-
1
-
-
0014640130
-
Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms A previously unrecognized heritable syndrome
-
Meretoja J. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. A previously unrecognized heritable syndrome. Ann Clin Res 1969;1:314-24
-
(1969)
Ann Clin Res
, vol.1
, pp. 314-324
-
-
Meretoja, J.1
-
3
-
-
0015806355
-
Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy
-
Meretoja J. Genetic aspects of familial amyloidosis with corneal lattice dystrophy and cranial neuropathy. Clin Genet 1973;4: 173-85
-
(1973)
Clin Genet
, vol.4
, pp. 173-185
-
-
Meretoja, J.1
-
4
-
-
33947627069
-
Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: A case report
-
DOI 10.1080/13506120601116393, PII 775701311
-
Tanskanen M, Paetau A, Salonen O, Salmi T, Lamminen A, Lindsberg P, Somer H, et al. Severe ataxia with neuropathy in hereditary gelsolin amyloidosis: B case report. Amyloid 2007;14:89-95 (Pubitemid 46491167)
-
(2007)
Amyloid
, vol.14
, Issue.1
, pp. 89-95
-
-
Tanskanen, M.1
Paetau, A.2
Salonen, O.3
Salmi, T.4
Lamminen, A.5
Lindsberg, P.6
Somer, H.7
Kiuru-Enari, S.8
-
5
-
-
79958716179
-
Gelsolin amyloidosis as a cause of early aging and progressive bilateral facial paralysis
-
Pihlamaa T, Rautio J, Kiuru-Enari S, Suominen S. Gelsolin amyloidosis as a cause of early aging and progressive bilateral facial paralysis. Plast Reconstr Surg 2011;127:2342-51
-
(2011)
Plast Reconstr Surg
, vol.127
, pp. 2342-2351
-
-
Pihlamaa, T.1
Rautio, J.2
Kiuru-Enari, S.3
Suominen, S.4
-
6
-
-
0026729321
-
Homozygosity for the Asn187 gelsolin mutation in Finnish-Type familial amyloidosis is associated with severe renal disease
-
Maury C P, Kere J, Tolvanen R, de la Chapelle A. Homozygosity for the Asn187 gelsolin mutation in Finnish-Type familial amyloidosis is associated with severe renal disease. Genomics 1992;13:902-3
-
(1992)
Genomics
, vol.13
, pp. 902-903
-
-
Maury, C.P.1
Kere, J.2
Tolvanen, R.3
De La Chapelle, A.4
-
7
-
-
33846029140
-
Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: The first report from the Middle East
-
DOI 10.1093/ndt/gfl548, Special Issue on Pediatric Overweight
-
Ardalan M R, Shoja M M, Kiuru-Enari S. Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: The first report from the Middle East. Nephrol Dial Transplant 2007;22: 272-5 (Pubitemid 46050357)
-
(2007)
Nephrology Dialysis Transplantation
, vol.22
, Issue.1
, pp. 272-275
-
-
Ardalan, M.R.1
Shoja, M.M.2
Kiuru-Enari, S.3
-
8
-
-
0025349996
-
Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein
-
DOI 10.1016/0006-291X(90)90612-Q
-
Haltia M, Prelli F, Ghiso J, Kiuru S, Somer H, Palo J, Frangione B. Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding protein. Biochem Biophys Res Commun 1990;167:927-32 (Pubitemid 20113270)
-
(1990)
Biochemical and Biophysical Research Communications
, vol.167
, Issue.3
, pp. 927-932
-
-
Haltia, M.1
Prelli, F.2
Ghiso, J.3
Kiuru, S.4
Somer, H.5
Palo, J.6
Frangione, B.7
-
9
-
-
84864861249
-
Multifunctional roles of gelsolin in health and diseases
-
Li G H, Arora P D, Chen Y, McCulloch C A, Liu P. Multifunctional roles of gelsolin in health and diseases. Med Res Rev 2012;32: 999-1025
-
(2012)
Med Res Rev
, vol.32
, pp. 999-1025
-
-
Li, G.H.1
Arora, P.D.2
Chen, Y.3
McCulloch, C.A.4
Liu, P.5
-
10
-
-
0025296194
-
Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin
-
Haltia M, Ghiso J, Prelli F, Gallo G, Kiuru S, Somer H, Palo J, et al. Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin. Am J Pathol 1990;136:1223-8 (Pubitemid 20210320)
-
(1990)
American Journal of Pathology
, vol.136
, Issue.6
, pp. 1223-1228
-
-
Haltia, M.1
Ghiso, J.2
Prelli, F.3
Gallo, G.4
Kiuru, S.5
Somer, H.6
Palo, J.7
Frangione, B.8
-
11
-
-
0025854054
-
Immunohistochemical localization of amyloid in Finnish hereditary amyloidosis with antibodies to gelsolin peptides
-
Maury CP. Immunohistochemical localization of amyloid in Finnish hereditary amyloidosis with antibodies to gelsolin peptides. Lab Invest 1991;64:400-4
-
(1991)
Lab Invest
, vol.64
, pp. 400-404
-
-
Maury, C.P.1
-
12
-
-
77953371033
-
Investigation of AGE, their receptor and NF-kappa B activation and apoptosis in patients with ATTR and gelsolin amyloidosis
-
Anan I, Kiuru-Enari S, Obayashi K, Ranlov P J, Ando Y. Investigation of AGE, their receptor and NF-kappa B activation and apoptosis in patients with ATTR and gelsolin amyloidosis. Histol Histopathol 2010;25:691-9
-
(2010)
Histol Histopathol
, vol.25
, pp. 691-699
-
-
Anan, I.1
Kiuru-Enari, S.2
Obayashi, K.3
Ranlov, P.J.4
Ando, Y.5
-
13
-
-
0032853001
-
Regulation of neural differentiation by normal and mutant (G654A, amyloidogenic) gelsolin
-
Westberg J A, Zhang K Z, Andersson LC. Regulation of neural differentiation by normal and mutant (G654A, amyloidogenic) gelsolin. FASEB J 1999;13:1621-6 (Pubitemid 29411796)
-
(1999)
FASEB Journal
, vol.13
, Issue.12
, pp. 1621-1626
-
-
Westberg, J.A.1
Zhang, K.-Z.2
Andersson, L.C.3
-
14
-
-
0034066624
-
Altered platelet shape change in hereditary gelsolin Asp 187 Asn-related amyloidosis
-
Kiuru S, Javela K, Somer H, Kekomaki R. Altered platelet shape change in hereditary gelsolin Asp187Asn-related amyloidosis. Thromb Haemost 2000;83:491-5 (Pubitemid 30148367)
-
(2000)
Thrombosis and Haemostasis
, vol.83
, Issue.3
, pp. 491-495
-
-
Kiuru, S.1
Javela, K.2
Somer, H.3
Kekomaki, R.4
-
15
-
-
84860128609
-
Gelsolin amyloidosis: Genetics, biochemistry, pathology and possible strategies for therapeutic intervention
-
Solomon J P, Page L J, Balch W E, Kelly JW. Gelsolin amyloidosis: Genetics, biochemistry, pathology and possible strategies for therapeutic intervention. Crit Rev Biochem Mol Biol 2012;47:282-96
-
(2012)
Crit Rev Biochem Mol Biol
, vol.47
, pp. 282-296
-
-
Solomon, J.P.1
Page, L.J.2
Balch, W.E.3
Kelly, J.W.4
-
16
-
-
0035092658
-
Corneal morphology and sensitivity in lattice dystrophy type II (familial amyloidosis, Finnish type)
-
Rosenberg M E, Tervo T M, Gallar J, Acosta M C, Muller LJ, Moilanen J A, Tarkkanen A H, et al. Corneal morphology and sensitivity in lattice dystrophy type II (familial amyloidosis, Finnish type). Invest Ophthalmol Vis Sci 2001;42:634-41 (Pubitemid 32206902)
-
(2001)
Investigative Ophthalmology and Visual Science
, vol.42
, Issue.3
, pp. 634-641
-
-
Rosenberg, M.E.1
Tervo, T.M.T.2
Gallar, J.3
Acosta, M.C.4
Muller, L.J.5
Moilanen, J.A.O.6
Tarkkanen, A.H.A.7
Vesaluoma, M.H.8
-
17
-
-
73349122594
-
Lattice corneal dystrophy, gelsolin type (Meretoja's syndrome
-
Carrwik C, Stenevi U. Lattice corneal dystrophy, gelsolin type (Meretoja's syndrome). Acta Ophthalmol 2009;87:813-9
-
(2009)
Acta Ophthalmol
, vol.87
, pp. 813-819
-
-
Carrwik, C.1
Stenevi, U.2
-
18
-
-
0026588330
-
Solid-phase minisequencing test reveals Asp187!Asn (G654!A) mutation of gelsolin in all affected individuals with Finnish type of familial amyloidosis
-
Paunio T, Kiuru S, Hongell V, Mustonen E, Syvänen AC, Bengström M, Palo J, et al. Solid-phase minisequencing test reveals Asp187!Asn (G654!A) mutation of gelsolin in all affected individuals with Finnish type of familial amyloidosis. Genomics 1992;13:237-9
-
(1992)
Genomics
, vol.13
, pp. 237-239
-
-
Paunio, T.1
Kiuru, S.2
Hongell, V.3
Mustonen, E.4
Syvänen, A.C.5
Bengström, M.6
Palo, J.7
-
19
-
-
0032840791
-
Xerostomia and hyposalivation: Causes, consequences and treatment in the elderly
-
DOI 10.2165/00002512-199915020-00004
-
Närhi T O, Meurman J H, Ainamo A. Xerostomia and hyposalivation: Causes, consequences and treatment in the elderly. Drugs Aging 1999;15:103-16 (Pubitemid 29396819)
-
(1999)
Drugs and Aging
, vol.15
, Issue.2
, pp. 103-116
-
-
Narhi, T.O.1
Meurman, J.H.2
Ainamo, A.3
-
20
-
-
0017803393
-
Individual diagnosis, prognosis and counselling for caries prevention
-
Ericsson Y, Hardwick L. Individual diagnosis, prognosis and counselling for caries prevention. Caries Res 1978;12:94-102 (Pubitemid 8364508)
-
(1978)
Caries Research
, vol.12
, Issue.SUPPL.1
, pp. 94-102
-
-
Ericsson, Y.1
Hardwick, L.2
-
21
-
-
0034584313
-
Xerostomia and hyposalivation
-
Nederfors T. Xerostomia and hyposalivation. Adv Dent Res 2000;14:48-56
-
(2000)
Adv Dent Res
, vol.14
, pp. 48-56
-
-
Nederfors, T.1
-
22
-
-
0021360822
-
Amount and avidity of salivary and serum antibodies against Streptococcus mutans in two groups of human subjects with different dental caries susceptibility
-
Lehtonen O P, Grahn E M, Stahlberg T H, Laitinen LA. Amount and avidity of salivary and serum antibodies against streptococcus mutans in two groups of human subjects with different dental caries susceptibility. Infect Immun 1984;43:308-13 (Pubitemid 14218733)
-
(1984)
Infection and Immunity
, vol.43
, Issue.1
, pp. 308-313
-
-
Lehtonen, O.P.J.1
Grahn, E.M.2
Stahlberg, T.H.3
Laitinen, L.A.4
-
23
-
-
0036022863
-
Circadian effects on the acute responses of salivary cortisol and IgA in well trained swimmers
-
DOI 10.1136/bjsm.36.4.260
-
Dimitriou L, Sharp N C, Doherty M. Circadian effects on the acute responses of salivary cortisol and IgA in well trained swimmers. Br J Sports Med 2002;36:260-4 (Pubitemid 34833119)
-
(2002)
British Journal of Sports Medicine
, vol.36
, Issue.4
, pp. 260-264
-
-
Dimitriou, L.1
Sharp, N.C.C.2
Doherty, M.3
-
25
-
-
0014330331
-
Labial salivary gland biopsy in sjogren's disease
-
Chisholm D M, Mason DK. Labial salivary gland biopsy in sjogren's disease. J Clin Pathol 1968;21:656-60
-
(1968)
J Clin Pathol
, vol.21
, pp. 656-660
-
-
Chisholm, D.M.1
Mason, D.K.2
-
26
-
-
0036106053
-
Dry eyes and mouth syndrome - A subgroup of patients presenting with sicca symptoms
-
Price E J, Venables PJ. Dry eyes and mouth syndrome - A subgroup of patients presenting with sicca symptoms. Rheumatology 2002;41:416-22 (Pubitemid 34537840)
-
(2002)
Rheumatology
, vol.41
, Issue.4
, pp. 416-422
-
-
Price, E.J.1
Venables, P.J.W.2
-
27
-
-
70349484790
-
Hereditary gelsolin amyloidosis mimicking Sjögren's syndrome
-
Juusela P, Tanskanen M, Nieminen A, Uitto V J, Blafield H, Kiuru-Enari S. Hereditary gelsolin amyloidosis mimicking Sjögren's syndrome. Clin Rheumatol 2009;28:1351-4
-
(2009)
Clin Rheumatol
, vol.28
, pp. 1351-1354
-
-
Juusela, P.1
Tanskanen, M.2
Nieminen, A.3
Uitto, V.J.4
Blafield, H.5
Kiuru-Enari, S.6
-
28
-
-
0027092852
-
Salivary hypofunction in patients with familial amyloidotic polyneuropathy
-
DOI 10.1016/0030-4220(92)90401-B
-
Johansson I, Ryberg M, Steen L, Wigren L. Salivary hypofunction in patients with familial amyloidotic polyneuropathy. Oral Surg Oral Med Oral Pathol 1992;74:742-8 (Pubitemid 23005443)
-
(1992)
Oral Surgery Oral Medicine and Oral Pathology
, vol.74
, Issue.6
, pp. 742-748
-
-
Johansson, I.1
Ryberg, M.2
Steen, L.3
Wigren, L.4
-
29
-
-
0036189848
-
Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a french family
-
DOI 10.1046/j.1523-1755.2002.00205.x
-
Valleix S, Drunat S, Philit J B, Adoue D, Piette J C, Droz D, MacGregor B, et al. Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family. Kidney Int 2002;61:907-12 (Pubitemid 34175459)
-
(2002)
Kidney International
, vol.61
, Issue.3
, pp. 907-912
-
-
Valleix, S.1
Drunat, S.2
Philit, J.-B.3
Adoue, D.4
Piette, J.-C.5
Droz, D.6
MacGregor, B.7
Canet, D.8
Delpech, M.9
Grateau, G.10
-
30
-
-
0021017031
-
Primary amyloidosis presenting as Sjogren's syndrome
-
DOI 10.1001/archinte.143.12.2325
-
Gogel H K, Searles R P, Volpicelli N A, Cornwell III GG. Primary amyloidosis presenting as Sjögren's syndrome. Arch Intern Med 1983;143:2325-6 (Pubitemid 14209743)
-
(1983)
Archives of Internal Medicine
, vol.143
, Issue.12
, pp. 2325-2326
-
-
Gogel, H.K.1
Searles, R.P.2
Volpicelli, N.A.3
Cornwell III, G.G.4
-
31
-
-
17444452171
-
Secondary amyloidosis and sicca syndrome
-
Catalano M A, Vaughan JH. Secondary amyloidosis and sicca syndrome. Arthritis Rheum 1980;23:1067
-
(1980)
Arthritis Rheum
, vol.23
, pp. 1067
-
-
Catalano, M.A.1
Vaughan, J.H.2
-
32
-
-
0034584313
-
Xerostomia and hyposalivation
-
Nederfors T. Xerostomia and hyposalivation. Adv Dent Res 2000;14:48-56
-
(2000)
Adv Dent Res
, vol.14
, pp. 48-56
-
-
Nederfors, T.1
-
33
-
-
58849142002
-
Feeling of dry mouth in relation to whole and minor gland saliva secretion rate
-
Eliasson L, Birkhed D, Carlen A. Feeling of dry mouth in relation to whole and minor gland saliva secretion rate. Arch Oral Biol 2009;54:263-7
-
(2009)
Arch Oral Biol
, vol.54
, pp. 263-267
-
-
Eliasson, L.1
Birkhed, D.2
Carlen, A.3
-
35
-
-
0026502439
-
Ontogeny of immunity to oral microbiota in humans
-
Smith D J, Taubman MA. Ontogeny of immunity to oral microbiota in humans. Crit Rev Oral Biol Med 1992;3:109-33
-
(1992)
Crit Rev Oral Biol Med
, vol.3
, pp. 109-133
-
-
Smith, D.J.1
Taubman, M.A.2
-
36
-
-
0034951954
-
The effect of pilocarpine on salivary constituents in patients with chronic graft-versus-host disease
-
DOI 10.1016/S0003-9969(01)00035-8, PII S0003996901000358
-
Nagler R M, Nagler A. The effect of pilocarpine on salivary constituents in patients with chronic graft-versus-host disease. Arch Oral Biol 2001;46:689-95 (Pubitemid 32587802)
-
(2001)
Archives of Oral Biology
, vol.46
, Issue.8
, pp. 689-695
-
-
Nagler, R.M.1
Nagler, A.2
-
37
-
-
1442348377
-
Sialochemical and Gustatory Analysis in Patients with Oral Sensory Complaints
-
DOI 10.1016/j.jpain.2003.09.002
-
Nagler R M, Hershkovich O. Sialochemical and gustatory analysis in patients with oral sensory complaints. J Pain 2004; 5:56-63 (Pubitemid 38280719)
-
(2004)
Journal of Pain
, vol.5
, Issue.1
, pp. 56-63
-
-
Nagler, R.M.1
Hershkovicht, O.2
-
38
-
-
0015175763
-
Histopathological findings of familial amyloidosis with cranial neuropathy as principal manifestation Report on three cases
-
Meretoja J, Teppo L. Histopathological findings of familial amyloidosis with cranial neuropathy as principal manifestation. Report on three cases. Acta Pathol Microbiol Scand [A] 1971;79:432-40
-
(1971)
Acta Pathol Microbiol Scand [A
, vol.79
, pp. 432-440
-
-
Meretoja, J.1
Teppo, L.2
-
40
-
-
0033028206
-
Gelsolin-related spinal and cerebral amyloid angiopathy
-
DOI 10.1002/1531-8249(199903)45:3<305::AID-ANA5>3.0.CO;2-E
-
Kiuru S, Salonen O, Haltia M. Gelsolin-related spinal and cerebral amyloid angiopathy. Ann Neurol 1999;45:305-11 (Pubitemid 29120034)
-
(1999)
Annals of Neurology
, vol.45
, Issue.3
, pp. 305-311
-
-
Kiuru, S.1
Salonen, O.2
Haltia, M.3
-
41
-
-
0034633008
-
Sjögren's syndrome
-
Fox R I, Michelson P, Casiano C A, Hayashi J, Stern M. Sjögren's syndrome. Clin Dermatol 2000;18:589-600
-
(2000)
Clin Dermatol
, vol.18
, pp. 589-600
-
-
Fox, R.I.1
Michelson, P.2
Casiano, C.A.3
Hayashi, J.4
Stern, M.5
-
42
-
-
0033621786
-
2+ signalling in labial salivary glands of healthy individuals and patients with primary Sjogren's syndrome (pSS)
-
DOI 10.1034/j.1600-0714.2000.290301.x
-
Pedersen A M, Dissing S, Fahrenkrug J, Hannibal J, Reibel J, Nauntofte B. Innervation pattern and Ca2 signalling in labial salivary glands of healthy individuals and patients with primary Sjögren's syndrome (pSS). J Oral Pathol Med 2000;29:97-109 (Pubitemid 30156929)
-
(2000)
Journal of Oral Pathology and Medicine
, vol.29
, Issue.3
, pp. 97-109
-
-
Pedersen, A.M.1
Dissing, S.2
Fahrenkrug, J.3
Hannibal, J.4
Reibel, J.5
Nauntofte, B.6
-
43
-
-
0003149450
-
Gastrointestinal system
-
Berne R M, Levy MN, eds. 4th e.d. St. Louis M.O. Mosby
-
Kutchai HC. The gastrointestinal system. In: Berne R M, Levy MN, eds. Physiology. 4th ed. St. Louis, MO: Mosby; 1998:617-22
-
(1998)
Physiology
, pp. 617-622
-
-
Kutchai, H.C.1
-
44
-
-
73349125776
-
Usefulness of labial salivary gland biopsy in familial amyloid polyneuropathy portuguese type
-
Do Amaral B, Coelho T, Sousa A, Guimaraes A. Usefulness of labial salivary gland biopsy in familial amyloid polyneuropathy Portuguese type. Amyloid 2009;16:232-8
-
(2009)
Amyloid
, vol.16
, pp. 232-238
-
-
Do Amaral, B.1
Coelho, T.2
Sousa, A.3
Guimaraes, A.4
|