Publications by authors named "Harutoshi Fujimura"

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Familial ALS With p. L127S (L126S) Variant of the Cu/Zn SOD1 Gene: A Report of Two New Cases and Literature Review.
Kimiko Inoue, Keiko Toyooka, Harutoshi Fujimura, Kayo Ueda, Misako Kaido

Neuropathology· December 2025

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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, Hisahide Nishio, Hiroya Naruse

Neuropathology· December 2025

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Transcriptome alterations underlying metabolic dysfunction and liver disease in myotonic dystrophy type 1.
Aono Fukumoto, Tomoki Yamanaka, Motoaki Yanaizu, Masayuki Nakamori, Manami Hama, Harutoshi Fujimura

Hum Mol Genet· October 2025

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Conventional magnetic resonance imaging key features for distinguishing pathologically confirmed corticobasal degeneration from its mimics: a retrospective analysis of the J-VAC study.
Keita Sakurai, Aya M Tokumaru, Mari Yoshida, Yuko Saito, Koichi Wakabayashi, Harutoshi Fujimura

Neuroradiology· November 2024

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An autopsy case of diffuse atypical argyrophilic grain disease (AGD) with presenile onset and three-year course of motor and cognitive impairment.
Kimiko Inoue, Satoko Sugase, Takashi Naka, Takeshi Ikeuchi, Shigeo Murayama, Harutoshi Fujimura

Neuropathology· June 2024

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Analysis of splicing abnormalities in the white matter of myotonic dystrophy type 1 brain using RNA sequencing.
Kazuki Yoshizumi, Masamitsu Nishi, Masataka Igeta, Masayuki Nakamori, Kimiko Inoue, Harutoshi Fujimura

Neurosci Res· March 2024

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Clinical course of pathologically confirmed corticobasal degeneration and corticobasal syndrome.
Ikuko Aiba, Yuichi Hayashi, Takayoshi Shimohata, Mari Yoshida, Yuko Saito, Harutoshi Fujimura

Brain Commun· November 2023

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[Antibody production capacity after COVID-19 vaccination in immune-mediated neuromuscular diseases under immunotherapy].
Misako Kaido, Yuta Kajiyama, Shinya Sasaki, Takako Saitou, Yoshiki Esa, Harutoshi Fujimura

Rinsho Shinkeigaku· March 2023

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Guillain-Barré Syndrome Associated with COVID-19 in a Japanese Male.
Yoshiki Esa, Yuta Kajiyama, Misako Kaido, Yushi Watanabe, Harutoshi Fujimura

Case Rep Neurol Med· October 2022

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Spinal muscular atrophy type 2 patient who survived 61 years: an autopsy case report.
Misaki Yamadera, Toshio Saito, Masakazu Shinohara, Hisahide Nishio, Shigeo Murayama, Harutoshi Fujimura

Neuropathology· April 2022

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Clinical trajectory of a patient with filaminopathy who developed arrhythmogenic cardiomyopathy, myofibrillar myopathy, and multiorgan tumors.
Tsuyoshi Matsumura, Kimiko Inoue, Keiko Toyooka, Michio Inoue, Aritoshi Iida, Harutoshi Fujimura

Neuromuscul Disord· December 2021

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Age-dependent decline in remyelination capacity is mediated by apelin-APJ signaling.
Masumi Ito, Rieko Muramatsu, Yuki Kato, Bikram Sharma, Akiko Uyeda, Harutoshi Fujimura

Nat Aging· March 2021

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Transcriptome alterations in myotonic dystrophy frontal cortex.
Brittney A Otero, Kiril Poukalov, Ryan P Hildebrandt, Charles A Thornton, Kenji Jinnai, Harutoshi Fujimura

Cell Rep· January 2021

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[An autopsy case of elderly-onset herpes simplex encephalitis with acute respiratory failure caused by brainstem lesions].
Yuto Hayashi, Katsuya Araki, Kimiko Inoue, Hiroka Ando, Harutoshi Fujimura

Rinsho Shinkeigaku· December 2020

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The secondary structural difference between Lewy body and glial cytoplasmic inclusion in autopsy brain with synchrotron FTIR micro-spectroscopy.
Katsuya Araki, Naoto Yagi, Yuka Ikemoto, Hideki Hayakawa, Harutoshi Fujimura

Sci Rep· November 2020

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Psychological Case Conference Following the Death of a Patient With Neuromuscular Disease: A Source of Emotional Support for Participating Medical Staff.
Haruo Fujino, Tsuyoshi Matsumura, Toshio Saito, Harutoshi Fujimura, Osamu Imura

J Patient Exp· October 2020

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Differences in splicing defects between the grey and white matter in myotonic dystrophy type 1 patients.
Masamitsu Nishi, Takashi Kimura, Masataka Igeta, Mitsuru Furuta, Koichi Suenaga, Harutoshi Fujimura

PLoS One· September 2020

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Mitochondrial DNA enhance innate immune responses in neuromyelitis optica by monocyte recruitment and activation.
Mikito Shimizu, Tatsusada Okuno, Makoto Kinoshita, Hisae Sumi, Harutoshi Fujimura

Sci Rep· August 2020

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A clinicopathological study of ALS with L126S mutation in the SOD1 gene presenting with isolated inferior olivary hypertrophy.
Makoto Hideshima, Goichi Beck, Misaki Yamadera, Yuichi Motoyama, Kensuke Ikenaka, Harutoshi Fujimura

Neuropathology· April 2020

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Response to the Letter: Confirmation of stroke-like lesions on MRI is a prerequisite for their histopathological assessment.
Misaki Yamadera, Harutoshi Fujimura

Neuropathology· February 2020

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Bile acid abnormality induced by intestinal dysbiosis might explain lipid metabolism in Parkinson's disease.
Yuhei Hasuike, Takuyuki Endo, Michiyo Koroyasu, Misa Matsui, Chiaki Mori, Harutoshi Fujimura

Med Hypotheses· January 2020

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Increased number of mitochondria in capillaries distributed in stroke-like lesions of two patients with MELAS.
Misaki Yamadera, Harutoshi Fujimura, Yuri Shimizu, Misa Matsui, Itsuko Nakamichi

Neuropathology· October 2019

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Parkinson's disease is a type of amyloidosis featuring accumulation of amyloid fibrils of α-synuclein.
Katsuya Araki, Naoto Yagi, Koki Aoyama, Chi-Jing Choong, Hideki Hayakawa, Harutoshi Fujimura

Proc Natl Acad Sci U S A· September 2019

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Pathological Findings in Male Patients With Anti-N-methyl-d-Aspartate Receptor Encephalitis.
Makito Hirano, Tatsuki Itoh, Harutoshi Fujimura, Kimiko Inoue, Makoto Samukawa

J Neuropathol Exp Neurol· August 2019

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Circulating transforming growth factor-β1 facilitates remyelination in the adult central nervous system.
Machika Hamaguchi, Rieko Muramatsu, Harutoshi Fujimura, Hideki Mochizuki, Hirotoshi Kataoka

Elife· May 2019

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