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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2021 | 2 |
2022 | 4 |
2024 | 0 |
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7 results
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Page 1
18F-THK5351 PET for visualizing predominant lesions of pathologically confirmed corticobasal degeneration presenting with frontal behavioral-spatial syndrome.
J Neurol. 2022 Sep;269(9):5157-5161. doi: 10.1007/s00415-022-11121-y. Epub 2022 Apr 13.
J Neurol. 2022.
PMID: 35416513
Free PMC article.
No abstract available.
Unique Lewy pathology in myotonic dystrophy type 1.
Sano T, Kawazoe T, Shioya A, Mori-Yoshimura M, Oya Y, Maruo K, Nishino I, Hoshino M, Murayama S, Saito Y.
Sano T, et al.
Neuropathology. 2022 Apr;42(2):104-116. doi: 10.1111/neup.12790. Epub 2022 Feb 23.
Neuropathology. 2022.
PMID: 35199386
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piRNA/PIWI Protein Complex as a Potential Biomarker in Sporadic Amyotrophic Lateral Sclerosis.
Abdelhamid RF, Ogawa K, Beck G, Ikenaka K, Takeuchi E, Yasumizu Y, Jinno J, Kimura Y, Baba K, Nagai Y, Okada Y, Saito Y, Murayama S, Mochizuki H, Nagano S.
Abdelhamid RF, et al.
Mol Neurobiol. 2022 Mar;59(3):1693-1705. doi: 10.1007/s12035-021-02686-2. Epub 2022 Jan 11.
Mol Neurobiol. 2022.
PMID: 35015250
Free PMC article.
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An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation in the SPG11 gene: widespread degeneration with eosinophilic inclusions.
Hayakawa M, Matsubara T, Mochizuki Y, Takeuchi C, Minamitani M, Imai M, Kosaki K, Arai T, Murayama S.
Hayakawa M, et al.
BMC Neurol. 2022 Jan 3;22(1):2. doi: 10.1186/s12883-021-02514-z.
BMC Neurol. 2022.
PMID: 34979968
Free PMC article.
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Parkinson's disease with a typical clinical course of 17 years overlapped by Creutzfeldt-Jakob disease: an autopsy case report.
Kubo SI, Matsubara T, Taguchi T, Sengoku R, Takeuchi A, Saito Y.
Kubo SI, et al.
BMC Neurol. 2021 Dec 10;21(1):480. doi: 10.1186/s12883-021-02504-1.
BMC Neurol. 2021.
PMID: 34893033
Free PMC article.
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An autopsy report of a familial amyotrophic lateral sclerosis case carrying VCP Arg487His mutation with a unique TDP-43 proteinopathy.
Matsubara T, Izumi Y, Oda M, Takahashi M, Maruyama H, Miyamoto R, Watanabe C, Tachiyama Y, Morino H, Kawakami H, Saito Y, Murayama S.
Matsubara T, et al.
Neuropathology. 2021 Apr;41(2):118-126. doi: 10.1111/neup.12710. Epub 2021 Jan 7.
Neuropathology. 2021.
PMID: 33415820
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Colocalization of BRCA1 with Tau Aggregates in Human Tauopathies.
Kurihara M, Mano T, Saito Y, Murayama S, Toda T, Iwata A.
Kurihara M, et al.
Brain Sci. 2019 Dec 20;10(1):7. doi: 10.3390/brainsci10010007.
Brain Sci. 2019.
PMID: 31861888
Free PMC article.
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