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28. Late onset lattice corneal dystrophy with systemic familial amyloidosis, amyloidosis V, in an English family. Stewart HS; Parveen R; Ridgway AE; Bonshek R; Black GC Br J Ophthalmol; 2000 Apr; 84(4):390-4. PubMed ID: 10729296 [TBL] [Abstract][Full Text] [Related]
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31. Clinical and genetical diagnosis of a case of Meretoja syndrome and frontotemporal lifting procedure. Galindo-Bocero J; García-Martínez I; Portillo M; Hernando Acero I; García-González N Arch Soc Esp Oftalmol (Engl Ed); 2022 Oct; 97(10):583-586. PubMed ID: 36114141 [TBL] [Abstract][Full Text] [Related]
32. [Neurological manifestations of AGel amyloidosis (Meretoja's syndrome) in a German family]. Bürmann J; Fassbender K; Henn W; Lohse P; Holzhoffer C; Fassbender K; Dillmann U Fortschr Neurol Psychiatr; 2011 Apr; 79(4):238-41. PubMed ID: 21480154 [TBL] [Abstract][Full Text] [Related]
33. Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: clinical and neurophysiological studies. Conceição I; Sales-Luis ML; De Carvalho M; Evangelista T; Fernandes R; Paunio T; Kangas H; Coutinho P; Neves C; Saraiva MJ Muscle Nerve; 2003 Dec; 28(6):715-21. PubMed ID: 14639586 [TBL] [Abstract][Full Text] [Related]
34. Gelsolin amyloidosis: genetics, biochemistry, pathology and possible strategies for therapeutic intervention. Solomon JP; Page LJ; Balch WE; Kelly JW Crit Rev Biochem Mol Biol; 2012; 47(3):282-96. PubMed ID: 22360545 [TBL] [Abstract][Full Text] [Related]
35. Exclusion of the gelsolin gene on 9q32-34 as the cause of familial lattice corneal dystrophy type I. Wiens A; Marles S; Safneck J; Kwiatkowski DJ; Maury CP; Zelinski T; Philipps S; Ekins MB; Greenberg CR Am J Hum Genet; 1992 Jul; 51(1):156-60. PubMed ID: 1319113 [TBL] [Abstract][Full Text] [Related]
36. [Familial amyloidosis, Finnish type with marked anhidrosis]. Ishiguchi H; Shimoya K; Ohnishi A; Murai Y; Nakazato M; Hoshii Y Rinsho Shinkeigaku; 1996 Mar; 36(3):436-41. PubMed ID: 8741346 [TBL] [Abstract][Full Text] [Related]
37. Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene. Maury CP; Kere J; Tolvanen R; de la Chapelle A FEBS Lett; 1990 Dec; 276(1-2):75-7. PubMed ID: 2176164 [TBL] [Abstract][Full Text] [Related]
38. Loss of a metal-binding site in gelsolin leads to familial amyloidosis-Finnish type. Kazmirski SL; Isaacson RL; An C; Buckle A; Johnson CM; Daggett V; Fersht AR Nat Struct Biol; 2002 Feb; 9(2):112-6. PubMed ID: 11753432 [TBL] [Abstract][Full Text] [Related]
39. Hereditary gelsolin amyloidosis (HGA): a neglected cause of bilateral progressive or recurrent facial palsy. Sagnelli A; Piscosquito G; Di Bella D; Fadda L; Melzi L; Morico A; Ciano C; Taroni F; Facchetti D; Salsano E; Pareyson D J Peripher Nerv Syst; 2017 Mar; 22(1):59-63. PubMed ID: 27982499 [TBL] [Abstract][Full Text] [Related]
40. Gelsolin gene mutation--at codon 187--in familial amyloidosis, Finnish: DNA-diagnostic assay. Haltia M; Levy E; Meretoja J; Fernandez-Madrid I; Koivunen O; Frangione B Am J Med Genet; 1992 Feb; 42(3):357-9. PubMed ID: 1311149 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]