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Items: 1 to 20 of 138

1.

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
2.

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
3.

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
4.

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.

6.

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
7.

Adjuvant chemotherapy in breast cancer patients induces temporary salivary gland hypofunction.

Jensen SB, Mouridsen HT, Reibel J, Brünner N, Nauntofte B.

Oral Oncol. 2008 Feb;44(2):162-73. Epub 2007 Jun 27.

PMID:
17588802
8.

Analysis of residual saliva and minor salivary gland secretions in patients with dry mouth.

Lee SK, Lee SW, Chung SC, Kim YK, Kho HS.

Arch Oral Biol. 2002 Sep;47(9):637-41.

PMID:
12243967
9.

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
10.

[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. doi: 10.1055/s-0029-1246083. Epub 2011 Apr 8. German.

PMID:
21480154
11.

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
12.

Minor gland saliva flow rate and proteins in subjects with hyposalivation due to Sjogren's syndrome and radiation therapy.

Eliasson L, Almståhl A, Lingström P, Wikström M, Carlén A.

Arch Oral Biol. 2005 Mar;50(3):293-9.

PMID:
15740707
13.

Subtle neuropsychiatric and neurocognitive changes in hereditary gelsolin amyloidosis (AGel amyloidosis).

Kantanen M, Kiuru-Enari S, Salonen O, Kaipainen M, Hokkanen L.

PeerJ. 2014 Jul 22;2:e493. doi: 10.7717/peerj.493. eCollection 2014.

14.

Primary Sjögren's syndrome: salivary gland function and clinical oral findings.

Pedersen AM, Reibel J, Nordgarden H, Bergem HO, Jensen JL, Nauntofte B.

Oral Dis. 1999 Apr;5(2):128-38.

PMID:
10522209
15.

Xerostomia in Sjögren's syndrome and lupus erythematosus: a comparative histological and immunofluorescence study of minor salivary glands alterations.

Fernandes JD, Nico MM, Aoki V, Bologna S, Romiti R, Levy-Neto M, Lourenço SV.

J Cutan Pathol. 2010 Apr;37(4):432-8. doi: 10.1111/j.1600-0560.2009.01368.x. Epub 2009 Jul 15.

PMID:
19614726
16.

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

Kiuru-Enari S, Haltia M.

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

PMID:
20597346
17.

Danish type gelsolin-related amyloidosis in a Brazilian family: case reports.

Solari HP, Ventura MP, Antecka E, Belfort Junior R, Burnier MN Jr.

Arq Bras Oftalmol. 2011 Jul-Aug;74(4):286-8.

18.

Gelsolin amyloidosis as a cause of early aging and progressive bilateral facial paralysis.

Pihlamaa T, Rautio J, Kiuru-Enari S, Suominen S.

Plast Reconstr Surg. 2011 Jun;127(6):2342-51. doi: 10.1097/PRS.0b013e318213a0a2.

PMID:
21617468
19.

Lattice corneal dystrophy type II: clinical, pathologic, and molecular study in a Spanish family.

Huerva V, Velasco A, Sánchez MC, Mateo AJ, Matías-Guiu X.

Eur J Ophthalmol. 2007 May-Jun;17(3):424-9.

PMID:
17534828
20.

Obstructive sleep apnoea syndrome in hereditary gelsolin-related amyloidosis.

Kiuru S, Nieminen T, Partinen M.

J Sleep Res. 1999 Jun;8(2):143-9.

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