These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
12. Hereditary amyloidosis with progressive peripheral neuropathy associated with apolipoprotein AI Gly26Arg: outcome of hepatorenal transplantation. Testro AG; Brennan SO; Macdonell RA; Hawkins PN; Angus PW Liver Transpl; 2007 Jul; 13(7):1028-31. PubMed ID: 17600344 [TBL] [Abstract][Full Text] [Related]
13. New clinical forms of hereditary apoA-I amyloidosis entail both glomerular and retinal amyloidosis. Colombat M; Aldigier JC; Rothschild PR; Javaugue V; Desport E; Frouget T; Goujon JM; Rioux-Leclercq N; Quellard N; Rerolle JP; Paraf F; Beugnet C; Tiple A; Durrbach A; Samuel D; Brézin A; Bridoux F; Valleix S Kidney Int; 2020 Jul; 98(1):195-208. PubMed ID: 32571483 [TBL] [Abstract][Full Text] [Related]
14. Tubulointerstitial nephritis is a dominant feature of hereditary apolipoprotein A-I amyloidosis. Gregorini G; Izzi C; Ravani P; Obici L; Dallera N; Del Barba A; Negrinelli A; Tardanico R; Nardi M; Biasi L; Scalvini T; Merlini G; Scolari F Kidney Int; 2015 Jun; 87(6):1223-9. PubMed ID: 25565309 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Solid organ transplantation for non-TTR hereditary amyloidosis: report from the 1st International Workshop on the Hereditary Renal Amyloidoses. Stangou AJ; Lobato L; Zeldenrust S; Rela M; Portmann B; Linke RP; Conceicao I; Otto G; Wilczek H; Suhr O; Azoulay D; Grateau G; Picken M; O'Grady J; Heaton N; Ericzon BG; Benson MD Amyloid; 2012 Jun; 19 Suppl 1():81-4. PubMed ID: 22540225 [TBL] [Abstract][Full Text] [Related]
17. Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene. Booth DR; Tan SY; Booth SE; Tennent GA; Hutchinson WL; Hsuan JJ; Totty NF; Truong O; Soutar AK; Hawkins PN; Bruguera M; Caballería J; Solé M; Campistol JM; Pepys MB J Clin Invest; 1996 Jun; 97(12):2714-21. PubMed ID: 8675681 [TBL] [Abstract][Full Text] [Related]
18. Amyloidogenic mutations in human apolipoprotein A-I are not necessarily destabilizing - a common mechanism of apolipoprotein A-I misfolding in familial amyloidosis and atherosclerosis. Das M; Mei X; Jayaraman S; Atkinson D; Gursky O FEBS J; 2014 Jun; 281(11):2525-42. PubMed ID: 24702826 [TBL] [Abstract][Full Text] [Related]