250 related articles for article (PubMed ID: 1626570)
1. A Danish kindred with familial amyloid cardiomyopathy revisited: identification of a mutant transthyretin-methionine111 variant in serum from patients and carriers.
Ranløv I; Alves IL; Ranløv PJ; Husby G; Costa PP; Saraiva MJ
Am J Med; 1992 Jul; 93(1):3-8. PubMed ID: 1626570
[TBL] [Abstract][Full Text] [Related]
2. Molecular diagnosis of the transthyretin (TTR) Met111 mutation in familial amyloid cardiomyopathy of Danish origin.
Nordvåg BY; Husby G; Ranløv I; el-Gewely MR
Hum Genet; 1992 Jun; 89(4):459-61. PubMed ID: 1618497
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. [Hereditary amyloid cardiomyopathy related to a mutation at transthyretin protein number 111. A clinical, genetic and echocardiographic study of an affected Danish family].
Svendsen IH; Steensgaard-Hansen F; Nordvåg BY
Ugeskr Laeger; 1999 Sep; 161(36):4995-9. PubMed ID: 10489791
[TBL] [Abstract][Full Text] [Related]
5. Family studies of the genetic abnormality in transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy.
Saraiva MJ; Birken S; Costa PP; Goodman DS
Ann N Y Acad Sci; 1984; 435():86-100. PubMed ID: 6099706
[TBL] [Abstract][Full Text] [Related]
6. A clinical, echocardiographic and genetic characterization of a Danish kindred with familial amyloid transthyretin methionine 111 linked cardiomyopathy.
Svendsen IH; Steensgaard-Hansen F; Nordvåg BY
Eur Heart J; 1998 May; 19(5):782-9. PubMed ID: 9717013
[TBL] [Abstract][Full Text] [Related]
7. Cardiac amyloidosis: a review and report of a new transthyretin (prealbumin) variant.
Hesse A; Altland K; Linke RP; Almeida MR; Saraiva MJ; Steinmetz A; Maisch B
Br Heart J; 1993 Aug; 70(2):111-5. PubMed ID: 8038017
[TBL] [Abstract][Full Text] [Related]
8. Retrospective molecular detection of Transthyretin Met 111 mutation in a Danish kindred with familial amyloid cardiomyopathy, using DNA from formalin-fixed and paraffin-embedded tissues.
Nordvåg BY; Ranløv I; Riise HM; Husby G; el-Gewely MR
Hum Genet; 1993 Oct; 92(3):265-8. PubMed ID: 8406434
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Glycosaminoglycans in extracts of cardiac amyloid fibrils from familial amyloid cardiomyopathy of Danish origin related to variant transthyretin Met 111.
Magnus JH; Stenstad T; Kolset SO; Husby G
Scand J Immunol; 1991 Jul; 34(1):63-9. PubMed ID: 2068532
[TBL] [Abstract][Full Text] [Related]
11. Biochemical marker in familial amyloidotic polyneuropathy, Portuguese type. Family studies on the transthyretin (prealbumin)-methionine-30 variant.
Saraiva MJ; Costa PP; Goodman DS
J Clin Invest; 1985 Dec; 76(6):2171-7. PubMed ID: 3908483
[TBL] [Abstract][Full Text] [Related]
12. A case of hereditary amyloidosis transthyretin variant Met 30 with amyloid cardiomyopathy, less polyneuropathy, and the presence of giant cells.
Nakamura Y; Yutani C; Nakazato M; Date Y; Baba T; Goto Y
Pathol Int; 1999 Oct; 49(10):898-902. PubMed ID: 10571824
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Late onset cardiomyopathy as presenting sign of ATTR A45G amyloidosis caused by a novel TTR mutation (p.A65G).
Klaassen SHC; Lemmink HH; Bijzet J; Glaudemans AWJM; Bos R; Plattel W; van den Berg MP; Slart RHJA; Nienhuis HLA; van Veldhuisen DJ; Hazenberg BPC
Cardiovasc Pathol; 2017; 29():19-22. PubMed ID: 28460244
[TBL] [Abstract][Full Text] [Related]
15. Familial amyloidosis in a large Spanish kindred resulting from a D38V mutation in the transthyretin gene.
Augustin S; Llige D; Andreu A; González A; Genescà J
Eur J Clin Invest; 2007 Aug; 37(8):673-8. PubMed ID: 17635579
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. A new transthyretin mutation associated with amyloid cardiomyopathy.
Saraiva MJ; Almeida Mdo R; Sherman W; Gawinowicz M; Costa P; Costa PP; Goodman DS
Am J Hum Genet; 1992 May; 50(5):1027-30. PubMed ID: 1570831
[TBL] [Abstract][Full Text] [Related]
19. A new prealbumin variant in familial amyloid cardiomyopathy of Danish origin.
Nordlie M; Sletten K; Husby G; Ranløv PJ
Scand J Immunol; 1988 Jan; 27(1):119-22. PubMed ID: 3340821
[TBL] [Abstract][Full Text] [Related]
20. Biochemical and molecular genetic characterization of a new variant prealbumin associated with hereditary amyloidosis.
Wallace MR; Dwulet FE; Conneally PM; Benson MD
J Clin Invest; 1986 Jul; 78(1):6-12. PubMed ID: 3722385
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]