-
1
-
-
0030820394
-
Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p
-
Amos CI, Balin D, Thiel TJ, Anderson JP, Gourley I, Frazier ML, Lynch PM, Luchtefeld MA, Young A, McGarrity TJ, Seldin MF. 1997. Fine mapping of a genetic locus for Peutz-Jeghers syndrome on chromosome 19p. Cancer Res 57:3653-3656.
-
(1997)
Cancer Res
, vol.57
, pp. 3653-3656
-
-
Amos, C.I.1
Balin, D.2
Thiel, T.J.3
Anderson, J.P.4
Gourley, I.5
Frazier, M.L.6
Lynch, P.M.7
Luchtefeld, M.A.8
Young, A.9
McGarrity, T.J.10
Seldin, M.F.11
-
2
-
-
0018251122
-
Oral hyperpigmentation and occult malignancy: Report of a case
-
Babin RW, Ceillery RI, DeSanto LW. 1978. Oral hyperpigmentation and occult malignancy: report of a case. J Otolaryngol 5:389-394.
-
(1978)
J Otolaryngol
, vol.5
, pp. 389-394
-
-
Babin, R.W.1
Ceillery, R.I.2
DeSanto, L.W.3
-
3
-
-
15444350943
-
Increased risk for cancer in patients with the Peutz-Jeghers syndrome
-
Boardman L, Thibodeau SN, Schaid DJ, Lindor NM, McDonnell SK, Burgart LJ, Ahlquist DA, Podratz KC, Pittelkow M, Hartmann LC. 1998. Increased risk for cancer in patients with the Peutz-Jeghers syndrome. Ann Intern Med 128:896-899.
-
(1998)
Ann Intern Med
, vol.128
, pp. 896-899
-
-
Boardman, L.1
Thibodeau, S.N.2
Schaid, D.J.3
Lindor, N.M.4
McDonnell, S.K.5
Burgart, L.J.6
Ahlquist, D.A.7
Podratz, K.C.8
Pittelkow, M.9
Hartmann, L.C.10
-
4
-
-
0030139524
-
BRCA2 germline mutations in male breast cancer cases and breast cancer families
-
Couch FJ, Farid LM, DeShano ML, Tavtigian SV, Calzone K, Campeau L, Peng Y, Bogden B, Chen Q, Neuhausen S, Shattuck-Eidens D, Godwin AK, Daly M, Radford DM, Sedlacek S, Rommens J, Simard J, Garber J, Merajver S, Weber BL. 1996. BRCA2 germline mutations in male breast cancer cases and breast cancer families. Nature Genet 13:123-125.
-
(1996)
Nature Genet
, vol.13
, pp. 123-125
-
-
Couch, F.J.1
Farid, L.M.2
DeShano, M.L.3
Tavtigian, S.V.4
Calzone, K.5
Campeau, L.6
Peng, Y.7
Bogden, B.8
Chen, Q.9
Neuhausen, S.10
Shattuck-Eidens, D.11
Godwin, A.K.12
Daly, M.13
Radford, D.M.14
Sedlacek, S.15
Rommens, J.16
Simard, J.17
Garber, J.18
Merajver, S.19
Weber, B.L.20
more..
-
5
-
-
0026034892
-
Peutz-Jeghers-like melanotic macules associated with esophageal adenocarcinoma
-
Eng A, Armin A, Massa M, Gradini R. 1991. Peutz-Jeghers-like melanotic macules associated with esophageal adenocarcinoma. Am J Path 13:152-157.
-
(1991)
Am J Path
, vol.13
, pp. 152-157
-
-
Eng, A.1
Armin, A.2
Massa, M.3
Gradini, R.4
-
6
-
-
0025943926
-
Acquired pigmentation simulating PJS: Initial manifestation of diffuse uveal melanocytic proliferation
-
Gass JDM, Glazer RJ. 1991. Acquired pigmentation simulating PJS: initial manifestation of diffuse uveal melanocytic proliferation. Brit J Ophth 75:693-695.
-
(1991)
Brit J Ophth
, vol.75
, pp. 693-695
-
-
Gass, J.D.M.1
Glazer, R.J.2
-
7
-
-
0023192463
-
Increased risk of cancer in the Peutz-Jeghers syndrome
-
Giardiello FM, Welsh SB, Hamilton SR, Offerhaus GJA, Gittelsohn KAM, Booker SV, Krush AJ, Yardley LH, Luk GD. 1987. Increased risk of cancer in the Peutz-Jeghers syndrome. N Engl J Med 316:1511-1515.
-
(1987)
N Engl J Med
, vol.316
, pp. 1511-1515
-
-
Giardiello, F.M.1
Welsh, S.B.2
Hamilton, S.R.3
Offerhaus, G.J.A.4
Gittelsohn, K.A.M.5
Booker, S.V.6
Krush, A.J.7
Yardley, L.H.8
Luk, G.D.9
-
8
-
-
0032403068
-
Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome
-
Gruber SB, Entius MM, Petersen GM, Laken SJ, Longo PA, Boyer R, Levin AM, Mujumda JU, Trent JM, Kinzler KW, Vogelstein B, Hamilton SR, Polymeropoulous MH. 1998. Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome. Cancer Res 58:5267-5270.
-
(1998)
Cancer Res
, vol.58
, pp. 5267-5270
-
-
Gruber, S.B.1
Entius, M.M.2
Petersen, G.M.3
Laken, S.J.4
Longo, P.A.5
Boyer, R.6
Levin, A.M.7
Mujumda, J.U.8
Trent, J.M.9
Kinzler, K.W.10
Vogelstein, B.11
Hamilton, S.R.12
Polymeropoulous, M.H.13
-
9
-
-
0028970197
-
The molecular basis of Turcot syndrome
-
Hamilton SR, Liu B, Parsons RE, Papadopoulos N, Jen J, Powell SM, Krush AJ, Berk T, Cohen Z, Tetu B, Burger PC, Wood PA, Taqi F, Booker SV, Petersen GM, Offerhaus GJA, Tersmette AC, Giardiello FM, Vogelstein B, Kinzler KW. 1995. The molecular basis of Turcot syndrome. N Engl J Med 332:839-847.
-
(1995)
N Engl J Med
, vol.332
, pp. 839-847
-
-
Hamilton, S.R.1
Liu, B.2
Parsons, R.E.3
Papadopoulos, N.4
Jen, J.5
Powell, S.M.6
Krush, A.J.7
Berk, T.8
Cohen, Z.9
Tetu, B.10
Burger, P.C.11
Wood, P.A.12
Taqi, F.13
Booker, S.V.14
Petersen, G.M.15
Offerhaus, G.J.A.16
Tersmette, A.C.17
Giardiello, F.M.18
Vogelstein, B.19
Kinzler, K.W.20
more..
-
10
-
-
0031012344
-
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis
-
Hemminki A, Tomlinson I, Markie D, Jarvinen H, Sistonen P, Bjorkqvist A-M, Knuutila S, Salovarra R, Bodmer W, Shibata D, de la Chapelle A, Aaltonen LA. 1997. Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis. Nature Genet 15:87-90.
-
(1997)
Nature Genet
, vol.15
, pp. 87-90
-
-
Hemminki, A.1
Tomlinson, I.2
Markie, D.3
Jarvinen, H.4
Sistonen, P.5
Bjorkqvist, A.-M.6
Knuutila, S.7
Salovarra, R.8
Bodmer, W.9
Shibata, D.10
De La Chapelle, A.11
Aaltonen, L.A.12
-
11
-
-
0032495530
-
A serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
Hemminki A, Markie D, Tomlinson I, Avizienyte E, Roth S, Loukola A, Bigenll G, Warren W, Aminoff M, Hoglund P, Jarvinen H, Kristo P, Pelin K, Ridanpaa M, Salovaara R, Toro T, Bodmer W, Olschwang S, Olsen AS, Stratton MR, de la Chapelle A, Aaltonen LA. 1998. A serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 391:184-187.
-
(1998)
Nature
, vol.391
, pp. 184-187
-
-
Hemminki, A.1
Markie, D.2
Tomlinson, I.3
Avizienyte, E.4
Roth, S.5
Loukola, A.6
Bigenll, G.7
Warren, W.8
Aminoff, M.9
Hoglund, P.10
Jarvinen, H.11
Kristo, P.12
Pelin, K.13
Ridanpaa, M.14
Salovaara, R.15
Toro, T.16
Bodmer, W.17
Olschwang, S.18
Olsen, A.S.19
Stratton, M.R.20
De La Chapelle, A.21
Aaltonen, L.A.22
more..
-
12
-
-
0027372058
-
Neoplastic transformation arising in Peutz-Jeghers polyposis
-
Hizawa K, Iida M, Matsumoto T, Kohrogi N, Yao T, Fujishima M. 1993. Neoplastic transformation arising in Peutz-Jeghers polyposis. Dis Colon Rectum 36:953-957.
-
(1993)
Dis Colon Rectum
, vol.36
, pp. 953-957
-
-
Hizawa, K.1
Iida, M.2
Matsumoto, T.3
Kohrogi, N.4
Yao, T.5
Fujishima, M.6
-
13
-
-
7844251203
-
Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases
-
Houlston R, Bevan S, Williams A, Young J, Dunlop M, Rozen P, Eng C, Markie D, Woodford-Richens K, Rodriguez-Bigas MA, Leggett B, Neale K, Phillips R, Sheridan E, Hodgson S, Iwama T, Eccles D, Bodmer W, Tomlinson I. 1998. Mutations in DPC4 (SMAD4) cause juvenile polyposis syndrome, but only account for a minority of cases. Hum Molec Genet 7:1907-1912.
-
(1998)
Hum Molec Genet
, vol.7
, pp. 1907-1912
-
-
Houlston, R.1
Bevan, S.2
Williams, A.3
Young, J.4
Dunlop, M.5
Rozen, P.6
Eng, C.7
Markie, D.8
Woodford-Richens, K.9
Rodriguez-Bigas, M.A.10
Leggett, B.11
Neale, K.12
Phillips, R.13
Sheridan, E.14
Hodgson, S.15
Iwama, T.16
Eccles, D.17
Bodmer, W.18
Tomlinson, I.19
-
14
-
-
76549223053
-
Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits
-
Jeghers H, McKusick VA, Katz KH. 1949. Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits. N Engl J Med 241:993-1031.
-
(1949)
N Engl J Med
, vol.241
, pp. 993-1031
-
-
Jeghers, H.1
McKusick, V.A.2
Katz, K.H.3
-
15
-
-
0031974516
-
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
-
Jenne DE, Reimann H, Nezu J, Friedel W, Loff S, Jeschke R, Muller O, Back W, Zimmer M. 1998. Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nature Genet 18:38-43.
-
(1998)
Nature Genet
, vol.18
, pp. 38-43
-
-
Jenne, D.E.1
Reimann, H.2
Nezu, J.3
Friedel, W.4
Loff, S.5
Jeschke, R.6
Muller, O.7
Back, W.8
Zimmer, M.9
-
16
-
-
0032876595
-
STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients
-
Jiang CY, Esufali S, Berk T, Gallinger S, Cohen Z, Tobi M, Redston M, Bapat B. 1999. STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients. Clin Genet 56:136-141.
-
(1999)
Clin Genet
, vol.56
, pp. 136-141
-
-
Jiang, C.Y.1
Esufali, S.2
Berk, T.3
Gallinger, S.4
Cohen, Z.5
Tobi, M.6
Redston, M.7
Bapat, B.8
-
17
-
-
0032604662
-
Peutz-Jeghers syndrome: Four inactivating germline mutations in the STK11 gene
-
Kruse R, Uhlhaas S, Lamberti C, Keller KM, Jackisch C, Steinhard J, Knopfle G, Loff S, Back W, Stolte M, Jungck M, Propping P, Friedl W, Jenne DE. 1999. Peutz-Jeghers syndrome: four inactivating germline mutations in the STK11 gene. Hum Mutat 13:257-258.
-
(1999)
Hum Mutat
, vol.13
, pp. 257-258
-
-
Kruse, R.1
Uhlhaas, S.2
Lamberti, C.3
Keller, K.M.4
Jackisch, C.5
Steinhard, J.6
Knopfle, G.7
Loff, S.8
Back, W.9
Stolte, M.10
Jungck, M.11
Propping, P.12
Friedl, W.13
Jenne, D.E.14
-
18
-
-
17344363637
-
Inherited mutations in PTEN that are associated with breast cancer, Cowden disease, and juvenile polyposis
-
Lynch ED, Ostermeyer EA, Lee MK, Arena JF, Ji H, Dann J, Swisshelm K, Suchard D, MacLeod PM, Kvinnsland S, Gjertsen BT, Heimdal K, Lubs H, Moller P, King MC. 1997. Inherited mutations in PTEN that are associated with breast cancer, Cowden disease, and juvenile polyposis. Am J Hum Genet 61:1254-1260.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1254-1260
-
-
Lynch, E.D.1
Ostermeyer, E.A.2
Lee, M.K.3
Arena, J.F.4
Ji, H.5
Dann, J.6
Swisshelm, K.7
Suchard, D.8
MacLeod, P.M.9
Kvinnsland, S.10
Gjertsen, B.T.11
Heimdal, K.12
Lubs, H.13
Moller, P.14
King, M.C.15
-
19
-
-
17344365130
-
Peutz-Jeghers Syndrome: Confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus on 19q13.4
-
Mehenni H, Blouin J-L, Radhakrishna U, Bhardwaj S, Bhardwaj K, Dixit VB, Richards KF, Bermejo-Fenoli A, Leal AS, Ravl RC, Antonarakis SE. 1997. Peutz-Jeghers Syndrome: confirmation of linkage to chromosome 19p13.3 and identification of a potential second locus on 19q13.4. Am J Hum Genet 61:1327-1334.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 1327-1334
-
-
Mehenni, H.1
Blouin, J.-L.2
Radhakrishna, U.3
Bhardwaj, S.4
Bhardwaj, K.5
Dixit, V.B.6
Richards, K.F.7
Bermejo-Fenoli, A.8
Leal, A.S.9
Ravl, R.C.10
Antonarakis, S.E.11
-
20
-
-
0032471851
-
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity
-
Mehenni H, Gehrig C, Nezu J, Oku A, Shimane M, Rossier C, Guex N, Blouin J-L, Scott HS, Antonarakis SE, 1998. Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity. Am J Hum Genet 63:1641-1650.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1641-1650
-
-
Mehenni, H.1
Gehrig, C.2
Nezu, J.3
Oku, A.4
Shimane, M.5
Rossier, C.6
Guex, N.7
Blouin, J.-L.8
Scott, H.S.9
Antonarakis, S.E.10
-
22
-
-
18344416870
-
Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3
-
Nakagawa H, Koyama K, Tanaka T, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Monden M, Nakamura Y. 1998a. Localization of the gene responsible for Peutz-Jeghers syndrome within a 6-cM region of chromosome 19p13.3. Hum Genet 102:203-206.
-
(1998)
Hum Genet
, vol.102
, pp. 203-206
-
-
Nakagawa, H.1
Koyama, K.2
Tanaka, T.3
Miyoshi, Y.4
Ando, H.5
Baba, S.6
Watatani, M.7
Yasutomi, M.8
Monden, M.9
Nakamura, Y.10
-
23
-
-
0031662147
-
Nine novel germline mutations of STK11 in 10 families with Peutz-Jeghers syndrome
-
Nakagawa H, Koyama K, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Matsuura N, Monden M, Nakamura Y. 1998b. Nine novel germline mutations of STK11 in 10 families with Peutz-Jeghers syndrome. Hum Genet 103:168-172.
-
(1998)
Hum Genet
, vol.103
, pp. 168-172
-
-
Nakagawa, H.1
Koyama, K.2
Miyoshi, Y.3
Ando, H.4
Baba, S.5
Watatani, M.6
Yasutomi, M.7
Matsuura, N.8
Monden, M.9
Nakamura, Y.10
-
24
-
-
0025791005
-
Peutz-Jeghers syndrome associated with adenocarcinoma of the cecum and focal carcinomas in hamartomatous polyps of the colon: A case report
-
Niimi K, Tomoda H, Furusawa M, Hayashi I, Okumura Y. 1991. Peutz-Jeghers syndrome associated with adenocarcinoma of the cecum and focal carcinomas in hamartomatous polyps of the colon: a case report. Jpn J Surg 21:220-223.
-
(1991)
Jpn J Surg
, vol.21
, pp. 220-223
-
-
Niimi, K.1
Tomoda, H.2
Furusawa, M.3
Hayashi, I.4
Okumura, Y.5
-
25
-
-
17344367301
-
Peutz-Jeghers disease: Most, but not all, families are compatible with linkage to 19p13.3
-
Olschwang S, Markie D, Seal S, Neale K, Phillips R, Cottrell S, Ellis I, Hodgson S, Zauber P, Spigelman A, Iwama T, Loff S, McKeown C, Marchese C, Sampson J, Davies S, Talbot I, Wyke J, Thomas G, Bodmer W, Hemminki A, Avizienyte E, de la Chapelle A, Aaltonen L, Tomlinson I. 1998. Peutz-Jeghers disease: most, but not all, families are compatible with linkage to 19p13.3. J Med Genet 35:42-44.
-
(1998)
J Med Genet
, vol.35
, pp. 42-44
-
-
Olschwang, S.1
Markie, D.2
Seal, S.3
Neale, K.4
Phillips, R.5
Cottrell, S.6
Ellis, I.7
Hodgson, S.8
Zauber, P.9
Spigelman, A.10
Iwama, T.11
Loff, S.12
McKeown, C.13
Marchese, C.14
Sampson, J.15
Davies, S.16
Talbot, I.17
Wyke, J.18
Thomas, G.19
Bodmer, W.20
Hemminki, A.21
Avizienyte, E.22
De La Chapelle, A.23
Aaltonen, L.24
Tomlinson, I.25
more..
-
26
-
-
14444272759
-
STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer
-
Resta N, Simone C, Mareni C, Montera M, Gentile M, Susca F, Gristina R, Pozzi S, Bertario L, Bufo P, Carlomagno N, Ingrosso M, Rossini FP, Tenconi R, Guanti G. 1998. STK11 mutations in Peutz-Jeghers syndrome and sporadic colon cancer. Cancer Res 58:4799-4801.
-
(1998)
Cancer Res
, vol.58
, pp. 4799-4801
-
-
Resta, N.1
Simone, C.2
Mareni, C.3
Montera, M.4
Gentile, M.5
Susca, F.6
Gristina, R.7
Pozzi, S.8
Bertario, L.9
Bufo, P.10
Carlomagno, N.11
Ingrosso, M.12
Rossini, F.P.13
Tenconi, R.14
Guanti, G.15
-
27
-
-
0024350881
-
Cancer and the Peutz-Jeghers syndrome
-
Spigelman AD, Murday V, Phillips RK. 1989. Cancer and the Peutz-Jeghers syndrome. Gut 30:1588-1590.
-
(1989)
Gut
, vol.30
, pp. 1588-1590
-
-
Spigelman, A.D.1
Murday, V.2
Phillips, R.K.3
-
28
-
-
0032895374
-
Peutz-Jeghers syndrome: Molecular analysis of three-generation kindred with a novel defect in serine threonine kinase gene STK11
-
Trojan J, Brieger A, Raedle J, Roth WK, Zeuzem S. 1999. Peutz-Jeghers syndrome: molecular analysis of three-generation kindred with a novel defect in serine threonine kinase gene STK11. Am J Gastrol 94:257-261.
-
(1999)
Am J Gastrol
, vol.94
, pp. 257-261
-
-
Trojan, J.1
Brieger, A.2
Raedle, J.3
Roth, W.K.4
Zeuzem, S.5
-
29
-
-
0026004638
-
Laugier-Hunziker syndrome: A clinical, histopathologic, and ultrastructural study of four cases and review of the literature
-
Veraldi S, Cavicchini S, Benelli C, Gasparini G. 1991. Laugier-Hunziker syndrome: a clinical, histopathologic, and ultrastructural study of four cases and review of the literature. J Am Acad Dermatol 25:632-636.
-
(1991)
J Am Acad Dermatol
, vol.25
, pp. 632-636
-
-
Veraldi, S.1
Cavicchini, S.2
Benelli, C.3
Gasparini, G.4
-
30
-
-
0032947283
-
Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients
-
Wang ZJ, Churchman M, Avizienyte E, McKeown C, Davies S, Evans DG, Ferguson A, Ellis I, Xu WH, Yan ZY, Aaltonen LA, Tomlinson IP. 1999. Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients. J Med Genet 36:365-368.
-
(1999)
J Med Genet
, vol.36
, pp. 365-368
-
-
Wang, Z.J.1
Churchman, M.2
Avizienyte, E.3
McKeown, C.4
Davies, S.5
Evans, D.G.6
Ferguson, A.7
Ellis, I.8
Xu, W.H.9
Yan, Z.Y.10
Aaltonen, L.A.11
Tomlinson, I.P.12
-
31
-
-
0033012429
-
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families
-
Westerman AM, Entius MM, Boor PPC, Koole R, de Baar E, Offerhaus GJA, Lubinski J, Lindhour D, Halley DJJ, de Rooij WM, Wilson JHP. 1999. Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families. Hum Mutat 13:476-481.
-
(1999)
Hum Mutat
, vol.13
, pp. 476-481
-
-
Westerman, A.M.1
Entius, M.M.2
Boor, P.P.C.3
Koole, R.4
De Baar, E.5
Offerhaus, G.J.A.6
Lubinski, J.7
Lindhour, D.8
Halley, D.J.J.9
De Rooij, W.M.10
Wilson, J.H.P.11
-
32
-
-
0032906537
-
Mutations and impaired function ofLKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer
-
Ylikorkala A, Avizienyte E, Tomlinson IPM, Tiainen M, Roth S, Loukola A, Hemminki A, Johansson M, Sistonen P, Markie D, Neale K, Phillips R, Zauber P, Twama T, Sampson J, Jarvinen H, Makela TP, Aaltonen LA. 1999. Mutations and impaired function ofLKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer. Hum Mol Genet 8:45-51.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 45-51
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Ylikorkala, A.1
Avizienyte, E.2
Tomlinson, I.P.M.3
Tiainen, M.4
Roth, S.5
Loukola, A.6
Hemminki, A.7
Johansson, M.8
Sistonen, P.9
Markie, D.10
Neale, K.11
Phillips, R.12
Zauber, P.13
Twama, T.14
Sampson, J.15
Jarvinen, H.16
Makela, T.P.17
Aaltonen, L.A.18
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