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29. [A sporadic case of late onset familial amyloidotic polyneuropathy preceded by cardiac involvement]. Aoki K; Koike R; Yuasa T; Ikeda S; Tsuji S Rinsho Shinkeigaku; 1993 Aug; 33(8):905-8. PubMed ID: 8261706 [TBL] [Abstract][Full Text] [Related]
30. [Amyloidosis of the vitreous body. Possibilities of diagnosis]. Soltau JB; Seiberth V; Knorz MC; Liesenhoff H Fortschr Ophthalmol; 1991; 88(4):408-10. PubMed ID: 1786932 [TBL] [Abstract][Full Text] [Related]
31. Onset in the seventh decade and lack of symptoms in heterozygotes for the TTRMet30 mutation in hereditary amyloid neuropathy-type I (Portuguese, Andrade). Sequeiros J; Saraiva MJ Am J Med Genet; 1987 Jun; 27(2):345-57. PubMed ID: 3037905 [TBL] [Abstract][Full Text] [Related]
32. Human transthyretin (prealbumin) gene and molecular genetics of familial amyloidotic polyneuropathy. Sakaki Y; Yoshioka K; Tanahashi H; Furuya H; Sasaki H Mol Biol Med; 1989 Apr; 6(2):161-8. PubMed ID: 2693890 [TBL] [Abstract][Full Text] [Related]
33. Transgenic mouse model of familial amyloidotic polyneuropathy. Shimada K; Maeda S; Murakami T; Nishiguchi S; Tashiro F; Yi S; Wakasugi S; Takahashi K; Yamamura K Mol Biol Med; 1989 Aug; 6(4):333-43. PubMed ID: 2560117 [TBL] [Abstract][Full Text] [Related]
34. Epidemiology of familial amyloid polyneuropathy in Japan: Identification of a novel endemic focus. Kato-Motozaki Y; Ono K; Shima K; Morinaga A; Machiya T; Nozaki I; Shibata-Hamaguchi A; Furukawa Y; Yanase D; Ishida C; Sakajiri K; Yamada M J Neurol Sci; 2008 Jul; 270(1-2):133-40. PubMed ID: 18410945 [TBL] [Abstract][Full Text] [Related]
35. Amyloid fibril protein in familial amyloidotic polyneuropathy, Portuguese type. Definition of molecular abnormality in transthyretin (prealbumin). Saraiva MJ; Birken S; Costa PP; Goodman DS J Clin Invest; 1984 Jul; 74(1):104-19. PubMed ID: 6736244 [TBL] [Abstract][Full Text] [Related]
36. Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy. Nakazato M; Kurihara T; Kangawa K; Matsuo H Lancet; 1984 Dec; 2(8414):1274-5. PubMed ID: 6150302 [No Abstract] [Full Text] [Related]
37. [Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence]. Adams D; Reilly M; Harding AE; Said G Rev Neurol (Paris); 1992; 148(12):736-41. PubMed ID: 1338934 [TBL] [Abstract][Full Text] [Related]
38. Ineffectiveness of dialysis in transthyretin (TTR) clearance in familial amyloid polyneuropathy type I, in spite of lower stability of the TTR Met30 variant. Beirão I; Lobato L; Riedstra S; Costa PM; Pimentel S; Guimarães S Clin Nephrol; 1999 Jan; 51(1):45-9. PubMed ID: 9988146 [TBL] [Abstract][Full Text] [Related]