-
1
-
-
16944366639
-
The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8p21
-
Saar K, Chrzanowska KH, Stumm M, Jung M, Nurnberg G, Wienker TF, Seemanova E, Wegner RD, Reis A, Sperling K. The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8p21. Am J Hum Genet 1997;60:605-10.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 605-610
-
-
Saar, K.1
Chrzanowska, K.H.2
Stumm, M.3
Jung, M.4
Nurnberg, G.5
Wienker, T.F.6
Seemanova, E.7
Wegner, R.D.8
Reis, A.9
Sperling, K.10
-
2
-
-
0032231476
-
Fine localization of the Nijmegen breakage syndrome gene to 8q21: Evidence for a common founder haplotype
-
Cerosaletti KM, Lange E, Stringham HM, Weemaes CM, Smeets D, Solder B, Belohradsky BH, Taylor AM, Karnes P, Eliott A, Komatsu K, Gatti RA, et al. Fine localization of the Nijmegen breakage syndrome gene to 8q21: evidence for a common founder haplotype. Am J Hum Genet 1998;63:125-34.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 125-134
-
-
Cerosaletti, K.M.1
Lange, E.2
Stringham, H.M.3
Weemaes, C.M.4
Smeets, D.5
Solder, B.6
Belohradsky, B.H.7
Taylor, A.M.8
Karnes, P.9
Eliott, A.10
Komatsu, K.11
Gatti, R.A.12
-
3
-
-
0019478575
-
A new chromosomal instability disorder. The Nijmegen breakage syndrome
-
Weemaes CM, Husting TW, Scheres JM, van Munster PJ, Bakkeren JA, Taalman RD. A new chromosomal instability disorder. The Nijmegen breakage syndrome. Acta Paediatr Scand 1981;70:557-64.
-
(1981)
Acta Paediatr Scand
, vol.70
, pp. 557-564
-
-
Weemaes, C.M.1
Husting, T.W.2
Scheres, J.M.3
Van Munster, P.J.4
Bakkeren, J.A.5
Taalman, R.D.6
-
5
-
-
0033710938
-
Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slavic populations
-
Varon R, Seemanova E, Chrzanowska K, Hnateyko O, Piekutowska-Abramczuk D, Krajewska-Walasek M, Sykut-Cegielska J, Sperling K, Reis A. Clinical ascertainment of Nijmegen breakage syndrome (NBS) and prevalence of the major mutation, 657del5, in three Slavic populations. Eur J Hum Genet 2000;8:900-2.
-
(2000)
Eur J Hum Genet
, vol.8
, pp. 900-902
-
-
Varon, R.1
Seemanova, E.2
Chrzanowska, K.3
Hnateyko, O.4
Piekutowska-Abramczuk, D.5
Krajewska-Walasek, M.6
Sykut-Cegielska, J.7
Sperling, K.8
Reis, A.9
-
6
-
-
0000770165
-
Nijmegen breakage syndrome
-
The International Nijmegen Breakage Syndrome Study Group. Nijmegen breakage syndrome. Arch Dis Child 2000;82:400-6
-
(2000)
Arch Dis Child
, vol.82
, pp. 400-406
-
-
-
7
-
-
0032076190
-
Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome
-
Varon R, Vissinga C, Platzer M, Cerosaletti KM, Chrzanowska KH, Saar K, Beckmann G, Seemanowa E, Cooper PR, Nowak NJ, Stumm M, Weemaes CM, et al. Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell 1998;93:467-76.
-
(1998)
Cell
, vol.93
, pp. 467-476
-
-
Varon, R.1
Vissinga, C.2
Platzer, M.3
Cerosaletti, K.M.4
Chrzanowska, K.H.5
Saar, K.6
Beckmann, G.7
Seemanowa, E.8
Cooper, P.R.9
Nowak, N.J.10
Stumm, M.11
Weemaes, C.M.12
-
8
-
-
3242892589
-
Nijmegen breakage syndrome: Clinical manifestation of defective response to DNA double-strand breaks
-
Digweed M, Sperling K. Nijmegen breakage syndrome: clinical manifestation of defective response to DNA double-strand breaks. DNA Repair (Amst) 2004;3:1207-17.
-
(2004)
DNA Repair (Amst)
, vol.3
, pp. 1207-1217
-
-
Digweed, M.1
Sperling, K.2
-
9
-
-
4444293274
-
Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex
-
Matsuura S, Kobayashi J, Tauchi H, Komatsu K. Nijmegen breakage syndrome and DNA double strand break repair by NBS1 complex. Adv Biophys 2004;38:65-80.
-
(2004)
Adv Biophys
, vol.38
, pp. 65-80
-
-
Matsuura, S.1
Kobayashi, J.2
Tauchi, H.3
Komatsu, K.4
-
10
-
-
4644345015
-
The Nijmegen breakage syndrome gene and its role in genome stability
-
Iijima K, Komatsu K, Matsuura S, Tauchi H. The Nijmegen breakage syndrome gene and its role in genome stability. Chromosoma 2004;113:53-61.
-
(2004)
Chromosoma
, vol.113
, pp. 53-61
-
-
Iijima, K.1
Komatsu, K.2
Matsuura, S.3
Tauchi, H.4
-
11
-
-
17644392463
-
Cell biology. Guiding ATM to broken DNA
-
Abraham RT, Tibbetts RS. Cell biology. Guiding ATM to broken DNA. Science 2005;308:510-11.
-
(2005)
Science
, vol.308
, pp. 510-511
-
-
Abraham, R.T.1
Tibbetts, R.S.2
-
12
-
-
33745183042
-
The frequency of heterozygous mutation 657del5 carriers of the NBS1 gene in the Wielkopolska voivodship
-
in press
-
Ziólkowska I, Mosor M, Nowak J. The frequency of heterozygous mutation 657del5 carriers of the NBS1 gene in the Wielkopolska voivodship. J Appl Genet, in press.
-
J Appl Genet
-
-
Ziólkowska, I.1
Mosor, M.2
Nowak, J.3
-
13
-
-
3042818662
-
Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland
-
Steffen J, Varon R, Mosor M, Maneva G, Maurer M, Stumm M, Nowakowska D, Rubach M, Kosakowska E, Ruka W, Nowecki Z, Rutkowski P, et al. Increased cancer risk of heterozygotes with NBS1 germline mutations in Poland. Int J Cancer 2004;111:67-71.
-
(2004)
Int J Cancer
, vol.111
, pp. 67-71
-
-
Steffen, J.1
Varon, R.2
Mosor, M.3
Maneva, G.4
Maurer, M.5
Stumm, M.6
Nowakowska, D.7
Rubach, M.8
Kosakowska, E.9
Ruka, W.10
Nowecki, Z.11
Rutkowski, P.12
-
14
-
-
17144442945
-
Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin
-
Dȩbniak T, Górski B, Cybulski C, Jakubowska A, Kurzawski G, Lener M, Mierzejewski M, Masojć B, Mȩdrek K, Kladny J, Zaluga E, Maleszka R, et al. Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin. Melanoma Res 2003; 13:365-70.
-
(2003)
Melanoma Res
, vol.13
, pp. 365-370
-
-
Dȩbniak, T.1
Górski, B.2
Cybulski, C.3
Jakubowska, A.4
Kurzawski, G.5
Lener, M.6
Mierzejewski, M.7
Masojć, B.8
Mȩdrek, K.9
Kladny, J.10
Zaluga, E.11
Maleszka, R.12
-
15
-
-
10744233070
-
NBS1 is a prostate cancer susceptibility gene
-
Cybulski C, Górski B, Dȩbniak T, Gliniewicz B, Mierzejewski M, Masojć B, Jakubowska A, Matyjasik J, Zlowocka E, Sikorski A, Narod SA, Lubiński J. NBS1 is a prostate cancer susceptibility gene. Cancer Res 2004;64:1215-19.
-
(2004)
Cancer Res
, vol.64
, pp. 1215-1219
-
-
Cybulski, C.1
Górski, B.2
Dȩbniak, T.3
Gliniewicz, B.4
Mierzejewski, M.5
Masojć, B.6
Jakubowska, A.7
Matyjasik, J.8
Zlowocka, E.9
Sikorski, A.10
Narod, S.A.11
Lubiński, J.12
-
16
-
-
0035328489
-
Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL)
-
Varon R, Reis A, Henze G, von Einsiedel HG, Sperling K, Seeger K. Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL). Cancer Res 2001;61: 3570-2.
-
(2001)
Cancer Res
, vol.61
, pp. 3570-3572
-
-
Varon, R.1
Reis, A.2
Henze, G.3
Von Einsiedel, H.G.4
Sperling, K.5
Seeger, K.6
-
17
-
-
0141918879
-
Letters to the editor
-
Taylor GM, O'Brien HP, Greaves MF, Ravetto PF, Eden OB. Letters to the editor. Cancer Res 2003;63:6563-4.
-
(2003)
Cancer Res
, vol.63
, pp. 6563-6564
-
-
Taylor, G.M.1
O'Brien, H.P.2
Greaves, M.F.3
Ravetto, P.F.4
Eden, O.B.5
-
18
-
-
0035328489
-
Mutation in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia
-
Correspondence re: Varon R, et al. Mutation in the Nijmegen breakage syndrome gene (NBS1) in childhood acute lymphoblastic leukemia. Cancer Res 2001;61:3570-3572.
-
(2001)
Cancer Res
, vol.61
, pp. 3570-3572
-
-
Varon, R.1
-
19
-
-
33645125102
-
Nijmegen Breakage syndrome (NBS) with immunological abnormalities and without chromosomal instability
-
in press
-
Seemanova E, Sperling K, Neitzel H, Varon R, Hadac J, Butova O, Schrock E, Seeman P, Digweed M. Nijmegen Breakage syndrome (NBS) with immunological abnormalities and without chromosomal instability. J Med Genet, in press..
-
J Med Genet
-
-
Seemanova, E.1
Sperling, K.2
Neitzel, H.3
Varon, R.4
Hadac, J.5
Butova, O.6
Schrock, E.7
Seeman, P.8
Digweed, M.9
-
20
-
-
0038505600
-
Germline 657del5 mutation in the NBS1 gene in breast cancer patients
-
Górski B, Dȩbniak T, Masojć B, Mierzejewski M, Mȩdrek K, Cybulski C, Jakubowska A, Kurzawski G, Chosia M, Scott R, Lubinski J. Germline 657del5 mutation in the NBS1 gene in breast cancer patients. Int J Cancer 2003;106:379-81.
-
(2003)
Int J Cancer
, vol.106
, pp. 379-381
-
-
Górski, B.1
Dȩbniak, T.2
Masojć, B.3
Mierzejewski, M.4
Mȩdrek, K.5
Cybulski, C.6
Jakubowska, A.7
Kurzawski, G.8
Chosia, M.9
Scott, R.10
Lubinski, J.11
-
21
-
-
20044366887
-
NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia
-
Buslov KG, Iyevleva AG, Chekmariova EV, Suspitsin EN, Togo AV, Kuligina ESh, Sokolenko AP, Matsko DE, Turkevich EA, Lazareva YR, Chagunava OL, Bit-Sava EM, et al. NBS1 657del5 mutation may contribute only to a limited fraction of breast cancer cases in Russia. Int J Cancer 2005;114:585-9.
-
(2005)
Int J Cancer
, vol.114
, pp. 585-589
-
-
Buslov, K.G.1
Iyevleva, A.G.2
Chekmariova, E.V.3
Suspitsin, E.N.4
Togo, A.V.5
Kuligina, E.Sh.6
Sokolenko, A.P.7
Matsko, D.E.8
Turkevich, E.A.9
Lazareva, Y.R.10
Chagunava, O.L.11
Bit-Sava, E.M.12
-
22
-
-
0032792820
-
Determination of the frequency of the common 657del5 Nijmegen breakage syndrome mutation in the German population: No association with risk of breast cancer
-
Carlomagno F, Chang-Claude J, Dunning AM, Ponder BA. Determination of the frequency of the common 657del5 Nijmegen breakage syndrome mutation in the German population: no association with risk of breast cancer. Genes Chromosomes Cancer 1999;25:393-5.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 393-395
-
-
Carlomagno, F.1
Chang-Claude, J.2
Dunning, A.M.3
Ponder, B.A.4
-
23
-
-
2942572799
-
A high proportion of founder BRCA1 mutations in Polish breast cancer families
-
Górski B, Jakubowska A, Huzarski T, Byrski T, Gronwald J, Grzybowska E, Mackiewicz A, Stawicka M, Bȩbenek M, Sorokin D, Fiszer-Maliszewska Ł, Haus O, et al. A high proportion of founder BRCA1 mutations in Polish breast cancer families. Int J Cancer 2004;110:683-6.
-
(2004)
Int J Cancer
, vol.110
, pp. 683-686
-
-
Górski, B.1
Jakubowska, A.2
Huzarski, T.3
Byrski, T.4
Gronwald, J.5
Grzybowska, E.6
Mackiewicz, A.7
Stawicka, M.8
Bȩbenek, M.9
Sorokin, D.10
Fiszer-Maliszewska, Ł.11
Haus, O.12
-
24
-
-
0030910022
-
The risk of cancer associated with the 185delAG and 5382insC mutations of BRCA1 and the 6174delT mutation of BRCA2 among Ashkenazi Jews
-
Struewing JP, Hange P, Wacholder S, Baker SM, Berlin M, McAdams M, Timmerman MM, Brody LC, Tucker MA. The risk of cancer associated with the 185delAG and 5382insC mutations of BRCA1 and the 6174delT mutation of BRCA2 among Ashkenazi Jews. N Engl J Med 1997;336:1401-8.
-
(1997)
N Engl J Med
, vol.336
, pp. 1401-1408
-
-
Struewing, J.P.1
Hange, P.2
Wacholder, S.3
Baker, S.M.4
Berlin, M.5
McAdams, M.6
Timmerman, M.M.7
Brody, L.C.8
Tucker, M.A.9
-
25
-
-
0036836572
-
Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma
-
Cerosaletti KM, Morrison VA, Sabath DE, Willerford DM, Concannon P. Mutations and molecular variants of the NBS1 gene in non-Hodgkin lymphoma. Genes Chromosomes Cancer 2002;35:282-6.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 282-286
-
-
Cerosaletti, K.M.1
Morrison, V.A.2
Sabath, D.E.3
Willerford, D.M.4
Concannon, P.5
-
26
-
-
9644294330
-
Cancer risk according to type and location of ATM mutation in ataxia-telangiectasia families
-
Cavaciuti E, Lauge A, Janin N, Ossian K, Hall J, Stoppa-Lyonnet D, Andrieu N. Cancer risk according to type and location of ATM mutation in ataxia-telangiectasia families. Genes Chromosomes Cancer 2005;42:1-9.
-
(2005)
Genes Chromosomes Cancer
, vol.42
, pp. 1-9
-
-
Cavaciuti, E.1
Lauge, A.2
Janin, N.3
Ossian, K.4
Hall, J.5
Stoppa-Lyonnet, D.6
Andrieu, N.7
-
27
-
-
20544474516
-
Cancer risk and mortality in heterozygous ATM mutation carriers
-
Thompson D, Duedal S, Kirner J, McGuffog L, Last J, Reiman A, Byrd P, Taylor M, Easton DF. Cancer risk and mortality in heterozygous ATM mutation carriers. J Natl Cancer Inst 2005;97:813-22.
-
(2005)
J Natl Cancer Inst
, vol.97
, pp. 813-822
-
-
Thompson, D.1
Duedal, S.2
Kirner, J.3
McGuffog, L.4
Last, J.5
Reiman, A.6
Byrd, P.7
Taylor, M.8
Easton, D.F.9
-
28
-
-
0142178215
-
Breast and ovarian cancer risk due to inherited mutations in BRCA1 and BRCA2
-
King MC, Marks JH, Mandell JB for the New York Breast Cancer Study Group. Breast and ovarian cancer risk due to inherited mutations in BRCA1 and BRCA2. Science 2003;302:643-6
-
(2003)
Science
, vol.302
, pp. 643-646
-
-
King, M.C.1
Marks, J.H.2
Mandell, J.B.3
-
30
-
-
33745191781
-
Preliminary evaluation of the frequencies and types of BRCA1 germline mutations among patients with familial and sporadic breast and ovarian cancers from 3 regions of Poland
-
(Abstract). Special issue on IV Polish Conference on Diagnosis and Treatment of Breast Cancer
-
Kluska A, Wojciechowska-Ła̧cka A, Pia̧tkowska M, Nowakowska D, Balabas A, Rachtan J, Molong I, Skasko E, Niwińska A, Kwiatkowska E, Steffen J. Preliminary evaluation of the frequencies and types of BRCA1 germline mutations among patients with familial and sporadic breast and ovarian cancers from 3 regions of Poland (in polish). Nowotwory J Oncol 2005;55 (Suppl 2)27 (Abstract). Special issue on IV Polish Conference on Diagnosis and Treatment of Breast Cancer.
-
(2005)
Nowotwory J Oncol
, vol.55
, Issue.SUPPL. 2
, pp. 27
-
-
Kluska, A.1
Wojciechowska-Ła̧cka, A.2
Pia̧tkowska, M.3
Nowakowska, D.4
Balabas, A.5
Rachtan, J.6
Molong, I.7
Skasko, E.8
Niwińska, A.9
Kwiatkowska, E.10
Steffen, J.11
-
31
-
-
0242610857
-
Nbn heterozygosity renders mice susceptible to tumor formation and ionizing radiation-induced tumorigenesis
-
Dumon-Jones V, Frappart PO, Tong WM, Sajithlal G, Hulla W, Schmid G, Herceg Z, Digweed M, Wang ZQ. Nbn heterozygosity renders mice susceptible to tumor formation and ionizing radiation-induced tumorigenesis. Cancer Res 2003;63:7263-9.
-
(2003)
Cancer Res
, vol.63
, pp. 7263-7269
-
-
Dumon-Jones, V.1
Frappart, P.O.2
Tong, W.M.3
Sajithlal, G.4
Hulla, W.5
Schmid, G.6
Herceg, Z.7
Digweed, M.8
Wang, Z.Q.9
-
32
-
-
0032728442
-
Therapy for non-Hodgkin lymphoma in children with primary immunodeficiency: Analysis of 19 patients from the BFM trials
-
Seidemann K, Tiemann M, Henze G, Sauerbrey A, Muller S, Reiter A. Therapy for non-Hodgkin lymphoma in children with primary immunodeficiency: analysis of 19 patients from the BFM trials. Med Pediatr Oncol 1999;33:536-44.
-
(1999)
Med Pediatr Oncol
, vol.33
, pp. 536-544
-
-
Seidemann, K.1
Tiemann, M.2
Henze, G.3
Sauerbrey, A.4
Muller, S.5
Reiter, A.6
-
33
-
-
0038748216
-
Fatal toxicity following radio- and chemotherapy of medulloblastoma in a child with unrecognized Nijmegen breakage syndrome
-
Distel L, Neubauer S, Varon R, Holler W, Grabenbauer G. Fatal toxicity following radio- and chemotherapy of medulloblastoma in a child with unrecognized Nijmegen breakage syndrome. Med Pediatr Oncol 2003;41:44-8.
-
(2003)
Med Pediatr Oncol
, vol.41
, pp. 44-48
-
-
Distel, L.1
Neubauer, S.2
Varon, R.3
Holler, W.4
Grabenbauer, G.5
-
34
-
-
0037337734
-
Medulloblastoma with adverse reaction to radiation therapy in Nijmegen breakage syndrome
-
Bakhshi S, Cerosaletti KM, Concannon P, Bawle EV, Fontanesi J, Gatti RA, Bhambhani K. Medulloblastoma with adverse reaction to radiation therapy in Nijmegen breakage syndrome. J Pediatr Hematol Oncol 2003;25:248-51.
-
(2003)
J Pediatr Hematol Oncol
, vol.25
, pp. 248-251
-
-
Bakhshi, S.1
Cerosaletti, K.M.2
Concannon, P.3
Bawle, E.V.4
Fontanesi, J.5
Gatti, R.A.6
Bhambhani, K.7
-
35
-
-
5144230063
-
Rhabdomyosarcoma in Nijmegen breakage syndrome: Strong association with perianal primary site
-
Meyer S, Kingston H, Taylor AM, Byrd PJ, Last JI, Brennan BM, Trueman S, Kelsey A, Taylor GM, Eden OB. Rhabdomyosarcoma in Nijmegen breakage syndrome: strong association with perianal primary site. Cancer Genet Cytogenet 2004;154:169-74.
-
(2004)
Cancer Genet Cytogenet
, vol.154
, pp. 169-174
-
-
Meyer, S.1
Kingston, H.2
Taylor, A.M.3
Byrd, P.J.4
Last, J.I.5
Brennan, B.M.6
Trueman, S.7
Kelsey, A.8
Taylor, G.M.9
Eden, O.B.10
-
36
-
-
16844384184
-
DNA lesion-specific colocalization of the Mre11/Rad50/Nbs1 (MRN) complex and replication protein A (RPA) to repair foci
-
Robinson JG, Lu L, Dixon K, Bissler JJ. DNA lesion-specific colocalization of the Mre11/Rad50/Nbs1 (MRN) complex and replication protein A (RPA) to repair foci. J Biol Chem 2005;280:12927-34.
-
(2005)
J Biol Chem
, vol.280
, pp. 12927-12934
-
-
Robinson, J.G.1
Lu, L.2
Dixon, K.3
Bissler, J.J.4
-
37
-
-
0035807219
-
Inhibition of BRCA1 leads to increased chemoresistance to microtubule-interfering agents, an effect that involves the JNK pathway
-
Lafarge S, Sylvain V, Ferrara M, Bignon YJ. Inhibition of BRCA1 leads to increased chemoresistance to microtubule-interfering agents, an effect that involves the JNK pathway. Oncogene 2001;20:6597-606.
-
(2001)
Oncogene
, vol.20
, pp. 6597-6606
-
-
Lafarge, S.1
Sylvain, V.2
Ferrara, M.3
Bignon, Y.J.4
-
38
-
-
0038147067
-
BRCA1 expression modulates chemosensitivity of BRCA1 defective HCC1937 human breast cancer cells
-
Tassone P, Tagliaferri P, Perricelli A, Blotta S, Quaresima B, Martelli ML, Goel A, Barbieri V, Costanzo F, Boland CR, Venuta S. BRCA1 expression modulates chemosensitivity of BRCA1 defective HCC1937 human breast cancer cells. Br J Cancer 2003;88:1285-91.
-
(2003)
Br J Cancer
, vol.88
, pp. 1285-1291
-
-
Tassone, P.1
Tagliaferri, P.2
Perricelli, A.3
Blotta, S.4
Quaresima, B.5
Martelli, M.L.6
Goel, A.7
Barbieri, V.8
Costanzo, F.9
Boland, C.R.10
Venuta, S.11
-
39
-
-
0037288936
-
Frequent disease progression and early recurrence in patients with familial ovarian cancer primarily treated with paclitaxel and cis- or carboplatin (preliminary report)
-
Wojciechowska-Ła̧cka A, Markowska J, Skasko E, Kruczek A, Steffen J. Frequent disease progression and early recurrence in patients with familial ovarian cancer primarily treated with paclitaxel and cis- or carboplatin (preliminary report). Eur J Gynaec Oncol 2002;20:21-4.
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(2002)
Eur J Gynaec Oncol
, vol.20
, pp. 21-24
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Wojciechowska-Ła̧cka, A.1
Markowska, J.2
Skasko, E.3
Kruczek, A.4
Steffen, J.5
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