243 related articles for article (PubMed ID: 1407590)
1. 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]
2. 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]
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. Familial amyloidotic polyneuropathy: report of patients heterozygous for the transthyretin Gly42 gene.
Murakami T; Yi S; Yamamoto K; Maruyama S; Araki S
Ann Neurol; 1992 Mar; 31(3):340-2. PubMed ID: 1637142
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. [Three siblings homozygous for the transthyretin-Met30 gene in familial amyloidotic polyneuropathy--evaluation of their clinical pictures with reference to those of other 10 cases reported].
Yoshinaga T; Nakazato M; Ikeda S; Ohnishi A
Rinsho Shinkeigaku; 1994 Feb; 34(2):99-105. PubMed ID: 8194279
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Systemic amyloidosis in transgenic mice carrying the human mutant transthyretin (Met30) gene. Pathologic similarity to human familial amyloidotic polyneuropathy, type I.
Yi S; Takahashi K; Naito M; Tashiro F; Wakasugi S; Maeda S; Shimada K; Yamamura K; Araki S
Am J Pathol; 1991 Feb; 138(2):403-12. PubMed ID: 1992765
[TBL] [Abstract][Full Text] [Related]
11. Homozygosity for the met30 transthyretin gene in a Turkish kindred with familial amyloidotic polyneuropathy.
Skare J; Yazici H; Erken E; Dede H; Cohen A; Milunsky A; Skinner M
Hum Genet; 1990 Nov; 86(1):89-90. PubMed ID: 2174830
[TBL] [Abstract][Full Text] [Related]
12. Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features.
Misu Ki; Hattori N; Nagamatsu M; Ikeda Si; Ando Y; Nakazato M; Takei Yi; Hanyu N; Usui Y; Tanaka F; Harada T; Inukai A; Hashizume Y; Sobue G
Brain; 1999 Oct; 122 ( Pt 10)():1951-62. PubMed ID: 10506096
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Familial amyloid polyneuropathy: alanine-for-threonine substitution in the transthyretin (prealbumin) molecule.
Koeppen AH; Wallace MR; Benson MD; Altland K
Muscle Nerve; 1990 Nov; 13(11):1065-75. PubMed ID: 2122246
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Familial amyloidotic polyneuropathy: a new transthyretin position 30 mutation (alanine for valine) in a family of German descent.
Jones LA; Skare JC; Cohen AS; Harding JA; Milunsky A; Skinner M
Clin Genet; 1992 Feb; 41(2):70-3. PubMed ID: 1544214
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel transthyretin variant (Val30----Leu) associated with familial amyloidotic polyneuropathy.
Nakazato M; Ikeda S; Shiomi K; Matsukura S; Yoshida K; Shimizu H; Atsumi T; Kangawa K; Matsuo H
FEBS Lett; 1992 Jul; 306(2-3):206-8. PubMed ID: 1633877
[TBL] [Abstract][Full Text] [Related]
19. Type I familial amyloidotic polyneuropathy in Japan.
Nakazato M; Shiomi K; Miyazato M; Matsukura S
Intern Med; 1992 Dec; 31(12):1335-8. PubMed ID: 1300167
[TBL] [Abstract][Full Text] [Related]
20. Vitreous amyloidosis associated with homozygosity for the transthyretin methionine-30 gene.
Sandgren O; Holmgren G; Lundgren E
Arch Ophthalmol; 1990 Nov; 108(11):1584-6. PubMed ID: 1978774
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
