128 related articles for article (PubMed ID: 27137880)
1. Causes of death and life span in Finnish gelsolin amyloidosis.
Schmidt EK; Atula S; Tanskanen M; Nikoskinen T; Notkola IL; Kiuru-Enari S
Ann Med; 2016 Aug; 48(5):352-8. PubMed ID: 27137880
[TBL] [Abstract][Full Text] [Related]
2. Gender differences in the clinical course of Finnish gelsolin amyloidosis.
Atula S; Nikoskinen T; Saastamoinen A; Strbian D; Schmidt EK; Kiuru-Enari S
Amyloid; 2016; 23(1):33-8. PubMed ID: 26805765
[TBL] [Abstract][Full Text] [Related]
3. Finnish gelsolin amyloidosis causes significant disease burden but does not affect survival: FIN-GAR phase II study.
Schmidt EK; Mustonen T; Kiuru-Enari S; Kivelä TT; Atula S
Orphanet J Rare Dis; 2020 Jan; 15(1):19. PubMed ID: 31952544
[TBL] [Abstract][Full Text] [Related]
4. [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]
5. Natural course of Finnish gelsolin amyloidosis.
Nikoskinen T; Schmidt EK; Strbian D; Kiuru-Enari S; Atula S
Ann Med; 2015; 47(6):506-11. PubMed ID: 26339870
[TBL] [Abstract][Full Text] [Related]
6. Cutis laxa in hereditary gelsolin amyloidosis.
Kiuru-Enari S; Keski-Oja J; Haltia M
Br J Dermatol; 2005 Feb; 152(2):250-7. PubMed ID: 15727635
[TBL] [Abstract][Full Text] [Related]
7. [Hereditary gelsolin amyloidosis--40 years of Meretoja disease].
Kiuru-Enari S; Haltia M
Duodecim; 2010; 126(10):1162-71. PubMed ID: 20597346
[TBL] [Abstract][Full Text] [Related]
8. Ocular amyloid deposition in familial amyloidosis, Finnish: an analysis of native and variant gelsolin in Meretoja's syndrome.
Kivelä T; Tarkkanen A; Frangione B; Ghiso J; Haltia M
Invest Ophthalmol Vis Sci; 1994 Sep; 35(10):3759-69. PubMed ID: 8088963
[TBL] [Abstract][Full Text] [Related]
9. Cardiac manifestations in Finnish gelsolin amyloidosis patients.
Mustonen T; Holkeri A; Holmström M; Atula S; Pakarinen S; Lehmonen L; Kiuru-Enari S; Aro AL
Amyloid; 2021 Sep; 28(3):168-172. PubMed ID: 33877023
[TBL] [Abstract][Full Text] [Related]
10. Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: a case report.
Tanskanen M; Paetau A; Salonen O; Salmi T; Lamminen A; Lindsberg P; Somer H; Kiuru-Enari S
Amyloid; 2007 Mar; 14(1):89-95. PubMed ID: 17453628
[TBL] [Abstract][Full Text] [Related]
11. Common origin of the gelsolin gene variant in 62 Finnish AGel amyloidosis families.
Mustonen T; Schmidt EK; Valori M; Tienari PJ; Atula S; Kiuru-Enari S
Eur J Hum Genet; 2018 Jan; 26(1):117-123. PubMed ID: 29167514
[TBL] [Abstract][Full Text] [Related]
12. Amyloid in parenchymal organs in gelsolin (AGel) amyloidosis.
Schmidt EK; Kiuru-Enari S; Atula S; Tanskanen M
Amyloid; 2019 Sep; 26(3):118-124. PubMed ID: 31122115
[No Abstract] [Full Text] [Related]
13. Xerostomia in hereditary gelsolin amyloidosis.
Juusela P; Tanskanen M; Nieminen A; Kari K; Suominen L; Uitto VJ; Kiuru-Enari S
Amyloid; 2013 Mar; 20(1):39-44. PubMed ID: 23356404
[TBL] [Abstract][Full Text] [Related]
14. Hereditary gelsolin amyloidosis.
Kiuru-Enari S; Haltia M
Handb Clin Neurol; 2013; 115():659-81. PubMed ID: 23931809
[TBL] [Abstract][Full Text] [Related]
15. Neuromuscular pathology in hereditary gelsolin amyloidosis.
Kiuru-Enari S; Somer H; Seppäläinen AM; Notkola IL; Haltia M
J Neuropathol Exp Neurol; 2002 Jun; 61(6):565-71. PubMed ID: 12071640
[TBL] [Abstract][Full Text] [Related]
16. Nanobody interaction unveils structure, dynamics and proteotoxicity of the Finnish-type amyloidogenic gelsolin variant.
Giorgino T; Mattioni D; Hassan A; Milani M; Mastrangelo E; Barbiroli A; Verhelle A; Gettemans J; Barzago MM; Diomede L; de Rosa M
Biochim Biophys Acta Mol Basis Dis; 2019 Mar; 1865(3):648-660. PubMed ID: 30625383
[TBL] [Abstract][Full Text] [Related]
17. Novel gelsolin variant as the cause of nephrotic syndrome and renal amyloidosis in a large kindred.
Efebera YA; Sturm A; Baack EC; Hofmeister CC; Satoskar A; Nadasdy T; Nadasdy G; Benson DM; Gillmore JD; Hawkins PN; Rowczenio D
Amyloid; 2014 Jun; 21(2):110-2. PubMed ID: 24601799
[TBL] [Abstract][Full Text] [Related]
18. Danish type gelsolin-related amyloidosis in a Brazilian family: case reports.
Solari HP; Ventura MP; Antecka E; Belfort Junior R; Burnier MN
Arq Bras Oftalmol; 2011; 74(4):286-8. PubMed ID: 22068858
[TBL] [Abstract][Full Text] [Related]
19. Severe elastolysis in hereditary gelsolin (AGel) amyloidosis.
Koskelainen S; Zhao F; Kalimo H; Baumann M; Kiuru-Enari S
Amyloid; 2020 Jun; 27(2):81-88. PubMed ID: 31814469
[TBL] [Abstract][Full Text] [Related]
20. Increasing amount of amyloid are associated with the severity of clinical features in hereditary gelsolin (AGel) amyloidosis.
Pihlamaa T; Suominen S; Kiuru-Enari S; Tanskanen M
Amyloid; 2016 Dec; 23(4):225-233. PubMed ID: 27879149
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]