Familial amyloid polyneuropathy associated with the novel transthyretin variant Arg34Gly

By Levy Jaime  

Amyloid: The Journal of Protein Folding Disorders, Vol. 19, Iss. 4, 2012-12 ,pp. : 201-203

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Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan

By Misu Ken-ichiro   Hattori Naoki   Nagamatsu Masaaki   Ikeda Shu-ichi   Ando Yukio   Nakazato Masamitsu   Takei Yo-ichi   Hanyu Norinao   Usui Yasuomi   Tanaka Fumiaki   Harada Toshihide   Inukai Akira   Hashizume Yoshio  

Brain, Vol. 122, Iss. 10, 1999-10 ,pp. : 1951-1962

Oxford University Press

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An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation

By Lozeron Pierre   Lacroix Catherine   Theaudin Marie   Richer Anne   Gugenheim Michel   Adams David   Misrahi Micheline  

Amyloid: The Journal of Protein Folding Disorders, Vol. 20, Iss. 3, 2013-09 ,pp. : 188-192

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A case of biopsy-proven leptomeningeal amyloidosis and intravenous Ig-responsive polyneuropathy associated with the Ala25Thr transthyretin gene mutation

By Shimizu Yuko   Takeuchi Megumi   Matsumura Miyuki   Tokuda Takahiko   Iwata Makoto  

Amyloid: The Journal of Protein Folding Disorders, Vol. 13, Iss. 1, 2006-03 ,pp. : 37-41

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Systemic delivery of transthyretin siRNA mediated by lactosylated dendrimer/-cyclodextrin conjugates into hepatocyte for familial amyloidotic polyneuropathy therapy

By Hayashi Yuya   Mori Yoshimasa   Higashi Taishi   Motoyama Keiichi   Jono Hirofumi   Sah Dinah W. Y.   Ando Yukio   Arima Hidetoshi  

Amyloid: The Journal of Protein Folding Disorders, Vol. 19, Iss. 1, 2012-06 ,pp. : 47-49

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