Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Yuta Ichinose"'
Autor:
Kazumasa Shindo, Yuto Morishima, Yumi Suwa, Toko Fukao, Takafumi Kurita, Akane Satake, Mai Tsuchiya, Yuta Ichinose, Takanori Hata, Kishin Koh, Takamura Nagasaka, Yoshihisa Takiyama
Publikováno v:
The Journal of Clinical Hypertension, Vol 23, Iss 1, Pp 175-178 (2021)
Abstract This study evaluated yearly changes in systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rates (HR) for patients with Parkinson's disease (PD). Data were collected for the last 10 years from medical records of 28 PD pa
Externí odkaz:
https://doaj.org/article/f6a9c89fcbb24158bb8a1d771260a69f
Autor:
Takanori Hata, Takamura Nagasaka, Kishin Koh, Mai Tsuchiya, Yuta Ichinose, Haitian Nan, Kazumasa Shindo, Yoshihisa Takiyama
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Non-dystrophic myotonias (NDMs) are skeletal muscle disorders involving myotonia distinct from myotonic dystrophy. It has been reported that the muscle pathology is usually normal or comprises mild myopathic changes in NDMs. We de
Externí odkaz:
https://doaj.org/article/bddeb86745e6419ea9205b1f861fbb32
Autor:
Kazumasa Shindo, Mai Tsuchiya, Takanori Hata, Yuta Ichinose, Kishin Koh, Jun Sone, Takamura Nagasaka, Gen Sobue, Yoshihisa Takiyama
Publikováno v:
Epilepsy and Behavior Case Reports, Vol 11, Iss , Pp 103-106 (2019)
We report a case of neuronal intranuclear inclusion disease (NIID) confirmed by detection of intranuclear inclusions in a skin biopsy specimen. Brain magnetic resonance imaging showed mild cerebral atrophy and linear hyperintensities at the corticome
Externí odkaz:
https://doaj.org/article/e9a5d3c59d68434fbaa02c915b3bf077
Autor:
Kazumasa Shindo, Tohko Sato, Hiroaki Murata, Yuta Ichinose, Takanori Hata, Yoshihisa Takiyama
Publikováno v:
BMC Neurology, Vol 19, Iss 1, Pp 1-4 (2019)
Abstract Background Spinocerebellar ataxia type 31 (SCA 31) is a slowly progressive neurodegenerative disorder characterized by pure cerebellar ataxia. Unlike other CAG repeat diseases, sleep-related problems have not been reported in patients with S
Externí odkaz:
https://doaj.org/article/d910d56666b74e43ab109a91218427a2
Autor:
Yuta Ichinose, Takafumi Kurita, Akane Satake, Takahiro Natori, Kazumasa Shindo, Yoshihisa Takiyama
Publikováno v:
Heliyon, Vol 6, Iss 12, Pp e05600- (2020)
A 44-year-old female developed mild gait disturbance. She had a history of a ventricular septum defect, deafness, epilepsy, schizophrenia and cataracts. Magnetic resonance imaging showed ventriculomegaly of the brain and lower thoracic spinal stenosi
Externí odkaz:
https://doaj.org/article/22ef5bd7e3414c1e9a20330dfcc51433
Autor:
Kishin Koh, Hiroyuki Ishiura, Haruo Shimazaki, Michiko Tsutsumiuchi, Yuta Ichinose, Haitian Nan, Shun Hamada, Toshihisa Ohtsuka, Shoji Tsuji, Yoshihisa Takiyama
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background Alterations of vacuolar protein sorting‐associated protein 13 (VPS13) family members including VPS13A, VPS13B, and VPS13C lead to chorea acanthocytosis, Cohen syndrome, and parkinsonism, respectively. Recently, VPS13D mutations
Externí odkaz:
https://doaj.org/article/9a9f5423d0174287ad053d9e3b0da0d6
Autor:
Takafumi Kurita, Mai Tsuchiya, Yuta Ichinose, Kazumasa Shindo, Yuto Morishima, Yoshihisa Takiyama, Yumi Suwa, Takamura Nagasaka, Takanori Hata, Kishin Koh, Toko Fukao, Akane Satake
Publikováno v:
The Journal of Clinical Hypertension. 23:175-178
This study evaluated yearly changes in systolic blood pressure (SBP), diastolic blood pressure (DBP), and heart rates (HR) for patients with Parkinson's disease (PD). Data were collected for the last 10 years from medical records of 28 PD patients an
Autor:
Yuto Morishima, Masaki Hashiyada, Kishin Koh, Lihua Gao, Haitian Nan, Yuta Ichinose, Kensho Okamoto, Yoshihisa Takiyama, Noboru Adachi
Publikováno v:
Internal Medicine. 59:2311-2315
Spastic paraplegia type 4 (SPG4) is caused by mutations of the SPAST gene and is the most common form of autosomal-dominantly inherited pure hereditary spastic paraplegia (HSP). We herein report a Japanese patient with SPG4 with a confirmed de novo m
Autor:
Yuta Ichinose, Yoshihisa Takiyama, Andrea Cortese, Mai Tsuchiya, Keisuke Shimozono, Toshihisa Ohtsuka, Yeon-Jeong Kim, Kishin Koh, Haitian Nan, Takanori Hata, Lihua Gao
Publikováno v:
Journal of Human Genetics. 65:1143-1147
Recently, the expansion of an intronic AAGGG repeat in the replication factor C subunit 1 (RFC1) gene was reported to cause cerebellar ataxia, neuropathy, vestibular areflexia syndrome (CANVAS). In Europeans, the expansion accounted for 22% of sporad
Autor:
Tatsuro Mutoh, Shigeto Sato, Yuanzhe Li, Taiji Tsunemi, Taku Hatano, Kishin Koh, Yasuo Uchiyama, Soichiro Kakuta, Tatsuya Hattori, Wado Akamatsu, Yoshihisa Takiyama, Yuta Ichinose, Tomoko Hino-Takai, Junko Matsuda, Matthew J. Farrer, Kenya Nishioka, Wataru Satake, Manabu Funayama, Sachiko Noda, Yasuaki Mizutani, Kei-Ichi Ishikawa, Tatsushi Toda, Yutaka Oji, Nobutaka Hattori, Hiroyo Yoshino, Masahito Yamada, Tsuyoshi Hamaguchi, Ayami Okuzumi, Shin Ichi Ueno, Kazumasa Shindo, Yih Ru Wu, Fusako Yokochi
Publikováno v:
Brain. 143:1190-1205
Recently, the genetic variability in lysosomal storage disorders has been implicated in the pathogenesis of Parkinson’s disease. Here, we found that variants in prosaposin (PSAP), a rare causative gene of various types of lysosomal storage disorder