Hiroya Naruse
7PUBLICATIONS
21CO-AUTHORS
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Publications (7)
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|Nov 15, 2025
An Autopsy Case of ALS Which Clinically Presented Sporadic Adult-Onset Lower Motor Neuron Disease and Genetically Had p. Leu127Ser (L126S) Variant in SOD1 and SMN2 Deletion.Kimiko Inoue, Harutoshi Fujimura, Kayo Ueda
|Dec 12, 2024
Genetic and functional analyses of SPTLC1 in juvenile amyotrophic lateral sclerosis.So Okubo, Hiroya Naruse, Hiroyuki Ishiura
|Feb 05, 2024
SPTLC2 variants are associated with early-onset ALS and FTD due to aberrant sphingolipid synthesis.Hiroya Naruse, Hiroyuki Ishiura, Kayoko Esaki
|Jul 20, 2023
LONRF2 is a protein quality control ubiquitin ligase whose deficiency causes late-onset neurological deficits.Dan Li, Yoshikazu Johmura, Satoru Morimoto
|May 30, 2023
Clinical features of a family with late-onset distal hereditary motor neuropathy harboring p.Pro39Leu variant of HSPB1.Hiroya Naruse, So Okubo, Atsushi Sudo
|May 12, 2023
Noncanonical splice-site variant in peripheral myelin protein 22 gene (PMP22) in a patient with hereditary neuropathy with liability to pressure palsies.Norifumi Kawamoto, Yuichi Hamada, Shunsuke Kobayashi
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Frequent Collaborators
2 joint publications
Takashi Matsukawa
2 joint publications
Shoji Tsuji
2 joint publications
Tatsushi Toda
1 joint publications
Hiroyuki Ishiura
1 joint publications
Jun Mitsui
1 joint publications
Norifumi Kawamoto
1 joint publications
Yuichi Hamada
1 joint publications
Masahiro Sonoo
1 joint publications
Yoshikazu Johmura
1 joint publications
Yukio Takeshita
