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Naruse, Hiroya
54
results:
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Format
Online (54)
Mediatypes
Articles (Online) (37)
OpenAccess-fulltext (17)
Sorted by: Relevance
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1
Correction to: RFC1‑related disorder presenting recurrent s..:
Tsuboyama, Yoko
;
Takahashi, Akiko
;
Furukawa, Sawako
...
Journal of Neurology. , 2024
Link:
https://doi.org/10.1007/..
?
2
RFC1-related disorder presenting recurrent syncope:
Tsuboyama, Yoko
;
Takahashi, Akiko
;
Furukawa, Sawako
...
Journal of Neurology. , 2024
Link:
https://doi.org/10.1007/..
?
3
SPTLC2 variants are associated with early‐onset ALS and FTD..:
Naruse, Hiroya
;
Ishiura, Hiroyuki
;
Esaki, Kayoko
...
Annals of Clinical and Translational Neurology. 11 (2024) 4 - p. 946-957 , 2024
Link:
https://doi.org/10.1002/..
?
4
Clinical features of a family with late‐onset distal heredi..:
Naruse, Hiroya
;
Okubo, So
;
Sudo, Atsushi
...
Journal of the Peripheral Nervous System. 28 (2023) 3 - p. 518-521 , 2023
Link:
https://doi.org/10.1111/..
?
5
Clinical and electrophysiological findings of facial palsy ..:
Yamakawa, Kaoru
;
Nishijima, Hironobu
;
Kubota, Akatsuki
...
Auris Nasus Larynx. 50 (2023) 2 - p. 305-308 , 2023
Link:
https://doi.org/10.1016/..
?
6
Noncanonical splice‐site variant in peripheral myelin prote..:
Kawamoto, Norifumi
;
Hamada, Yuichi
;
Kobayashi, Shunsuke
...
Journal of the Peripheral Nervous System. 28 (2023) 3 - p. 513-517 , 2023
Link:
https://doi.org/10.1111/..
?
7
High-dose ubiquinol supplementation in multiple-system atro..:
Mitsui, Jun
;
Matsukawa, Takashi
;
Uemura, Yukari
...
eClinicalMedicine. 59 (2023) - p. 101920 , 2023
Link:
https://doi.org/10.1016/..
?
8
LONRF2 is a protein quality control ubiquitin ligase whose ..:
Li, Dan
;
Johmura, Yoshikazu
;
Morimoto, Satoru
...
Nature Aging. 3 (2023) 8 - p. 1001-1019 , 2023
Link:
https://doi.org/10.1038/..
?
9
Valosin-containing protein Asp395Gly mutation in a patient ..:
Kobayashi, Ryota
;
Naruse, Hiroya
;
Kawakatsu, Shinobu
...
BMC Neurology. 22 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1186/..
?
10
Randomized, double‐blind, placebo‐controlled phase 1 study ..:
Mitsui, Jun
;
Matsukawa, Takashi
;
Tanaka, Masaki
...
Neurology and Clinical Neuroscience. 10 (2021) 1 - p. 14-24 , 2021
Link:
https://doi.org/10.1111/..
?
11
Loss-of-function variants in NEK1 are associated with an in..:
Naruse, Hiroya
;
Ishiura, Hiroyuki
;
Mitsui, Jun
...
Journal of Human Genetics. 66 (2020) 3 - p. 237-241 , 2020
Link:
https://doi.org/10.1038/..
?
12
Familial dementia with Lewy bodies with VPS13C mutations:
Kobayashi, Ryota
;
Naruse, Hiroya
;
Koyama, Shingo
...
Parkinsonism & Related Disorders. 81 (2020) - p. 31-33 , 2020
Link:
https://doi.org/10.1016/..
?
13
Splice-site mutations in KIF5A in the Japanese case series ..:
Naruse, Hiroya
;
Ishiura, Hiroyuki
;
Mitsui, Jun
...
neurogenetics. 22 (2020) 1 - p. 11-17 , 2020
Link:
https://doi.org/10.1007/..
?
14
Association of ATXN2 intermediate-length CAG repeats with a..:
Naruse, Hiroya
;
Matsukawa, Takashi
;
Ishiura, Hiroyuki
...
neurogenetics. 20 (2019) 2 - p. 65-71 , 2019
Link:
https://doi.org/10.1007/..
?
15
Prominent Spasticity and Hyperreflexia of the Legs in a Nep..:
Naruse, Hiroya
;
Takahashi, Yuji
;
Ishiura, Hiroyuki
...
Internal Medicine. 58 (2019) 19 - p. 2865-2869 , 2019
Link:
https://doi.org/10.2169/..
1-15