S, Petri, Susanne, Povedano, M.Onica, Reviers, Evy, Riva, Nilo, Roes, Kit C.B, Rubio, Miguel A, Salachas, FranCois, Sarafov, Stayko, SorarU, Gianni, Stevic, Zorica, Svenstrup, Kirsten, Moller, Anette Torvin, Turner, Martin R, Van Damme, Philip, Van Leeuwen, Lucie A.G, Varona, Luis, Costa, Juan F. V.Azquez, Weber, Markus, Hardiman, Orla, Van den Berg, Leonard H

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