These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
95 related articles for article (PubMed ID: 8290065)
1. Genetic expression of a transthyretin mutation in a case of amyloidotic polyneuropathy occurring in an African. Léger JM; Grateau G; Gugenheim M; Hauw JJ; Bouche P; Brunet P Neurology; 1994 Jan; 44(1):181. PubMed ID: 8290065 [No Abstract] [Full Text] [Related]
3. A new mutation causing familial amyloidotic polyneuropathy. Skare JC; Saraiva MJ; Alves IL; Skare IB; Milunsky A; Cohen AS; Skinner M Biochem Biophys Res Commun; 1989 Nov; 164(3):1240-6. PubMed ID: 2590199 [TBL] [Abstract][Full Text] [Related]
4. A novel transthyretin mutation associated with familial amyloidotic polyneuropathy. Murakami T; Maeda S; Yi S; Ikegawa S; Kawashima E; Onodera S; Shimada K; Araki S Biochem Biophys Res Commun; 1992 Jan; 182(2):520-6. PubMed ID: 1734866 [TBL] [Abstract][Full Text] [Related]
5. Mass spectrometric detection of the plasma prealbumin (transthyretin) variant associated with familial amyloidotic polyneuropathy. Wada Y; Matsuo T; Katakuse I; Suzuki T; Azuma T; Tsujino S; Kishimoto S; Matsuda H; Hayashi A Biochim Biophys Acta; 1986 Sep; 873(2):316-9. PubMed ID: 3756182 [TBL] [Abstract][Full Text] [Related]
6. Familial amyloidotic polyneuropathy with late-onset and well-preserved autonomic function: a Japanese kindred with novel mutant transthyretin (Ala97 to Gly). Yasuda T; Sobue G; Doyu M; Nakazato M; Shiomi K; Yanagi T; Mitsuma T J Neurol Sci; 1994 Jan; 121(1):97-102. PubMed ID: 8133316 [TBL] [Abstract][Full Text] [Related]
7. Structure and expression of the mutant prealbumin gene associated with familial amyloidotic polyneuropathy. Maeda S; Mita S; Araki S; Shimada K Mol Biol Med; 1986 Aug; 3(4):329-38. PubMed ID: 3022108 [TBL] [Abstract][Full Text] [Related]
8. [Molecular and genetic bases for deposition of amyloid fibrils in familial amyloidotic polyneuropathy]. Maeda S; Araki S; Shimada K Rinsho Shinkeigaku; 1986 Dec; 26(12):1298-301. PubMed ID: 3829529 [No Abstract] [Full Text] [Related]
9. Direct sequencing of the gene for Maryland/German familial amyloidotic polyneuropathy type II and genotyping by allele-specific enzymatic amplification. Nichols WC; Liepnieks JJ; McKusick VA; Benson MD Genomics; 1989 Oct; 5(3):535-40. PubMed ID: 2613237 [TBL] [Abstract][Full Text] [Related]
10. Genetic expression of a transthyretin mutation in typical and late-onset Portuguese families with familial amyloidotic polyneuropathy. Saraiva MJ; Costa PP; Goodman DS Neurology; 1986 Nov; 36(11):1413-7. PubMed ID: 3762958 [TBL] [Abstract][Full Text] [Related]
11. Familial amyloidotic polyneuropathy: report of patients heterozygous for the transthyretin Gly42 gene. Murakami T; Yi S; Yamamoto K; Maruyama S; Araki S Ann Neurol; 1992 Mar; 31(3):340-2. PubMed ID: 1637142 [TBL] [Abstract][Full Text] [Related]
12. Identification of a novel transthyretin variant (Val30----Leu) associated with familial amyloidotic polyneuropathy. Nakazato M; Ikeda S; Shiomi K; Matsukura S; Yoshida K; Shimizu H; Atsumi T; Kangawa K; Matsuo H FEBS Lett; 1992 Jul; 306(2-3):206-8. PubMed ID: 1633877 [TBL] [Abstract][Full Text] [Related]
13. Structure of the mutant prealbumin gene responsible for familial amyloidotic polyneuropathy. Yoshioka K; Sasaki H; Yoshioka N; Furuya H; Harada T; Kito S; Sakaki Y Mol Biol Med; 1986 Aug; 3(4):319-28. PubMed ID: 3022107 [TBL] [Abstract][Full Text] [Related]
15. Homozygosity for the transthyretin-Met30 gene in three Japanese siblings with type I familial amyloidotic polyneuropathy. Yoshinaga T; Nakazato M; Ikeda S; Ohnishi A Neurology; 1992 Oct; 42(10):2045-7. PubMed ID: 1407590 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. Two novel variants of transthyretin identified in Japanese cases with familial amyloidotic polyneuropathy: transthyretin (Glu42 to Gly) and transthyretin (Ser50 to Arg). Ueno S; Uemichi T; Takahashi N; Soga F; Yorifuji S; Tarui S Biochem Biophys Res Commun; 1990 Jun; 169(3):1117-21. PubMed ID: 2363717 [TBL] [Abstract][Full Text] [Related]
18. Transthyretin (prealbumin) in familial amyloidotic polyneuropathy: genetic and functional aspects. Saraiva MJ; Costa PP; Goodman DS Adv Neurol; 1988; 48():189-200. PubMed ID: 3334781 [No Abstract] [Full Text] [Related]
19. Familial amyloidotic polyneuropathy presenting with carpal tunnel syndrome and a new transthyretin mutation, asparagine 70. Izumoto S; Younger D; Hays AP; Martone RL; Smith RT; Herbert J Neurology; 1992 Nov; 42(11):2094-102. PubMed ID: 1436517 [TBL] [Abstract][Full Text] [Related]
20. Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met30) gene. Pathologic similarity to human familial amyloidotic polyneuropathy, type I. Yi S; Takahashi K; Naito M; Tashiro F; Wakasugi S; Maeda S; Shimada K; Yamamura K; Araki S Am J Pathol; 1991 Feb; 138(2):403-12. PubMed ID: 1992765 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]