Citations (68)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (10)
Daniells Erazo, Jaime Luna, Pierre-Marie Preux, Farid Boumediene & Philippe Couratier. (2022) Epidemiological and genetic features of amyotrophic lateral sclerosis in Latin America and the Caribbean: a systematic review. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 23:1-2, pages 4-15.
Read now
Read now
Renshi Xu, Bei Shao, Chengsi Wu, Yunzhu Yang, Hanmin Wang, Rongwei Yang, Xiong Zhang, Juan Yi & Jingjing Liu. (2013) Identification of Tau and SOD1 gene mutation in a small Chinese Han pedigree of adult amyotrophic lateral sclerosis. Neurocase 19:5, pages 497-504.
Read now
Read now
Mariusz Berdyński, Magdalena Kuźma-Kozakiewicz, Claudia Ricci, Justyna Kubiszewska, Stéphanie Millecamps, François Salachas, Anna Łusakowska, Paola Carrera, Vincent Meininger, Stefania Battistini, Hubert Kwieciński & Cezary Żekanowski. (2012) Recurrent G41S mutation in Cu/Zn superoxide dismutase gene (SOD1) causing familial amyotrophic lateral sclerosis in a large Polish family. Amyotrophic Lateral Sclerosis 13:1, pages 132-136.
Read now
Read now
. (2011) SESSION 6A BEYOND GUAM: NEW ASPECTS OF THE BMAA HYPOTHESIS. Amyotrophic Lateral Sclerosis 12:sup1, pages 20-22.
Read now
Read now
Michio Hirano, Catarina M. Quinzii, Hiroshi Mitsumoto, Arthur P. Hays, J. Kirk Roberts, Patricia Richard & Lewis P. Rowland. (2011) Senataxin mutations and amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis 12:3, pages 223-227.
Read now
Read now
Veronica Alonso, Ana Villaverde-Hueso, Manuel J. Hens, Antonio Morales-Piga, Ignacio Abaitua & Manuel Posada de la Paz. (2011) Increase in motor neuron disease mortality in Spain: Temporal and geographical analysis (1990–2005). Amyotrophic Lateral Sclerosis 12:3, pages 192-198.
Read now
Read now
Josep Gamez, Claudia Caponnetto, Loretta Ferrera, Enrique Syriani, Valeria Marini, Miguel Morales, Domenico Bordo, Cristina Pirro, Cecilia Garre & Paola Origone. (2011) I112M SOD1 mutation causes ALS with rapid progression and reduced penetrance in four Mediterranean families. Amyotrophic Lateral Sclerosis 12:1, pages 70-75.
Read now
Read now
Louise Atkins, Richard G. Brown, P. Nigel Leigh & Laura H. Goldstein. (2010) Marital relationships in amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis 11:4, pages 344-350.
Read now
Read now
Fabio Coppedè, Francesca Migheli, Annalisa Lo Gerfo, Maria Rita Fabbrizi, Cecilia Carlesi, Michelangelo Mancuso, Stefania Corti, Nicoletta Mezzina, Roberto del Bo, Giacomo P. Comi, Gabriele Siciliano & Lucia Migliore. (2010) Association study between XRCC1 gene polymorphisms and sporadic amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis 11:1-2, pages 122-124.
Read now
Read now
Stefania Battistini, Claudia Ricci, Fabio Giannini, Silvia Calzavara, Giuseppe Greco, Alberto Del Corona, Michelangelo Mancuso, Noè Battistini, Gabriele Siciliano & Paola Carrera. (2010) G41S SOD1 mutation: A common ancestor for six ALS Italian families with an aggressive phenotype. Amyotrophic Lateral Sclerosis 11:1-2, pages 210-215.
Read now
Read now
Articles from other publishers (58)
Shilpa Sharma, Vijay Raj Tomar, Abhilash Jayaraj & Shashank Deep. (2023) A computational strategy for therapeutic development against superoxide dismutase (SOD1) amyloid formation: effect of polyphenols on the various events in the aggregation pathway. Physical Chemistry Chemical Physics 25:8, pages 6232-6246.
Crossref
Crossref
Donatella Ciarmoli & Fabrizio Stasolla. 2022. Analyzing Multidisciplinary Uses and Impact of Innovative Technologies. Analyzing Multidisciplinary Uses and Impact of Innovative Technologies
69
94
.
Andrew D. Schweitzer & A. John Tsiouris. 2022. Hybrid PET/MR Neuroimaging. Hybrid PET/MR Neuroimaging
397
410
.
Kathryn E. Dean, Beiyi Shen, Gulce Askin, Andrew D. Schweitzer, Mona Shahbazi, Yi Wang, Dale Lange & Apostolos John Tsiouris. (2021) A specific biomarker for amyotrophic lateral sclerosis: Quantitative susceptibility mapping. Clinical Imaging 75, pages 125-130.
Crossref
Crossref
Akhlaq A. Farooqui. 2021. Molecular Aspects of Neurodegeneration, Neuroprotection, and Regeneration in Neurological Disorders. Molecular Aspects of Neurodegeneration, Neuroprotection, and Regeneration in Neurological Disorders
1
40
.
Md. Tanvir Kabir, Md. Sahab Uddin, Ahmed Abdeen, Ghulam Md Ashraf, Asma Perveen, Abdul Hafeez, May N. Bin-Jumah & Mohamed M. Abdel-Daim. (2020) Evidence Linking Protein Misfolding to Quality Control in Progressive Neurodegenerative Diseases. Current Topics in Medicinal Chemistry 20:23, pages 2025-2043.
Crossref
Crossref
Banaja P. Dash, Marcel Naumann, Jared Sterneckert & Andreas Hermann. (2020) Genome Wide Analysis Points towards Subtype-Specific Diseases in Different Genetic Forms of Amyotrophic Lateral Sclerosis. International Journal of Molecular Sciences 21:18, pages 6938.
Crossref
Crossref
Zeynep Öztürk, Cahir J. O’Kane & Juan José Pérez-Moreno. (2020) Axonal Endoplasmic Reticulum Dynamics and Its Roles in Neurodegeneration. Frontiers in Neuroscience 14.
Crossref
Crossref
Yasmeena Akhter, Jahangir Nabi, Hinna Hamid, Nahida Tabassum, Faheem Hyder Pottoo & Aashish Sharma. 2020. Quality Control of Cellular Protein in Neurodegenerative Disorders. Quality Control of Cellular Protein in Neurodegenerative Disorders
1
24
.
Radwa Reda, Manal Tantawi, Howida Shedeed & Mohamed F. Tolba. 2020. Proceedings of the International Conference on Artificial Intelligence and Computer Vision (AICV2020). Proceedings of the International Conference on Artificial Intelligence and Computer Vision (AICV2020)
490
500
.
Tedeschi, Petrozziello & Secondo. (2019) Calcium Dyshomeostasis and Lysosomal Ca2+ Dysfunction in Amyotrophic Lateral Sclerosis. Cells 8:10, pages 1216.
Crossref
Crossref
Haibo Zhang, Yaling Liu, Zhenfei Li, Na Liang, Xiaomeng Zhou, Xiangyu Nie, Ting Zhang & Weijing Qi. (2019) Amyotrophic Lateral Sclerosis and Primary Biliary Cirrhosis Overlap Syndrome: Two Cases Report. Frontiers in Neurology 10.
Crossref
Crossref
Dulika S. Sumathipala & Vajira H. W. Dissanayake. 2019. Pathology, Prevention and Therapeutics of Neurodegenerative Disease. Pathology, Prevention and Therapeutics of Neurodegenerative Disease
73
79
.
Sumeet Kumar, Navneesh Yadav, Sanjay Pandey & B. K. Thelma. (2018) Advances in the discovery of genetic risk factors for complex forms of neurodegenerative disorders: contemporary approaches, success, challenges and prospects. Journal of Genetics 97:3, pages 625-648.
Crossref
Crossref
J. Luna, G. Logroscino, P. Couratier & B. Marin. (2017) Current issues in ALS epidemiology: Variation of ALS occurrence between populations and physical activity as a risk factor. Revue Neurologique 173:5, pages 244-253.
Crossref
Crossref
Stefanie M. A. Willekens, Donatienne Van Weehaeghe, Philip Van Damme & Koen Van Laere. (2016) Positron emission tomography in amyotrophic lateral sclerosis: Towards targeting of molecular pathological hallmarks. European Journal of Nuclear Medicine and Molecular Imaging 44:3, pages 533-547.
Crossref
Crossref
Christine Brütting, Alexander Emmer, Malte E. Kornhuber & Martin S. Staege. (2017) Cooccurrences of Putative Endogenous Retrovirus-Associated Diseases. BioMed Research International 2017, pages 1-11.
Crossref
Crossref
Meena Kumari Kotni, Mingzhu Zhao & Dong-Qing Wei. (2016) Gene expression profiles and protein-protein interaction networks in amyotrophic lateral sclerosis patients with C9orf72 mutation. Orphanet Journal of Rare Diseases 11:1.
Crossref
Crossref
Håvard Torvik Gotaas, Geir Olve Skeie & Nils Erik Gilhus. (2016) Myasthenia gravis and amyotrophic lateral sclerosis: A pathogenic overlap. Neuromuscular Disorders 26:6, pages 337-341.
Crossref
Crossref
James B. Hilton, Anthony R. White & Peter J. Crouch. (2015) Metal-deficient SOD1 in amyotrophic lateral sclerosis. Journal of Molecular Medicine 93:5, pages 481-487.
Crossref
Crossref
Aaron Ciechanover & Yong Tae Kwon. (2015) Degradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies. Experimental & Molecular Medicine 47:3, pages e147-e147.
Crossref
Crossref
Miguel Mitne-Neto. 2015. Stem Cells in Modeling Human Genetic Diseases. Stem Cells in Modeling Human Genetic Diseases
29
44
.
Jianfeng Liang, Dongman Chao, Harleen K Sandhu, Yanbing Yu, Li Zhang, Gianfranco Balboni, Dong H Kim & Ying Xia. (2014) δ-Opioid receptors up-regulate excitatory amino acid transporters in mouse astrocytes. British Journal of Pharmacology 171:23, pages 5417-5430.
Crossref
Crossref
Ming-Dong Wang, James Gomes, Neil R. Cashman, Julian Little & Daniel Krewski. (2014) A Meta-Analysis of Observational Studies of the Association Between Chronic Occupational Exposure to Lead and Amyotrophic Lateral Sclerosis. Journal of Occupational & Environmental Medicine 56:12, pages 1235-1242.
Crossref
Crossref
Ming-Dong Wang, James Gomes, Neil R. Cashman, Julian Little & Daniel Krewski. (2014) Intermediate CAG Repeat Expansion in the ATXN2 Gene Is a Unique Genetic Risk Factor for ALS−A Systematic Review and Meta-Analysis of Observational Studies. PLoS ONE 9:8, pages e105534.
Crossref
Crossref
Chundi Vinay Kumar, K.M. Kumar, Rayapadi Swetha, Sudha Ramaiah & Anand Anbarasu. (2014) Protein aggregation due to nsSNP resulting in P56S VABP protein is associated with amyotrophic lateral sclerosis. Journal of Theoretical Biology 354, pages 72-80.
Crossref
Crossref
Orhan Tansel Korkmaz, Nurgul Aytan, Isabel Carreras, Ji-Kyung Choi, Neil W. Kowall, Bruce G. Jenkins & Alpaslan Dedeoglu. (2014) 7,8-Dihydroxyflavone improves motor performance and enhances lower motor neuronal survival in a mouse model of amyotrophic lateral sclerosis. Neuroscience Letters 566, pages 286-291.
Crossref
Crossref
Yanling Sui, Zichun Zhao, Rong Liu, Bin Cai & Dongsheng Fan. (2014) Adenosine monophosphate-activated protein kinase activation enhances embryonic neural stem cell apoptosis in a mouse model of amyotrophic lateral sclerosis. Neural Regeneration Research 9:19, pages 1770.
Crossref
Crossref
Eitan Lilo, Shane Wald-Altman, Leonardo J. Solmesky, Keren Ben Yaakov, Noga Gershoni-Emek, Shlomo Bulvik, Ibrahim Kassis, Dimitrios Karussis, Eran Perlson & Miguel Weil. (2013) Characterization of human sporadic ALS biomarkers in the familial ALS transgenic mSOD1G93A mouse model. Human Molecular Genetics 22:23, pages 4720-4725.
Crossref
Crossref
Patricia S. Estes, Scott G. Daniel, Abigail P. Mccallum, Ashley V. Boehringer, Alona S. Sukhina, Rebecca A. Zwick & Daniela C. Zarnescu. (2013)
Motor neurons and glia exhibit specific individualized responses to TDP-43 expression in a
Drosophila
model of amyotrophic lateral sclerosis
. Disease Models & Mechanisms.
Crossref
Crossref
Syuichi Tetsuka, Mitsuya Morita, Aritoshi Iida, Ritei Uehara, Shiro Ikegawa & Imaharu Nakano. (2013) ZNF512B gene is a prognostic factor in patients with amyotrophic lateral sclerosis. Journal of the Neurological Sciences 324:1-2, pages 163-166.
Crossref
Crossref
Beatrice Nefussy & Vivian E. Drory. 2013. Neurodegenerative Diseases: Integrative PPPM Approach as the Medicine of the Future. Neurodegenerative Diseases: Integrative PPPM Approach as the Medicine of the Future
205
233
.
Massimo Buscema, Silvana Penco & Enzo Grossi. (2012) A Novel Mathematical Approach to Define the Genes/SNPs Conferring Risk or Protection in Sporadic Amyotrophic Lateral Sclerosis Based on Auto Contractive Map Neural Networks and Graph Theory. Neurology Research International 2012, pages 1-13.
Crossref
Crossref
Rachel L. Redler & Nikolay V. Dokholyan. 2012. Molecular Biology of Neurodegenerative Diseases. Molecular Biology of Neurodegenerative Diseases
215
262
.
Aaron Kerman & Avijit Chakrabartty. 2012. Non-fibrillar Amyloidogenic Protein Assemblies - Common Cytotoxins Underlying Degenerative Diseases. Non-fibrillar Amyloidogenic Protein Assemblies - Common Cytotoxins Underlying Degenerative Diseases
257
288
.
Guijie Ren, Zhongcai Ma, Maria Hui, Lili C Kudo, Koon-Sea Hui & Stanislav L Karsten. (2011) Cu, Zn-superoxide dismutase 1 (SOD1) is a novel target of Puromycin-sensitive aminopeptidase (PSA/NPEPPS): PSA/NPEPPS is a possible modifier of amyotrophic lateral sclerosis. Molecular Neurodegeneration 6:1.
Crossref
Crossref
Orla Hardiman, Leonard H. van den Berg & Matthew C. Kiernan. (2011) Clinical diagnosis and management of amyotrophic lateral sclerosis. Nature Reviews Neurology 7:11, pages 639-649.
Crossref
Crossref
Mamede de Carvalho & Michael Swash. (2011) Amyotrophic lateral sclerosis. Current Opinion in Neurology 24:5, pages 497-503.
Crossref
Crossref
Genevieve Gowing & Clive N. Svendsen. (2011) Stem Cell Transplantation for Motor Neuron Disease: Current Approaches and Future Perspectives. Neurotherapeutics 8:4, pages 591-606.
Crossref
Crossref
Miguel Mitne-Neto, Marcela Machado-Costa, Maria C.N. Marchetto, Mario H. Bengtson, Claudio A. Joazeiro, Hiroshi Tsuda, Hugo J. Bellen, Helga C.A. Silva, Acary S.B. Oliveira, Monize Lazar, Alysson R. Muotri & Mayana Zatz. (2011) Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients. Human Molecular Genetics 20:18, pages 3642-3652.
Crossref
Crossref
Aritoshi Iida, Atsushi Takahashi, Michiaki Kubo, Susumu Saito, Naoya Hosono, Yozo Ohnishi, Kazuma Kiyotani, Taisei Mushiroda, Masahiro Nakajima, Kouichi Ozaki, Toshihiro Tanaka, Tatsuhiko Tsunoda, Shuichi Oshima, Motoki Sano, Tetsumasa Kamei, Torao Tokuda, Masashi Aoki, Kazuko Hasegawa, Koichi Mizoguchi, Mitsuya Morita, Yuji Takahashi, Masahisa Katsuno, Naoki Atsuta, Hirohisa Watanabe, Fumiaki Tanaka, Ryuji Kaji, Imaharu Nakano, Naoyuki Kamatani, Shoji Tsuji, Gen Sobue, Yusuke Nakamura & Shiro Ikegawa. (2011) A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese. Human Molecular Genetics 20:18, pages 3684-3692.
Crossref
Crossref
Michael J. Strong, Tibor Hortobágyi, Koichi Okamoto & Shinsuke Kato. 2011. Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders. Neurodegeneration: The Molecular Pathology of Dementia and Movement Disorders
418
433
.
Xiaohua Xu, Arthur E. Warrington, Allan J. Bieber & Moses Rodriguez. (2011) Enhancing CNS Repair in Neurological Disease. CNS Drugs 25:7, pages 555-573.
Crossref
Crossref
Patricia S. Estes, Ashley Boehringer, Rebecca Zwick, Jonathan E. Tang, Brianna Grigsby & Daniela C. Zarnescu. (2011) Wild-type and A315T mutant TDP-43 exert differential neurotoxicity in a Drosophila model of ALS. Human Molecular Genetics 20:12, pages 2308-2321.
Crossref
Crossref
Giovanni De Marco, Elisa Lupino, Andrea Calvo, Cristina Moglia, Barbara Buccinnà, Silvia Grifoni, Cristina Ramondetti, Annarosa Lomartire, Maria Teresa Rinaudo, Marco Piccinini, Maria Teresa Giordana & Adriano Chiò. (2010) Cytoplasmic accumulation of TDP-43 in circulating lymphomonocytes of ALS patients with and without TARDBP mutations. Acta Neuropathologica 121:5, pages 611-622.
Crossref
Crossref
Lucia Corrado, Yari Carlomagno, Luca Falasco, Simona Mellone, Michela Godi, Emanuela Cova, Cristina Cereda, Lucia Testa, Letizia Mazzini & Sandra D'Alfonso. (2011) A novel peripherin gene (PRPH) mutation identified in one sporadic amyotrophic lateral sclerosis patient. Neurobiology of Aging 32:3, pages 552.e1-552.e6.
Crossref
Crossref
Claudia Ricci, Stefania Battistini, Lorena Cozzi, Michele Benigni, Paola Origone, Lorenzo Verriello, Christian Lunetta, Cristina Cereda, Pamela Milani, Giuseppe Greco, Maria Cristina Patrosso, Renzo Causarano, Claudia Caponnetto, Fabio Giannini, Massimo Corbo & Silvana Penco. (2011) Lack of association of PON polymorphisms with sporadic ALS in an Italian population. Neurobiology of Aging 32:3, pages 552.e7-552.e13.
Crossref
Crossref
Matthew C Kiernan, Steve Vucic, Benjamin C Cheah, Martin R Turner, Andrew Eisen, Orla Hardiman, James R Burrell & Margaret C Zoing. (2011) Amyotrophic lateral sclerosis. The Lancet 377:9769, pages 942-955.
Crossref
Crossref
Jian Liu, Armin Akhavan, Mengde Lu, Arie Gruzman, Vishwanath R. Lingappa, Jiyan An & Robert Bowser. (2010) Carbonic Anhydrase I Is Recognized by an SOD1 Antibody upon Biotinylation of Human Spinal Cord Extracts. International Journal of Molecular Sciences 11:10, pages 4051-4062.
Crossref
Crossref
Richard S Bedlack. (2010) Amyotrophic lateral sclerosis: current practice and future treatments. Current Opinion in Neurology 23:5, pages 524-529.
Crossref
Crossref
Takuto Hideyama, Takenari Yamashita, Takeshi Suzuki, Shoji Tsuji, Miyoko Higuchi, Peter H. Seeburg, Ryosuke Takahashi, Hidemi Misawa & Shin Kwak. (2010) Induced Loss of ADAR2 Engenders Slow Death of Motor Neurons from Q/R Site-Unedited GluR2. The Journal of Neuroscience 30:36, pages 11917-11925.
Crossref
Crossref
F. Agosta, E. Pagani, M. Petrolini, D. Caputo, M. Perini, A. Prelle, F. Salvi & M. Filippi. (2010) Assessment of White Matter Tract Damage in Patients with Amyotrophic Lateral Sclerosis: A Diffusion Tensor MR Imaging Tractography Study: Fig 1.. American Journal of Neuroradiology 31:8, pages 1457-1461.
Crossref
Crossref
Lili C. Kudo, Liubov Parfenova, Nancy Vi, Kimbley Lau, Justine Pomakian, Paul Valdmanis, Guy A. Rouleau, Harry V. Vinters, Martina Wiedau-Pazos & Stanislav L. Karsten. (2010) Integrative gene–tissue microarray-based approach for identification of human disease biomarkers: application to amyotrophic lateral sclerosis. Human Molecular Genetics 19:16, pages 3233-3253.
Crossref
Crossref
Beatrice Nefussy & Vivian E. Drory. (2010) Moving toward a predictive and personalized clinical approach in amyotrophic lateral sclerosis: novel developments and future directions in diagnosis, genetics, pathogenesis and therapies. EPMA Journal 1:2, pages 329-341.
Crossref
Crossref
Orla Hardiman. 2005. Encyclopedia of Life Sciences. Encyclopedia of Life Sciences.
Takanori Takazawa, Ken Ikeda, Takehisa Hirayama, Kiyokazu Kawabe, Yoshikazu Nakamura, Hirono Ito, Osamu Kano, Yasuhiro Yoshii, Fumiaki Tanaka, Gen Sobue & Yasuo Iwasaki. (2010) Familial Amyotrophic Lateral Sclerosis with a Novel G85S Mutation of Superoxide Dismutase 1 Gene: Clinical Features of Lower Motor Neuron Disease. Internal Medicine 49:2, pages 183-186.
Crossref
Crossref
M. Sabatelli, F. Eusebi, A. Al-Chalabi, A. Conte, F. Madia, M. Luigetti, I. Mancuso, C. Limatola, F. Trettel, F. Sobrero, S. Di Angelantonio, F. Grassi, A. Di Castro, C. Moriconi, S. Fucile, S. Lattante, G. Marangi, M. Murdolo, D. Orteschi, A. Del Grande, P. Tonali, G. Neri & M. Zollino. (2009) Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis. Human Molecular Genetics 18:20, pages 3997-4006.
Crossref
Crossref
Albert C. LudolphSarah Jesse. (2009) Review: Evidence-based drug treatment in amyotrophic lateral sclerosis and upcoming clinical trials. Therapeutic Advances in Neurological Disorders 2:5, pages 319-326.
Crossref
Crossref