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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2020 | 2 |
2021 | 4 |
2022 | 1 |
2023 | 1 |
2024 | 1 |
Search Results
7 results
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Page 1
Current Knowledge of Endolysosomal and Autophagy Defects in Hereditary Spastic Paraplegia.
Cells. 2021 Jul 2;10(7):1678. doi: 10.3390/cells10071678.
Cells. 2021.
PMID: 34359848
Free PMC article.
Review.
Stem Cell Models and Gene Targeting for Human Motor Neuron Diseases.
Karpe Y, Chen Z, Li XJ.
Karpe Y, et al.
Pharmaceuticals (Basel). 2021 Jun 12;14(6):565. doi: 10.3390/ph14060565.
Pharmaceuticals (Basel). 2021.
PMID: 34204831
Free PMC article.
Review.
Item in Clipboard
The presymptomatic phase of amyotrophic lateral sclerosis: are we merely scratching the surface?
Chipika RH, Siah WF, McKenna MC, Li Hi Shing S, Hardiman O, Bede P.
Chipika RH, et al.
J Neurol. 2021 Dec;268(12):4607-4629. doi: 10.1007/s00415-020-10289-5. Epub 2020 Oct 31.
J Neurol. 2021.
PMID: 33130950
Review.
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Thalamic pathology in frontotemporal dementia: Predilection for specific nuclei, phenotype-specific signatures, clinical correlates, and practical relevance.
McKenna MC, Lope J, Bede P, Tan EL.
McKenna MC, et al.
Brain Behav. 2023 Feb;13(2):e2881. doi: 10.1002/brb3.2881. Epub 2023 Jan 7.
Brain Behav. 2023.
PMID: 36609810
Free PMC article.
Review.
Item in Clipboard
Neural Correlates of Motor Imagery of Gait in Amyotrophic Lateral Sclerosis.
Abidi M, de Marco G, Grami F, Termoz N, Couillandre A, Querin G, Bede P, Pradat PF.
Abidi M, et al.
J Magn Reson Imaging. 2021 Jan;53(1):223-233. doi: 10.1002/jmri.27335. Epub 2020 Sep 7.
J Magn Reson Imaging. 2021.
PMID: 32896088
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The impact of age on genetic testing decisions in amyotrophic lateral sclerosis.
Mehta PR, Iacoangeli A, Opie-Martin S, van Vugt JJFA, Al Khleifat A, Bredin A, Ossher L, Andersen PM, Hardiman O, Mehta AR, Fratta P, Talbot K; Project MinE ALS Sequencing Consortium; Al-Chalabi A.
Mehta PR, et al.
Brain. 2022 Dec 19;145(12):4440-4447. doi: 10.1093/brain/awac279.
Brain. 2022.
PMID: 36162820
Free PMC article.
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Mutations in the tail and rod domains of the neurofilament heavy-chain gene increase the risk of ALS.
Marriott H, Spargo TP, Al Khleifat A, Andersen PM, Başak NA, Cooper-Knock J, Corcia P, Couratier P, de Carvalho M, Drory V, Gotkine M, Landers JE, McLaughlin R, Pardina JSM, Morrison KE, Pinto S, Shaw CE, Shaw PJ, Silani V, Ticozzi N, van Damme P, van den Berg LH, Vourc'h P, Weber M, Veldink JH; Project MinE ALS Sequencing Consortium; Dobson RJ, Schwab P, Al-Chalabi A, Iacoangeli A.
Marriott H, et al.
Ann Clin Transl Neurol. 2024 May 22. doi: 10.1002/acn3.52083. Online ahead of print.
Ann Clin Transl Neurol. 2024.
PMID: 38775181
Free article.
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