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5. Biochemical and genetic characterization of type I familial amyloidotic polyneuropathy. Nakazato M; Sasaki H; Furuya H; Sakaki Y; Kurihara T; Matsukura S; Kangawa K; Matsuo H Ann Neurol; 1987 Jun; 21(6):596-8. PubMed ID: 3037992 [TBL] [Abstract][Full Text] [Related]
6. Prenatal detection of a gene for hereditary amyloidosis. Nichols WC; Padilla LM; Benson MD Am J Med Genet; 1989 Dec; 34(4):520-4. PubMed ID: 2516414 [TBL] [Abstract][Full Text] [Related]
7. Molecular detection of carriers of hereditary amyloidosis in a Swedish-American family. Wallace MR; Conneally PM; Long GL; Benson MD Am J Med Genet; 1986 Oct; 25(2):335-41. PubMed ID: 2877582 [TBL] [Abstract][Full Text] [Related]
15. Non-senile wild-type transthyretin systemic amyloidosis presenting as bilateral carpal tunnel syndrome. Kodaira M; Sekijima Y; Tojo K; Tsuchiya A; Yazaki M; Ikeda S; Sekijima Y; Hoshii Y; Tachibana S J Peripher Nerv Syst; 2008 Jun; 13(2):148-50. PubMed ID: 18601659 [No Abstract] [Full Text] [Related]
16. [Diagnosis by recombinant DNA techniques and clinical features of familial amyloid polyneuropathy]. Harada T No To Shinkei; 1988 Jul; 40(7):617-21. PubMed ID: 2852018 [TBL] [Abstract][Full Text] [Related]
17. [Identification of genetic carriers in familial amyloidosis with polyneuropathy is possible with the DNA technic]. Holmgren G; Drugge U; Lundgren E; Sandgren O; Steen L Lakartidningen; 1988 Nov; 85(44):3677-9. PubMed ID: 2904519 [No Abstract] [Full Text] [Related]
18. A case of late onset cardiac amyloidosis with a new transthyretin variant (lysine 92). Saito F; Nakazato M; Akiyama H; Kitahara Y; Date Y; Iwasaki Y; Harasawa S; Hisaki R; Horie T; Kinukawa N; Watanabe T; Sakamaki T; Yagi H; Hoshii Y; Yutani C; Kanmatsuse K Hum Pathol; 2001 Feb; 32(2):237-9. PubMed ID: 11230714 [TBL] [Abstract][Full Text] [Related]