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Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene.
Shimizu H, Toyoshima Y, Shiga A, Yokoseki A, Arakawa K, Sekine Y, Shimohata T, Ikeuchi T, Nishizawa M, Kakita A, Onodera O, Takahashi H. Shimizu H, et al. Acta Neuropathol. 2013 Sep;126(3):453-9. doi: 10.1007/s00401-013-1150-5. Epub 2013 Jun 28. Acta Neuropathol. 2013. PMID: 23812289
Significant association of cadaveric dura mater grafting with subpial Aβ deposition and meningeal amyloid angiopathy.
Hamaguchi T, Taniguchi Y, Sakai K, Kitamoto T, Takao M, Murayama S, Iwasaki Y, Yoshida M, Shimizu H, Kakita A, Takahashi H, Suzuki H, Naiki H, Sanjo N, Mizusawa H, Yamada M. Hamaguchi T, et al. Among authors: shimizu h. Acta Neuropathol. 2016 Aug;132(2):313-315. doi: 10.1007/s00401-016-1588-3. Epub 2016 Jun 17. Acta Neuropathol. 2016. PMID: 27314593 No abstract available.
Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes.
Takeuchi R, Tada M, Shiga A, Toyoshima Y, Konno T, Sato T, Nozaki H, Kato T, Horie M, Shimizu H, Takebayashi H, Onodera O, Nishizawa M, Kakita A, Takahashi H. Takeuchi R, et al. Among authors: shimizu h. Acta Neuropathol Commun. 2016 Jun 23;4(1):61. doi: 10.1186/s40478-016-0335-2. Acta Neuropathol Commun. 2016. PMID: 27338935 Free PMC article.
Biallelic TBCD Mutations Cause Early-Onset Neurodegenerative Encephalopathy.
Miyake N, Fukai R, Ohba C, Chihara T, Miura M, Shimizu H, Kakita A, Imagawa E, Shiina M, Ogata K, Okuno-Yuguchi J, Fueki N, Ogiso Y, Suzumura H, Watabe Y, Imataka G, Leong HY, Fattal-Valevski A, Kramer U, Miyatake S, Kato M, Okamoto N, Sato Y, Mitsuhashi S, Nishino I, Kaneko N, Nishiyama A, Tamura T, Mizuguchi T, Nakashima M, Tanaka F, Saitsu H, Matsumoto N. Miyake N, et al. Among authors: shimizu h. Am J Hum Genet. 2016 Oct 6;99(4):950-961. doi: 10.1016/j.ajhg.2016.08.005. Epub 2016 Sep 22. Am J Hum Genet. 2016. PMID: 27666374 Free PMC article.
6,230 results