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Research Article

Neuropathology of amyotrophic lateral sclerosis with extra-motor system degeneration: Characteristics and differences in the molecular pathology between ALS with dementia and Guamanian ALS

Pages 97-104 | Published online: 10 Jul 2009

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N. Chernoff, D. J. Hill, D. L. Diggs, B. D. Faison, B. M. Francis, J. R Lang, M. M. Larue, T.-T. Le, K. A. Loftin, J. N. Lugo, J. E. Schmid & W. M. Winnik. (2017) A critical review of the postulated role of the non-essential amino acid, β-N-methylamino-L-alanine, in neurodegenerative disease in humans. Journal of Toxicology and Environmental Health, Part B 20:4, pages 183-229.
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Fang Cui, Wenjia Zhu, Zhibin Zhou, Yuting Ren, Yifan Li, Mao Li, Yunyun Huo & Xusheng Huang. (2015) Frequency and risk factor analysis of cognitive and anxiety-depressive disorders in patients with amyotrophic lateral sclerosis/motor neuron disease. Neuropsychiatric Disease and Treatment 11, pages 2847-2854.
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Lewis P. Rowland. (2009) T.L. Bunina, Asao Hirano, and the post mortem cellular diagnosis of amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis 10:2, pages 74-78.
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Articles from other publishers (11)

Audrey M. G. Ragagnin, Sina Shadfar, Marta Vidal, Md Shafi Jamali & Julie D. Atkin. (2019) Motor Neuron Susceptibility in ALS/FTD. Frontiers in Neuroscience 13.
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Varan Govind. 2016. Magnetic Resonance Spectroscopy of Degenerative Brain Diseases. Magnetic Resonance Spectroscopy of Degenerative Brain Diseases 121 150 .
Ida E Holm, Aage Kristian Olsen Alstrup & Yonglun Luo. (2016) Genetically modified pig models for neurodegenerative disorders. The Journal of Pathology 238:2, pages 267-287.
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Angela L. Shamchuk & Keith B. Tierney. 2013. Animal Models for the Study of Human Disease. Animal Models for the Study of Human Disease 651 678 .
N. Sudharshan, C. Hanstock, B. Hui, T. Pyra, W. Johnston & S. Kalra. (2011) Degeneration of the Mid-Cingulate Cortex in Amyotrophic Lateral Sclerosis Detected In Vivo with MR Spectroscopy. American Journal of Neuroradiology 32:2, pages 403-407.
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Meng-nan YU. (2010) Motor neuron disease complicated by frontotemporal dementia:a case report. Academic Journal of Second Military Medical University 29:1, pages 115-116.
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Satomi Maekawa, P. Nigel Leigh, Andrew King, Edith Jones, John C. Steele, Istvan Bodi, Christopher E. Shaw, Tibor Hortobagyi & Safa Al-Sarraj. (2009) TDP-43 is consistently co-localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations. Neuropathology 29:6, pages 672-683.
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Anna-Lena Ström, Ping Shi, Fujian Zhang, Jozsef Gal, Renee Kilty, Lawrence J. Hayward & Haining Zhu. (2008) Interaction of Amyotrophic Lateral Sclerosis (ALS)-related Mutant Copper-Zinc Superoxide Dismutase with the Dynein-Dynactin Complex Contributes to Inclusion Formation. Journal of Biological Chemistry 283:33, pages 22795-22805.
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Robert A. Boyajian, Carlos Amo, Shirley M. Otis, John S. Romine & Richard A. Smith. (2008) Magnetic Source Imaging of Cortical Dysfunction in Amyotrophic Lateral Sclerosis. American Journal of Physical Medicine & Rehabilitation 87:6, pages 427-437.
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Safa Al‐Sarraj. 2008. Dementias. Dementias 431 441 .
N. J. CairnsM. GrossmanS. E. ArnoldD. J. BurnE. JarosR. H. PerryC. DuyckaertsB. StankoffB. PillonK. SkullerudF. F. Cruz-SanchezE. H. BigioI. R.A. MackenzieM. GearingJ. L. JuncosJ. D. GlassH. YokooY. NakazatoS. MosahebJ. R. ThorpeK. UryuV. M.-Y. LeeJ .Q. Trojanowski. (2004) Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease. Neurology 63:8, pages 1376-1384.
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