Thomas Meyer, Matthias Boentert, Julian Großkreutz, Patrick Weydt, Sarah Bernsen, Peter Reilich, Robert Steinbach, Annekathrin Rödiger, Joachim Wolf, Ute Weyen, Albert C. Ludolph, Jochen Weishaupt, Susanne Petri, Paul Lingor, René Günther, Wolfgang Löscher, Markus Weber, Christoph Münch, André Maier, Torsten Grehl: Motor phenotypes of amyotrophic lateral sclerosis – a three-determinant anatomical classification based on the region of onset, propagation of motor symptoms, and the degree of upper and lower motor neuron dysfunction. In: Neurological Research and Practice. Band7, Nr.1, 28. April 2025, ISSN2524-3489, S.27, doi:10.1186/s42466-025-00389-w, PMID 40289140, PMC 12036282 (freier Volltext) – (biomedcentral.com [abgerufen am 17. Mai 2025]).
Michael A. van Es, Orla Hardiman, Adriano Chio, Ammar Al-Chalabi, R. Jeroen Pasterkamp: Amyotrophic lateral sclerosis. In: The Lancet. Band390, Nr.10107, 4. November 2017, S.2084–2098, doi:10.1016/S0140-6736(17)31287-4, PMID 28552366.
Thomas Meyer, Matthias Boentert, Julian Großkreutz, Patrick Weydt, Sarah Bernsen, Peter Reilich, Robert Steinbach, Annekathrin Rödiger, Joachim Wolf, Ute Weyen, Albert C. Ludolph, Jochen Weishaupt, Susanne Petri, Paul Lingor, René Günther, Wolfgang Löscher, Markus Weber, Christoph Münch, André Maier, Torsten Grehl: Motor phenotypes of amyotrophic lateral sclerosis – a three-determinant anatomical classification based on the region of onset, propagation of motor symptoms, and the degree of upper and lower motor neuron dysfunction. In: Neurological Research and Practice. Band7, Nr.1, 28. April 2025, ISSN2524-3489, S.27, doi:10.1186/s42466-025-00389-w, PMID 40289140, PMC 12036282 (freier Volltext) – (biomedcentral.com [abgerufen am 17. Mai 2025]).
P. G. Ince, J. R. Highley u. a.: Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology. In: Acta neuropathologica. Band 122, Nummer 6, Dezember 2011, S. 657–671, ISSN1432-0533. doi:10.1007/s00401-011-0913-0. PMID 22105541. (Review).
R. A. Radford, M. Morsch, S. L. Rayner, N. J. Cole, D. L. Pountney, R. S. Chung: The established and emerging roles of astrocytes and microglia in amyotrophic lateral sclerosis and frontotemporal dementia. In: Frontiers in cellular neuroscience. Band 9, 2015, S. 414, doi:10.3389/fncel.2015.00414, PMID 26578880, PMC 4621294 (freier Volltext) (Review), speziell Bild 2.
D. R. Rosen, T. Siddique, D. Patterson, D. A. Figlewicz, P. Sapp, A. Hentati, D. Donaldson, J. Goto, J. P. O’Regan, H. X. Deng: Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. In: Nature, Band 362, Nummer 6415, März 1993, S. 59–62; doi:10.1038/362059a0. PMID 8446170.
J. Sreedharan, I. P. Blair, V. B. Tripathi, X. Hu, C. Vance, B. Rogelj, S. Ackerley, J. C. Durnall, K. L. Williams, E. Buratti, F. Baralle, J. de Belleroche, J. D. Mitchell, P. N. Leigh, A. Al-Chalabi, C. C. Miller, G. Nicholson, C. E. Shaw: TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. In: Science, Band 319, Nummer 5870, März 2008, S. 1668–1672, doi:10.1126/science.1154584. PMID 18309045.
Han-Xiang Deng, Wenjie Chen u. a.: Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia. In: Nature. 2011, doi:10.1038/nature10353.
J. Mitchell, P. Paul, H. J. Chen u. a.: Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase. In: Proc. Natl. Acad. Sci. U.S.A. Band107, Nr.16, 2010, S.7556–7561, doi:10.1073/pnas.0914128107, PMID 20368421, PMC 2867752 (freier Volltext).
J. Sasabe, Y. Miyoshi, M. Suzuki u. a.: D-amino acid oxidase controls motoneuron degeneration through D-serine. In: Proc. Natl. Acad. Sci. U.S.A. Band109, Nr.2, 2012, S.627–632, doi:10.1073/pnas.1114639109, PMID 22203986, PMC 3258611 (freier Volltext).
Feng-Chiao Su, Stephen A. Goutman u. a.: Association of Environmental Toxins With Amyotrophic Lateral Sclerosis. In: JAMA Neurology. 2016. doi:10.1001/jamaneurol.2016.0594.
E. Lagrange, J.P. Vernoux, J. Reis, V. Palmer, W. Camu, P.S. Spencer: An amyotrophic lateral sclerosis hot spot in the French Alps associated with genotoxic fungi. In: Journal of the Neurological Sciences. Band427, 15. August 2021, 117558, doi:10.1016/j.jns.2021.117558 (englisch).
Witzel S, Maier A, Steinbach R et al. Safety and Effectiveness of Long-term Intravenous Administration of Edaravone for Treatment of Patients With Amyotrophic Lateral Sclerosis. JAMA Neurol. 2022;79(2):121–130. doi:10.1001/jamaneurol.2021.4893
Patent EP3119797B1: Zusammensetzungen und Verfahren zur Behandlung von amyotropher Lateralsklerose. Angemeldet am 18. März 2015, veröffentlicht am 23. Dezember 2020, Anmelder: University of Massachusetts, Erfinder: Christian Mueller, Robert H. Brown Jr.
Michael A. van Es, Orla Hardiman, Adriano Chio, Ammar Al-Chalabi, R. Jeroen Pasterkamp: Amyotrophic lateral sclerosis. In: The Lancet. Band390, Nr.10107, 4. November 2017, S.2084–2098, doi:10.1016/S0140-6736(17)31287-4, PMID 28552366.
Thomas Meyer, Matthias Boentert, Julian Großkreutz, Patrick Weydt, Sarah Bernsen, Peter Reilich, Robert Steinbach, Annekathrin Rödiger, Joachim Wolf, Ute Weyen, Albert C. Ludolph, Jochen Weishaupt, Susanne Petri, Paul Lingor, René Günther, Wolfgang Löscher, Markus Weber, Christoph Münch, André Maier, Torsten Grehl: Motor phenotypes of amyotrophic lateral sclerosis – a three-determinant anatomical classification based on the region of onset, propagation of motor symptoms, and the degree of upper and lower motor neuron dysfunction. In: Neurological Research and Practice. Band7, Nr.1, 28. April 2025, ISSN2524-3489, S.27, doi:10.1186/s42466-025-00389-w, PMID 40289140, PMC 12036282 (freier Volltext) – (biomedcentral.com [abgerufen am 17. Mai 2025]).
A. Chio, G. Benzi, M. Dossena, R. Mutani, G. Mora: Severely increased risk of amyotrophic lateral sclerosis among Italian professional football players. In: Brain. 2005 Mar;128(Pt 3), S. 472–476. PMID 15634730
P. G. Ince, J. R. Highley u. a.: Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology. In: Acta neuropathologica. Band 122, Nummer 6, Dezember 2011, S. 657–671, ISSN1432-0533. doi:10.1007/s00401-011-0913-0. PMID 22105541. (Review).
R. A. Radford, M. Morsch, S. L. Rayner, N. J. Cole, D. L. Pountney, R. S. Chung: The established and emerging roles of astrocytes and microglia in amyotrophic lateral sclerosis and frontotemporal dementia. In: Frontiers in cellular neuroscience. Band 9, 2015, S. 414, doi:10.3389/fncel.2015.00414, PMID 26578880, PMC 4621294 (freier Volltext) (Review), speziell Bild 2.
D. R. Rosen, T. Siddique, D. Patterson, D. A. Figlewicz, P. Sapp, A. Hentati, D. Donaldson, J. Goto, J. P. O’Regan, H. X. Deng: Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis. In: Nature, Band 362, Nummer 6415, März 1993, S. 59–62; doi:10.1038/362059a0. PMID 8446170.
H. X. Deng, A. Hentati, J. A. Tainer, Z. Iqbal, A. Cayabyab, W. Y. Hung, E. D. Getzoff, P. Hu, B. Herzfeldt, R. P. Roos: Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase. In: Science, Band 261, Nummer 5124, August 1993, S. 1047–1051; PMID 8351519.
J. Sreedharan, I. P. Blair, V. B. Tripathi, X. Hu, C. Vance, B. Rogelj, S. Ackerley, J. C. Durnall, K. L. Williams, E. Buratti, F. Baralle, J. de Belleroche, J. D. Mitchell, P. N. Leigh, A. Al-Chalabi, C. C. Miller, G. Nicholson, C. E. Shaw: TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. In: Science, Band 319, Nummer 5870, März 2008, S. 1668–1672, doi:10.1126/science.1154584. PMID 18309045.
J. Mitchell, P. Paul, H. J. Chen u. a.: Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase. In: Proc. Natl. Acad. Sci. U.S.A. Band107, Nr.16, 2010, S.7556–7561, doi:10.1073/pnas.0914128107, PMID 20368421, PMC 2867752 (freier Volltext).
J. Sasabe, Y. Miyoshi, M. Suzuki u. a.: D-amino acid oxidase controls motoneuron degeneration through D-serine. In: Proc. Natl. Acad. Sci. U.S.A. Band109, Nr.2, 2012, S.627–632, doi:10.1073/pnas.1114639109, PMID 22203986, PMC 3258611 (freier Volltext).
N. G. Hockstein, D. S. Samadi, K. Gendron, S. D. Handler: Sialorrhea: a management challenge. In: American family physician, Band 69, Nummer 11, Juni 2004, S. 2628–2634, ISSN0002-838X. PMID 15202698.
Thomas Meyer, Matthias Boentert, Julian Großkreutz, Patrick Weydt, Sarah Bernsen, Peter Reilich, Robert Steinbach, Annekathrin Rödiger, Joachim Wolf, Ute Weyen, Albert C. Ludolph, Jochen Weishaupt, Susanne Petri, Paul Lingor, René Günther, Wolfgang Löscher, Markus Weber, Christoph Münch, André Maier, Torsten Grehl: Motor phenotypes of amyotrophic lateral sclerosis – a three-determinant anatomical classification based on the region of onset, propagation of motor symptoms, and the degree of upper and lower motor neuron dysfunction. In: Neurological Research and Practice. Band7, Nr.1, 28. April 2025, ISSN2524-3489, S.27, doi:10.1186/s42466-025-00389-w, PMID 40289140, PMC 12036282 (freier Volltext) – (biomedcentral.com [abgerufen am 17. Mai 2025]).
P. G. Ince, J. R. Highley u. a.: Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology. In: Acta neuropathologica. Band 122, Nummer 6, Dezember 2011, S. 657–671, ISSN1432-0533. doi:10.1007/s00401-011-0913-0. PMID 22105541. (Review).
N. G. Hockstein, D. S. Samadi, K. Gendron, S. D. Handler: Sialorrhea: a management challenge. In: American family physician, Band 69, Nummer 11, Juni 2004, S. 2628–2634, ISSN0002-838X. PMID 15202698.