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The Utility of Long-Read Sequencing in Diagnosing Early Onset Parkinson's Disease.
Daida K, Yoshino H, Malik L, Baker B, Ishiguro M, Genner R, Paquette K, Li Y, Nishioka K, Masuzugawa S, Hirano M, Takahashi K, Kolmogorov M, Billingsley KJ, Funayama M, Blauwendraat C, Hattori N. Daida K, et al. Among authors: ishiguro m. Ann Neurol. 2024 Dec 19. doi: 10.1002/ana.27155. Online ahead of print. Ann Neurol. 2024. PMID: 39699073
Long-read sequencing resolves a complex structural variant in PRKN Parkinson's disease.
Daida K, Funayama M, Billingsley KJ, Malik L, Miano-Burkhardt A, Leonard HL, Makarious MB, Iwaki H, Ding J, Gibbs JR, Ishiguro M, Yoshino H, Ogaki K, Oyama G, Nishioka K, Nonaka R, Akamatsu W, Blauwendraat C, Hattori N. Daida K, et al. Among authors: ishiguro m. medRxiv [Preprint]. 2023 Aug 21:2023.08.14.23293948. doi: 10.1101/2023.08.14.23293948. medRxiv. 2023. Update in: Mov Disord. 2023 Dec;38(12):2249-2257. doi: 10.1002/mds.29610 PMID: 37790330 Free PMC article. Updated. Preprint.
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease.
Daida K, Funayama M, Billingsley KJ, Malik L, Miano-Burkhardt A, Leonard HL, Makarious MB, Iwaki H, Ding J, Gibbs JR, Ishiguro M, Yoshino H, Ogaki K, Oyama G, Nishioka K, Nonaka R, Akamatsu W, Blauwendraat C, Hattori N. Daida K, et al. Among authors: ishiguro m. Mov Disord. 2023 Dec;38(12):2249-2257. doi: 10.1002/mds.29610. Epub 2023 Nov 5. Mov Disord. 2023. PMID: 37926948 Free PMC article.
The Utility of Long-Read Sequencing in Diagnosing Genetic Autosomal Recessive Parkinson's Disease: a genetic screening study.
Daida K, Yoshino H, Malik L, Baker B, Ishiguro M, Genner R, Paquette K, Li Y, Nishioka K, Masuzugawa S, Hirano M, Takahashi K, Kolmogolv M, Billingsley KJ, Funayama M, Blauwendraat C, Hattori N. Daida K, et al. Among authors: ishiguro m. medRxiv [Preprint]. 2024 Jun 15:2024.06.14.24308784. doi: 10.1101/2024.06.14.24308784. medRxiv. 2024. PMID: 39108517 Free PMC article. Preprint.
Genetic analysis of ATP10B for Parkinson's disease in Japan.
Ishiguro M, Yoshino H, Li Y, Ikeda A, Funayama M, Nishioka K, Hattori N. Ishiguro M, et al. Parkinsonism Relat Disord. 2021 Jul;88:10-12. doi: 10.1016/j.parkreldis.2021.05.020. Epub 2021 May 29. Parkinsonism Relat Disord. 2021. PMID: 34091411
Genetic and clinical study of PARK7 in Japanese Parkinson's disease.
Ishiguro M, Funayama M, Hatano T, Nishida H, Wada Y, Noda K, Tomiyama M, Yoshino H, Li Y, Ong S, Cioffi E, Nishioka K, Hattori N. Ishiguro M, et al. Heliyon. 2024 Jul 26;10(15):e35271. doi: 10.1016/j.heliyon.2024.e35271. eCollection 2024 Aug 15. Heliyon. 2024. PMID: 39170205 Free PMC article.
Clinical characteristics and pathophysiological properties of newly discovered LRRK2 variants associated with Parkinson's disease.
Tezuka T, Ishiguro M, Taniguchi D, Osogaguchi E, Shiba-Fukushima K, Ogata J, Ishii R, Ikeda A, Li Y, Yoshino H, Matsui T, Kaida K, Funayama M, Nishioka K, Kumazawa F, Matsubara T, Tsuda H, Saito Y, Murayama S, Imai Y, Hattori N. Tezuka T, et al. Among authors: ishiguro m. Neurobiol Dis. 2024 Sep;199:106571. doi: 10.1016/j.nbd.2024.106571. Epub 2024 Jun 18. Neurobiol Dis. 2024. PMID: 38901781 Free article.
CD8+ T-cell encephalitis mimicking PRES in AIDS: a case report.
Ishiguro M, Ueno Y, Ishiguro Y, Takanashi M, Murai K, Taieb G, Daida K, Suda A, Yokoyama K, Naito T, Hattori N. Ishiguro M, et al. Among authors: ishiguro y. BMC Neurol. 2020 May 12;20(1):179. doi: 10.1186/s12883-020-01756-7. BMC Neurol. 2020. PMID: 32397957 Free PMC article.
644 results