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24. A new genetic variant of hereditary apolipoprotein A-I amyloidosis: a case-report followed by discussion of diagnostic challenges and therapeutic options. Moutafi M; Ziogas DC; Michopoulos S; Bagratuni T; Vasileiou V; Verga L; Merlini G; Palladini G; Matsouka C; Dimopoulos MA; Kastritis E BMC Med Genet; 2019 Jan; 20(1):23. PubMed ID: 30665372 [TBL] [Abstract][Full Text] [Related]
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26. Cardiac amyloidosis with the E526V mutation of the fibrinogen A alpha-chain. Mourad G; Delabre JP; Garrigue V N Engl J Med; 2008 Dec; 359(26):2847-8. PubMed ID: 19109585 [No Abstract] [Full Text] [Related]
27. Prevalence of germline mutations in the TTR gene in a consecutive series of surgical pathology specimens with ATTR amyloid. Eriksson M; Büttner J; Todorov T; Yumlu S; Schönland S; Hegenbart U; Kristen AV; Dengler T; Lohse P; Helmke B; Schmidt H; Röcken C Am J Surg Pathol; 2009 Jan; 33(1):58-65. PubMed ID: 18830126 [TBL] [Abstract][Full Text] [Related]
28. Infertility and hypergonadotropic hypogonadism as first evidence of hereditary apolipoprotein A-I amyloidosis. Scalvini T; Martini PR; Obici L; Tardanico R; Biasi L; Gregorini G; Scolari F; Merlini G J Urol; 2007 Jul; 178(1):344-8. PubMed ID: 17507040 [TBL] [Abstract][Full Text] [Related]
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