Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Hidetsuna, Utsunomiya"'
Publikováno v:
Acta Radiologica Open
To discuss the computed tomography (CT) and magnetic resonance (MR) findings of posterior fossa epidural hematoma (PFEDH) mimicking sinus thrombosis, we present two pediatric cases with the PFEDH extending along the sigmoid sinus groove evaluated by
Autor:
Yoshihiro Ikura, Tomoko Hashimoto-Tamaoki, Jiro Tsugawa, Yuka Yotsumoto, Hidetsuna Utsunomiya, Satoko Miyatake, Yonehiro Kanemura, Naomichi Matsumoto, Atsuko Harada
Publikováno v:
Molecular and Clinical Oncology.
A heterozygous loss-of-function mutation of the PTEN gene, one of the tumor suppressor genes, causes a wide variety of disorders, ranging from macrocephaly/autism syndrome to PTEN hamartoma tumor syndrome, including Cowden disease that causes thyroid
Autor:
Keita Sakurai, Kentaro Yamada, Keiko Toyoda, Hidetsuna Utsunomiya, Masahiro Muto, Hiroyuki Yuasa, Yoshio Hashizume, Ikuko Aiba, Yuto Uchida, Masaki Takao, Yufuko Saito, Motoo Nakagawa, Shohei Inui, Mari Yoshida, Hiroshi Oba, Asako Yamamoto, Satoru Morimoto, Takuya Oguri, Aya M. Tokumaru
Publikováno v:
Neuroradiology. 61(11)
This short report clarifies the heterogeneity of structural magnetic resonance imaging (MRI) findings in seven demented patients due to pathologically accumulated TAR DNA-binding protein-43 (TDP-43) protein using visual analyses including visual rati
Autor:
Yuka, Yotsumoto, Atsuko, Harada, Jiro, Tsugawa, Yoshihiro, Ikura, Hidetsuna, Utsunomiya, Satoko, Miyatake, Naomichi, Matsumoto, Yonehiro, Kanemura, Tomoko, Hashimoto-Tamaoki
Publikováno v:
Molecular and Clinical Oncology
A heterozygous loss-of-function mutation of the PTEN gene, one of the tumor suppressor genes, causes a wide variety of disorders, ranging from macrocephaly/autism syndrome to PTEN hamartoma tumor syndrome, including Cowden disease that causes thyroid
Autor:
Atsuko Harada, Koichi Ueda, Jun Sugasawa, Takumi Yamanaka, Mami Yamasaki, Tetsuya Sugiyama, Yuka Shigemura, Hidehiro Oku, Shota Kojima, Hidetsuna Utsunomiya, Mari Ueki, Tsunehiko Ikeda, Kensuke Tajiri, Tomoko Miyake
Publikováno v:
International Medical Case Reports Journal
Introduction The incidence of facial cleft is rare and ranges between 1.43 and 4.85 per 100,000 births. To date, there have been few reports of detailed ophthalmologic examinations performed in cases of facial cleft. Here, we report a case of optic-n
Autor:
Mami Yamasaki, Hidetsuna Utsunomiya
Publikováno v:
Japanese Journal of Neurosurgery. 25:338-345
Autor:
Makoto Tamari, Hidetsuna Utsunomiya
Publikováno v:
International Journal of Physical Medicine & Rehabilitation.
Autor:
Atsuko Harada, Yonehiro Kanemura, Takumi Yamanaka, Fuyuki Miya, Tatsuhiko Tsunoda, Mitsuhiro Kato, Hidetsuna Utsunomiya, Mami Yamasaki, Kenjiro Kosaki
Publikováno v:
Child's Nervous System. 31:465-471
Megalencephaly capillary malformation (MCAP) is a syndrome involving brain overgrowth, characterized by megalencephaly, capillary malformations, asymmetric growth, polymicrogyria, polydactyly, and syndactyly. Cerebellar tonsillar herniation (CTH) and
Publikováno v:
Journal of Neuroimaging. 24:590-594
BACKGROUND AND PURPOSE Impairment of orientation for time (OT) is a characteristic symptom of Alzheimer disease (AD). However, the brain regions underlying OT remain to be elucidated. Using single photon emission computed tomography (SPECT), we exami
Identification of Nerve Fibers Using Diffusion Tensor Imaging and its Application for Rehabilitation
Autor:
Hidetsuna Utsunomiya, Makoto Tamari
Publikováno v:
Rigakuryoho Kagaku. 29:841-845