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34. Molecular analysis of a variant type of familial amyloidotic polyneuropathy showing cerebellar ataxia and pyramidal tract signs. Furuya H; Yoshioka K; Sasaki H; Sakaki Y; Nakazato M; Matsuo H; Nakadai A; Ikeda S; Yanagisawa N J Clin Invest; 1987 Dec; 80(6):1706-11. PubMed ID: 3479441 [TBL] [Abstract][Full Text] [Related]
35. Production of recombinant human transthyretin with biological activities toward the understanding of the molecular basis of familial amyloidotic polyneuropathy (FAP). Furuya H; Saraiva MJ; Gawinowicz MA; Alves IL; Costa PP; Sasaki H; Goto I; Sakaki Y Biochemistry; 1991 Mar; 30(9):2415-21. PubMed ID: 1848097 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. Transthyretin gene mutations in British and French patients with amyloid neuropathy. Bhatia K; Reilly M; Adams D; Davis MB; Hawkes CH; Thomas PK; Said G; Harding AE J Neurol Neurosurg Psychiatry; 1993 Jun; 56(6):694-7. PubMed ID: 8509786 [TBL] [Abstract][Full Text] [Related]
38. Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin. Tanaka M; Hirai S; Matsubara E; Okamoto K; Morimatsu M; Nakazato M J Neurol Neurosurg Psychiatry; 1988 Apr; 51(4):576-8. PubMed ID: 3379433 [TBL] [Abstract][Full Text] [Related]