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2. Prenatal diagnosis of hereditary amyloidosis in a Portuguese family living in France. Lucotte G; Berriche S; David F; Rouquet H; Turpin JC Genet Couns; 1993; 4(4):285-7. PubMed ID: 8110416 [TBL] [Abstract][Full Text] [Related]
3. Transthyretin VAL107, a new variant associated with familial cardiac and neuropathic amyloidosis. Jacobson DR; Gertz MA; Buxbaum JN Hum Mutat; 1994; 3(4):399-401. PubMed ID: 8081397 [No Abstract] [Full Text] [Related]
10. 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]
11. A case of hereditary amyloidosis transthyretin variant Met 30 with amyloid cardiomyopathy, less polyneuropathy, and the presence of giant cells. Nakamura Y; Yutani C; Nakazato M; Date Y; Baba T; Goto Y Pathol Int; 1999 Oct; 49(10):898-902. PubMed ID: 10571824 [TBL] [Abstract][Full Text] [Related]
15. [Indications for simultaneous origin of a German and American family with type II hereditary amyloid neuropathy]. Seddigh S; Dahmen N; Goebel HH; Hopf HC; Benson MD Nervenarzt; 1999 Oct; 70(10):899-902. PubMed ID: 10554781 [TBL] [Abstract][Full Text] [Related]
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17. [Meretoja syndrome: Identification of a family and description of the corneal involvement by confocal microscopy]. Bonnin N; Borel A; Daniel E; Tiple A; Joubert R; Heng AE; Chiambaretta F J Fr Ophtalmol; 2015 Jun; 38(6):e111-5. PubMed ID: 25913657 [No Abstract] [Full Text] [Related]
18. [Variant transthyretin genes associated with familial amyloid polyneuropathy]. Ueno S No To Shinkei; 1994 May; 46(5):415-23. PubMed ID: 8060680 [No Abstract] [Full Text] [Related]
19. Hereditary amyloidosis: some words on the history and present status of our eminent subject. Benson MD Amyloid; 2000 Mar; 7(1):15-6. PubMed ID: 10842698 [No Abstract] [Full Text] [Related]
20. 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] [Next] [New Search]