110 related articles for article (PubMed ID: 25510352)
1. Most recent common ancestor of TTR Val30Met mutation in Italian population and its potential role in genotype-phenotype correlation.
Iorio A; De Angelis F; Di Girolamo M; Luigetti M; Pradotto L; Mauro A; Manfellotto D; Fuciarelli M; Polimanti R
Amyloid; 2015; 22(2):73-8. PubMed ID: 25510352
[TBL] [Abstract][Full Text] [Related]
2. On the origin of the transthyretin Val30Met familial amyloid polyneuropathy.
Zaros C; Genin E; Hellman U; Saporta MA; Languille L; Wadington-Cruz M; Suhr O; Misrahi M; Planté-Bordeneuve V
Ann Hum Genet; 2008 Jul; 72(Pt 4):478-84. PubMed ID: 18460047
[TBL] [Abstract][Full Text] [Related]
3. Haplotypes and DNA sequence variation within and surrounding the transthyretin gene: genotype-phenotype correlations in familial amyloid polyneuropathy (V30M) in Portugal and Sweden.
Soares ML; Coelho T; Sousa A; Holmgren G; Saraiva MJ; Kastner DL; Buxbaum JN
Eur J Hum Genet; 2004 Mar; 12(3):225-37. PubMed ID: 14673473
[TBL] [Abstract][Full Text] [Related]
4. Origin of sporadic late-onset hereditary ATTR Val30Met amyloidosis in Japan.
Ueda M; Yamashita T; Misumi Y; Masuda T; Ando Y
Amyloid; 2018 Sep; 25(3):143-147. PubMed ID: 30486687
[TBL] [Abstract][Full Text] [Related]
5. Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis.
Iorio A; De Angelis F; Di Girolamo M; Luigetti M; Pradotto LG; Mazzeo A; Frusconi S; My F; Manfellotto D; Fuciarelli M; Polimanti R
BMC Genomics; 2017 Mar; 18(1):254. PubMed ID: 28335735
[TBL] [Abstract][Full Text] [Related]
6. Haplotype analysis of common transthyretin mutations.
Almeida MR; Aoyama-Oishi N; Sakaki Y; Holmgren G; Ulf D; Ferlini A; Salvi F; Munar-Oués M; Benson MD; Skinner M
Hum Genet; 1995 Sep; 96(3):350-4. PubMed ID: 7649556
[TBL] [Abstract][Full Text] [Related]
7. Non-coding variants contribute to the clinical heterogeneity of TTR amyloidosis.
Iorio A; De Lillo A; De Angelis F; Di Girolamo M; Luigetti M; Sabatelli M; Pradotto L; Mauro A; Mazzeo A; Stancanelli C; Perfetto F; Frusconi S; My F; Manfellotto D; Fuciarelli M; Polimanti R
Eur J Hum Genet; 2017 Sep; 25(9):1055-1060. PubMed ID: 28635949
[TBL] [Abstract][Full Text] [Related]
8. Functional variation of the transthyretin gene among human populations and its correlation with amyloidosis phenotypes.
Polimanti R; Di Girolamo M; Manfellotto D; Fuciarelli M
Amyloid; 2013 Dec; 20(4):256-62. PubMed ID: 24111657
[TBL] [Abstract][Full Text] [Related]
9. A natural history analysis of asymptomatic
Coelho T; Conceição I; Waddington-Cruz M; Keohane D; Sultan MB; Chapman D; Amass L;
Amyloid; 2022 Dec; 29(4):228-236. PubMed ID: 35730447
[TBL] [Abstract][Full Text] [Related]
10. Liver transplantation for hereditary transthyretin amyloidosis.
Suhr OB; Herlenius G; Friman S; Ericzon BG
Liver Transpl; 2000 May; 6(3):263-76. PubMed ID: 10827225
[TBL] [Abstract][Full Text] [Related]
11. THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis.
Coelho T; Maurer MS; Suhr OB
Curr Med Res Opin; 2013 Jan; 29(1):63-76. PubMed ID: 23193944
[TBL] [Abstract][Full Text] [Related]
12. Heterogeneity of penetrance in familial amyloid polyneuropathy, ATTR Val30Met, in the Swedish population.
Hellman U; Alarcon F; Lundgren HE; Suhr OB; Bonaiti-Pellié C; Planté-Bordeneuve V
Amyloid; 2008 Sep; 15(3):181-6. PubMed ID: 18925456
[TBL] [Abstract][Full Text] [Related]
13. TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance?
Bonaïti B; Olsson M; Hellman U; Suhr O; Bonaïti-Pellié C; Planté-Bordeneuve V
Eur J Hum Genet; 2010 Aug; 18(8):948-52. PubMed ID: 20234390
[TBL] [Abstract][Full Text] [Related]
14. Familial amyloidotic polyneuropathy type 1 in Brazil is associated with the transthyretin Val30Met variant.
Palácios SA; Bittencourt PL; Cançado EL; Farias AQ; Massarollo PC; Mies S; Kalil J; Goldberg AC
Amyloid; 1999 Dec; 6(4):289-91. PubMed ID: 10611951
[TBL] [Abstract][Full Text] [Related]
15. In silico analysis of TTR gene (coding and non-coding regions, and interactive network) and its implications in transthyretin-related amyloidosis.
Polimanti R; Di Girolamo M; Manfellotto D; Fuciarelli M
Amyloid; 2014 Sep; 21(3):154-62. PubMed ID: 24779883
[TBL] [Abstract][Full Text] [Related]
16. Liver Transplantation for Hereditary Transthyretin Amyloidosis: After 20 Years Still the Best Therapeutic Alternative?
Ericzon BG; Wilczek HE; Larsson M; Wijayatunga P; Stangou A; Pena JR; Furtado E; Barroso E; Daniel J; Samuel D; Adam R; Karam V; Poterucha J; Lewis D; Ferraz-Neto BH; Cruz MW; Munar-Ques M; Fabregat J; Ikeda S; Ando Y; Heaton N; Otto G; Suhr O
Transplantation; 2015 Sep; 99(9):1847-54. PubMed ID: 26308415
[TBL] [Abstract][Full Text] [Related]
17. Screening and biochemical characterization of transthyretin variants in the Portuguese population.
Alves IL; Altland K; Almeida MR; Winter P; Saraiva MJ
Hum Mutat; 1997; 9(3):226-33. PubMed ID: 9090525
[TBL] [Abstract][Full Text] [Related]
18. Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met.
Dardiotis E; Koutsou P; Zamba-Papanicolaou E; Vonta I; Hadjivassiliou M; Hadjigeorgiou G; Cariolou M; Christodoulou K; Kyriakides T
J Neurol Sci; 2009 Sep; 284(1-2):158-62. PubMed ID: 19493541
[TBL] [Abstract][Full Text] [Related]
19. Transthyretin familial amyloid polyneuropathy.
Planté-Bordeneuve V; Kerschen P
Handb Clin Neurol; 2013; 115():643-58. PubMed ID: 23931808
[TBL] [Abstract][Full Text] [Related]
20. Cysteine 10 is a key residue in amyloidogenesis of human transthyretin Val30Met.
Takaoka Y; Ohta M; Miyakawa K; Nakamura O; Suzuki M; Takahashi K; Yamamura K; Sakaki Y
Am J Pathol; 2004 Jan; 164(1):337-45. PubMed ID: 14695346
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]