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.
42. A new mutation (TTR Ala-47) in the transthyretin gene associated with hereditary amyloidosis. Ferlini A; Patrosso MC; Repetto M; Frattini A; Villa A; Fini S; Salvi F; Vezzoni P; Forabosco A Hum Mutat; 1994; 4(1):61-4. PubMed ID: 7951260 [No Abstract] [Full Text] [Related]
43. 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]
44. 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]
45. Transthyretin Ile 122 and cardiac amyloidosis in African-Americans. 2 case reports. Jacobson DR; Ittmann M; Buxbaum JN; Wieczorek R; Gorevic PD Tex Heart Inst J; 1997; 24(1):45-52. PubMed ID: 9068139 [TBL] [Abstract][Full Text] [Related]
46. Molecular strategies in genetic diagnosis of transthyretin-related hereditary amyloidosis. Ferlini A; Fini S; Salvi F; Patrosso MC; Vezzoni P; Forabosco A FASEB J; 1992 Jul; 6(10):2864-6. PubMed ID: 1353040 [TBL] [Abstract][Full Text] [Related]
47. Homozygosity for the transthyretin-Met30-gene in seven individuals with familial amyloidosis with polyneuropathy detected by restriction enzyme analysis of amplified genomic DNA sequences. Holmgren G; Bergström S; Drugge U; Lundgren E; Nording-Sikström C; Sandgren O; Steen L Clin Genet; 1992 Jan; 41(1):39-41. PubMed ID: 1353008 [TBL] [Abstract][Full Text] [Related]
48. Characterization of a basic transthyretin variant--TTR Arg 102--in the German population. Almeida MR; Altland K; Rauh S; Gawinowicz M; Moreira P; Costa PP; Saraiva MJ Biochim Biophys Acta; 1991 Oct; 1097(3):224-6. PubMed ID: 1681909 [TBL] [Abstract][Full Text] [Related]
49. Familial carpal tunnel syndrome due to amyloidogenic transthyretin His 114 variant. Murakami T; Tachibana S; Endo Y; Kawai R; Hara M; Tanase S; Ando M Neurology; 1994 Feb; 44(2):315-8. PubMed ID: 8309582 [TBL] [Abstract][Full Text] [Related]
50. 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]
51. Transthyretin Ser 6 gene frequency in individuals without amyloidosis. Jacobson DR; Alves IL; Saraiva MJ; Thibodeau SN; Buxbaum JN Hum Genet; 1995 Mar; 95(3):308-12. PubMed ID: 7868124 [TBL] [Abstract][Full Text] [Related]
52. Purification and characterization of amyloid-related transthyretin associated with familial amyloidotic cardiomyopathy. Hermansen LF; Bergman T; Jörnvall H; Husby G; Ranløv I; Sletten K Eur J Biochem; 1995 Feb; 227(3):772-9. PubMed ID: 7867637 [TBL] [Abstract][Full Text] [Related]
53. Familial amyloid with a transthyretin leucine 33 mutation presenting with ascites. Myers TJ; Kyle RA; Jacobson DR Am J Hematol; 1998 Nov; 59(3):249-51. PubMed ID: 9798666 [TBL] [Abstract][Full Text] [Related]
54. Transthyretin amyloidosis associated with a novel variant (Trp41Leu) presenting with vitreous opacities. Yazaki M; Connors LH; Eagle RC; Leff SR; Skinner M; Benson MD Amyloid; 2002 Dec; 9(4):263-7. PubMed ID: 12557756 [TBL] [Abstract][Full Text] [Related]
55. Biochemical and clinical characterization of prealbuminCHICAGO: an apparently benign variant of serum prealbumin (transthyretin) discovered with high-resolution two-dimensional electrophoresis. Harrison HH; Gordon ED; Nichols WC; Benson MD Am J Med Genet; 1991 Jun; 39(4):442-52. PubMed ID: 1877623 [TBL] [Abstract][Full Text] [Related]
56. Systemic senile amyloidosis. Identification of a new prealbumin (transthyretin) variant in cardiac tissue: immunologic and biochemical similarity to one form of familial amyloidotic polyneuropathy. Gorevic PD; Prelli FC; Wright J; Pras M; Frangione B J Clin Invest; 1989 Mar; 83(3):836-43. PubMed ID: 2646319 [TBL] [Abstract][Full Text] [Related]
57. A new ATTR Phe64Ile mutation with late-onset multiorgan involvement. Tarquini R; Perfetto F; Bergesio F; Miliani A; Del Pace S; Frusconi S; Minuti B; Pelo E; Torricelli F Amyloid; 2007 Dec; 14(4):289-92. PubMed ID: 17968689 [TBL] [Abstract][Full Text] [Related]
58. Hereditary amyloidosis: detection of variant prealbumin genes by restriction enzyme analysis of amplified genomic DNA sequences. Nichols WC; Benson MD Clin Genet; 1990 Jan; 37(1):44-53. PubMed ID: 2154345 [TBL] [Abstract][Full Text] [Related]
59. A novel variant of transthyretin (Glu42Asp) associated with sporadic late-onset cardiac amyloidosis. Dupuy O; Blétry O; Blanc AS; Droz D; Viémont M; Delpech M; Grateau G Amyloid; 1998 Dec; 5(4):285-7. PubMed ID: 10036587 [TBL] [Abstract][Full Text] [Related]