398 related articles for article (PubMed ID: 3011930)
1. 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]
2. 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]
3. 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]
4. Familial amyloidotic polyneuropathy: transthyretin (prealbumin) variants in kindreds of Italian origin.
Saraiva MJ; Costa PP; Almeida Mdo R; Banzhoff A; Altland K; Ferlini A; Rubboli G; Plasmati R; Tassinari CA; Romeo G
Hum Genet; 1988 Dec; 80(4):341-3. PubMed ID: 2848756
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Homozygosity for the transthyretin-met30-gene in two Swedish sibs with familial amyloidotic polyneuropathy.
Holmgren G; Haettner E; Nordenson I; Sandgren O; Steen L; Lundgren E
Clin Genet; 1988 Nov; 34(5):333-8. PubMed ID: 3229002
[TBL] [Abstract][Full Text] [Related]
7. Studies on plasma transthyretin (prealbumin) in familial amyloidotic polyneuropathy, Portuguese type.
Saraiva MJ; Costa PP; Goodman DS
J Lab Clin Med; 1983 Oct; 102(4):590-603. PubMed ID: 6311926
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. 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]
11. Simplified method for screening populations at risk for transthyretin Met30-associated familial amyloidotic polyneuropathy.
Saraiva MJ; Alves IL; Costa PP
Clin Chem; 1989 Jun; 35(6):1033-5. PubMed ID: 2543515
[TBL] [Abstract][Full Text] [Related]
12. Structure of Met30 variant of transthyretin and its amyloidogenic implications.
Terry CJ; Damas AM; Oliveira P; Saraiva MJ; Alves IL; Costa PP; Matias PM; Sakaki Y; Blake CC
EMBO J; 1993 Feb; 12(2):735-41. PubMed ID: 8382610
[TBL] [Abstract][Full Text] [Related]
13. Proline at position 36: a new transthyretin mutation associated with familial amyloidotic polyneuropathy.
Jones LA; Skare JC; Harding JA; Cohen AS; Milunsky A; Skinner M
Am J Hum Genet; 1991 May; 48(5):979-82. PubMed ID: 1850191
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Diagnostic radioimmunoassay and DNA-analysis in Swedish and Japanese patients with familial amyloidotic polyneuropathy. Homozygosity for the TTR met30 gene.
Holmgren G; Lundgren E; Kangawa K; Kurihara T; Matsukura S; Matsuo H; Nakazato M; Steen L
Acta Neurol Scand; 1993 Feb; 87(2):124-7. PubMed ID: 8095120
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Presence of an abnormal transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy.
Saraiva MJ; Costa PP; Birken S; Goodman DS
Trans Assoc Am Physicians; 1983; 96():261-70. PubMed ID: 6208668
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy.
Nakazato M; Sasaki H; Furuya H; Sakaki Y; Kurihara T; Matsukura S; Kangawa K; Matsuo H
Ann Neurol; 1987 Jun; 21(6):596-8. PubMed ID: 3037992
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
