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Items: 1 to 20 of 129

1.

Pituicytoma with gelsolin amyloid deposition.

Ida CM, Yan X, Jentoft ME, Kip NS, Scheithauer BW, Morris JM, Dogan A, Parisi JE, Kovacs K.

Endocr Pathol. 2013 Sep;24(3):149-55. doi: 10.1007/s12022-013-9254-y.

PMID:
23817895
2.

Hereditary gelsolin amyloidosis.

Kiuru-Enari S, Haltia M.

Handb Clin Neurol. 2013;115:659-81. doi: 10.1016/B978-0-444-52902-2.00039-4. Review.

PMID:
23931809
3.

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.

PMID:
17453628
4.

[Hereditary gelsolin amyloidosis--40 years of Meretoja disease].

Kiuru-Enari S, Haltia M.

Duodecim. 2010;126(10):1162-71. Review. Finnish.

PMID:
20597346
5.

Cutis laxa in hereditary gelsolin amyloidosis.

Kiuru-Enari S, Keski-Oja J, Haltia M.

Br J Dermatol. 2005 Feb;152(2):250-7.

PMID:
15727635
6.

[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. Japanese.

PMID:
8741346
7.

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.

PMID:
8088963
8.

[Familial amyloidotic polyneuropathy type IV (Finnish type)--the first description of a large kindred in Japan].

Sunada Y, Shimizu T, Mannen T, Kanazawa I.

Rinsho Shinkeigaku. 1992 Aug;32(8):826-33. Japanese.

PMID:
1337023
9.

Familial systemic amyloidosis associated with bilateral sensorineural hearing loss and bilateral facial palsies.

Hornigold R, Patel AV, Ward VM, O'Connor AF.

J Laryngol Otol. 2006 Sep;120(9):778-80. Epub 2006 Jul 26. Review.

PMID:
16870032
11.

Pituicytoma: a distinctive low-grade glioma of the neurohypophysis.

Brat DJ, Scheithauer BW, Staugaitis SM, Holtzman RN, Morgello S, Burger PC.

Am J Surg Pathol. 2000 Mar;24(3):362-8.

PMID:
10716149
12.

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. Epub 2016 Nov 23.

PMID:
27879149
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. doi: 10.3109/13506129.2013.764284. Epub 2013 Jan 28.

PMID:
23356404
14.

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. doi: 10.1111/jns.12200.

PMID:
27982499
15.

Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein.

Haltia M, Prelli F, Ghiso J, Kiuru S, Somer H, Palo J, Frangione B.

Biochem Biophys Res Commun. 1990 Mar 30;167(3):927-32.

PMID:
2157434
16.

Hereditary gelsolin amyloidosis mimicking Sjögren's syndrome.

Juusela P, Tanskanen M, Nieminen A, Uitto VJ, Blåfield H, Kiuru-Enari S.

Clin Rheumatol. 2009 Nov;28(11):1351-4. doi: 10.1007/s10067-009-1260-6. Epub 2009 Aug 23.

PMID:
19701715
18.

An immunohistochemical study of gelsolin immunoreactivity in corneal amyloidosis.

Loeffler KU, Edward DP, Tso MO.

Am J Ophthalmol. 1992 May 15;113(5):546-54.

PMID:
1315488
20.

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