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25. Lattice corneal dystrophy type II with familial amyloid polyneuropathy type IV. Asaoka T; Amano S; Sunada Y; Sawa M Jpn J Ophthalmol; 1993; 37(4):426-31. PubMed ID: 8145387 [TBL] [Abstract][Full Text] [Related]
28. Clinical value of immunohistochemistry with AF-antibody in the diagnosis of familial amyloid neuropathy. Feurle GE; Linke RP; Kuhn E; Wagner A J Neurol; 1984; 231(5):237-43. PubMed ID: 6394723 [TBL] [Abstract][Full Text] [Related]
29. Presence of an abnormal transthyretin (prealbumin) in Portuguese patients with familial amyloidotic polyneuropathy. Saraiva MJ; Costa PP; Birken S; Goodman DS Trans Assoc Am Physicians; 1983; 96():261-70. PubMed ID: 6208668 [TBL] [Abstract][Full Text] [Related]
30. Immunohistochemical analysis of lattice corneal dystrophies types I and II. Kivelä T; Tarkkanen A; McLean I; Ghiso J; Frangione B; Haltia M Br J Ophthalmol; 1993 Dec; 77(12):799-804. PubMed ID: 8110676 [TBL] [Abstract][Full Text] [Related]
31. [Diagnosis of familial amyloid polyneuropathy--gene analysis with primer-directed enzymatic amplification of DNA, isolation of plasma variant prealbumin and immunohistochemical identification of tissue amyloid protein]. Ikeda S; Nakano T; Yanagisawa N; Hanyu N; Suzuki T; Sakaki Y Rinsho Shinkeigaku; 1991 Apr; 31(4):363-71. PubMed ID: 1655325 [TBL] [Abstract][Full Text] [Related]
32. Characterization of a transthyretin (prealbumin) variant associated with familial amyloidotic polyneuropathy type II (Indiana/Swiss). Dwulet FE; Benson MD J Clin Invest; 1986 Oct; 78(4):880-6. PubMed ID: 3760189 [TBL] [Abstract][Full Text] [Related]