204 related articles for article (PubMed ID: 3379433)
1. Familial amyloidotic polyneuropathy without familial occurrence: carrier detection by the radioimmunoassay of variant transthyretin.
Tanaka M; Hirai S; Matsubara E; Okamoto K; Morimatsu M; Nakazato M
J Neurol Neurosurg Psychiatry; 1988 Apr; 51(4):576-8. PubMed ID: 3379433
[TBL] [Abstract][Full Text] [Related]
2. Asymptomatic homozygous gene carrier in a family with type I familial amyloid polyneuropathy.
Ikeda S; Nakano T; Yanagisawa N; Nakazato M; Tsukagoshi H
Eur Neurol; 1992; 32(6):308-13. PubMed ID: 1490495
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. An Italian family with Ala-47 transthyretin mutation associated with cardiomyopathy and polyneuropathy.
Solaro C; Schenone A; Di Sapio A; Pradotto L; Mancardi GL; Primavera A; Mauro A
Neuromuscul Disord; 2000 Jan; 10(1):52-5. PubMed ID: 10677864
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Familial amyloidotic polyneuropathy (ATTR Ser50Ile): the first autopsy case report.
Sakashita N; Ando Y; Obayashi K; Terazaki H; Yamashita T; Takei M; Kinjo M; Takahashi K
Virchows Arch; 2000 Apr; 436(4):345-50. PubMed ID: 10834537
[TBL] [Abstract][Full Text] [Related]
7. [Familial amyloidotic polyneuropathy without familial occurrence but with asymptomatic carriers discovered by radioimmunoassay of variant transthyretin].
Matsubara E; Tanaka M; Hirai S; Okamoto K; Nakazato M
Rinsho Shinkeigaku; 1988 Mar; 28(3):275-9. PubMed ID: 2841056
[No Abstract] [Full Text] [Related]
8. 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]
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. [A late onset familial amyloidotic polyneuropathy (FAP) with a novel variant transthyretin characterized by a basic-for-acidic amino acid substitution (Glu61-->Lys)].
Yamamoto T; Matsunaga K; Ohnishi A; Nakazato M; Murai Y
Rinsho Shinkeigaku; 1996 Sep; 36(9):1065-8. PubMed ID: 8976129
[TBL] [Abstract][Full Text] [Related]
11. Diagnostic radioimmunoassay for familial amyloidotic polyneuropathy before clinical onset.
Nakazato M; Kurihara T; Matsukura S; Kangawa K; Matsuo H
J Clin Invest; 1986 May; 77(5):1699-703. PubMed ID: 3457802
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Abnormal transthyretin in asymptomatic relatives in familial amyloidotic polyneuropathy.
Nakazato M; Tanaka M; Yamamura Y; Kurihara T; Matsukura S; Kangawa K; Matsuo H
Arch Neurol; 1987 Dec; 44(12):1275-8. PubMed ID: 2823755
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Familial amyloid polyneuropathy related to transthyretin Gly42 in a Japanese family.
Uemichi T; Ueno S; Fujimura H; Umekage T; Yorifuji S; Matsuzawa Y; Tarui S
Muscle Nerve; 1992 Aug; 15(8):904-11. PubMed ID: 1353861
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. 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]
20. 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]
[Next] [New Search]