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Neurological Research
A Journal of Progress in Neurosurgery, Neurology and Neurosciences
Volume 32, 2010 - Issue 5
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Articles

Familial amyloid polyneuropathy (Finnish type) presenting multiple cranial nerve deficits with carpal tunnel syndrome and orthostatic hypotension

Kouki MakiokaDepartment of Neurology Graduate School of Medicine Gunma University, Maebashi, Gunma, Japan
,
Masaki IkedaDepartment of Neurology Graduate School of Medicine Gunma University, Maebashi, Gunma, Japan
,
Yoshio IkedaDepartment of Neurology Graduate School of Medicine and Dentistry, Okayma University, Okayama, Japan
,
Ai NakasoneDepartment of Neurology Graduate School of Medicine Gunma University, Maebashi, Gunma, Japan
,
Tenshi OsawaDepartment of Neurology Graduate School of Medicine Gunma University, Maebashi, Gunma, Japan
,
Atsushi SasakiDepartment of Human Pathology Graduate School of Medicine Gunma University, Maebashi, Gunma, Japan
,
Tomohiro OtaniDepartment of Ophthalmology Graduate School of Medicine, Gunma University, Maebashi, Gunma, Japan
,
Masashi AraiDepartment of Neurology Isesaki Municipal Hospital, Isesaki, Gunma, Japan
&
Koichi OkamotoDepartment of Neurology Graduate School of Medicine Gunma University, Maebashi, Gunma, Japan
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Pages 472-475 | Published online: 19 Jul 2013

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Read on this site (1)

James P. Solomon, Lesley J. Page, William E. Balch & Jeffery W. Kelly. (2012) Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention. Critical Reviews in Biochemistry and Molecular Biology 47:3, pages 282-296.
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Articles from other publishers (7)

Yaling Jiang, Meidan Wan, XueWen Xiao, Zhuojie Lin, Xixi Liu, Yafang Zhou, Xinxin Liao, Jingyi Lin, Hui Zhou, Lu Zhou, Ling Weng, Junling Wang, Jifeng Guo, Hong Jiang, Zhuohua Zhang, Kun Xia, Jiada Li, Beisha Tang, Bin Jiao & Lu Shen. (2023) GSN gene frameshift mutations in Alzheimer’s disease . Journal of Neurology, Neurosurgery & Psychiatry 94:6, pages 436-447.
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Tuuli Mustonen, Ville Sivonen, Sari Atula, Sari Kiuru-Enari & Saku T. Sinkkonen. (2021) Hearing problems in patients with hereditary gelsolin amyloidosis. Orphanet Journal of Rare Diseases 16:1.
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Yaling Jiang, Bin Jiao, Xinxin Liao, Xuewen Xiao, Xixi Liu & Lu Shen. (2020) Analyses Mutations in GSN, CST3, TTR, and ITM2B Genes in Chinese Patients With Alzheimer’s Disease. Frontiers in Aging Neuroscience 12.
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Alan Thurston. (2013) Carpal tunnel syndrome. Orthopaedics and Trauma 27:5, pages 332-341.
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Brent P. Goodman & Eduardo E. Benarroch. 2013. Neurological Disorders due to Systemic Disease. Neurological Disorders due to Systemic Disease 239 260 .
Sari Kiuru-Enari & Matti Haltia. 2013. Peripheral Nerve Disorders. Peripheral Nerve Disorders 659 681 .
Makiko Taira, Hiroyuki Ishiura, Jun Mitsui, Yuji Takahashi, Toshihiro Hayashi, Jun Shimizu, Takashi Matsukawa, Naoko Saito, Kazumasa Okada, Sadatoshi Tsuji, Hiromasa Sawamura, Shiro Amano, Jun Goto & Shoji Tsuji. (2012) Clinical features and haplotype analysis of newly identified Japanese patients with gelsolin-related familial amyloidosis of Finnish type. neurogenetics 13:3, pages 237-243.
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