Zobrazeno 1 - 10
of 17
pro vyhledávání: '"MND/motor neuron disease"'
Autor:
Rupesh Kumar, Shazia Haider
Publikováno v:
IBRO Neuroscience Reports, Vol 12, Iss, Pp 25-44 (2022)
IBRO Neuroscience Reports
IBRO Neuroscience Reports
Amyotrophic Lateral Sclerosis (ALS) is a fatal disease, progressive nature characterizes by loss of both upper and lower motor neuron functions. One of the major challenge is to understand the mechanism of ALS multifactorial nature. We aimed to explo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c23dbfa5e2c81d371bd122e6d9e27c4d
https://doi.org/10.1016/j.ibneur.2021.12.002
https://doi.org/10.1016/j.ibneur.2021.12.002
Autor:
Masahisa, Nozaki, Asako, Otomo, Shun, Mitsui, Suzuka, Ono, Ryohei, Shirakawa, YongPing, Chen, Yutaro, Hama, Kai, Sato, XuePing, Chen, Toshiyasu, Suzuki, Hui-Fang, Shang, Shinji, Hadano
Publikováno v:
eNeurologicalSci
Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are genetically, pathologically and clinically-related progressive neurodegenerative diseases. Thus far, several SQSTM1 variations have been identified in patients with ALS and FTD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0559a3914a18e9cbb7aec0bb21736d3f
https://pubmed.ncbi.nlm.nih.gov/33319079
https://pubmed.ncbi.nlm.nih.gov/33319079
Autor:
Adriano Chiò, Tamara Thurn, Christopher J McDermott, Johanna Anneser, Andrea Sylvia Winkler, Gabriele Mora, Walter Sermeus, Miriam Galvin, Gian Domenico Borasio
Objective: This study aims (1) to assess physicians’ attitudes toward different palliative end-of-life (EOL) practices in amyotrophic lateral sclerosis (ALS) care, including forgoing artificial nutrition and hydration (FANH), continuous sedation un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4658a1c386b05fa09b44e98affad6d60
Publikováno v:
Muñoz-Neira, C, Tedde, A, Coulthard, E J, Thai, N J & Pennington, C M 2019, ' Neural correlates of altered insight in frontotemporal dementia : a systematic review ', NeuroImage: Clinical, vol. 24, 102066 . https://doi.org/10.1016/j.nicl.2019.102066
NeuroImage : Clinical
Muñoz-Neira, C, Tedde, A, Coulthard, E, Thai, N J & Pennington, C 2019, ' Neural correlates of altered insight in frontotemporal dementia: a systematic review ', NeuroImage: Clinical, vol. 24, pp. 102066 . https://doi.org/10.1016/j.nicl.2019.102066
NeuroImage: Clinical, Vol 24, Iss, Pp-(2019)
NeuroImage : Clinical
Muñoz-Neira, C, Tedde, A, Coulthard, E, Thai, N J & Pennington, C 2019, ' Neural correlates of altered insight in frontotemporal dementia: a systematic review ', NeuroImage: Clinical, vol. 24, pp. 102066 . https://doi.org/10.1016/j.nicl.2019.102066
NeuroImage: Clinical, Vol 24, Iss, Pp-(2019)
Highlights • Fractionating insight into objects aids its neuroanatomical exploration in dementia. • Distinctive neural correlates seem to underpin different insight objects in FTD. • Altered insight into disease/health condition mostly involves
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0089015e0250327e8f25ded62dfd45c
https://hdl.handle.net/1983/8a977835-b0a2-4cc5-9b1b-7ac6db21ed67
https://hdl.handle.net/1983/8a977835-b0a2-4cc5-9b1b-7ac6db21ed67
Autor:
Rabab Debs, Jean-Yves Hogrel, Gaëlle Bruneteau, Tanya Stojkovic, Maria del Mar Amador, Julien Cohen-Adad, Lucette Lacomblez, David Devos, Nadine Le Forestier, Peter Bede, Timothée Lenglet, Menghan Li, Sophie Blancho, Pierre-François Pradat, Pascal Laforêt, Anthony Behin, François Salachas, Habib Benali, Martin Catala, Véronique Marchand-Pauvert, Mohamed-Mounir El Mendili, Stéphane Lehéricy, Vincent Meininger, Giorgia Querin
Publikováno v:
Neuroimage-Clinical
Neuroimage-Clinical, Elsevier, 2019, 21, pp.101618. ⟨10.1016/j.nicl.2018.101618⟩
Neuroimage-Clinical, 2019, 21, pp.101618. ⟨10.1016/j.nicl.2018.101618⟩
NeuroImage : Clinical
NeuroImage: Clinical, Vol 21, Iss, Pp-(2019)
Neuroimage-Clinical, Elsevier, 2019, 21, pp.101618. ⟨10.1016/j.nicl.2018.101618⟩
Neuroimage-Clinical, 2019, 21, pp.101618. ⟨10.1016/j.nicl.2018.101618⟩
NeuroImage : Clinical
NeuroImage: Clinical, Vol 21, Iss, Pp-(2019)
Spinal muscular atrophy (SMA) type III and IV are autosomal recessive, slowly progressive lower motor neuron syndromes. Nevertheless, wider cerebral involvement has been consistently reported in mouse models. The objective of this study is the charac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6d677f059efc03030b5919d29d82dbe
https://hal.sorbonne-universite.fr/hal-02090969
https://hal.sorbonne-universite.fr/hal-02090969
Autor:
Russell L. McLaughlin, Mark A. Doherty, Rangariroyashe H. Chipika, Jennifer C. Hengeveld, Alice Vajda, Colette Donaghy, Siobhan Hutchinson, Eoin Finegan, Peter Bede, Stacey Li Hi Shing, Orla Hardiman
Publikováno v:
NeuroImage: Clinical, Vol 24, Iss, Pp-(2019)
NeuroImage : Clinical
NeuroImage : Clinical
Highlights • Computational neuroimaging captures focal brainstem pathology in motor neuron diseases in contrast to both healthy- and disease controls. • ALS patients exhibit progressive medulla oblongata, pontine and mesencephalic volume loss ove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12ccd1464ded8b70a9e45b34320d117f
https://doi.org/10.1016/j.nicl.2019.102054
https://doi.org/10.1016/j.nicl.2019.102054
Autor:
Rosa Rademakers, Daniel H. Geschwind, Mochtar Pribadi, Maria Luisa Gorno-Tempini, Theodore P. Zanto, Anna Karydas, Jesse A. Brown, Giovanni Coppola, Suzee E. Lee, Alainna B. Brown, Howard J. Rosen, Ana C. Sias, Bruce L. Miller, Anna A. Vidovszky, Anna M. Khazenzon, Maria Luisa Mandelli, Deepika Dokuru, William W. Seeley
Publikováno v:
Lee, SE; Sias, AC; Mandelli, ML; Brown, JA; Brown, AB; Khazenzon, AM; et al.(2017). Network degeneration and dysfunction in presymptomatic C9ORF72 expansion carriers. NEUROIMAGE-CLINICAL, 14, 286-297. doi: 10.1016/j.nicl.2016.12.006. UCLA: Retrieved from: http://www.escholarship.org/uc/item/6jp2p38g
NeuroImage : Clinical
NeuroImage: Clinical
NeuroImage: Clinical, Vol 14, Iss C, Pp 286-297 (2017)
NeuroImage : Clinical
NeuroImage: Clinical
NeuroImage: Clinical, Vol 14, Iss C, Pp 286-297 (2017)
Hexanucleotide repeat expansions in C9ORF72 are the most common known genetic cause of familial and sporadic frontotemporal dementia and amyotrophic lateral sclerosis. Previous work has shown that patients with behavioral variant frontotemporal demen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::498fed2df2b2cfd95644af84f5038e42
Akademický článek
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Autor:
Jürgen Götz, Naeman N. Götz
Publikováno v:
ASN NEURO
ASN Neuro, Vol 1 (2009)
ASN Neuro, Vol 1 (2009)
In dementia research, animal models have become indispensable tools. They not only model aspects of the human condition, but also simulate processes that occur in humans and hence provide insight into how disease is initiated and propagated. The pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c66b5657ec65249461d665642e7de232
http://europepmc.org/articles/PMC2785514
http://europepmc.org/articles/PMC2785514
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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