Clinicopathological features of adult-onset neuronal intranuclear inclusion disease von Sone, Jun, Mori, Keiko, Inagaki, Tomonori, Katsumata, Ryu, Takagi, Shinnosuke, Yokoi, Satoshi, Araki, Kunihiko, Kato, Toshiyasu, Nakamura, Tomohiko, Koike, Haruki, Takashima, Hiroshi, Hashiguchi, Akihiro, Kohno, Yutaka, Kurashige, Takashi, Kuriyama, Masaru, Takiyama, Yoshihisa, Tsuchiya, Mai, Kitagawa, Naoyuki, Kawamoto, Michi, Yoshimura, Hajime, Suto, Yutaka, Nakayasu, Hiroyuki, Uehara, Naoko, Sugiyama, Hiroshi, Takahashi, Makoto, Kokubun, Norito, Konno, Takuya, Katsuno, Masahisa, Tanaka, Fumiaki, Iwasaki, Yasushi, Yoshida, Mari, Sobue, Gen

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Temporal Changes in Brain Magnetic Resonance Imaging Findings over 16 Years in a Patient with Neuronal Intranuclear Inclusion Disease von Tamura, Aiko, Fujino, Yuzo, Sone, Jun, Shiga, Kensuke

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Acute Reversible Encephalopathy with Neuronal Intranuclear Inclusion Disease Diagnosed by a Brain Biopsy: Inferring the Mechanism of Encephalopathy from Radiological and Histologic... von Orihara, Azusa, Miyakoshi, Natsuki, Sunami, Yoko, Kimura, Hideki, Nakata, Yasuhiro, Komori, Takashi, Sone, Jun, Takahashi, Kazushi

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Motor neuron TDP-43 proteinopathy in progressive supranuclear palsy and corticobasal degeneration von Riku, Yuichi, Iwasaki, Yasushi, Ishigaki, Shinsuke, Akagi, Akio, Hasegawa, Masato, Nishioka, Kenya, Li, Yuanzhe, Riku, Miho, Ikeuchi, Takeshi, Fujioka, Yusuke, Miyahara, Hiroaki, Sone, Jun, Hattori, Nobutaka, Yoshida, Mari, Katsuno, Masahisa, Sobue, Gen

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First detailed case report of a pediatric patient with neuronal intranuclear inclusion disease diagnosed by NOTCH2NLC genetic testing von Miyamoto, Yosuke, Okazaki, Tetsuya, Watanabe, Keisuke, Togawa, Masami, Adachi, Tadashi, Kato, Ayumi, Ochiai, Ryoya, Tamai, Chisato, Sone, Jun, Maegaki, Yoshihiro

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Blepharoptosis As an Early Manifestation of Neuronal Intranuclear Inclusion Disease von Miyaue, Noriyuki, Ochi, Chikako, Ito, Yuko H., Ando, Rina, Sone, Jun, Nagai, Masahiro

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FXTAS is difficult to differentiate from neuronal intranuclear inclusion disease through skin biopsy: a case report von Toko, Megumi, Ohshita, Tomohiko, Kurashige, Takashi, Morino, Hiroyuki, Kume, Kodai, Yamashita, Hiroshi, Sobue, Gen, Iwasaki, Yasushi, Sone, Jun, Kawakami, Hideshi, Maruyama, Hirofumi

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Nuclear Expression of TDP-43 Is Linked with Morphology and Ubiquitylation of Cytoplasmic Aggregates in Amyotrophic Lateral Sclerosis von Yabata, Hiroyuki, Riku, Yuichi, Miyahara, Hiroaki, Akagi, Akio, Sone, Jun, Urushitani, Makoto, Yoshida, Mari, Iwasaki, Yasushi

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Clinicopathological features of progressive supranuclear palsy with asymmetrical atrophy of the superior cerebellar peduncle von Koizumi, Ryuichi, Akagi, Akio, Riku, Yuichi, Sone, Jun, Miyahara, Hiroaki, Tanaka, Fumiaki, Yoshida, Mari, Iwasaki, Yasushi

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A case of neuronal intranuclear inclusion disease with recurrent vomiting and without apparent DWI abnormality for the first seven years von Okamura, Shun, Takahashi, Makoto, Abe, Keisuke, Inaba, Akira, Sone, Jun, Orimo, Satoshi

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Unilateral Wing-Beating Tremor in Neuronal Intranuclear Inclusion Disease von Sugiyama, Atsuhiko, Kojima, Kazuho, Hirano, Shigeki, Sone, Jun, Kuwabara, Satoshi

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Memory Loss and Frontal Cognitive Dysfunction in a Patient with Adult-onset Neuronal Intranuclear Inclusion Disease von Araki, Kunihiko, Sone, Jun, Fujioka, Yusuke, Masuda, Michihito, Ohdake, Reiko, Tanaka, Yasuhiro, Nakamura, Tomohiko, Watanabe, Hirohisa, Sobue, Gen

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Reply: Neuronal intranuclear (hyaline) inclusion disease and fragile X-associated tremor/ataxia syndrome: a morphological and molecular dilemma von Sone, Jun, Nakamura, Tomohiko, Koike, Haruki, Katsuno, Masahisa, Tanaka, Fumiaki, Iwasaki, Yasushi, Yoshida, Mari, Sobue, Gen

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Next-generation sequencing of 28 ALS-related genes in a Japanese ALS cohort von Nakamura, Ryoichi, Sone, Jun, Atsuta, Naoki, Tohnai, Genki, Watanabe, Hazuki, Yokoi, Daichi, Nakatochi, Masahiro, Watanabe, Hirohisa, Ito, Mizuki, Senda, Jo, Katsuno, Masahisa, Tanaka, Fumiaki, Li, Yuanzhe, Izumi, Yuishin, Morita, Mitsuya, Taniguchi, Akira, Kano, Osamu, Oda, Masaya, Kuwabara, Satoshi, Abe, Koji, Aiba, Ikuko, Okamoto, Koichi, Mizoguchi, Kouichi, Hasegawa, Kazuko, Aoki, Masashi, Hattori, Nobutaka, Tsuji, Shoji, Nakashima, Kenji, Kaji, Ryuji, Sobue, Gen

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Long-term MRI findings of adult-onset neuronal intranuclear inclusion disease von Tachi, Kisaki, Takata, Tadayuki, Kume, Kodai, Sone, Jun, Kobara, Hideki, Deguchi, Kazushi, Kawakami, Hideshi, Masaki, Tsutomu

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Pathological background of subcortical hyperintensities on diffusion-weighted images in a case of neuronal intranuclear inclusion disease von Yokoi, Satoshi, Yasui, Keizo, Hasegawa, Yasuhiro, Niwa, Kazuki, Noguchi, Yoshinori, Tsuzuki, Toyonori, Mimuro, Maya, Sone, Jun, Watanabe, Hirohisa, Katsuno, Masahisa, Yoshida, Mari, Sobue, Gen

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A case of unusual renal manifestation in a patient with neuronal intranuclear inclusion disease treated with steroids von Morita, Keisuke, Shinzato, Takahiro, Endo, Yuzo, Suzuki, Makoto, Yoshida, Hidefumi, Sone, Jun, Nagai, Kojiro

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Pathological observations of a long spinal cord lesion in a patient with multiple sclerosis von Yabata, Hiroyuki, Saito, Yufuko, Fukuoka, Takaaki, Akagi, Akio, Riku, Yuichi, Sone, Jun, Miyahara, Hiroaki, Doyu, Manabu, Yoshida, Mari, Iwasaki, Yasushi

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Disulfide Bond Mediates Aggregation, Toxicity, and Ubiquitylation of Familial Amyotrophic Lateral Sclerosis-linked Mutant SOD1 von Niwa, Jun-ichi, Yamada, Shin-ichi, Ishigaki, Shinsuke, Sone, Jun, Takahashi, Miho, Katsuno, Masahisa, Tanaka, Fumiaki, Doyu, Manabu, Sobue, Gen

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Reply to “GGC Repeat Expansion of NOTCH2NLC is Rare in European Leukoencephalopathy” von Doi, Hiroshi, Okubo, Masaki, Fukai, Ryoko, Fujita, Atsushi, Mitsuhashi, Satomi, Takahashi, Keita, Kunii, Misako, Tada, Mikiko, Fukuda, Hiromi, Mizuguchi, Takeshi, Miyatake, Satoko, Miyake, Noriko, Sone, Jun, Sobue, Gen, Takeuchi, Hideyuki, Matsumoto, Naomichi, Tanaka, Fumiaki

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