-
1
-
-
0033093762
-
Maladies associées aux tumeurs annexielles. Tumeurs folliculaires
-
Cribier B. Maladies associées aux tumeurs annexielles. Tumeurs folliculaires. Ann Dermatol Venereol 126 (1999) 270-279
-
(1999)
Ann Dermatol Venereol
, vol.126
, pp. 270-279
-
-
Cribier, B.1
-
2
-
-
0032771551
-
Maladies associées aux tumeurs annexielles. Tumeurs sébacées, tumeurs sudorales
-
Cribier B. Maladies associées aux tumeurs annexielles. Tumeurs sébacées, tumeurs sudorales. Ann Dermatol Venereol 126 (1999) 455-462
-
(1999)
Ann Dermatol Venereol
, vol.126
, pp. 455-462
-
-
Cribier, B.1
-
4
-
-
0036751607
-
Cowden disease or multiple hamartoma syndrome - cutaneous clue to internal malignancy
-
Fistarol S.K., Anliker M.D., and Itin P.H. Cowden disease or multiple hamartoma syndrome - cutaneous clue to internal malignancy. Eur J Dermatol 12 (2002) 411-421
-
(2002)
Eur J Dermatol
, vol.12
, pp. 411-421
-
-
Fistarol, S.K.1
Anliker, M.D.2
Itin, P.H.3
-
5
-
-
0033738748
-
Will the real Cowden syndrome please stand up: revised diagnostic criteria
-
Eng C. Will the real Cowden syndrome please stand up: revised diagnostic criteria. J Med Genet 37 (2000) 828-830
-
(2000)
J Med Genet
, vol.37
, pp. 828-830
-
-
Eng, C.1
-
6
-
-
2342458960
-
Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome
-
Pilarski R., and Eng C. Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome. J Med Genet 41 (2004) 323-326
-
(2004)
J Med Genet
, vol.41
, pp. 323-326
-
-
Pilarski, R.1
Eng, C.2
-
9
-
-
0344069686
-
Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic study
-
Rütten A., Burgdorf W., Hügel H., Kutzner H., Hosseiny-Malayeri H.R., Friedl W., et al. Cystic sebaceous tumors as marker lesions for the Muir-Torre syndrome: a histopathologic and molecular genetic study. Am J Dermatopathol 21 (1999) 405-413
-
(1999)
Am J Dermatopathol
, vol.21
, pp. 405-413
-
-
Rütten, A.1
Burgdorf, W.2
Hügel, H.3
Kutzner, H.4
Hosseiny-Malayeri, H.R.5
Friedl, W.6
-
10
-
-
33747618448
-
An illustrative case of Muir-Torre Syndrome: contribution of immunohistochemical analysis in identifying indicator sebaceous lesions
-
Marazza G., Masouyé I., Taylor S., Prins C., Gaudin T., Saurat J.H., and French L.E. An illustrative case of Muir-Torre Syndrome: contribution of immunohistochemical analysis in identifying indicator sebaceous lesions. Arch Dermatol 142 (2006) 1039-1042
-
(2006)
Arch Dermatol
, vol.142
, pp. 1039-1042
-
-
Marazza, G.1
Masouyé, I.2
Taylor, S.3
Prins, C.4
Gaudin, T.5
Saurat, J.H.6
French, L.E.7
-
11
-
-
0036020476
-
Microsatellite instability and its relevance to cutaneous tumorigenesis
-
Hussein M.R., and Wood G.S. Microsatellite instability and its relevance to cutaneous tumorigenesis. J Cutan Pathol 29 (2002) 257-267
-
(2002)
J Cutan Pathol
, vol.29
, pp. 257-267
-
-
Hussein, M.R.1
Wood, G.S.2
-
12
-
-
45249103326
-
BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reports
-
Toro J.R., Wei M.H., Glenn G.M., Weinreich M., Toure O., Vocke C., et al. BHD mutations, clinical and molecular genetic investigations of Birt-Hogg-Dubé syndrome: a new series of 50 families and a review of published reports. J Med Genet 45 (2008) 321-331
-
(2008)
J Med Genet
, vol.45
, pp. 321-331
-
-
Toro, J.R.1
Wei, M.H.2
Glenn, G.M.3
Weinreich, M.4
Toure, O.5
Vocke, C.6
-
13
-
-
47749095900
-
Birt-Hogg-Dubé (BHD) syndrome: report of two novel germline mutations in the folliculin (FLCN) gene
-
Palmirotta R., Donati P., Savonarola A., Cota C., Ferroni P., and Guadagni F. Birt-Hogg-Dubé (BHD) syndrome: report of two novel germline mutations in the folliculin (FLCN) gene. Eur J Dermatol 18 (2008) 382-386
-
(2008)
Eur J Dermatol
, vol.18
, pp. 382-386
-
-
Palmirotta, R.1
Donati, P.2
Savonarola, A.3
Cota, C.4
Ferroni, P.5
Guadagni, F.6
-
14
-
-
37049023196
-
Birt-Hogg-Dubé syndrome: clinical and genetic studies of 20 families
-
Leter E.M., Koopmans A.K., Gille J.J.P., Van Os T.A., Vittoz G.G., David E.F., et al. Birt-Hogg-Dubé syndrome: clinical and genetic studies of 20 families. J Invest Dermatol 128 (2008) 45-49
-
(2008)
J Invest Dermatol
, vol.128
, pp. 45-49
-
-
Leter, E.M.1
Koopmans, A.K.2
Gille, J.J.P.3
Van Os, T.A.4
Vittoz, G.G.5
David, E.F.6
-
15
-
-
0032808944
-
Acrochordons are not a component of the Birt-Hogg-Dubé syndrome: does this syndrome exist? Case reports and review of the literature
-
De la Torre C., Ocampo C., Doval I.G., Losada A., and Cruces M.J. Acrochordons are not a component of the Birt-Hogg-Dubé syndrome: does this syndrome exist? Case reports and review of the literature. Am J Dermatopathol 21 (1999) 369-374
-
(1999)
Am J Dermatopathol
, vol.21
, pp. 369-374
-
-
De la Torre, C.1
Ocampo, C.2
Doval, I.G.3
Losada, A.4
Cruces, M.J.5
-
16
-
-
0032942317
-
Birt-Hogg-Dubé syndrome and Hornstein-Knickenberg syndrome are the same. Different sectioning technique as the cause of different histology
-
Schulz T., and Hartschuch W. Birt-Hogg-Dubé syndrome and Hornstein-Knickenberg syndrome are the same. Different sectioning technique as the cause of different histology. J Cutan Pathol 26 (1999) 55-61
-
(1999)
J Cutan Pathol
, vol.26
, pp. 55-61
-
-
Schulz, T.1
Hartschuch, W.2
-
17
-
-
0036799242
-
Histomorphologic and immunophenotypic analysis of fibrofolliculomas and trichodiscomas in Birt-Hogg-Dubé syndrome and sporadic disease
-
Collins G.L., Somach S., and Morgan M.B. Histomorphologic and immunophenotypic analysis of fibrofolliculomas and trichodiscomas in Birt-Hogg-Dubé syndrome and sporadic disease. J Cutan Pathol 29 (2002) 529-533
-
(2002)
J Cutan Pathol
, vol.29
, pp. 529-533
-
-
Collins, G.L.1
Somach, S.2
Morgan, M.B.3
-
18
-
-
33645981272
-
Pleuropulmonary pathology of Birt-Hogg-Dubé syndrome
-
Butnor K.J., and Guinee D.G. Pleuropulmonary pathology of Birt-Hogg-Dubé syndrome. Am J Surg Pathol 30 (2006) 395-399
-
(2006)
Am J Surg Pathol
, vol.30
, pp. 395-399
-
-
Butnor, K.J.1
Guinee, D.G.2
-
19
-
-
0035143345
-
Birt-Hogg-Dubé syndrome: treatment of cutaneous manifestations with laser sking resurfacing
-
Jacob C.I., and Dover J.S. Birt-Hogg-Dubé syndrome: treatment of cutaneous manifestations with laser sking resurfacing. Arch Dermatol 137 (2001) 98-99
-
(2001)
Arch Dermatol
, vol.137
, pp. 98-99
-
-
Jacob, C.I.1
Dover, J.S.2
-
20
-
-
0029561613
-
Multiple familial pilomatricomas: a cutaneous marker for Gardner syndrome?
-
Pujol R.M., Casanova J.M., Egido R., Pujol J., and de Moragas J.M. Multiple familial pilomatricomas: a cutaneous marker for Gardner syndrome?. Pediatr Dermatol 12 (1995) 331-335
-
(1995)
Pediatr Dermatol
, vol.12
, pp. 331-335
-
-
Pujol, R.M.1
Casanova, J.M.2
Egido, R.3
Pujol, J.4
de Moragas, J.M.5
-
21
-
-
34249908936
-
Intraosseous pilomatricoma: a possible rare skeletal manifestation of Gardner syndrome
-
Ishida T., Abe S., Miki Y., and Imamura T. Intraosseous pilomatricoma: a possible rare skeletal manifestation of Gardner syndrome. Skeletal Radiol 36 (2007) 693-698
-
(2007)
Skeletal Radiol
, vol.36
, pp. 693-698
-
-
Ishida, T.1
Abe, S.2
Miki, Y.3
Imamura, T.4
-
22
-
-
0028988154
-
Cutaneous cysts of Gardner's syndrome are similar to follicular stem cells
-
Narisawa Y., and Kohda H. Cutaneous cysts of Gardner's syndrome are similar to follicular stem cells. J Cutan Pathol 22 (1995) 115-121
-
(1995)
J Cutan Pathol
, vol.22
, pp. 115-121
-
-
Narisawa, Y.1
Kohda, H.2
-
23
-
-
1842736915
-
Pilomatricoma-like changes in the epidermoid cysts of Gardner syndrome with an APC gene mutation
-
Urabe K., Xia J., Masuda T., Moroi Y., Furue M., and Matsumoto T. Pilomatricoma-like changes in the epidermoid cysts of Gardner syndrome with an APC gene mutation. J Dermatol 31 (2004) 255-257
-
(2004)
J Dermatol
, vol.31
, pp. 255-257
-
-
Urabe, K.1
Xia, J.2
Masuda, T.3
Moroi, Y.4
Furue, M.5
Matsumoto, T.6
-
24
-
-
35348992639
-
The genetics of hereditary colon cancer
-
Rustgi A.K. The genetics of hereditary colon cancer. Gene Dev 21 (2007) 2525-2538
-
(2007)
Gene Dev
, vol.21
, pp. 2525-2538
-
-
Rustgi, A.K.1
-
25
-
-
31944448351
-
Familial adenomatous polyposis (FAP): genotype correlation to FAP phenotype with osteomas and sebaceous cysts
-
Bisgaard M.L., and Bülow S. Familial adenomatous polyposis (FAP): genotype correlation to FAP phenotype with osteomas and sebaceous cysts. Am J Med Genet 140 (2006) 200-204
-
(2006)
Am J Med Genet
, vol.140
, pp. 200-204
-
-
Bisgaard, M.L.1
Bülow, S.2
-
26
-
-
0242635631
-
The concomitant occurrence of multiple epidermal cysts, osteomas and thyroid gland nodules is not diagnostic for Gardner syndrome in the absence of intestinal polyposis: a clinical and genetic report
-
Herrmann S.M., Adler Y.D., Schmidt-Petersen K., Nicaud V., Morrison C., Paul M., and Zouboulis C.C. The concomitant occurrence of multiple epidermal cysts, osteomas and thyroid gland nodules is not diagnostic for Gardner syndrome in the absence of intestinal polyposis: a clinical and genetic report. Br J Dermatol 149 (2003) 877-883
-
(2003)
Br J Dermatol
, vol.149
, pp. 877-883
-
-
Herrmann, S.M.1
Adler, Y.D.2
Schmidt-Petersen, K.3
Nicaud, V.4
Morrison, C.5
Paul, M.6
Zouboulis, C.C.7
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