-
1
-
-
0001182707
-
Cowden's disease. A possible new symptom complex with multiple system involvement
-
Lloyd KM 2nd, Dennis M. Cowden's disease. A possible new symptom complex with multiple system involvement. Ann Intern Med 1963;58:136-42.
-
(1963)
Ann Intern Med
, vol.58
, pp. 136-142
-
-
Lloyd 2nd, K.M.1
Dennis, M.2
-
2
-
-
0028941317
-
-
Hanssen AM, Fryns JP. Cowden syndrome. J Med Genet 1995;32:117-19.
-
Hanssen AM, Fryns JP. Cowden syndrome. J Med Genet 1995;32:117-19.
-
-
-
-
3
-
-
0031975070
-
Clinical and pathological features of breast disease in Cowden's syndrome: An underrecognized syndrome with an increased risk of breast cancer
-
Schrager CA, Schneider D, Gruener AC, et al. Clinical and pathological features of breast disease in Cowden's syndrome: an underrecognized syndrome with an increased risk of breast cancer. Hum Pathol 1998;29:47-53.
-
(1998)
Hum Pathol
, vol.29
, pp. 47-53
-
-
Schrager, C.A.1
Schneider, D.2
Gruener, A.C.3
-
4
-
-
0031766247
-
Similarities of cutaneous and breast pathology in Cowden's syndrome
-
Schrager CA, Schneider D, Gruener AC, et al. Similarities of cutaneous and breast pathology in Cowden's syndrome. Exp Dermatol 1998;7:380-90.
-
(1998)
Exp Dermatol
, vol.7
, pp. 380-390
-
-
Schrager, C.A.1
Schneider, D.2
Gruener, A.C.3
-
5
-
-
0025865691
-
Lhermitte-Duclos disease and Cowden disease: A single phakomatosis
-
Padberg GW, Schot JD, Vielvoye GJ, et al. Lhermitte-Duclos disease and Cowden disease: a single phakomatosis. Ann Neurol 1991;29:517-23.
-
(1991)
Ann Neurol
, vol.29
, pp. 517-523
-
-
Padberg, G.W.1
Schot, J.D.2
Vielvoye, G.J.3
-
6
-
-
0022649866
-
The Cowden syndrome: A clinical and genetic study in 21 patients
-
Starink TM, van der Veen JP, Arwert F, et al. The Cowden syndrome: a clinical and genetic study in 21 patients. Clin Genet 1986;29:222-33.
-
(1986)
Clin Genet
, vol.29
, pp. 222-233
-
-
Starink, T.M.1
van der Veen, J.P.2
Arwert, F.3
-
7
-
-
0032853452
-
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
-
Marsh DJ, Kum JB, Lunetta KL, et al. PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome. Hum Mol Genet 1999;8:1461-72.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1461-1472
-
-
Marsh, D.J.1
Kum, J.B.2
Lunetta, K.L.3
-
12
-
-
0029148158
-
Cutaneous sclerotic fibroma. Immunohistochemical evidence of a fibroblastic neoplasm with ongoing type I collagen synthesis
-
Shitabata PK, Crouch EC, Fitzgibbon JF, et al. Cutaneous sclerotic fibroma. Immunohistochemical evidence of a fibroblastic neoplasm with ongoing type I collagen synthesis. Am J Dermatopathol 1995;17:339-43.
-
(1995)
Am J Dermatopathol
, vol.17
, pp. 339-343
-
-
Shitabata, P.K.1
Crouch, E.C.2
Fitzgibbon, J.F.3
-
13
-
-
0030451834
-
Solitary sclerotic fibroma of the skin: A sclerotic dermatofibroma?
-
Pujol RM, de Castro F, Schroeter AL, et al. Solitary sclerotic fibroma of the skin: a sclerotic dermatofibroma? Am J Dermatopathol 1996;18:620-4.
-
(1996)
Am J Dermatopathol
, vol.18
, pp. 620-624
-
-
Pujol, R.M.1
de Castro, F.2
Schroeter, A.L.3
-
15
-
-
0026787939
-
Multiple sclerotic fibromas of the skin. A cutaneous marker of Cowden's disease
-
Requena L, Gutierrez J, Sanchez YE. Multiple sclerotic fibromas of the skin. A cutaneous marker of Cowden's disease. J Cutan Pathol 1992;19:346-51.
-
(1992)
J Cutan Pathol
, vol.19
, pp. 346-351
-
-
Requena, L.1
Gutierrez, J.2
Sanchez, Y.E.3
|