Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Misa Nakano"'
Autor:
Saori Itoi-Ochi, MD, PhD, Yukiho Kurosaki, MD, Asako Ota, MD, Akiko Miyazaki, MD, Akiko Hosokawa, MD, PhD, Misa Nakano, MD, PhD, Toshiyuki Takahashi, MD, PhD, Noriko Umegaki-Arao, MD, PhD, Manabu Fujimoto, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 46, Iss , Pp 1-4 (2024)
Externí odkaz:
https://doaj.org/article/a3892310ccb34a059ea459f7dd601e5c
Publikováno v:
Case Reports in Dermatology, Vol 6, Iss 2, Pp 140-144 (2014)
Spindle cell melanoma, which is a rare form of melanoma, is clinically and histopathologically difficult to diagnose from a variety of nonmelanocytic spindle cell tumors. We describe a 42-year-old Japanese woman with amelanotic melanoma that comprise
Externí odkaz:
https://doaj.org/article/0b1daf6e0b224855ab2dbaff9b9c8eff
Autor:
Yasutaka Mitamura, Masakazu Takahara, Takamichi Ito, Misa Nakano, Yoichi Moroi, Masutaka Furue
Publikováno v:
Case Reports in Dermatology, Vol 5, Iss 2, Pp 198-202 (2013)
Antiphospholipid syndrome (APS) with pleural effusion is extremely rare. A 75-year-old man was admitted to our hospital for spreading erythema on his trunk and extremities, as well as dyspnea. One year before admission, he had visited us with a 1-yea
Externí odkaz:
https://doaj.org/article/a27b6fa521a84f75a7e0af21396c62c3
Publikováno v:
Journal of the Japan Epilepsy Society. 37:755-765
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24c0719728eb307101a86f9b78158271
https://doi.org/10.3805/jjes.37.755
https://doi.org/10.3805/jjes.37.755
Publikováno v:
The Journal of Dermatology. 48
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35ac2b68dbcaf474a7071e207d1482ce
https://doi.org/10.1111/1346-8138.15842
https://doi.org/10.1111/1346-8138.15842
Autor:
Akane Terasaki, Masayuki Nakamura, Yuka Urata, Hanae Hiwatashi, Izumi Yokoyama, Takeshi Yasuda, Teiichi Onuma, Kazumaru Wada, Sunao Kaneko, Rumiko Kan, Shin-ichi Niwa, Ohiko Hashimoto, Osamu Komure, Yu-ichi Goto, Yuko Yamagishi, Misa Nakano, Yoshihiko Furusawa, Akira Sano
Publikováno v:
Journal of human genetics. 66(4)
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant disease characterized by adult-onset tremulous hand movement, myoclonus, and infrequent epileptic seizures. Recently, intronic expansion of unstable TTTCA/TTTTA pentanucleotide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::733ef800b7fd6c3b7520f9d4fdc0c9a9
https://pubmed.ncbi.nlm.nih.gov/33184460
https://pubmed.ncbi.nlm.nih.gov/33184460
Autor:
Teiichi Onuma, Shin-Ichi Niwa, Akira Sano, Sunao Kaneko, Izumi Yokoyama, Yu-ichi Goto, Takeshi Yasuda, Yuko Yamagishi, Misa Nakano, Rumiko Kan, Yoshihiko Furusawa, Akane Terasaki, Ohiko Hashimoto, Kazumaru Wada, Hanae Hiwatashi, Masayuki Nakamura, Osamu Komure, Yuka Urata
Publikováno v:
Journal of Human Genetics. 66:449-450
Benign adult familial myoclonic epilepsy (BAFME) is an autosomal dominant disease characterized by adult-onset tremulous hand movement, myoclonus, and infrequent epileptic seizures. Recently, intronic expansion of unstable TTTCA/TTTTA pentanucleotide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4599326677160d46b13af9d730f77c62
https://doi.org/10.1038/s10038-020-00867-w
https://doi.org/10.1038/s10038-020-00867-w
Publikováno v:
Case Reports in Dermatology, Vol 6, Iss 2, Pp 140-144 (2014)
Case Reports in Dermatology
Case Reports in Dermatology
Spindle cell melanoma, which is a rare form of melanoma, is clinically and histopathologically difficult to diagnose from a variety of nonmelanocytic spindle cell tumors. We describe a 42-year-old Japanese woman with amelanotic melanoma that comprise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::085b376f792a680c54e3df5512df5fee
http://www.karger.com/Article/FullText/363097
http://www.karger.com/Article/FullText/363097
Autor:
Misa Nakano-Nakamura, Makiko Kido-Nakahara, Yoichi Moroi, Masakazu Takahara, Maho Murata, Masutaka Furue, Takeshi Nakahara
Publikováno v:
Nishi Nihon Hifuka. 76:565-568
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0ab9038e818643e6bb123e5ec2a12b1
https://doi.org/10.2336/nishinihonhifu.76.565
https://doi.org/10.2336/nishinihonhifu.76.565
Autor:
Keiko Yaka, Ichizo Nishino, Masayuki Moriya, Yuko Kawasaki, Misa Nakano, Shingo Azuma, Ichiro Naba, Chikao Tatsumi
Publikováno v:
Neurology and Clinical Neuroscience. 3:131-133
A 53-year-old man presented with bilateral ptosis, diffuse muscle weakness and easy fatigability, and was admitted to Toyonaka Municipal Hospital, Osaka, Japan. The patient was diagnosed with myasthenia gravis in his childhood. Since then, he had bee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80a4bd13c0cce201938a0923889e3919
https://doi.org/10.1111/ncn3.162
https://doi.org/10.1111/ncn3.162