Bereich
Muskelzentrum | ALS Clinic
MUSKEL · Dept. III
Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations
German ALS network MND-NET, Weis J, Dorst J, Volk A, Borck G, Sperfeld A, de Carvalho M, Klopstock T, Sendtner M, Otto M, Schuster J, Weishaupt J, Andersen P, Ludolph A, Meitinger T, Freischmidt A, Danzer K, Braak H, Del Tredici K, Jablonka S, Kubisch C, Zeller D, Weydt P, Grosskreutz J, Meyer T, Petri S, Grehl T, Müller K, Yilmaz R, Rosenbohm A, Ruf W, Neuwirth C, Hübers A, Günther K, Knehr A, Jordan B, Schrank B, Claeys K, Pinto S, Weber M, Brenner D. Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations. Brain 2019; 142:e67.
01.01.2019Reply: Adult-onset distal spinal muscular atrophy: a new phenotype associated with KIF5A mutations
01.01.2019Brain 2019; 142:e67
German ALS network MND-NET, Weis Joachim, Dorst Johannes, Volk Alexander E, Borck Guntram, Sperfeld Anne, de Carvalho Mamede, Klopstock Thomas, Sendtner Michael, Otto Markus, Schuster Joachim, Weishaupt Jochen H, Andersen Peter M, Ludolph Albert C, Meitinger Thomas, Freischmidt Axel, Danzer Karin M, Braak Heiko, Del Tredici Kelly, Jablonka Sibylle, Kubisch Christian, Zeller Daniel, Weydt Patrick, Grosskreutz Julian, Meyer Thomas, Petri Susanne, Grehl Torsten, Müller Kathrin, Yilmaz Rüstem, Rosenbohm Angela, Ruf Wolfgang, Neuwirth Christoph, Hübers Annemarie, Günther Kornelia, Knehr Antje, Jordan Berit, Schrank Berthold, Claeys Kristl G, Pinto Susana, Weber Markus, Brenner David
Diagnostic criteria for amyotrophic lateral sclerosis: A multicentre study of inter-rater variation and sensitivity
Johnsen B, Swash M, Abraham A, Drory V, Weber M, Neuwirth C, Czell D, Maderna L, Schofield I, Liguori R, Nix W, Camdessanché J, Dengler R, Paracka L, Kollewe K, Fuglsang-Frederiksen A, Pugdahl K, DE CARVALHO M. Diagnostic criteria for amyotrophic lateral sclerosis: A multicentre study of inter-rater variation and sensitivity. Clin Neurophysiol 2018
09.12.2018Diagnostic criteria for amyotrophic lateral sclerosis: A multicentre study of inter-rater variation and sensitivity
09.12.2018Clin Neurophysiol 2018
Johnsen B, Swash M, Abraham A, Drory V E, Weber Markus, Neuwirth Christoph, Czell D, Maderna L, Schofield I, Liguori R, Nix W, Camdessanché J P, Dengler R, Paracka L, Kollewe K, Fuglsang-Frederiksen A, Pugdahl K, DE CARVALHO M
A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis
Maier M, Nitsch R, Christoph H, Weber M, Perrin S, Stehle T, Späni C, Kulic L, Vieira F, McAfoose J, Preisig D, Montrasio F, Wirth F, Welt T, Grimm J. A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis. Sci Transl Med 2018; 10
05.12.2018A human-derived antibody targets misfolded SOD1 and ameliorates motor symptoms in mouse models of amyotrophic lateral sclerosis
05.12.2018Sci Transl Med 2018; 10
Maier Marcel, Nitsch Roger M, Christoph Hock, Weber Markus, Perrin Steve, Stehle Thilo, Späni Claudia, Kulic Luka, Vieira Fernando G, McAfoose Jordan, Preisig Daniel, Montrasio Fabio, Wirth Fabian, Welt Tobias, Grimm Jan
Motor Unit Number Index (MUNIX) of hand muscles is a disease biomarker for adult spinal muscular atrophy
Günther R, Neuwirth C, Koch J, Lingor P, Braun N, Untucht R, Petzold D, Weber M, Hermann A. Motor Unit Number Index (MUNIX) of hand muscles is a disease biomarker for adult spinal muscular atrophy. Clin Neurophysiol 2018
24.11.2018Motor Unit Number Index (MUNIX) of hand muscles is a disease biomarker for adult spinal muscular atrophy
24.11.2018Clin Neurophysiol 2018
Günther René, Neuwirth Christoph, Koch Jan Christoph, Lingor Paul, Braun Nathalie, Untucht Robert, Petzold Daniel, Weber Markus, Hermann Andreas
Metabotropic glutamate receptor subtype 5 is altered in LPS-induced murine neuroinflammation model and in the brains of AD and ALS patients
Müller Herde A, Schibli R, Weber M, Ametamey S. Metabotropic glutamate receptor subtype 5 is altered in LPS-induced murine neuroinflammation model and in the brains of AD and ALS patients. Eur J Nucl Med Mol Imaging 2018
05.10.2018Metabotropic glutamate receptor subtype 5 is altered in LPS-induced murine neuroinflammation model and in the brains of AD and ALS patients
05.10.2018Eur J Nucl Med Mol Imaging 2018
Müller Herde Adrienne, Schibli Roger, Weber Markus, Ametamey Simon M
In-vivo evaluation of neuronal and glial changes in amyotrophic lateral sclerosis with diffusion tensor spectroscopy
Reischauer C, Gutzeit A, Neuwirth C, Fuchs A, Sartoretti-Schefer S, Weber M, Czell D. In-vivo evaluation of neuronal and glial changes in amyotrophic lateral sclerosis with diffusion tensor spectroscopy. Neuroimage Clin 2018; 20:993-1000.
03.10.2018In-vivo evaluation of neuronal and glial changes in amyotrophic lateral sclerosis with diffusion tensor spectroscopy
03.10.2018Neuroimage Clin 2018; 20:993-1000
Reischauer Carolin, Gutzeit Andreas, Neuwirth Christoph, Fuchs Alexander, Sartoretti-Schefer Sabine, Weber Markus, Czell David
Amyotrophe Lateralsklerose - eine Krankheit mit besonderen Herausforderungen
Braun N, Neuwirth C, Weber M. Amyotrophe Lateralsklerose - eine Krankheit mit besonderen Herausforderungen. palliative ch 2018
30.07.2018Amyotrophe Lateralsklerose - eine Krankheit mit besonderen Herausforderungen
30.07.2018palliative ch 2018
Braun Nathalie, Neuwirth Christoph, Weber Markus
Implementing Motor Unit Number Index (MUNIX) in a large clinical trial: Real world experience from 27 centres
Neuwirth C, Finegan E, Glass J, Babu S, Ladha S, Kwast-Rabben O, Juntas-Morales R, Coffey A, Chaudhry V, Vu T, Saephanh C, Newhard C, Zakrzewski M, Rosier E, Hamel N, Raheja D, Raaijman J, Ferguson T, Tümmler A, Appelfeller M, Braun N, Claeys K, Bucelli R, Fournier C, Bromberg M, Petri S, Goedee S, Lenglet T, Leppanen R, Canosa A, Goodman I, Al-Lozi M, Ohkubo T, Hübers A, Atassi N, Abrahao A, Funke A, Weber M. Implementing Motor Unit Number Index (MUNIX) in a large clinical trial: Real world experience from 27 centres. Clin Neurophysiol 2018; 129:1756-1762.
03.05.2018Implementing Motor Unit Number Index (MUNIX) in a large clinical trial: Real world experience from 27 centres
03.05.2018Clin Neurophysiol 2018; 129:1756-1762
Neuwirth Christoph, Finegan Eoin, Glass Jonathan D, Babu Suma, Ladha Shafeeq S, Kwast-Rabben Olga, Juntas-Morales Raul, Coffey Amina, Chaudhry Vinay, Vu Tuan, Saephanh Chow, Newhard Colleen, Zakrzewski Marion, Rosier Esther, Hamel Nancy, Raheja Divisha, Raaijman Jesper, Ferguson Toby, Tümmler Anke, Appelfeller Martin, Braun Nathalie, Claeys Kristl G, Bucelli Robert, Fournier Christina, Bromberg Mark, Petri Susanne, Goedee Stephan, Lenglet Timothée, Leppanen Ron, Canosa Antonio, Goodman Ira, Al-Lozi Muhammad, Ohkubo Takuya, Hübers Annemarie, Atassi Nazem, Abrahao Agessandro, Funke Andreas, Weber Markus
Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model
van den Berg L, Grosskreutz J, Weber M, Couratier P, Corcia P, van Es M, Bredenoord A, Shaw C, Gunkel A, Rödiger A, Ludolph A, Petri S, de Carvalho M, Veldink J, Moons K, Hardiman O, Chio A, Al-Chalabi A, Shaw P, Turner M, Talbot K, Van Damme P, Ringer T, Körner S, Gromicho M, Pinto S, Thompson A, McDermott C, Martin S, Calvo A, Rooney J, van Eijk R, Visser A, Debray T, Kobeleva X, Rosenbohm A, Stubendorff B, Hollinger H, Kazoka M, Heverin M, Vajda A, van Rheenen W, Van Vugt J, Dekker A, Middelkoop B, Sommer H, Westeneng H. Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model. Lancet Neurol 2018; 17:423-433.
26.03.2018Prognosis for patients with amyotrophic lateral sclerosis: development and validation of a personalised prediction model
26.03.2018Lancet Neurol 2018; 17:423-433
van den Berg Leonard H, Grosskreutz Julian, Weber Markus, Couratier Philippe, Corcia Philippe, van Es Michael A, Bredenoord Annelien L, Shaw Christopher E, Gunkel Anne, Rödiger Annekathrin, Ludolph Albert C, Petri Susanne, de Carvalho Mamede, Veldink Jan H, Moons Karel G M, Hardiman Orla, Chio Adriano, Al-Chalabi Ammar, Shaw Pamela J, Turner Martin R, Talbot Kevin, Van Damme Philip, Ringer Thomas M, Körner Sonja, Gromicho Marta, Pinto Susana, Thompson Alexander G, McDermott Christopher J, Martin Sarah, Calvo Andrea, Rooney James P K, van Eijk Ruben P A, Visser Anne E, Debray Thomas P A, Kobeleva Xenia, Rosenbohm Angela, Stubendorff Beatrice, Hollinger Hannah, Kazoka Mbombe, Heverin Mark, Vajda Alice, van Rheenen Wouter, Van Vugt Joke J F A, Dekker Annelot M, Middelkoop Bas M, Sommer Helma, Westeneng Henk-Jan
Unmasking the silent motor neuron loss in ALS
Neuwirth C, Weber M. Unmasking the silent motor neuron loss in ALS. Muscle Nerve 2018
23.03.2018Unmasking the silent motor neuron loss in ALS
23.03.2018Muscle Nerve 2018
Neuwirth Christoph, Weber Markus
Investigation of Neurodegenerative Processes in Amyotrophic Lateral Sclerosis Using White Matter Fiber Density
Stämpfli P, Gutzeit A, Seifritz E, Sartoretti-Schefer S, Weber M, Neuwirth C, Kozerke S, Czell D, Sommer S, Reischauer C. Investigation of Neurodegenerative Processes in Amyotrophic Lateral Sclerosis Using White Matter Fiber Density. Clin Neuroradiol 2018; 29:493-503.
19.02.2018Investigation of Neurodegenerative Processes in Amyotrophic Lateral Sclerosis Using White Matter Fiber Density
19.02.2018Clin Neuroradiol 2018; 29:493-503
Stämpfli Philipp, Gutzeit Andreas, Seifritz Erich, Sartoretti-Schefer Sabine, Weber Markus, Neuwirth Christoph, Kozerke Sebastian, Czell David, Sommer Stefan, Reischauer Carolin
Motor Unit Number Index (MUNIX): Guidelines for Recording Signals and Their Analysis
Nandedkar S, Barkhaus P, Stålberg E, Neuwirth C, Weber M. Motor Unit Number Index (MUNIX): Guidelines for Recording Signals and Their Analysis. Muscle Nerve 2018
10.02.2018Motor Unit Number Index (MUNIX): Guidelines for Recording Signals and Their Analysis
10.02.2018Muscle Nerve 2018
Nandedkar Sanjeev D, Barkhaus Paul E, Stålberg Erik V, Neuwirth Christoph, Weber Markus
Hot-spot KIF5A mutations cause familial ALS
Weishaupt J, Weis J, Dorst J, Volk A, Borck G, Sperfeld A, de Carvalho M, Klopstock T, Sendtner M, Otto M, Schuster J, Andersen P, Ludolph A, Strom T, Meitinger T, Freischmidt A, Danzer K, Braak H, Del Tredici K, Jablonka S, Kubisch C, German ALS network MND-NET, Ruf W, Weydt P, Grosskreutz J, Meyer T, Petri S, Grehl T, Müller K, Yilmaz R, Neuwirth C, Weber M, Zeller D, Hübers A, Günther K, Knehr A, Jordan B, Schrank B, Claeys K, Pinto S, Brenner D. Hot-spot KIF5A mutations cause familial ALS. Brain 2018
12.01.2018Hot-spot KIF5A mutations cause familial ALS
12.01.2018Brain 2018
Weishaupt Jochen H, Weis Joachim, Dorst Johannes, Volk Alexander E, Borck Guntram, Sperfeld Anne, de Carvalho Mamede, Klopstock Thomas, Sendtner Michael, Otto Markus, Schuster Joachim, Andersen Peter M, Ludolph Albert C, Strom Tim M, Meitinger Thomas, Freischmidt Axel, Danzer Karin M, Braak Heiko, Del Tredici Kelly, Jablonka Sibylle, Kubisch Christian, German ALS network MND-NET, Ruf Wolfgang, Weydt Patrick, Grosskreutz Julian, Meyer Thomas, Petri Susanne, Grehl Torsten, Müller Kathrin, Yilmaz Rüstem, Neuwirth Christoph, Weber Markus, Zeller Daniel, Hübers Annemarie, Günther Kornelia, Knehr Antje, Jordan Berit, Schrank Berthold, Claeys Kristl G, Pinto Susana, Brenner David
Atypical periodic paralysis and myalgia: A novel RYR1 phenotype
Matthews E, Houlden H, Schaefer A, Healy E, Palace J, Quinlivan R, Treves S, Holton J, Jungbluth H, Mein R, Spiegel R, Neuwirth C, Jaffer F, Scalco R, Fialho D, Parton M, Raja Rayan D, Suetterlin K, Sud R, Hanna M. Atypical periodic paralysis and myalgia: A novel RYR1 phenotype. Neurology 2018
03.01.2018Atypical periodic paralysis and myalgia: A novel RYR1 phenotype
03.01.2018Neurology 2018
Matthews Emma, Houlden Henry, Schaefer Andrew, Healy Estelle, Palace Jacqueline, Quinlivan Ros, Treves Susan, Holton Janice L, Jungbluth Heinz, Mein Rachel, Spiegel Roland, Neuwirth Christoph, Jaffer Fatima, Scalco Renata S, Fialho Doreen, Parton Matt, Raja Rayan Dipa, Suetterlin Karen, Sud Richa, Hanna Michael G
Reconsidering the causality of TIA1 mutations in ALS
Van Der Spek R, Hardiman O, Mora J, Morrison K, Mitne-Neto M, Robberecht W, Shaw P, Panadés M, Van Damme P, Silani V, Gotkine M, Weber M, van Es M, Landers J, Al-Chalabi A, van den Berg L, Veldink J, Glass J, Drory V, van Rheenen W, Pulit S, Kenna K, Ticozzi N, Kooyman M, McLaughlin R, Moisse M, van Eijk K, Van Vugt J, Andersen P, Nazli Basak A, Blair I, de Carvalho M, Chio A, Corcia P, Couratier P, PROJECT MINE ALS SEQUENCING CONSORTIUM. Reconsidering the causality of TIA1 mutations in ALS. Amyotroph Lateral Scler Frontotemporal Degener 2017:1-3.
13.12.2017Reconsidering the causality of TIA1 mutations in ALS
13.12.2017Amyotroph Lateral Scler Frontotemporal Degener 2017:1-3
Van Der Spek Rick A, Hardiman Orla, Mora Jesus S, Morrison Karen E, Mitne-Neto Miguel, Robberecht Wim, Shaw Pamela J, Panadés Monica P, Van Damme Philip, Silani Vincenzo, Gotkine Marc, Weber Markus, van Es Michael A, Landers John E, Al-Chalabi Ammar, van den Berg Leonard H, Veldink Jan H, Glass Jonathan D, Drory Vivian E, van Rheenen Wouter, Pulit Sara L, Kenna Kevin P, Ticozzi Nicola, Kooyman Maarten, McLaughlin Russell L, Moisse Matthieu, van Eijk Kristel R, Van Vugt Joke J F A, Andersen Peter, Nazli Basak A, Blair Ian, de Carvalho Mamede, Chio Adriano, Corcia Philippe, Couratier Phillipe, PROJECT MINE ALS SEQUENCING CONSORTIUM
July 2017 ENCALS statement on edaravone
van den Berg L, Silani V, Shaw P, Salachas F, Povedano Panades M, Petri S, Nygren I, Mora Pardina J, Mitre Ropero B, Staaf G, Svenstrup K, Hardiman O, Wolf J, Weydt P, Weber M, van der Kooi A, Van Damme P, Tysnes O, Talbot K, Meyer T, McDermott C, Ludolph A, Desnuelle C, de Carvalho M, Danielsson O, Couratier P, Corcia P, Chio A, Chandran S, Andersen P, Grehl T, Grosskreutz J, Laaksovirta H, KuzmaKozakiewicz M, Koritnik B, Koch J, Kleveland G, Karlsborg M, Ingre C, Holmøy T, Al-Chalabi A. July 2017 ENCALS statement on edaravone. Amyotroph Lateral Scler Frontotemporal Degener 2017; 18:471-474.
04.10.2017July 2017 ENCALS statement on edaravone
04.10.2017Amyotroph Lateral Scler Frontotemporal Degener 2017; 18:471-474
van den Berg Leonard H, Silani Vincenzo, Shaw Pamela, Salachas François, Povedano Panades Mónica, Petri Susanne, Nygren Ingela, Mora Pardina Jesus, Mitre Ropero Bernardo, Staaf Gert, Svenstrup Kirsten, Hardiman Orla, Wolf Joachim, Weydt Patrick, Weber Markus, van der Kooi Anneke, Van Damme Philip, Tysnes Ole-Bjørn, Talbot Kevin, Meyer Thomas, McDermott Christopher, Ludolph Albert, Desnuelle Claude, de Carvalho Mamede, Danielsson Olof, Couratier Philippe, Corcia Philippe, Chio Adriano, Chandran Siddharthan, Andersen Peter M, Grehl Torsten, Grosskreutz Julian, Laaksovirta Hannu, KuzmaKozakiewicz Magdalena, Koritnik Blaž, Koch Jan Christoph, Kleveland Grethe, Karlsborg Merete, Ingre Caroline, Holmøy Trygve, Al-Chalabi Ammar
Is survival improved by the use of NIV and PEG in amyotrophic lateral sclerosis (ALS)? A post-mortem study of 80 ALS patients
Burkhardt C, Neuwirth C, Sommacal A, Andersen P, Weber M. Is survival improved by the use of NIV and PEG in amyotrophic lateral sclerosis (ALS)? A post-mortem study of 80 ALS patients. PloS one 2017; 12:e0177555.
23.05.2017Is survival improved by the use of NIV and PEG in amyotrophic lateral sclerosis (ALS)? A post-mortem study of 80 ALS patients
23.05.2017PloS one 2017; 12:e0177555
Burkhardt Christian, Neuwirth Christoph, Sommacal Andreas, Andersen Peter M, Weber Markus
Longitudinal assessment of the Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen (ECAS): lack of practice effect in ALS patients?
Burkhardt C, Neuwirth C, Weber M. Longitudinal assessment of the Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen (ECAS): lack of practice effect in ALS patients?. Amyotroph Lateral Scler Frontotemporal Degener 2017:1-8.
06.02.2017Longitudinal assessment of the Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen (ECAS): lack of practice effect in ALS patients?
06.02.2017Amyotroph Lateral Scler Frontotemporal Degener 2017:1-8
Burkhardt Christian, Neuwirth Christoph, Weber Markus
Further analysis of KIFAP3 gene in ALS patients from Switzerland and Sweden
Czell D, Sapp P, Neuwirth C, Weber M, Andersen P, Brown R. Further analysis of KIFAP3 gene in ALS patients from Switzerland and Sweden. Amyotroph Lateral Scler Frontotemporal Degener 2017; 18:302-304.
31.01.2017Further analysis of KIFAP3 gene in ALS patients from Switzerland and Sweden
31.01.2017Amyotroph Lateral Scler Frontotemporal Degener 2017; 18:302-304
Czell David, Sapp Peter C, Neuwirth Christoph, Weber Markus, Andersen Peter M, Brown Robert H
Motor Unit Number Index (MUNIX) detects motor neuron loss in pre-symptomatic muscles in Amyotrophic Lateral Sclerosis
Neuwirth C, Barkhaus P, Burkhardt C, Castro J, Czell D, de Carvalho M, Nandedkar S, Stålberg E, Weber M. Motor Unit Number Index (MUNIX) detects motor neuron loss in pre-symptomatic muscles in Amyotrophic Lateral Sclerosis. Clin Neurophysiol 2016
18.12.2016Motor Unit Number Index (MUNIX) detects motor neuron loss in pre-symptomatic muscles in Amyotrophic Lateral Sclerosis
18.12.2016Clin Neurophysiol 2016
Neuwirth Christoph, Barkhaus Paul E, Burkhardt Christian, Castro José, Czell David, de Carvalho Mamede, Nandedkar Sanjeev, Stålberg Erik, Weber Markus