Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Junya Kawada"'
Publikováno v:
The American Journal of Case Reports
Patient: Male, 54 Final Diagnosis: Guillain-Barré syndrome Symptoms: Paresthesia of extremities • unilateral facial palsy Medication: — Clinical Procedure: — Specialty: Neurology Objective: Unusual clinical course Background: A rare variant of
Publikováno v:
Journal of Advanced Concrete Technology. 14:634-642
Autor:
Izumi Kitagawa, Yasuharu Tokuda, Joel Branch, Shuku Sato, Junya Kawada, Aya Terane, Sho Nishiguchi
Publikováno v:
Journal of General and Family Medicine. 17:99-104
Publikováno v:
Journal of Neurology and Neuroscience.
Background: Parkinson’s disease (PD) is a common movement disorder with a wide range of non-motor symptoms. Depression is one of these symptoms; however, its pathomechanism and management remains to be elucidated. We evaluated of istradefylline (IS
Autor:
Junya Kawada, Tsuyoshi Watanabe, Masahiko Tanaka, Kazuaki Yamamoto, Satoshi Tanaka, Satoshi Endo, Gakuji Gondo
Publikováno v:
Cephalalgia : an international journal of headache. 37(9)
Introduction We report a case of cervicogenic headache caused by an intradural extramedullary tumor of the middle cervical spine, which has not previously been reported. Case presentation The patient was a 73-year-old male who visited a physician for
Publikováno v:
Nihon Naika Gakkai Zasshi. 102:1223-1225
Autor:
Halmagyi Gm, Tomoyasu Shirakawa, Junya Kawada, Tomoko Ogasawara, Akira Yoshioka, Genjiro Hirose, Satoshi Kataoka
Publikováno v:
Annals of Neurology. 43:403-406
We report on a patient who developed primary position upbeat nystagmus (ppUBN) due to a unilateral medial medullary infarction. On oculography, the slow phases of the nystagmus sometimes had an exponentially decreasing velocity waveform, indicating t
Publikováno v:
American Journal of Case Reports; 2017, Vol. 18, p1048-1052, 5p
Autor:
Jiro, Fukae, Hideki, Mochizuki, Rina, Ohashi, Kazuko, Mitani, Junya, Kawada, Yoshikuni, Mizuno
Publikováno v:
Rinsho shinkeigaku = Clinical neurology. 45(5)
Hemiparkinsonism-hemiatrophy syndrome (HPHA) is a rare form of parkinsonism, characterized by unilateral parkinsonism, ipsilateral body atrophy and early age of onset. We report a 59-year-old woman with hemiatrophy of her face and upper limb on the l
Autor:
Yukiko K. Hayashi, Junya Kawada, Ritsuko Koga, Toshifumi Tsukahara, Kiichi Arahata, Atsushi Nagano, Ryozo Okada, Yoshihiro Kurano, Megumu Ogawa
Publikováno v:
Nature genetics. 12(3)
Mutations in the STA gene at the Xq28 locus have been found in patients with X-linked Emery-Dreifuss muscular dystrophy (EDMD). This gene encodes a hitherto unknown protein named 'emerin'. To elucidate the subcellular localization of emerin, we raise