Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Mikako, Enokizono"'
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-5 (2022)
Abstract Background Sinus pericranii is a rare cranial venous malformation resulting in a subcutaneous mass due to abnormal communication between intracranial and subperiosteal/interperiosteal veins. To date, to the best of our knowledge, there are n
Externí odkaz:
https://doaj.org/article/4fcbf4adbbf24d0f81e036d9cd1a7e62
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background Neonatal encephalopathy due to acute perinatal asphyxia is a major cause of perinatal brain damage. Moderate to severe neonatal encephalopathy is associated with high mortality and morbidity rates. However, the neurodevelopmental
Externí odkaz:
https://doaj.org/article/22ab189659e64a4f8b06c7891c9ea61f
Publikováno v:
Children, Vol 10, Iss 3, p 506 (2023)
Background: Transplantation-associated thrombotic microangiopathy (TA-TMA) is a severe complication of hematopoietic stem cell transplantation and is sometimes fatal. Observations: A 4-year-old, male patient with stage M neuroblastoma (NBL) who had r
Externí odkaz:
https://doaj.org/article/e9a36b83e35c44509ec8b4dc07a7d368
Autor:
Tetsuhiko Okabe, Taiki Nozaki, Noriko Aida, Jay Starkey, Mikako Enokizono, Tetsu Niwa, Atsuhiko Handa, Yuji Numaguchi, Yasuyuki Kurihara
Publikováno v:
Insights into Imaging, Vol 9, Iss 3, Pp 313-324 (2018)
Abstract Neurological complications of paediatric cancers are a substantial problem. Complications can be primary from central nervous system (CNS) spread or secondary from indirect or remote effects of cancer, as well as cancer treatments such as ch
Externí odkaz:
https://doaj.org/article/a3f16a85321648969234a1fe7ec4e08d
Autor:
Yuko, Tsujioka, Taiki, Nozaki, Yasunari, Niimi, Jay, Starkey, Daisuke, Hasegawa, Mutsuko, Kondo, Mikako, Enokizono, Akari, Makidono, Tatsuo, Kono, Masahiro, Jinzaki
Publikováno v:
Clinical Imaging. 89:162-173
Vascular malformations are a complex and diverse group of disorders. They may enlarge with time, impair quality of life, and even be fatal. While many are sporadic, others are part of inherited syndromes; several gene mutations responsible for vascul
Autor:
Yukio Kimura, Noriko Sato, Miho Ota, Norihide Maikusa, Tomoko Maekawa, Daichi Sone, Mikako Enokizono, Atsuhiko Sugiyama, Etsuko Imabayashi, Hiroshi Matsuda, Tomoko Okamoto, Takashi Yamamura, Hideharu Sugimoto
Publikováno v:
eNeurologicalSci, Vol 8, Iss , Pp 11-16 (2017)
Background: White matter hyperintensities (WMH) in the cholinergic pathways are associated with cognitive performance in Alzheimer's disease. This study aimed to evaluate the relationship between the volume reduction of cholinergic pathways and cogni
Externí odkaz:
https://doaj.org/article/ba24f8d9ac9b42a5b37bb73e452a6371
Autor:
Daichi Sone, Masako Watanabe, Norihide Maikusa, Noriko Sato, Yukio Kimura, Mikako Enokizono, Mitsutoshi Okazaki, Hiroshi Matsuda
Publikováno v:
PLoS ONE, Vol 14, Iss 2, p e0212494 (2019)
PurposeThe pathophysiology of idiopathic generalized epilepsy (IGE) is still unclear, but graph theory may help to understand it. Here, we examined the graph-theoretical findings of the gray matter network in IGE using anatomical covariance methods.M
Externí odkaz:
https://doaj.org/article/a91339577ec34fd9b0db2c3b023e5142
Acute encephalopathy with biphasic seizures and reduced diffusion (AESD) is characterized by biphasic seizures following febrile viral infections and delayed reduced diffusion of the cerebral white matter on magnetic resonance imaging (MRI) diffusion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c97922d0c3adabb05ccf53caa963571d
https://doi.org/10.20944/preprints202305.0182.v1
https://doi.org/10.20944/preprints202305.0182.v1
Autor:
Mikako Enokizono, Noriko Aida, Akira Yagishita, Yasuhiro Nakata, Reiko Ideguchi, Ryo Kurokawa, Tatsuo Kono, Toshio Moritani, Harushi Mori
Publikováno v:
Japanese Journal of Radiology.
Although there are many types of inborn errors of metabolism (IEMs) affecting the central nervous system, also referred to as neurometabolic disorders, individual cases are rare, and their diagnosis is often challenging. However, early diagnosis is m
Autor:
Hideaki Mashimo, Mitsuhiro Kato, Kazuki Watanabe, Hirotomo Saitsu, Keitaro Yamada, Satoko Kumada, Mitsuko Nakashima, Mikako Enokizono
Publikováno v:
Journal of Human Genetics. 66:1193-1197
Heterozygous variants in TUBB encoding one of β-tubulin isotypes are known to cause two overlapping developmental brain disorders, complex cortical dysplasia with other brain malformations (CDCBM) and congenital symmetric circumferential skin crease