281 related articles for article (PubMed ID: 19018796)
1. Mitochondrial haplogroup is associated with the phenotype of familial amyloidosis with polyneuropathy in Swedish and French patients.
Olsson M; Hellman U; Planté-Bordeneuve V; Jonasson J; Lång K; Suhr OB
Clin Genet; 2009 Feb; 75(2):163-8. PubMed ID: 19018796
[TBL] [Abstract][Full Text] [Related]
2. 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]
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. Modeling familial amyloidotic polyneuropathy (Transthyretin V30M) in Drosophila melanogaster.
Berg I; Thor S; Hammarström P
Neurodegener Dis; 2009; 6(3):127-38. PubMed ID: 19372706
[TBL] [Abstract][Full Text] [Related]
5. Epidemiology of familial amyloid polyneuropathy in Japan: Identification of a novel endemic focus.
Kato-Motozaki Y; Ono K; Shima K; Morinaga A; Machiya T; Nozaki I; Shibata-Hamaguchi A; Furukawa Y; Yanase D; Ishida C; Sakajiri K; Yamada M
J Neurol Sci; 2008 Jul; 270(1-2):133-40. PubMed ID: 18410945
[TBL] [Abstract][Full Text] [Related]
6. Distinct characteristics of amyloid deposits in early- and late-onset transthyretin Val30Met familial amyloid polyneuropathy.
Koike H; Ando Y; Ueda M; Kawagashira Y; Iijima M; Fujitake J; Hayashi M; Yamamoto M; Mukai E; Nakamura T; Katsuno M; Hattori N; Sobue G
J Neurol Sci; 2009 Dec; 287(1-2):178-84. PubMed ID: 19709674
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Regional differences and similarities of FAP in Sweden.
Hellman U; Suhr O
Amyloid; 2012 Jun; 19 Suppl 1():53-4. PubMed ID: 22468675
[TBL] [Abstract][Full Text] [Related]
9. Epidemiological, clinical and genetic study of familial amyloidotic polyneuropathy in Cyprus.
Dardiotis E; Koutsou P; Papanicolaou EZ; Vonta I; Kladi A; Vassilopoulos D; Hadjigeorgiou G; Christodoulou K; Kyriakides T
Amyloid; 2009 Mar; 16(1):32-7. PubMed ID: 19291512
[TBL] [Abstract][Full Text] [Related]
10. Myocardial hypertrophy and function are related to age at onset in familial amyloidotic polyneuropathy.
Suhr OB; Lindqvist P; Olofsson BO; Waldenström A; Backman C
Amyloid; 2006 Sep; 13(3):154-9. PubMed ID: 17062381
[TBL] [Abstract][Full Text] [Related]
11. A Swedish family with the rare Phe33Leu transthyretin mutation.
Holmgren G; Hellman U; Jonasson J; Lundgren HE; Westermark P; Suhr OB
Amyloid; 2005 Sep; 12(3):189-92. PubMed ID: 16194875
[TBL] [Abstract][Full Text] [Related]
12. Regional difference and similarity of familial amyloidosis with polyneuropathy in France.
Adams D; Lozeron P; Theaudin M; Mincheva Z; Cauquil C; Adam C; Signate A; Vial C; Maisonobe T; Delmont E; Franques J; Vallat JM; Sole G; Pereon Y; Lacour A; Echaniz-Laguna A; Misrahi M; Lacroix C;
Amyloid; 2012 Jun; 19 Suppl 1():61-4. PubMed ID: 22620968
[TBL] [Abstract][Full Text] [Related]
13. Continuous development of arrhythmia is observed in Swedish transplant patients with familial amyloidotic polyneuropathy (amyloidogenic transthyretin Val30Met variant).
Okamoto S; Hörnsten R; Obayashi K; Wijayatunga P; Suhr OB
Liver Transpl; 2011 Feb; 17(2):122-8. PubMed ID: 21280184
[TBL] [Abstract][Full Text] [Related]
14. [Application to transthyretin analysis].
Ueda M; Ando Y
Rinsho Byori; 2006 Jun; 54(6):601-8. PubMed ID: 16872010
[TBL] [Abstract][Full Text] [Related]
15. Late-onset familial amyloid polyneuropathy in Japan.
Koike H; Sobue G
Amyloid; 2012 Jun; 19 Suppl 1():55-7. PubMed ID: 22506939
[TBL] [Abstract][Full Text] [Related]
16. Diagnostic pitfalls in sporadic transthyretin familial amyloid polyneuropathy (TTR-FAP).
Planté-Bordeneuve V; Ferreira A; Lalu T; Zaros C; Lacroix C; Adams D; Said G
Neurology; 2007 Aug; 69(7):693-8. PubMed ID: 17698792
[TBL] [Abstract][Full Text] [Related]
17. Clinicopathologic and genetic features of early- and late-onset FAP type I (FAP ATTR Val30Met) in Japan.
Sobue G; Koike H; Misu K; Hattori N; Yamamoto M; Ikeda S; Ando Y; Nakazato M; Inukai A
Amyloid; 2003 Aug; 10 Suppl 1():32-8. PubMed ID: 14640040
[TBL] [Abstract][Full Text] [Related]
18. Cardiac phenotype and clinical outcome of familial amyloid polyneuropathy associated with transthyretin alanine 60 variant.
Sattianayagam PT; Hahn AF; Whelan CJ; Gibbs SD; Pinney JH; Stangou AJ; Rowczenio D; Pflugfelder PW; Fox Z; Lachmann HJ; Wechalekar AD; Hawkins PN; Gillmore JD
Eur Heart J; 2012 May; 33(9):1120-7. PubMed ID: 21992998
[TBL] [Abstract][Full Text] [Related]
19. Analysis of mitochondrial haplogroups associated with TTR Val30Ala familial amyloidotic polyneuropathy in Chinese patients.
Liu JY; Jiang XM; Zhang M; Guo YJ
Int J Neurosci; 2012 Dec; 122(12):716-8. PubMed ID: 22784244
[TBL] [Abstract][Full Text] [Related]
20. [Clinical phenotype of Charcot-Marie-Tooth disease (CMT) and familial amyloid polyneuropathy (FAP)].
Sobue G
Rinsho Shinkeigaku; 2003 Nov; 43(11):769-74. PubMed ID: 15152460
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
