-
1
-
-
0030140025
-
Localization of the gene for Cowden disease to chromosome 10q22-23
-
Nelen MR, Padberg GW, Peeters EA, et al. Localization of the gene for Cowden disease to chromosome 10q22-23. Nat Genet. 1996;13(1):114-116. (Pubitemid 126528240)
-
(1996)
Nature Genetics
, vol.13
, Issue.1
, pp. 114-116
-
-
Nelen, M.R.1
Padberg, G.W.2
Peeters, E.A.J.3
Lin, A.Y.4
Van Den, H.B.5
Frants, R.R.6
Coulon, V.7
Goldstein, A.M.8
Van Reen, M.M.M.9
Easton, D.F.10
Eeles, R.A.11
Hodgson, S.12
Mulvihill, J.J.13
Murday, V.A.14
Tucker, M.A.15
Mariman, E.C.M.16
Starink, T.M.17
Ponder, B.A.J.18
Ropers, H.H.19
Kremer, H.20
Longy, M.21
Eng, C.22
more..
-
2
-
-
70350238781
-
PTEN hamartoma tumor syndrome: An overview
-
Hobert JA, Eng C. PTEN hamartoma tumor syndrome: an overview. Genet Med. 2009;11(10):687-694.
-
(2009)
Genet Med
, vol.11
, Issue.10
, pp. 687-694
-
-
Hobert, J.A.1
Eng, C.2
-
3
-
-
0032905101
-
Novel PTEN mutations in patients with Cowden disease: Absence of clear genotype-phenotype correlations
-
DOI 10.1038/sj.ejhg.5200289
-
Nelen MR, Kremer H, Konings IB, et al. Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations. Eur J Hum Genet. 1999;7(3):267-273. (Pubitemid 29213732)
-
(1999)
European Journal of Human Genetics
, vol.7
, Issue.3
, pp. 267-273
-
-
Nelen, M.R.1
Kremer, H.2
Konings, I.B.M.3
Schoute, F.4
Van Essen, A.J.5
Koch, R.6
Woods, C.G.7
Fryns, J.-P.8
Hamel, B.9
Hoefsloot, L.H.10
Peeters, E.A.J.11
Padberg, G.W.12
-
4
-
-
79951903547
-
Oncophenotypic review and clinical correlates of phosphatase and tensin homolog on chromosome 10 hamartoma tumor syndrome
-
Patnaik MM, Raza SS, Khambatta S, Stanich PP, Goetz MP. Oncophenotypic review and clinical correlates of phosphatase and tensin homolog on chromosome 10 hamartoma tumor syndrome. J Clin Oncol. 2010;28(36):e767-e768.
-
(2010)
J Clin Oncol
, vol.28
, Issue.36
-
-
Patnaik, M.M.1
Raza, S.S.2
Khambatta, S.3
Stanich, P.P.4
Goetz, M.P.5
-
5
-
-
58849157647
-
Cowden syndrome: A critical review of the clinical literature
-
Pilarski R. Cowden syndrome: a critical review of the clinical literature. J Genet Couns. 2009;18(1):13-27.
-
(2009)
J Genet Couns
, vol.18
, Issue.1
, pp. 13-27
-
-
Pilarski, R.1
-
6
-
-
0021707317
-
Colorectal polyps in Cowden's disease (multiple hamartoma syndrome)
-
Carlson GJ, Nivatvongs S, Snover DC. Colorectal polyps in Cowden's disease (multiple hamartoma syndrome). Am J Surg Pathol. 1984;8(10):763-770.
-
(1984)
Am J Surg Pathol
, vol.8
, Issue.10
, pp. 763-770
-
-
Carlson, G.J.1
Nivatvongs, S.2
Snover, D.C.3
-
7
-
-
0028009373
-
Gastrointestinal manifestations of Cowden's disease: Report of four cases
-
Hizawa K, Iida M, Matsumoto T, et al. Gastrointestinal manifestations of Cowden's disease: report of four cases. J Clin Gastroenterol. 1994;18(1):13-18. (Pubitemid 24004297)
-
(1994)
Journal of Clinical Gastroenterology
, vol.18
, Issue.1
, pp. 13-18
-
-
Hizawa, K.1
Iida, M.2
Matsumoto, T.3
Kohrogi, N.4
Suekane, H.5
Yao, T.6
Fujishima, M.7
-
8
-
-
0028158105
-
Cowden's disease with extensive gastrointestinal polyposis
-
Marra G, Armelao F, Vecchio FM, Percesepe A, Anti M. Cowden's disease with extensive gastrointestinal polyposis. J Clin Gastroenterol. 1994;18(1):42-47. (Pubitemid 24004303)
-
(1994)
Journal of Clinical Gastroenterology
, vol.18
, Issue.1
, pp. 42-47
-
-
Marra, G.1
Armelao, F.2
Vecchio, F.M.3
Percesepe, A.4
Anti, M.5
-
9
-
-
0023248731
-
Cowden's disease: A case report an literature review
-
Chen YM, Ott DJ, Wu WC, Gelfand DW. Cowden's disease: a case report and literature review. Gastrointest Radiol. 1987;12(4):325-329. (Pubitemid 17101216)
-
(1987)
Gastrointestinal Radiology
, vol.12
, Issue.4
, pp. 325-329
-
-
Chen, Y.M.1
Ott, D.J.2
Wu, W.C.3
Gelfand, D.W.4
-
10
-
-
30344437009
-
Cowden syndrome: Report of two cases and review of clinical presentation and management of a rare colorectal polyposis
-
DOI 10.1016/j.cursur.2005.04.015, PII S0149794405000747
-
Campos FG, Habr-Gama A, Kiss DR, et al. Cowden syndrome: report of two cases and review of clinical presentation and management of a rare colorectal polyposis. Curr Surg. 2006;63(1):15-19. (Pubitemid 43055592)
-
(2006)
Current Surgery
, vol.63
, Issue.1
, pp. 15-19
-
-
Campos, F.G.1
Habr-Gama, A.2
Kiss, D.R.3
Atui, F.C.4
Rawet, V.5
Goldstein, P.J.6
Gama-Rodrigues, J.7
-
12
-
-
13944265646
-
The hamartomatous polyposis syndromes: A clinical and molecular review
-
DOI 10.1111/j.1572-0241.2005.40237.x
-
Schreibman IR, Baker M, Amos C, McGarrity TJ. The hamartomatous polyposis syndromes: a clinical and molecular review. Am J Gastroenterol. 2005;100(2):476-490. (Pubitemid 40314537)
-
(2005)
American Journal of Gastroenterology
, vol.100
, Issue.2
, pp. 476-490
-
-
Schreibman, I.R.1
Baker, M.2
Amos, C.3
McGarrity, T.J.4
-
13
-
-
0022997995
-
Cowden disease. A hereditary polyposis syndrome diagnosable by mucocutaneous inspection
-
Hover AR, Cawthern T, McDanial W. Cowden disease: a hereditary polyposis syndrome diagnosable by mucocutaneous inspection. J Clin Gastroenterol. 1986;8(5):576-579. (Pubitemid 17180563)
-
(1986)
Journal of Clinical Gastroenterology
, vol.8
, Issue.5
, pp. 576-579
-
-
Hover, A.R.1
Cawthern, T.2
McDanial, W.3
-
15
-
-
34548513847
-
Multiple colon carcinomas in a patient with Cowden syndrome
-
Bosserhoff AK, Grussendorf-Conen EI, Rubben A, et al. Multiple colon carcinomas in a patient with Cowden syndrome. Int J Mol Med. 2006;18(4):643-647.
-
(2006)
Int J Mol Med
, vol.18
, Issue.4
, pp. 643-647
-
-
Bosserhoff, A.K.1
Grussendorf-Conen, E.I.2
Rubben, A.3
-
16
-
-
78649707989
-
Frequent gastrointestinal polyps and colorectal adenocarcinomas in a prospective series of PTEN mutation carriers
-
Heald B, Mester J, Rybicki L, Orloff MS, Burke CA, Eng C. Frequent gastrointestinal polyps and colorectal adenocarcinomas in a prospective series of PTEN mutation carriers. Gastroenterology. 2010;139(6):1927-1933.
-
(2010)
Gastroenterology
, vol.139
, Issue.6
, pp. 1927-1933
-
-
Heald, B.1
Mester, J.2
Rybicki, L.3
Orloff, M.S.4
Burke, C.A.5
Eng, C.6
-
17
-
-
78650887621
-
Cancer and Lhermitte-Duclos disease are common in Cowden syndrome patients
-
Riegert-Johnson DL, Gleeson FC, Roberts M, et al. Cancer and Lhermitte-Duclos disease are common in Cowden syndrome patients. Hered Cancer Clin Pract. 2010;8(1):6.
-
(2010)
Hered Cancer Clin Pract
, vol.8
, Issue.1
, pp. 6
-
-
Riegert-Johnson, D.L.1
Gleeson, F.C.2
Roberts, M.3
-
18
-
-
84863944009
-
Genetic/familial high-risk assessment: Breast and ovarian
-
Published March 8, Accessed May 14. 2010
-
National Comprehensive Cancer Network. Genetic/familial high-risk assessment: breast and ovarian. NCCN Clinical Practice Guidelines in Oncology. Published March 8, 2010. http://www.nccn.org/professionals/physician-gls/PDF/ genetics-screening.pdf. Accessed May 14. 2010.
-
(2010)
NCCN Clinical Practice Guidelines in Oncology
-
-
-
19
-
-
77957118417
-
-
7th ed. New York, NY: Springer
-
Edge SB, Byrd DR, Compton CC, Green FL, Trotti A. Cancer Staging Manual. 7th ed. New York, NY: Springer; 2010.
-
(2010)
Cancer Staging Manual
-
-
Edge, S.B.1
Byrd, D.R.2
Compton, C.C.3
Green, F.L.4
Trotti, A.5
-
20
-
-
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. 2000;37(11):828-830.
-
(2000)
J Med Genet
, vol.37
, Issue.11
, pp. 828-830
-
-
Eng, C.1
-
21
-
-
21344470459
-
Hereditary colorectal cancer syndromes
-
DOI 10.1007/s10552-004-3488-4
-
Strate LL, Syngal S. Hereditary colorectal cancer syndromes. Cancer Causes Control. 2005;16(3):201-213. (Pubitemid 40903116)
-
(2005)
Cancer Causes and Control
, vol.16
, Issue.3
, pp. 201-213
-
-
Strate, L.L.1
Syngal, S.2
-
22
-
-
0034222104
-
Cowden's disease diagnosed through mucocutaneous lesions and gastrointestinal polyposis with recurrent hematochezia, unrevealed by initial diagnosis
-
Kato M, Mizuki A, Hayashi T, et al. Cowden's disease diagnosed through mucocutaneous lesions and gastrointestinal polyposis with recurrent hematochezia, unrevealed by initial diagnosis. Intern Med. 2000;39(7):559-563.
-
(2000)
Intern Med
, vol.39
, Issue.7
, pp. 559-563
-
-
Kato, M.1
Mizuki, A.2
Hayashi, T.3
-
23
-
-
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(3):222-233. (Pubitemid 16136974)
-
(1986)
Clinical Genetics
, vol.29
, Issue.3
, pp. 222-233
-
-
Starink T.., M.1
Van Der, V.J.P.W.2
Arwert, F.3
-
24
-
-
0003537117
-
Germline PTEN/MMAC1/TEP1 mutations and association with gastrointestinal manifestations in Cowden disease
-
[abstract G2902]
-
Weber HC, Marsh D, Lubensky I, Lin A, Eng C. Germline PTEN/MMAC1/TEP1 mutations and association with gastrointestinal manifestations in Cowden disease [abstract G2902]. Gastroenterology. 1998;114(suppl 1):A702.
-
(1998)
Gastroenterology
, vol.114
, Issue.SUPPL. 1
-
-
Weber, H.C.1
Marsh, D.2
Lubensky, I.3
Lin, A.4
Eng, C.5
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