Search Results - Müller, Kathrin

Effects of tofersen treatment in patients with <i>SOD1</i>-ALS in a “real-world” setting - a 12-month multicenter cohort study from the German early access program by Wiesenfarth, Maximilian (Author) , Dorst, Johannes (Author) , Brenner, David (Author) , Elmas, Zeynep (Author) , Parlak, Özlem (Author) , Uzelac, Zeljko (Author) , Kandler, Katharina (Author) , Mayer, Kristina (Author) , Weiland, Ulrike (Author) , Herrmann, Christine (Author) , Schuster, Joachim (Author) , Freischmidt, Axel (Author) , Müller, Kathrin (Author) , Siebert, Reiner (Author) , Bachhuber, Franziska (Author) , Simak, Tatiana (Author) , Günther, Kornelia (Author) , Fröhlich, Elke (Author) , Knehr, Antje (Author) , Regensburger, Martin (Author) , German, Alexander (Author) , Petri, Susanne (Author) , Grosskreutz, Julian (Author) , Klopstock, Thomas (Author) , Reilich, Peter (Author) , Schöberl, Florian (Author) , Hagenacker, Tim (Author) , Weyen, Ute (Author) , Günther, René (Author) , Vidovic, Maximilian (Author) , Jentsch, Martin (Author) , Haarmeier, Thomas (Author) , Weydt, Patrick (Author) , Valkadinov, Ivan (Author) , Hesebeck-Brinckmann, Jasper (Author) , Conrad, Julian (Author) , Weishaupt, Jochen H. (Author) , Schumann, Peggy (Author) , Körtvélyessy, Peter (Author) , Meyer, Thomas (Author) , Ruf, Wolfgang Philipp (Author) , Witzel, Simon (Author) , Senel, Makbule (Author) , Tumani, Hayrettin (Author) , Ludolph, Albert Christian (Author) ,

• kostenfrei
• kostenfrei

Integrative genetic analysis illuminates ALS heritability and identifies risk genes by Megat, Salim (Author) , Mora, Natalia (Author) , Sanogo, Jason (Author) , Roman, Olga (Author) , Catanese, Alberto (Author) , Alami, Najwa Ouali (Author) , Freischmidt, Axel (Author) , Mingaj, Xhuljana (Author) , De Calbiac, Hortense (Author) , Muratet, François (Author) , Dirrig-Grosch, Sylvie (Author) , Dieterle, Stéphane (Author) , Van Bakel, Nick (Author) , Müller, Kathrin (Author) , Sieverding, Kirsten (Author) , Weishaupt, Jochen H. (Author) , Andersen, Peter Munch (Author) , Weber, Markus (Author) , Neuwirth, Christoph (Author) , Margelisch, Markus (Author) , Sommacal, Andreas (Author) , Van Eijk, Kristel R. (Author) , Veldink, Jan H. (Author) , Lautrette, Géraldine (Author) , Couratier, Philippe (Author) , Camuzat, Agnès (Author) , Le Ber, Isabelle (Author) , Grassano, Maurizio (Author) , Chio, Adriano (Author) , Böckers, Tobias M. (Author) , Ludolph, Albert C. (Author) , Roselli, Francesco (Author) , Yilmazer-Hanke, Deniz (Author) , Millecamps, Stéphanie (Author) , Kabashi, Edor (Author) , Storkebaum, Erik (Author) , Sellier, Chantal (Author) , Dupuis, Luc (Author) ,

• kostenfrei
• kostenfrei

Metabolic alterations precede neurofilament changes in presymptomatic ALS gene carriers by Dorst, Johannes (Author) , Weydt, Patrick (Author) , Brenner, David (Author) , Witzel, Simon (Author) , Kandler, Katharina (Author) , Huss, André (Author) , Herrmann, Christine (Author) , Wiesenfarth, Maximilian (Author) , Knehr, Antje (Author) , Günther, Kornelia (Author) , Müller, Kathrin (Author) , Weishaupt, Jochen H. (Author) , Prudlo, Johannes (Author) , Forsberg, Karin (Author) , Andersen, Peter M. (Author) , Rosenbohm, Angela (Author) , Schuster, Joachim (Author) , Roselli, Francesco (Author) , Dupuis, Luc (Author) , Mayer, Benjamin (Author) , Tumani, Hayrettin (Author) , Kassubek, Jan Rainer (Author) , Ludolph, Albert C. (Author) ,

• lizenzpflichtig
• lizenzpflichtig

Author correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes by Megat, Salim (Author) , Mora, Natalia (Author) , Sanogo, Jason (Author) , Roman, Olga (Author) , Catanese, Alberto (Author) , Alami, Najwa Ouali (Author) , Freischmidt, Axel (Author) , Mingaj, Xhuljana (Author) , De Calbiac, Hortense (Author) , Muratet, François (Author) , Dirrig-Grosch, Sylvie (Author) , Dieterle, Stéphane (Author) , Van Bakel, Nick (Author) , Müller, Kathrin (Author) , Sieverding, Kirsten (Author) , Weishaupt, Jochen H. (Author) , Andersen, Peter Munch (Author) , Weber, Markus (Author) , Neuwirth, Christoph (Author) , Margelisch, Markus (Author) , Sommacal, Andreas (Author) , Van Eijk, Kristel R. (Author) , Veldink, Jan H. (Author) , Lautrette, Géraldine (Author) , Couratier, Philippe (Author) , Camuzat, Agnès (Author) , Le Ber, Isabelle (Author) , Grassano, Maurizio (Author) , Chio, Adriano (Author) , Böckers, Tobias M. (Author) , Ludolph, Albert C. (Author) , Roselli, Francesco (Author) , Yilmazer-Hanke, Deniz (Author) , Millecamps, Stéphanie (Author) , Kabashi, Edor (Author) , Storkebaum, Erik (Author) , Sellier, Chantal (Author) , Dupuis, Luc (Author) ,

• lizenzpflichtig
• lizenzpflichtig

Heterozygous DHTKD1 variants in two European cohorts of amyotrophic lateral sclerosis patients by Osmanovic, Alma (Author) , Gogol, Isabel (Author) , Martens, Helge (Author) , Widjaja, Maylin (Author) , Müller, Kathrin (Author) , Schreiber-Katz, Olivia (Author) , Feuerhake, Friedrich (Author) , Langhans, Claus-Dieter (Author) , Schmidt, Gunnar (Author) , Andersen, Peter M. (Author) , Ludolph, Albert C. (Author) , Weishaupt, Jochen H. (Author) , Brand, Frank (Author) , Petri, Susanne (Author) , Weber, Ruthild (Author) ,

• lizenzpflichtig
• lizenzpflichtig

FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees by Brenner, David (Author) , Müller, Kathrin (Author) , Lattante, Serena (Author) , Yılmaz, Rüstem (Author) , Knehr, Antje (Author) , Freischmidt, Axel (Author) , Ludolph, Albert C. (Author) , Andersen, Peter M. (Author) , Weishaupt, Jochen H. (Author) ,

• lizenzpflichtig

Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cells by Ruf, Wolfgang (Author) , Hannon, Eilis (Author) , Freischmidt, Axel (Author) , Grozdanov, Veselin (Author) , Brenner, David (Author) , Müller, Kathrin (Author) , Knehr, Antje (Author) , Günther, Kornelia (Author) , Dorst, Johannes (Author) , Ammerpohl, Ole (Author) , Danzer, Karin M. (Author) , Mill, Jonathan (Author) , Ludolph, Albert C. (Author) , Weishaupt, Jochen H. (Author) ,

• lizenzpflichtig
• lizenzpflichtig

J wave syndromes in patients with spinal and bulbar muscular atrophy: original communication by Steinmetz, Karoline (Author) , Rudic, Boris (Author) , Borggrefe, Martin (Author) , Müller, Kathrin (Author) , Siebert, Reiner (Author) , Rottbauer, Wolfgang (Author) , Ludolph, Albert C. (Author) , Buckert, Dominik (Author) , Rosenbohm, Angela (Author) ,

• lizenzpflichtig
• lizenzpflichtig

In vivo histopathological staging in C9orf72-associated ALS: A tract of interest DTI study by Müller, Hans-Peter (Author) , Del Tredici, Kelly (Author) , Lulé, Dorothée (Author) , Müller, Kathrin (Author) , Weishaupt, Jochen H. (Author) , Ludolph, Albert C. (Author) , Kassubek, Jan Rainer (Author) ,

• lizenzpflichtig
• lizenzpflichtig

SQSTM1/p62 variants in 486 patients with familial ALS from Germany and Sweden by Yılmaz, Rüstem (Author) , Müller, Kathrin (Author) , Brenner, David (Author) , Volk, Alexander E. (Author) , Borck, Guntram (Author) , Hermann, Andreas (Author) , Meitinger, Thomas (Author) , Strom, Tim M. (Author) , Danzer, Karin M. (Author) , Ludolph, Albert C. (Author) , Andersen, Peter M. (Author) , Weishaupt, Jochen H. (Author) , Weyen, Ute (Author) , Regensburger, Martin (Author) , Winkler, Jürgen (Author) , Linker, Ralf (Author) , Winner, Beate (Author) , Hagenacker, Tim (Author) , Koch, Jan Christoph (Author) , Lingor, Paul (Author) , Göricke, Bettina (Author) , Zierz, Stephan (Author) , Jordan, Berit (Author) , Baum, Petra (Author) , Wolf, Joachim (Author) , Winkler, Andrea (Author) , Young, Peter (Author) , Bogdahn, Ulrich (Author) , Prudlo, Johannes (Author) , Kassubek, Jan Rainer (Author) ,

• lizenzpflichtig
• lizenzpflichtig

Genotypes of amyotrophic lateral sclerosis in Mongolia by Daria, Tselmen (Author) , Müller, Kathrin (Author) , Oidovdorj, Gansuvd (Author) , Baatar, Khandsuren (Author) , Boldbaatar, Punsaldulam (Author) , Sarangerel, Jambal (Author) , Rentsenbat, Munkhbayar (Author) , Turbat, Sarantsetseg (Author) , Yadamsuren, Erdenechimeg (Author) , Weydt, Patrick (Author) , Dambasuren, Bolormaa (Author) , Bosookhuu, Oyungerel (Author) , Banzrai, Chimeglkham (Author) , Damchaa, Baasanjav (Author) , Pinkhardt, Elmar Hans (Author) , Rosenbohm, Angela (Author) , Högel, Josef (Author) , Andersen, Peter (Author) , Borck, Guntram (Author) , Batmunkh, Munkhbat (Author) , Ludolph, Albert C. (Author) , Weishaupt, Jochen H. (Author) ,

• lizenzpflichtig
• lizenzpflichtig

Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations: letter to the editor by Brenner, David (Author) , Rosenbohm, Angela (Author) , Yılmaz, Rüstem (Author) , Müller, Kathrin (Author) , Grehl, Torsten (Author) , Petri, Susanne (Author) , Meyer, Thomas (Author) , Großkreutz, Julian (Author) , Weydt, Patrick (Author) , Ruf, Wolfgang (Author) , Neuwirth, Christoph (Author) , Weber, Markus (Author) , Pinto, Susana (Author) , Claeys, Kristl G (Author) , Schrank, Berthold (Author) , Jordan, Berit (Author) , Knehr, Antje (Author) , Günther, Kornelia (Author) , Hübers, Annemarie (Author) , Zeller, Daniel (Author) , Kubisch, Christian (Author) , Jablonka, Sibylle (Author) , Sendtner, Michael (Author) , Klopstock, Thomas (Author) , de Carvalho, Mamede (Author) , Sperfeld, Anne (Author) , Borck, Guntram (Author) , Volk, Alexander E. (Author) , Dorst, Johannes (Author) , Weis, Joachim (Author) , Otto, Markus (Author) , Schuster, Joachim (Author) , Del Tredici, Kelly (Author) , Braak, Heiko (Author) , Danzer, Karin M (Author) , Freischmidt, Axel (Author) , Meitinger, Thomas (Author) , Ludolph, Albert C. (Author) , Andersen, Peter M (Author) , Weishaupt, Jochen H. (Author) ,

• lizenzpflichtig

A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification: letter to the editor by Forouhideh, Yalda (Author) , Müller, Kathrin (Author) , Ruf, Wolfgang (Author) , Assi, Muhannad (Author) , Şeker, Tuncay (Author) , Tunca, Ceren (Author) , Knehr, Antje (Author) , Strom, Tim M (Author) , Gorges, Martin (Author) , Schradt, Falk (Author) , Meitinger, Thomas (Author) , Ludolph, Albert C. (Author) , Pinkhardt, Elmar H (Author) , Başak, A Nazlı (Author) , Kassubek, Jan Rainer (Author) , Uttner, Ingo (Author) , Weishaupt, Jochen H. (Author) ,

• lizenzpflichtig

Hot-spot KIF5A mutations cause familial ALS by Brenner, David (Author) , Yılmaz, Rüstem (Author) , Müller, Kathrin (Author) , Grehl, Torsten (Author) , Petri, Susanne (Author) , Meyer, Thomas (Author) , Großkreutz, Julian (Author) , Weydt, Patrick (Author) , Ruf, Wolfgang (Author) , Neuwirth, Christoph (Author) , Weber, Markus (Author) , Pinto, Susana (Author) , Claeys, Kristl G. (Author) , Schrank, Berthold (Author) , Jordan, Berit (Author) , Knehr, Antje (Author) , Günther, Kornelia (Author) , Hübers, Annemarie (Author) , Zeller, Daniel (Author) , Kubisch, Christian (Author) , Jablonka, Sibylle (Author) , Sendtner, Michael (Author) , Klopstock, Thomas (Author) , de Carvalho, Mamede (Author) , Sperfeld, Anne (Author) , Borck, Guntram (Author) , Volk, Alexander E. (Author) , Dorst, Johannes (Author) , Weis, Joachim (Author) , Otto, Markus (Author) , Schuster, Joachim (Author) , Del Tredici, Kelly (Author) , Braak, Heiko (Author) , Danzer, Karin M. (Author) , Freischmidt, Axel (Author) , Meitinger, Thomas (Author) , Strom, Tim M. (Author) , Ludolph, Albert C. (Author) , Andersen, Peter M. (Author) , Weishaupt, Jochen H. (Author) ,

CHCHD10 mutations p.R15L and p.G66V cause motoneuron disease by haploinsufficiency by Brockmann, Sarah J. (Author) , Freischmidt, Axel (Author) , Oeckl, Patrick (Author) , Müller, Kathrin (Author) , Ponna, Srinivas K (Author) , Helferich, Anika Marie (Author) , Paone, Christoph (Author) , Reinders, Jörg (Author) , Kojer, Kerstin (Author) , Orth, Michael (Author) , Jokela, Manu (Author) , Auranen, Mari (Author) , Udd, Bjarne (Author) , Hermann, Andreas (Author) , Danzer, Karin M (Author) , Lichtner, Peter (Author) , Walther, Paul (Author) , Ludolph, Albert C. (Author) , Andersen, Peter M (Author) , Otto, Markus (Author) , Kursula, Petri (Author) , Just, Steffen (Author) , Weishaupt, Jochen H. (Author) ,

• lizenzpflichtig

Comprehensive analysis of the mutation spectrum in 301 German ALS families by Müller, Kathrin (Author) , Brenner, David (Author) , Weydt, Patrick (Author) , Meyer, Thomas (Author) , Grehl, Torsten (Author) , Petri, Susanne (Author) , Großkreutz, Julian (Author) , Schuster, Joachim (Author) , Volk, Alexander E. (Author) , Borck, Guntram (Author) , Kubisch, Christian (Author) , Klopstock, Thomas (Author) , Zeller, Daniel (Author) , Jablonka, Sibylle (Author) , Sendtner, Michael (Author) , Klebe, Stephan (Author) , Knehr, Antje (Author) , Günther, Kornelia (Author) , Weis, Joachim (Author) , Claeys, Kristl G. (Author) , Schrank, Berthold (Author) , Sperfeld, Anne-Dorte (Author) , Hübers, Annemarie (Author) , Otto, Markus (Author) , Dorst, Johannes (Author) , Meitinger, Thomas (Author) , Strom, Tim M. (Author) , Andersen, Peter M. (Author) , Ludolph, Albert C. (Author) , Weishaupt, Jochen H. (Author) ,

• lizenzpflichtig
• lizenzpflichtig

Association of mutations in TBK1 with sporadic and familial amyotrophic lateral sclerosis and frontotemporal dementia by Freischmidt, Axel (Author) , Müller, Kathrin (Author) , Ludolph, Albert C. (Author) , Weishaupt, Jochen H. (Author) , Andersen, Peter M. (Author) ,

• lizenzpflichtig

Instability of C154Y variant of aldo-keto reductase 1C3 by Endo, Satoshi (Author) , Takada, Sayaka (Author) , Honda, Ryo P. (Author) , Müller, Kathrin (Author) , Weishaupt, Jochen H. (Author) , Andersen, Peter M. (Author) , Ludolph, Albert C. (Author) , Kamatari, Yuji O. (Author) , Matsunaga, Toshiyuki (Author) , Kuwata, Kazuo (Author) , El-Kabbani, Ossama (Author) , Ikari, Akira (Author) ,

• lizenzpflichtig
• lizenzpflichtig

NEK1 mutations in familial amyotrophic lateral sclerosis: letter to the editor by Brenner, David (Author) , Müller, Kathrin (Author) , Wieland, Thomas (Author) , Weydt, Patrick (Author) , Böhm, Sarah (Author) , Lulé, Dorothée (Author) , Hübers, Annemarie (Author) , Neuwirth, Christoph (Author) , Weber, Markus (Author) , Borck, Guntram (Author) , Wahlqvist, Magnus (Author) , Danzer, Karin M. (Author) , Volk, Alexander E. (Author) , Meitinger, Thomas (Author) , Strom, Tim M. (Author) , Otto, Markus (Author) , Kassubek, Jan (Author) , Ludolph, Albert C. (Author) , Andersen, Peter M. (Author) , Weishaupt, Jochen H. (Author) ,

• lizenzpflichtig

Neurofilament levels as biomarkers in asymptomatic and symptomatic familial amyotrophic lateral sclerosis by Weydt, Patrick (Author) , Oeckl, Patrick (Author) , Huss, Andre (Author) , Müller, Kathrin (Author) , Volk, Alexander E. (Author) , Kuhle, Jens (Author) , Knehr, Antje (Author) , Andersen, Peter M. (Author) , Prudlo, Johannes (Author) , Steinacker, Petra (Author) , Weishaupt, Jochen H. (Author) , Ludolph, Albert C. (Author) , Otto, Markus (Author) ,