Výsledky vyhledávání - "Kazuhiro Tashima"

Susac's Syndrome: Beneficial Effects of Corticosteroid Therapy in a Japanese Case

Autor: Eiichiro Uyama, Makoto Uchino, Yoichiro Hashimoto, Kazuhiro Tashima, Toshiro Yonehara

Publikováno v: Internal Medicine. 40:135-139

Susac's syndrome is a rare disorder characterized by the triad of microangiopathy of the brain and retina with hearing loss. More than 50 affected individuals have been reported worldwide, all Caucasians. We herein identify the first Japanese patient

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ecd9e5523609d938cdf8057042bdd56
https://doi.org/10.2169/internalmedicine.40.135

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Endothelium-dependent vasodilatation in patients with familial amyloidotic polyneuropathy

Autor: Masayuki Ando, Moritaka Suga, Yukio Ando, Masaaki Nakamura, Hisayasu Terazaki, Konen Obayashi, Kazuhiro Tashima, Makoto Uchino, Taro Yamashita

Publikováno v: Muscle & Nerve. 23:1084-1088

We examined endothelium-dependent vasodilatation in 15 familial amyloidotic polyneuropathy (FAP) amyloidogenic transthyretin (ATTR) Valine30Methionine (Val30Met) patients and 12 healthy volunteers. Using ultrasonography, we measured the radial artery

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ab01d6fd42c44c9d4adb1a044646a8d
https://doi.org/10.1002/1097-4598(200007)23:7<1084::aid-mus11>3.0.co

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Outcome of liver transplantation for transthyretin amyloidosis: follow-up of Japanese familial amyloidotic polyneuropathy patients

Autor: Shin Ichi Yoshimatsu, Yukio Ando, Hisayasu Terazaki, Eiko Ando, Ole B Suhr, Konen Obayashi, Makoto Uchino, Taro Yamashita, Masayuki Ando, Kazuhiro Tashima

Publikováno v: Journal of the Neurological Sciences. 171:19-23

Since 1990, liver transplantation for familial amyloidotic polyneuropathy (FAP) has been carried out world-wide, and the outcome of the procedure seems to be promising. FAP is inherited systemic disease caused by mutated transthyretin. The most commo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7904b9f051d0bcb229a7e32a73cc09fa
https://doi.org/10.1016/s0022-510x(99)00231-2

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Gastrointestinal dysfunction in familial amyloidotic polyneuropathy (ATTR Val3 et) - comparison of Swedish and Japanese patients

Autor: Yukio Ando, Hisayasu Terazaki, Gösta Holmgren, Ole B. Suhr, Kazuhiro Tashima, Taro Yamashita, Makoto Uchino, Konen Obayashi

Publikováno v: Amyloid. 6:124-129

The aim of the present study was to compare the clinical symptoms of Swedish and Japanese patients with familial amyloidotic polyneuropathy (ATTR Val Met), especially gastrointestinal disturbances, and to correlate the findings with survival.Seventy-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::11ad532c689cbdafe499cc3d9af1a4f4
https://doi.org/10.3109/13506129909007313

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Familial amyloidotic polyneuropathy type I with extracellular superoxide dismutase mutation: A case report

Autor: Naomi Sakashita, Kiyoshi Takahashi, Taro Yamashita, Kazuhiro Tashima, Peter Nilsson, Stefan L. Marklund, Yukio Ando

Publikováno v: Human Pathology. 29:1169-1172

We report an autopsy case of familial amyloidotic polyneuropathy (FAP) Type I with mutations in both transthyretin (TTR) and extracellular superoxide dismutase (EC-SOD). This patient started to develop peripheral neuropathy at age 25, followed by car

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eae0614e4df170d157fc45f527a2b116
https://doi.org/10.1016/s0046-8177(98)90433-6

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An atypical case of adult Moyamoya disease with initial onset of brain stem ischemia

Autor: Eiichiro Uyama, Teruyuki Hirano, Shuji Mita, Makoto Uchino, Kazuhiro Tashima

Publikováno v: Journal of the Neurological Sciences. 157:100-104

We present an atypical case of adult moyamoya disease whose clinical onset consisted of ischemic symptoms of the brain stem. She initially presented with left hemisensory disturbance caused by a pontine lesion, followed by a myelopathy of the upper c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d187acdddaa2f8cd42b85f1cd8fc8550
https://doi.org/10.1016/s0022-510x(98)00057-4

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Heterogeneity of clinical symptoms in patients with familial amyloidotic polyneuropathy (FAP TTR Met30)

Autor: Masayuki Ando, Makoto Uchino, Yoshiya Tanaka, Yukio Ando, Kazuhiro Tashima, Eiko Ando

Publikováno v: Amyloid. 4:108-111

Patients with familial amyloidotic polyneuropathy (FAP TTR Met 30) manifest clinical jindings, such as auto-nomic dysfunction, sensori-motor polyneuropathy, and visceral organ impairment with the progression of the disease. to clarih the clinical fea

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3ce1ca03d0bc42d59492629095ae0123
https://doi.org/10.3109/13506129708995279

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Letters to the editor

Publikováno v: Muscle & Nerve. 19:1636-1642

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::22c645cc1b93e72826d1a2f15c92cf54
https://doi.org/10.1002/mus.880191206

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Autonomic dysfunction and anemia in neurologic disorders

Autor: Yukio Ando, Konen Obayashi, Ole B. Suhr, Kazuhiro Tashima, Masayuki Ando, Taro Yamashita, Keiko Asahara, Makoto Uchino, Mizue Yonemitsu

Publikováno v: Journal of the Autonomic Nervous System. 61:145-148

The effect of autonomic dysfunctions on anemia in various neurological disorders, such as familial amyloidotic polyneuropathy (FAP) Type I, pandysautonomia, and Shy-Drager syndrome was examined. As a control, hemograms of patients with amyotrophic la

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ed30f016426ebda9cd97351b3854be7
https://doi.org/10.1016/s0165-1838(96)00070-7

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