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25. Presymptomatic diagnosis of heterozygosity for familial amyloidotic polyneuropathy by recombinant DNA techniques. Sasaki H; Sakaki Y; Takagi Y; Sahashi K; Takahashi A; Isobe T; Shinoda T; Matsuo H; Goto I; Kuroiwa Y Lancet; 1985 Jan; 1(8420):100. PubMed ID: 2856994 [No Abstract] [Full Text] [Related]
26. Familial amyloid polyneuropathy associated with the transthyretin Cys114 gene in a Japanese kindred. Ueno S; Fujimura H; Yorifuji S; Nakamura Y; Takahashi M; Tarui S; Yanagihara T Brain; 1992 Oct; 115 ( Pt 5)():1275-89. PubMed ID: 1330202 [TBL] [Abstract][Full Text] [Related]
27. Prenatal detection of a gene for hereditary amyloidosis. Nichols WC; Padilla LM; Benson MD Am J Med Genet; 1989 Dec; 34(4):520-4. PubMed ID: 2516414 [TBL] [Abstract][Full Text] [Related]
28. Presence of a plasma transthyretin (prealbumin) variant in familial amyloidotic polyneuropathy in a kindred of Greek origin. Saraiva MJ; Sherman W; Goodman DS J Lab Clin Med; 1986 Jul; 108(1):17-22. PubMed ID: 3011930 [TBL] [Abstract][Full Text] [Related]
29. Detection of three transthyretin gene mutations in familial amyloidotic polyneuropathy by analysis of DNA extracted from formalin-fixed and paraffin-embedded tissues. Date Y; Nakazato M; Kangawa K; Shirieda K; Fujimoto T; Matsukura S J Neurol Sci; 1997 Sep; 150(2):143-8. PubMed ID: 9268242 [TBL] [Abstract][Full Text] [Related]
30. Identification of carriers of a variant plasma prealbumin (transthyretin) associated with familial amyloidotic polyneuropathy type I. Benson MD; Dwulet FE J Clin Invest; 1985 Jan; 75(1):71-5. PubMed ID: 2981253 [TBL] [Abstract][Full Text] [Related]
32. Primary structure of an amyloid prealbumin variant in familial polyneuropathy of Jewish origin. Pras M; Prelli F; Franklin EC; Frangione B Proc Natl Acad Sci U S A; 1983 Jan; 80(2):539-42. PubMed ID: 6300852 [TBL] [Abstract][Full Text] [Related]
33. Transthyretin Pro 36 associated with familial amyloidotic polyneuropathy in an Ashkenazic Jewish kindred. Jacobson DR; Rosenthal CJ; Buxbaum JN Hum Genet; 1992; 90(1-2):158-60. PubMed ID: 1358785 [TBL] [Abstract][Full Text] [Related]
34. Structural comparisons between mouse and human prealbumin. Wakasugi S; Maeda S; Shimada K; Nakashima H; Migita S J Biochem; 1985 Dec; 98(6):1707-14. PubMed ID: 3005251 [TBL] [Abstract][Full Text] [Related]
36. A transthyretin variant (alanine 71) associated with familial amyloidotic polyneuropathy in a French family. Benson MD; Turpin JC; Lucotte G; Zeldenrust S; LeChevalier B; Benson MD J Med Genet; 1993 Feb; 30(2):120-2. PubMed ID: 8095302 [TBL] [Abstract][Full Text] [Related]
37. 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]
38. [Identification of genetic carriers in familial amyloidosis with polyneuropathy is possible with the DNA technic]. Holmgren G; Drugge U; Lundgren E; Sandgren O; Steen L Lakartidningen; 1988 Nov; 85(44):3677-9. PubMed ID: 2904519 [No Abstract] [Full Text] [Related]
39. Identification of a prealbumin variant in the serum of a Japanese patient with familial amyloidotic polyneuropathy. Nakazato M; Kangawa K; Minamino N; Tawara S; Matsuo H; Araki S Biochem Biophys Res Commun; 1984 Jul; 122(2):712-8. PubMed ID: 6087810 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]