PubMed

Early onset vitreous amyloidosis in familial amyloidotic polyneuropathy with a transthyretin Glu54Gly mutation is associated with elevated vitreous VEGF.

O'Hearn TM, Fawzi A, He S, Rao NA, Lim JI.

Br J Ophthalmol. 2007 Dec;91(12):1607-9. Epub 2007 May 23.PMID: 17522146 [PubMed - indexed for MEDLINE]Related articles

Oculoleptomeningeal amyloidosis in a patient with a TTR Val30Gly mutation in the transthyretin gene.

Roe RH, Fisher Y, Eagle RC Jr, Fine HF, Cunningham ET Jr.

Ophthalmology. 2007 Nov;114(11):e33-7.PMID: 17980738 [PubMed - indexed for MEDLINE]Related articles

Characterisation and management of vitreous and nerve amyloid in familial amyloid polyneuropathy due to variant transthyretin, Phe33Val.

Gregory ME, Carey M, Hawkins PN, Banerjee S, Gillmore JD.

Br J Ophthalmol. 2008 Jan;92(1):34-5, 142. No abstract available. PMID: 18156374 [PubMed - indexed for MEDLINE]Related articles

Secondary glaucoma in patients with familial amyloidotic polyneuropathy.

Kimura A, Ando E, Fukushima M, Koga T, Hirata A, Arimura K, Ando Y, Negi A, Tanihara H.

Arch Ophthalmol. 2003 Mar;121(3):351-6.PMID: 12617705 [PubMed - indexed for MEDLINE]Related articles

Vitreous opacities and outcome of vitreous surgery in patients with familial amyloidotic polyneuropathy.

Koga T, Ando E, Hirata A, Fukushima M, Kimura A, Ando Y, Negi A, Tanihara H.

Am J Ophthalmol. 2003 Feb;135(2):188-93.PMID: 12566023 [PubMed - indexed for MEDLINE]Related articles

Vitreous amyloidosis in familial amyloidotic polyneuropathy. Report of a case with the Val30Met transthyretin mutation.

Ciulla TA, Tolentino F, Morrow JF, Dryja TP.

Surv Ophthalmol. 1995 Nov-Dec;40(3):197-206. Review.PMID: 8599155 [PubMed - indexed for MEDLINE]Related articles

An aggressive form of familial amyloid polyneuropathy caused by a Glu54Gly mutation in the transthyretin gene.

Kim HS, Kim SM, Kang SW, Jung SC, Lee KS, Kim TS, Choi YC.

Eur J Neurol. 2005 Aug;12(8):657-9.PMID: 16053476 [PubMed - indexed for MEDLINE]Related articles

A case of vitreous amyloidosis without systemic symptoms in familial amyloidotic polyneuropathy.

Kawaji T, Ando Y, Ando E, Nakamura M, Hirata A, Tanihara H.

Amyloid. 2004 Dec;11(4):257-9.PMID: 15678760 [PubMed - indexed for MEDLINE]Related articles

Ocular amyloid angiopathy associated with familial amyloidotic polyneuropathy caused by amyloidogenic transthyretin Y114C.

Kawaji T, Ando Y, Nakamura M, Yamashita T, Wakita M, Ando E, Hirata A, Tanihara H.

Ophthalmology. 2005 Dec;112(12):2212. Epub 2005 Oct 12.PMID: 16225929 [PubMed - indexed for MEDLINE]Related articles

Oculoleptomeningeal amyloidosis in 3 individuals with the transthyretin variant Tyr69His.

Schweitzer K, Ehmann D, Garcia R, Alport E.

Can J Ophthalmol. 2009 Jun;44(3):317-9.PMID: 19491989 [PubMed - indexed for MEDLINE]Related articlesFree article

Transthyretin Ala97Ser in Chinese-Taiwanese patients with familial amyloid polyneuropathy: genetic studies and phenotype expression.

Liu YT, Lee YC, Yang CC, Chen ML, Lin KP.

J Neurol Sci. 2008 Apr 15;267(1-2):91-9. Epub 2007 Nov 26.PMID: 18022643 [PubMed - indexed for MEDLINE]Related articles

Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: a clinicopathologic study.

Motozaki Y, Sugiyama Y, Ishida C, Komai K, Matsubara S, Yamada M.

J Neurol Sci. 2007 Sep 15;260(1-2):236-9. Epub 2007 Apr 26.PMID: 17466336 [PubMed - indexed for MEDLINE]Related articles

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 15;270(1-2):133-40. Epub 2008 Apr 14.PMID: 18410945 [PubMed - indexed for MEDLINE]Related articles

Vitreous amyloidosis after liver transplantation in patients with familial amyloid polyneuropathy: ocular synthesis of mutant transthyretin.

Munar-Qués M, Salva-Ladaria L, Mulet-Perera P, Solé M, López-Andreu FR, Saraiva MJ.

Amyloid. 2000 Dec;7(4):266-9.PMID: 11132095 [PubMed - indexed for MEDLINE]Related articles

Clinical picture and outcome of transthyretin-related familial amyloid polyneuropathy (FAP) in Japanese patients.

Ikeda S.

Clin Chem Lab Med. 2002 Dec;40(12):1257-61. Review.PMID: 12553427 [PubMed - indexed for MEDLINE]Related articles

Late-onset familial amyloid polyneuropathy (FAP) Val30Met without family history.

Rudolph T, Kurz MW, Farbu E.

Clin Med Res. 2008 Sep;6(2):80-2. Epub 2008 Jul 7.PMID: 18606975 [PubMed - indexed for MEDLINE]Related articlesFree article

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. Epub 2008 Nov 1.PMID: 19018796 [PubMed - indexed for MEDLINE]Related articles

Familial amyloid polyneuropathy with genetic anticipation associated to a gly47glu transthyretin variant in an Italian kindred.

Pelo E, Da Prato L, Ciaccheri M, Castelli G, Gori F, Pizzi A, Torricelli F, Marconi G.

Amyloid. 2002 Mar;9(1):35-41.PMID: 12000196 [PubMed - indexed for MEDLINE]Related articles

An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy.

Frigerio R, Fabrizi GM, Ferrarini M, Cavallaro T, Brighina L, Santoro P, Agostoni E, Cavaletti G, Rizzuto N, Ferrarese C.

Amyloid. 2004 Jun;11(2):121-4.PMID: 15478468 [PubMed - indexed for MEDLINE]Related articles

Familial transthyretin-type amyloid polyneuropathy in Japan: clinical and genetic heterogeneity.

Ikeda S, Nakazato M, Ando Y, Sobue G.

Neurology. 2002 Apr 9;58(7):1001-7. Review.PMID: 11940682 [PubMed - indexed for MEDLINE]Related articles