Lower urinary tract dysfunction in type 1 familial amyloidotic polyneuropathy in Kumamoto, Japan

WADA Yoshihiro; ANDO Yukio; KAI Nobuyuki; TAKAHASHI Wataru; KIKUKAWA Hiroaki; NAKANISHI Juro; HONDA Jiro; JINNOUCHI Yoshiteru; UEDA Shoichi

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J-GLOBAL ID：200902205955216337 Reference number：07A0016352

Lower urinary tract dysfunction in type 1 familial amyloidotic polyneuropathy in Kumamoto, Japan

熊本における1型家族性アミロイドポリニューロパシー患者の下部尿路機能障害

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Material：
Volume： 13 Issue： 12 Page： 1475-1478 Publication year： Dec. 2006
JST Material Number： W1347A ISSN： 0919-8172 Document type： Article
Article type：原著論文 Country of issue： Australia (AUS) Language： ENGLISH (EN)

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Urogenital diseases , Nervous system diseases

Reference (20)：

ANDRADE, C. A peculiar form of peripheral neuropathy : familial atypical generalized amyloidosis with special involvement of the peripheral nerves. Brain. 1952, 75, 408-427
HOFER, PA. Postmortem findings in primary familial amyloidosis with polyneuropathy. Acta Pathol. Microbiol. Scand. 1975, 83, 309-322
RUKAVINA, JG. Primary systemic amyloidosis : a review and an experimental, genetic and clinical study of 29 cases with particular emphasis on the familial form. Medicine. 1956, 35, 239-334
MERETOJA, J. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin change and various internal symptoms. Ann. Clin. Res. 1969, 1, 314-324
ARAKI, S. Polyneuritic amyloidosis in a Japanese family. Arch. Neurol. 1968, 18, 593-602

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