Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Kenta Orimo"'
Autor:
Daisuke Yoshioka, Takehiko Yamanashi, Kenta Taneda, Takashi Matsukawa, Kenta Orimo, Masaaki Iwata
Publikováno v:
PCN Reports, Vol 3, Iss 1, Pp n/a-n/a (2024)
Abstract Background Idiopathic basal ganglia calcification (IBGC), also known as Farh's disease, is a rare neurodegenerative disorder characterized by calcification of the basal ganglia and other brain regions. This disease usually occurs in middle
Externí odkaz:
https://doaj.org/article/c39e9718a6344666aca4e539d478b28f
Autor:
Haruka Masuzawa, MD, Fumio Suzuki, MD, PhD, Shiori Amemiya, MD, PhD, Kenta Orimo, MD, Hiroyuki Ishiura, MD, PhD, Ryo Hara, MD, Tatsushi Toda, MD, PhD, Teruo Nakazawa, MD, Akira Honda, MD, PhD, Mariko Tanaka, MD, PhD, Munetoshi Hinata, MD, PhD, Osamu Abe, MD, PhD
Publikováno v:
Radiology Case Reports, Vol 18, Iss 5, Pp 1929-1932 (2023)
Intravascular lymphoma (IVL) is difficult to diagnose because its clinical presentation and laboratory and imaging findings are nonspecific. Herein, we report a case of IVL presenting as a lesion in the splenium of the corpus callosum. A 52-year-old
Externí odkaz:
https://doaj.org/article/72225dd3080c4d418722da4c60b055af
Autor:
Masanori Kurihara, Kenta Orimo, Tatsuo Mano, Ryoji Miyano, Aya Kamisawa Sato, Kenichiro Sato, Ryoko Ihara, Toshihiro Hayashi, Tatsushi Toda
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 3, Iss , Pp 100080- (2020)
Externí odkaz:
https://doaj.org/article/f09955d1e67448ec8db36f32a8882057
Autor:
Keiko Hatano, Kenta Orimo, Mizuki Ogura, Shingo Okabe, Tadao Ishida, Akatsuki Kubota, Jun Shimizu, Hideji Hashida
Publikováno v:
Internal Medicine. 62:475-479
A 36-year-old man developed polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes (POEMS) syndrome after conversion from solitary plasmacytoma of bone to multiple myeloma. Twenty-four days following the neurological onset, he lost
Autor:
Kenta Orimo, Katsuhiko Takeda, Mizuho Kawai, Hideki Nakajima, Nobue K. Iwata, Hiroyuki Murai, Jun Goto
Publikováno v:
Internal Medicine
Anti-leucine-rich glioma-inactivated 1 (LGI1) antibody is associated with limbic encephalitis. We herein report a patient with anti-LGI1 encephalitis who developed severe orthostatic hypotension (OH) responsive to immunoglobulin therapy five years af
Publikováno v:
Internal Medicine
Autor:
Ryoji Miyano, Toshihiro Hayashi, Kenta Orimo, Tatsuo Mano, Aya Kamisawa Sato, Ryoko Ihara, Masanori Kurihara, Kenichiro Sato, Tatsushi Toda
Publikováno v:
Clinical Parkinsonism & Related Disorders, Vol 3, Iss, Pp 100080-(2020)
Clinical Parkinsonism & Related Disorders
Clinical Parkinsonism & Related Disorders
Progressive supranuclear palsy (PSP) is a neurodegenerative disease that presents with various clinical symptoms. Although Richardson’s syndrome is the most common, other presentations include parkinsonism (PSP-P) and progressive gait freezing [1].
Autor:
Hironobu Nishijima, Miwako Takahashi, Masashi Hamada, Harushi Mori, Toshikatsu Kaburaki, Tatsuro Mutoh, Rie Tanaka, Tatsuo Mano, Masako Ikemura, Ryoji Miyano, Kenta Orimo, Masanori Kurihara, Toshihiro Hayashi, Tatsushi Toda
Publikováno v:
Neurology and Clinical Neuroscience. 7:75-77
Autor:
Hideji Hashida, Kenta Orimo, Naoko Saito-Sato, Hideki Nakayama, Tadao Ishida, Mizuki Ogura, Keiko Hatano
Publikováno v:
Journal of Stroke and Cerebrovascular Diseases. 30:105637
Immune thrombocytopenic purpura (ITP) can increase the risk of not only hemorrhagic incidents but also thrombotic events. Although several patients with ITP who developed cerebral infarction have been reported, concurrence of spinal cord infarction a
Autor:
Keishi Horiguchi, Sumihito Nobusawa, Hayato Ikota, Junko Hirato, Kenta Orimo, Yoichi Nakazato, Hideaki Yokoo
Publikováno v:
Pathology International. 64:472-477
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) is a very aggressive embryonal central nervous system (CNS) tumor, histologically featuring ependymoblastic rosettes and neuronal differentiation in a neuropil-like background. 19q13.4