-
1
-
-
12644292106
-
The two histological main types of gastric carcinoma: Diffuse and so-called Intestinal-type carcinoma an attempt at a histo-clinical classification
-
Lauren P. The two histological main types of gastric carcinoma: diffuse and so-called Intestinal-type carcinoma. An attempt at a histo-clinical classification. Acta Pathol Microbiol Scand. 1965;64:31Y49.
-
(1965)
Acta. Pathol. Microbiol. Scand.
, vol.64
, pp. 31-49
-
-
Lauren, P.1
-
2
-
-
0029082877
-
Newelements for an updated classification of the carcinomas of the stomach
-
Carneiro F, Seixas M, Sobrinho-Simoes M. Newelements for an updated classification of the carcinomas of the stomach. Pathol Res Pract. 1995; 191:571Y584.
-
(1995)
Pathol. Res. Pract.
, vol.191
, pp. 571-584
-
-
Carneiro, F.1
Seixas, M.2
Sobrinho-Simoes, M.3
-
3
-
-
67650410007
-
Stomach carcinoma incidence patterns in the united states by histologic type and anatomic site
-
Wu H, Rusiecki JA, Zhu K, et al. Stomach carcinoma incidence patterns in the United States by histologic type and anatomic site. Cancer Epidemiol Biomarkers Prev. 2009;18:1945Y1952.
-
(2009)
Cancer Epidemiol. Biomarkers Prev.
, vol.18
, pp. 1945-1952
-
-
Wu, H.1
Rusiecki, J.A.2
Zhu, K.3
-
4
-
-
0032900798
-
E-cadherin gene mutations provide a genetic basis for the phenotypic divergence of mixed gastric carcinomas
-
Machado JC, Soares P, Carneiro F, et al. E-cadherin gene mutations provide a genetic basis for the phenotypic divergence of mixed gastric carcinomas. Lab Invest. 1999;79:459Y465.
-
(1999)
Lab. Invest.
, vol.79
, pp. 459-465
-
-
MacHado, J.C.1
Soares, P.2
Carneiro, F.3
-
5
-
-
0027977943
-
E-cadherin gene mutations provide clues to diffuse type gastric carcinomas
-
Becker KF, Atkinson MJ, Reich U, et al. E-cadherin gene mutations provide clues to diffuse type gastric carcinomas. Cancer Res. 1994;54: 3845Y3852.
-
(1994)
Cancer Res.
, vol.54
, pp. 3845-3852
-
-
Becker, K.F.1
Atkinson, M.J.2
Reich, U.3
-
6
-
-
0029957442
-
Inactivation of the E-cadherin gene in primary gastric carcinomas and gastric carcinoma cell lines
-
Tamura G, Sakata K, Nishizuka S, et al. Inactivation of the E-cadherin gene in primary gastric carcinomas and gastric carcinoma cell lines. Jpn J Cancer Res. 1996;87:1153Y1159.
-
(1996)
Jpn J. Cancer Res.
, vol.87
, pp. 1153-1159
-
-
Tamura, G.1
Sakata, K.2
Nishizuka, S.3
-
7
-
-
0029790319
-
E-cadherin gene mutations in signet ring cell carcinoma of the stomach
-
Muta H, Noguchi M, Kanai Y, et al. E-cadherin gene mutations in signet ring cell carcinoma of the stomach. Jpn J Cancer Res. 1996;87:843Y848.
-
(1996)
Jpn J. Cancer Res.
, vol.87
, pp. 843-848
-
-
Muta, H.1
Noguchi, M.2
Kanai, Y.3
-
8
-
-
0028285556
-
T thomsen-friedenreich antigen and other simple mucin-type carbohydrate antigens in precursor lesions of gastric carcinoma
-
Carneiro F, Santos L, David L, et al. T (Thomsen-Friedenreich) antigen and other simple mucin-type carbohydrate antigens in precursor lesions of gastric carcinoma. Histopathology. 1994;24:105Y113.
-
(1994)
Histopathology
, vol.24
, pp. 105-113
-
-
Carneiro, F.1
Santos, L.2
David, L.3
-
9
-
-
82055185791
-
Molecular pathology of gastric carcinoma
-
Jang BG, Kim WH. Molecular pathology of gastric carcinoma. Pathobiology. 2011;78:302Y310.
-
(2011)
Pathobiology
, vol.78
, pp. 302-310
-
-
Jang, B.G.1
Kim, W.H.2
-
10
-
-
82255183148
-
Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer
-
Wang K, Kan J, Yuen ST, et al. Exome sequencing identifies frequent mutation of ARID1A in molecular subtypes of gastric cancer. Nat Genet. 2011;43:1219Y1223.
-
(2011)
Nat. Genet.
, vol.43
, pp. 1219-1223
-
-
Wang, K.1
Kan, J.2
Yuen, S.T.3
-
11
-
-
84860327480
-
Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes
-
Zang ZJ, Cutcutache I, Poon SL, et al. Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes. Nat Genet. 2012;44:570Y574.
-
(2012)
Nat. Genet.
, vol.44
, pp. 570-574
-
-
Zang, Z.J.1
Cutcutache, I.2
Poon, S.L.3
-
12
-
-
68449100164
-
Evidence of tumor microsatellite instability in gastric cancer with familial aggregation
-
Pedrazzani C, Corso G, Velho S, et al. Evidence of tumor microsatellite instability in gastric cancer with familial aggregation. Fam Cancer. 2009;8:215Y220.
-
(2009)
Fam. Cancer
, vol.8
, pp. 215-220
-
-
Pedrazzani, C.1
Corso, G.2
Velho, S.3
-
13
-
-
0035879041
-
Red meat family history and increased risk of gastric cancer with microsatellite instability
-
Palli D, Russo A, Ottini L, et al. Red meat, family history, and increased risk of gastric cancer with microsatellite instability. Cancer Res. 2001; 61:5415Y5419.
-
(2001)
Cancer Res.
, vol.61
, pp. 5415-5419
-
-
Palli, D.1
Russo, A.2
Ottini, L.3
-
15
-
-
63449103412
-
Smoking status and gastric cancer risk: An updated meta-analysis of case-control studies published in the past ten years
-
La Torre G, Chiaradia G, Gianfagna F, et al. Smoking status and gastric cancer risk: an updated meta-analysis of case-control studies published in the past ten years. Tumori. 2009;95:13Y22.
-
(2009)
Tumori
, vol.95
, pp. 13-22
-
-
La Torre, G.1
Chiaradia, G.2
Gianfagna, F.3
-
16
-
-
0018844274
-
Patterns of gastrointestinal cancer in european migrants to australia: The role of dietary change
-
McMichael AJ, McCall MG, Hartshorne JM, et al. Patterns of gastrointestinal cancer in European migrants to Australia: the role of dietary change. Int J Cancer. 1980;25:431Y437.
-
(1980)
Int. J. Cancer.
, vol.25
, pp. 431-437
-
-
McMichael, A.J.1
McCall, M.G.2
Hartshorne, J.M.3
-
17
-
-
0026050956
-
Helicobacter pylori infection and gastric carcinoma among japanese americans in hawaii
-
Nomura A, Stemmermann GN, Chyou PH, et al. Helicobacter pylori infection and gastric carcinoma among Japanese Americans in Hawaii. N Engl J Med. 1991;325:1132Y1136.
-
(1991)
N. Engl. J. Med.
, vol.325
, pp. 1132-1136
-
-
Nomura, A.1
Stemmermann, G.N.2
Chyou, P.H.3
-
18
-
-
0025945933
-
Helicobacter pylori infection and the risk of gastric carcinoma
-
Parsonnet J, Friedman GD, Vandersteen DP, et al. Helicobacter pylori infection and the risk of gastric carcinoma. N Engl J Med. 1991;325: 1127Y1131.
-
(1991)
N. Engl. J. Med.
, vol.325
, pp. 1127-1131
-
-
Parsonnet, J.1
Friedman, G.D.2
Vandersteen, D.P.3
-
19
-
-
0034878894
-
Gastric cancer and helicobacter pylori: A combined analysis of 12 case control studies nested within prospective cohorts
-
Helicobacter and Cancer Collaborative Group.
-
Helicobacter and Cancer Collaborative Group. Gastric cancer and Helicobacter pylori: a combined analysis of 12 case control studies nested within prospective cohorts. Gut. 2001;49:347Y353.
-
(2001)
Gut.
, vol.49
, pp. 347-353
-
-
-
20
-
-
79955782286
-
Helicobacter pylori infection and gastric cardia cancer: Systematic review and meta-analysis
-
Cavaleiro-Pinto M, Peleteiro B, Lunet N, et al. Helicobacter pylori infection and gastric cardia cancer: systematic review and meta-analysis. Cancer Causes Control. 2011;22:375Y387.
-
(2011)
Cancer Causes Control.
, vol.22
, pp. 375-387
-
-
Cavaleiro-Pinto, M.1
Peleteiro, B.2
Lunet, N.3
-
21
-
-
84862801280
-
Epstein-barr virus-associated gastric carcinoma: A newly defined entity
-
Chen JN, He D, Tang F, et al. Epstein-Barr virusYassociated gastric carcinoma: a newly defined entity. J Clin Gastroenterol. 2010;46:262Y271.
-
(2010)
J. Clin Gastroenterol.
, vol.46
, pp. 262-271
-
-
Chen, J.N.1
He, D.2
Tang, F.3
-
22
-
-
78049485263
-
Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008
-
Ferlay J, Shin HR, Bray F, et al. Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer. 2008;127:2893Y2917.
-
(2008)
Int. J. Cancer.
, vol.127
, pp. 2893-2917
-
-
Ferlay, J.1
Shin, H.R.2
Bray, F.3
-
24
-
-
4344704061
-
Is gastric cancer preventable
-
Correa P. Is gastric cancer preventable? Gut. 2004;53:1217Y1219.
-
(2004)
Gut.
, vol.53
, pp. 1217-1219
-
-
Correa, P.1
-
25
-
-
3042778739
-
Differential trends in the intestinal and diffuse types of gastric carcinoma in the united states 1973-2000: Increase in the signet ring cell type
-
Henson DE, Dittus C, Younes M, et al. Differential trends in the intestinal and diffuse types of gastric carcinoma in the United States, 1973Y2000: increase in the signet ring cell type. Arch Pathol Lab Med. 2004;128:765Y770.
-
(2004)
Arch. Pathol. Lab. Med.
, vol.128
, pp. 765-770
-
-
Henson, D.E.1
Dittus, C.2
Younes, M.3
-
26
-
-
0030864984
-
Helicobacter pylori and the birth cohort effect: Evidence of a continuous decrease of infection rates in childhood
-
Roosendaal R, Kuipers EJ, Buitenwerf J, et al. Helicobacter pylori and the birth cohort effect: evidence of a continuous decrease of infection rates in childhood. Am J Gastroenterol. 1997;92:1480Y1482.
-
(1997)
Am. J. Gastroenterol.
, vol.92
, pp. 1480-1482
-
-
Roosendaal, R.1
Kuipers, E.J.2
Buitenwerf, J.3
-
27
-
-
0034104414
-
Changing pattern of histological type location stage and outcome of surgical treatment of gastric carcinoma
-
Borch K, Jonsson B, Tarpila E, et al. Changing pattern of histological type, location, stage and outcome of surgical treatment of gastric carcinoma. Br J Surg. 2000;87:618Y626.
-
(2000)
Br. J. Surg.
, vol.87
, pp. 618-626
-
-
Borch, K.1
Jonsson, B.2
Tarpila, E.3
-
29
-
-
0345256389
-
Swedish empiric risks: Familial risk of cancer: Data for clinical counseling and cancer genetics
-
Hemminki K, Li X, Czene K. Swedish empiric risks: familial risk of cancer: data for clinical counseling and cancer genetics. Int J Cancer. 2004;108:109Y114.
-
(2004)
Int. J. Cancer.
, vol.108
, pp. 109-114
-
-
Hemminki, K.1
Li, X.2
Czene, K.3
-
30
-
-
75749126169
-
Stomach cancer risk in gastric cancer relatives: Interaction between helicobacter pylori infection and family history of gastric cancer for the risk of stomach cancer
-
Shin CM, Kim N, Yang HJ, et al. Stomach cancer risk in gastric cancer relatives: interaction between Helicobacter pylori infection and family history of gastric cancer for the risk of stomach cancer. J Clin Gastroenterol. 2010;44:e34Ye39.
-
(2010)
J. Clin. Gastroenterol.
, vol.44
-
-
Shin, C.M.1
Kim, N.2
Yang, H.J.3
-
31
-
-
0034303865
-
Significant prognostic factors in patients with early gastric cancer
-
Yokota T, Kunii Y, Teshima S, et al. Significant prognostic factors in patients with early gastric cancer. Int Surg. 2000;85:286Y290.
-
(2000)
Int. Surg.
, vol.85
, pp. 286-290
-
-
Yokota, T.1
Kunii, Y.2
Teshima, S.3
-
32
-
-
0033432725
-
Familial gastric cancer: Overview and guidelines for management
-
Caldas C, Carneiro F, Lynch HT, et al. Familial gastric cancer: overview and guidelines for management. J Med Genet. 1999;36:873Y880.
-
(1999)
J. Med. Genet.
, vol.36
, pp. 873-880
-
-
Caldas, C.1
Carneiro, F.2
Lynch, H.T.3
-
33
-
-
0032568370
-
E-cadherin germline mutations in familial gastric cancer
-
Guilford P, Hopkins J, Harraway J, et al. E-cadherin germline mutations in familial gastric cancer. Nature. 1998;392:402Y405.
-
(1998)
Nature
, vol.392
, pp. 402-405
-
-
Guilford, P.1
Hopkins, J.2
Harraway, J.3
-
34
-
-
19244377605
-
Identification of germ-line E-cadherin mutations in gastric cancer families of european origin
-
Gayther SA, Gorringe KL, Ramus SJ, et al. Identification of germ-line E-cadherin mutations in gastric cancer families of European origin. Cancer Res. 1998;58:4086Y4089.
-
(1998)
Cancer Res.
, vol.58
, pp. 4086-4089
-
-
Gayther, S.A.1
Gorringe, K.L.2
Ramus, S.J.3
-
35
-
-
0032865483
-
E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer
-
Guilford PJ, Hopkins JB, Grady WM, et al. E-cadherin germline mutations define an inherited cancer syndrome dominated by diffuse gastric cancer. Hum Mutat. 1999;14:249Y255.
-
(1999)
Hum Mutat.
, vol.14
, pp. 249-255
-
-
Guilford, P.J.1
Hopkins, J.B.2
Grady, W.M.3
-
36
-
-
0032806475
-
Diffuse type gastric and lobular breast carcinoma in a familial gastric cancer patient with an E-cadherin germline mutation
-
Keller G, Vogelsang H, Becker I, et al. Diffuse type gastric and lobular breast carcinoma in a familial gastric cancer patient with an E-cadherin germline mutation. Am J Pathol. 1999;155:337Y342.
-
(1999)
Am. J. Pathol.
, vol.155
, pp. 337-342
-
-
Keller, G.1
Vogelsang, H.2
Becker, I.3
-
37
-
-
0033029710
-
Germline E-cadherin gene CDH1 mutations predispose to familial gastric cancer and colorectal cancer
-
Richards FM, McKee SA, Rajpar MH, et al. Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancer. Hum Mol Genet. 1999;8:607Y610.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 607-610
-
-
Richards, F.M.1
McKee, S.A.2
Rajpar, M.H.3
-
38
-
-
0032985112
-
Familial gastric cancer: Clinicopathological characteristics RER phenotype and germline p53 and E-cadherin mutations
-
Shinmura K, Kohno T, Takahashi M, et al. Familial gastric cancer: clinicopathological characteristics, RER phenotype and germline p53 and E-cadherin mutations. Carcinogenesis. 1999;20:1127Y1131.
-
(1999)
Carcinogenesis
, vol.20
, pp. 1127-1131
-
-
Shinmura, K.1
Kohno, T.2
Takahashi, M.3
-
39
-
-
0032920262
-
Germline mutations of E-cadherin gene in korean familial gastric cancer patients
-
Yoon KA, Ku JL, Yang HK, et al. Germline mutations of E-cadherin gene in Korean familial gastric cancer patients. J Hum Genet. 1999; 44:177Y180.
-
(1999)
J. Hum. Genet.
, vol.44
, pp. 177-180
-
-
Yoon, K.A.1
Ku, J.L.2
Yang, H.K.3
-
40
-
-
84873610953
-
CDH1-related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling published online ahead of print
-
August 30 2011
-
Kluijt I, Siemerink EJ, Ausems MG, et al. CDH1-related hereditary diffuse gastric cancer syndrome: Clinical variations and implications for counseling [published online ahead of print August 30, 2011]. Int J Cancer. 2011.
-
(2011)
Int. J. Cancer.
-
-
Kluijt, I.1
Siemerink, E.J.2
Ausems, M.G.3
-
41
-
-
77954673384
-
Hereditary diffuse gastric cancer: Translation of CDH1 germline mutations into clinical practice
-
Guilford P, Humar B, Blair V. Hereditary diffuse gastric cancer: translation of CDH1 germline mutations into clinical practice. Gastric Cancer. 2010;13:1Y10.
-
(2010)
Gastric Cancer
, vol.13
, pp. 1-10
-
-
Guilford, P.1
Humar, B.2
Blair, V.3
-
42
-
-
0027682590
-
The structural and functional analysis of cadherin calciumdependent cell adhesion molecules
-
GrunwaldGB. The structural and functional analysis of cadherin calciumdependent cell adhesion molecules. Curr Opin Cell Biol. 1993;5: 797Y805.
-
(1993)
Curr. Opin. Cell. Biol.
, vol.5
, pp. 797-805
-
-
Grunwald, G.B.1
-
43
-
-
0029240438
-
E-cadherin as a tumor invasion suppressor gene
-
Birchmeier W. E-cadherin as a tumor (invasion) suppressor gene. Bioessays. 1995;17:97Y99.
-
(1995)
Bioessays
, vol.17
, pp. 97-99
-
-
Birchmeier, W.1
-
44
-
-
77956110372
-
Hereditary diffuse gastric cancer: Updated consensus guidelines for clinical management and directions for future research
-
Fitzgerald RC, Hardwick R, Huntsman D, et al. Hereditary diffuse gastric cancer: updated consensus guidelines for clinical management and directions for future research. J Med Genet. 2010;47:436Y444.
-
(2010)
J. Med. Genet.
, vol.47
, pp. 436-444
-
-
Fitzgerald, R.C.1
Hardwick, R.2
Huntsman, D.3
-
45
-
-
3142695439
-
Germline E-cadherin mutations in hereditary diffuse gastric cancer: Assessment of 42 new families and review of genetic screening criteria
-
Brooks-Wilson AR, Kaurah P, Suriano G, et al. Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria. J Med Genet. 2004; 41:508Y517.
-
(2004)
J. Med. Genet.
, vol.41
, pp. 508-517
-
-
Brooks-Wilson, A.R.1
Kaurah, P.2
Suriano, G.3
-
46
-
-
1842591223
-
Intragenic deletion of CDH1 as the inactivating mechanism of the wild-type allele in an HDGC tumour
-
Oliveira C, de Bruin J, Nabais S, et al. Intragenic deletion of CDH1 as the inactivating mechanism of the wild-type allele in an HDGC tumour. Oncogene. 2004;23:2236Y2240.
-
(2004)
Oncogene
, vol.23
, pp. 2236-2240
-
-
Oliveira, C.1
De Bruin, J.2
Nabais, S.3
-
47
-
-
23044486914
-
Characterization of a recurrent germ line mutation of the E-cadherin gene: Implications for genetic testing and clinical management
-
Suriano G, Yew S, Ferreira P, et al. Characterization of a recurrent germ line mutation of the E-cadherin gene: implications for genetic testing and clinical management. Clin Cancer Res. 2005;11:5401Y5409.
-
(2005)
Clin. Cancer Res.
, vol.11
, pp. 5401-5409
-
-
Suriano, G.1
Yew, S.2
Ferreira, P.3
-
48
-
-
66149108352
-
Quantification of epigenetic and genetic 2nd hits in CDH1 during hereditary diffuse gastric cancer syndrome progression
-
Oliveira C, Sousa S, Pinheiro H, et al. Quantification of epigenetic and genetic 2nd hits in CDH1 during hereditary diffuse gastric cancer syndrome progression. Gastroenterology. 2009;136:2137Y2148.
-
(2009)
Gastroenterology
, vol.136
, pp. 2137-2148
-
-
Oliveira, C.1
Sousa, S.2
Pinheiro, H.3
-
49
-
-
19444376902
-
Germline mutations of the Ecadherin CDH1 and TP53 genes rather than of RUNX3 and HPP1 contribute to genetic predisposition in german gastric cancer patients
-
Keller G, Vogelsang H, Becker I, et al. Germline mutations of the Ecadherin (CDH1) and TP53 genes, rather than of RUNX3 and HPP1, contribute to genetic predisposition in German gastric cancer patients. J Med Genet. 2004;41:e89.
-
(2004)
J. Med. Genet.
, vol.41
-
-
Keller, G.1
Vogelsang, H.2
Becker, I.3
-
50
-
-
0142248852
-
A novel germline mutation in the MET extracellular domain in a korean patient with the diffuse type of familial gastric cancer
-
Kim IJ, Park JH, Kang HC, et al. A novel germline mutation in the MET extracellular domain in a Korean patient with the diffuse type of familial gastric cancer. J Med Genet. 2003;40:e97.
-
(2003)
J. Med. Genet.
, vol.40
-
-
Kim, I.J.1
Park, J.H.2
Kang, H.C.3
-
51
-
-
3843061612
-
E-cadherin CDH1 and p53 rather than SMAD4 and caspase-10 germlinemutations contribute to genetic predisposition in portuguese gastric cancer patients
-
Oliveira C, Ferreira P, Nabais S, et al. E-cadherin (CDH1) and p53 rather thanSMAD4 and caspase-10 germlinemutations contribute to genetic predisposition in Portuguese gastric cancer patients. Eur J Cancer. 2004; 40:1897Y1903.
-
(2004)
Eur. J. Cancer
, vol.40
, pp. 1897-1903
-
-
Oliveira, C.1
Ferreira, P.2
Nabais, S.3
-
52
-
-
64549109715
-
Germline CDH1 deletions in hereditary diffuse gastric cancer families
-
Oliveira C, Senz J, Kaurah P, et al. Germline CDH1 deletions in hereditary diffuse gastric cancer families. Hum Mol Genet. 2009;18: 1545Y1555.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1545-1555
-
-
Oliveira, C.1
Senz, J.2
Kaurah, P.3
-
53
-
-
0035211026
-
Incidence of gastric cancer and breast cancer in CDH1 E-cadherin mutation carriers from hereditary diffuse gastric cancer families
-
Pharoah PD, Guilford P, Caldas C. Incidence of gastric cancer and breast cancer in CDH1 (E-cadherin) mutation carriers from hereditary diffuse gastric cancer families. Gastroenterology. 2001;121:1348Y1353.
-
(2001)
Gastroenterology
, vol.121
, pp. 1348-1353
-
-
Pharoah, P.D.1
Guilford, P.2
Caldas, C.3
-
54
-
-
34249989159
-
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer
-
Kaurah P, MacMillan A, Boyd N, et al. Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer. JAMA. 2007;297:2360Y2372.
-
(2007)
JAMA
, vol.297
, pp. 2360-2372
-
-
Kaurah, P.1
MacMillan, A.2
Boyd, N.3
-
55
-
-
46449107403
-
Hereditary diffuse gastric cancer: Association with lobular breast cancer
-
Schrader KA, Masciari S, Boyd N, et al. Hereditary diffuse gastric cancer: association with lobular breast cancer. Fam Cancer. 2008; 7:73Y82.
-
(2008)
Fam. Cancer
, vol.7
, pp. 73-82
-
-
Schrader, K.A.1
Masciari, S.2
Boyd, N.3
-
56
-
-
0031686121
-
Mutations of the human E-cadherin CDH1 gene
-
Berx G, Becker KF, Hofler H, et al. Mutations of the human E-cadherin (CDH1) gene. Hum Mutat. 1998;12:226Y237.
-
(1998)
Hum. Mutat.
, vol.12
, pp. 226-237
-
-
Berx, G.1
Becker, K.F.2
Hofler, H.3
-
57
-
-
0029951738
-
E-cadherin is inactivated in a majority of invasive human lobular breast cancers by truncation mutations throughout its extracellular domain
-
Berx G, Cleton-Jansen AM, Strumane K, et al. E-cadherin is inactivated in a majority of invasive human lobular breast cancers by truncation mutations throughout its extracellular domain. Oncogene. 1996;13: 1919Y1925.
-
(1996)
Oncogene
, vol.13
, pp. 1919-1925
-
-
Berx, G.1
Cleton-Jansen, A.M.2
Strumane, K.3
-
58
-
-
78751704485
-
Germline mutations in CDH1 are infrequent in women with early-onset or familial lobular breast cancers
-
Schrader KA, Masciari S, Boyd N, et al. Germline mutations in CDH1 are infrequent in women with early-onset or familial lobular breast cancers. J Med Genet. 2011;48:64Y68.
-
(2011)
J. Med. Genet.
, vol.48
, pp. 64-68
-
-
Schrader, K.A.1
Masciari, S.2
Boyd, N.3
-
59
-
-
18344384564
-
Screening E-cadherin in gastric cancer families reveals germline mutations only in hereditary diffuse gastric cancer kindred
-
Oliveira C, Bordin MC, Grehan N, et al. Screening E-cadherin in gastric cancer families reveals germline mutations only in hereditary diffuse gastric cancer kindred. Hum Mutat. 2002;19:510Y517.
-
(2002)
Hum. Mutat.
, vol.19
, pp. 510-517
-
-
Oliveira, C.1
Bordin, M.C.2
Grehan, N.3
-
60
-
-
32944469779
-
Cleft lip palate and CDH1 E-cadherin mutations in families with hereditary diffuse gastric cancer
-
Frebourg T, Oliveira C, Hochain P, et al. Cleft lip/palate and CDH1/E-cadherin mutations in families with hereditary diffuse gastric cancer. J Med Genet. 2006;43:138Y142.
-
(2006)
J. Med. Genet.
, vol.43
, pp. 138-142
-
-
Frebourg, T.1
Oliveira, C.2
Hochain, P.3
-
61
-
-
53949103559
-
Hereditary diffuse gastric cancer: Implications of genetic testing for screening and prophylactic surgery
-
Cisco RM, Ford JM, Norton JA. Hereditary diffuse gastric cancer: implications of genetic testing for screening and prophylactic surgery. Cancer. 2008;113:1850Y1856.
-
(2008)
Cancer
, vol.113
, pp. 1850-1856
-
-
Cisco, R.M.1
Ford, J.M.2
Norton, J.A.3
-
62
-
-
0035927967
-
Early gastric cancer in young asymptomatic carriers of germ-line E-cadherin mutations
-
HuntsmanDG, Carneiro F, Lewis FR, et al. Early gastric cancer in young, asymptomatic carriers of germ-line E-cadherin mutations. N Engl J Med. 2001;344:1904Y1909.
-
(2001)
N. Engl. J. Med.
, vol.344
, pp. 1904-1909
-
-
Huntsman, D.G.1
Carneiro, F.2
Lewis, F.R.3
-
63
-
-
34249302080
-
CDH1 truncating mutations in the E-cadherin gene: An indication for total gastrectomy to treat hereditary diffuse gastric cancer
-
Norton J, Ham C, Van Dam J, et al. CDH1 truncating mutations in the E-cadherin gene: an indication for total gastrectomy to treat hereditary diffuse gastric cancer. Ann Surg. 2007;45:873Y879.
-
(2007)
Ann Surg.
, vol.45
, pp. 873-879
-
-
Norton, J.1
Ham, C.2
Van Dam, J.3
-
64
-
-
46249087094
-
Risk-reducing total gastrectomy for germline mutations in E-cadherin CDH1: Pathologic findings with clinical implications
-
Rogers W, Dobo E, Norton J, et al. Risk-reducing total gastrectomy for germline mutations in E-cadherin (CDH1): pathologic findings with clinical implications. Am J Surg Pathol. 2008;32:799Y809.
-
(2008)
Am. J. Surg. Pathol.
, vol.32
, pp. 799-809
-
-
Rogers, W.1
Dobo, E.2
Norton, J.3
-
65
-
-
78650222510
-
Pregnancy after prophylactic total gastrectomy
-
Kaurah P, Fitzgerald R, Dwerryhouse S, et al. Pregnancy after prophylactic total gastrectomy. Fam Cancer. 2010;9:331Y334.
-
(2010)
Fam. Cancer
, vol.9
, pp. 331-334
-
-
Kaurah, P.1
Fitzgerald, R.2
Dwerryhouse, S.3
-
66
-
-
34047137002
-
-
American cancer society guidelines for breast screening with MRI as an adjunct to mammography
-
Saslow D, Boetes C, Burke W, et al. American Cancer Society guidelines for breast screening with MRI as an adjunct to mammography. CA Cancer J Clin. 2007;57:75Y89.
-
(2007)
CA Cancer J. Clin.
, vol.57
, pp. 75-89
-
-
Saslow, D.1
Boetes, C.2
Burke, W.3
-
67
-
-
77952982796
-
Genetic familial high-risk assessment: Breast and ovarian
-
Daly M, Axilbund J, Buys S, et al. Genetic/familial high-risk assessment: breast and ovarian. J Natl Compr Cancer Netw. 2010;8:562Y594.
-
(2010)
J. Natl. Compr. Cancer Netw.
, vol.8
, pp. 562-594
-
-
Daly, M.1
Axilbund, J.2
Buys, S.3
-
68
-
-
0035680457
-
The role of tamoxifen in breast cancer prevention: Issues sparked by the NSABP breast cancer prevention trial P-1
-
Wolmark N, Dunn BK. The role of tamoxifen in breast cancer prevention: issues sparked by the NSABP Breast Cancer Prevention Trial (P-1). Ann N Y Acad Sci. 2001;949:99Y108.
-
(2001)
Ann. N. Y. Acad. Sci.
, vol.949
, pp. 99-108
-
-
Wolmark, N.1
Dunn, B.K.2
-
69
-
-
0018774362
-
The cancer-family syndrome: A pragmatic basis for syndrome identification
-
Lynch HT, Lynch PM. The cancer-family syndrome: a pragmatic basis for syndrome identification. Dis Colon Rectum. 1979;22:106Y110.
-
(1979)
Dis. Colon Rectum.
, vol.22
, pp. 106-110
-
-
Lynch, H.T.1
Lynch, P.M.2
-
70
-
-
59849129653
-
EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from lynch syndrome
-
Palomaki GE, McClain MR, Melillo S, et al. EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome. Genet Med. 2009;11:42Y65.
-
(2009)
Genet. Med.
, vol.11
, pp. 42-65
-
-
Palomaki, G.E.1
McClain, M.R.2
Melillo, S.3
-
71
-
-
61449320520
-
Endometrial cancer and Lynch syndrome: Clinical and pathologic considerations
-
Meyer LA, Broaddus RR, Lu KH. Endometrial cancer and Lynch syndrome: clinical and pathologic considerations. Cancer Control. 2009; 16:14Y22.
-
(2009)
Cancer Control.
, vol.16
, pp. 14-22
-
-
Meyer, L.A.1
Broaddus, R.R.2
Lu, K.H.3
-
72
-
-
33749066191
-
Prediction of germline mutations and cancer risk in the lynch syndrome
-
Chen S, Wang W, Lee S, et al. Prediction of germline mutations and cancer risk in the Lynch syndrome. JAMA. 2006;296:1479Y1487.
-
(2006)
JAMA
, vol.296
, pp. 1479-1487
-
-
Chen, S.1
Wang, W.2
Lee, S.3
-
73
-
-
0030659081
-
Features of gastric cancer in hereditary non-polyposis colorectal cancer syndrome
-
Aarnio M, Salovaara R, Aaltonen LA, et al. Features of gastric cancer in hereditary non-polyposis colorectal cancer syndrome. Int J Cancer. 1997;74:551Y555.
-
(1997)
Int. J. Cancer.
, vol.74
, pp. 551-555
-
-
Aarnio, M.1
Salovaara, R.2
Aaltonen, L.A.3
-
74
-
-
0032941343
-
Cancer risk in mutation carriers of DNA-mismatch-repair genes
-
Aarnio M, Sankila R, Pukkala E, et al. Cancer risk in mutation carriers of DNA-mismatch-repair genes. Int J Cancer. 1999;81:214Y218.
-
(1999)
Int. J. Cancer
, vol.81
, pp. 214-218
-
-
Aarnio, M.1
Sankila, R.2
Pukkala, E.3
-
75
-
-
0033897383
-
Risk of gastric cancer in hereditary nonpolyposis colorectal cancer in korea
-
Park YJ, Shin KH, Park JG. Risk of gastric cancer in hereditary nonpolyposis colorectal cancer in Korea. Clin Cancer Res. 2000;6: 2994Y2998.
-
(2000)
Clin. Cancer Res.
, vol.6
, pp. 2994-2998
-
-
Park, Y.J.1
Shin, K.H.2
Park, J.G.3
-
76
-
-
0029862873
-
Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis
-
Vasen HF, Wijnen JT, Menko FH, et al. Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis. Gastroenterology. 1996;110:1020Y1027.
-
(1996)
Gastroenterology
, vol.110
, pp. 1020-1027
-
-
Vasen, H.F.1
Wijnen, J.T.2
Menko, F.H.3
-
77
-
-
44949202465
-
The risk of extra-colonic extraendometrial cancer in the lynch syndrome
-
Watson P, Vasen HF, Mecklin JP, et al. The risk of extra-colonic, extraendometrial cancer in the Lynch syndrome. Int J Cancer. 2008;123: 444Y449.
-
(2008)
Int. J. Cancer.
, vol.123
, pp. 444-449
-
-
Watson, P.1
Vasen, H.F.2
Mecklin, J.P.3
-
78
-
-
34347209468
-
Is gastric cancer part of the tumour spectrum of hereditary non-polyposis colorectal cancer a molecular genetic study
-
Gylling A, Abdel-Rahman WM, Juhola M, et al. Is gastric cancer part of the tumour spectrum of hereditary non-polyposis colorectal cancer? A molecular genetic study. Gut. 2007;56:926Y933.
-
(2007)
Gut.
, vol.56
, pp. 926-933
-
-
Gylling, A.1
Abdel-Rahman, W.M.2
Juhola, M.3
-
79
-
-
0031551963
-
A national cancer institute workshop on hereditary nonpolyposis colorectal cancer syndrome: Meeting highlights and bethesda guidelines
-
Rodriguez-Bigas MA, Boland CR, Hamilton SR, et al. A National Cancer Institute Workshop on Hereditary Nonpolyposis Colorectal Cancer Syndrome: meeting highlights and Bethesda guidelines. J Natl Cancer Inst. 1997;89:1758Y1762.
-
(1997)
J. Natl. Cancer Inst.
, vol.89
, pp. 1758-1762
-
-
Rodriguez-Bigas, M.A.1
Boland, C.R.2
Hamilton, S.R.3
-
80
-
-
10744233937
-
Revised bethesda guidelines for hereditary nonpolyposis colorectal cancer lynch syndrome and microsatellite instability
-
Umar A, Boland CR, Terdiman JP, et al. Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst. 2004;96:261Y268.
-
(2004)
J. Natl. Cancer Inst.
, vol.96
, pp. 261-268
-
-
Umar, A.1
Boland, C.R.2
Terdiman, J.P.3
-
81
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Eidens D, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science. 1994; 266:66Y71.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
-
82
-
-
0006713602
-
Identification of the breast cancer susceptibility gene BRCA2
-
Wooster R, Bignell G, Lancaster J, et al. Identification of the breast cancer susceptibility gene BRCA2. Nature. 1995;378:789Y792.
-
(1995)
Nature
, vol.378
, pp. 789-792
-
-
Wooster, R.1
Bignell, G.2
Lancaster, J.3
-
83
-
-
0033523268
-
Cancer risks in BRCA2 mutation carriers
-
The Breast Cancer Linkage Consortium
-
The Breast Cancer Linkage Consortium. Cancer risks in BRCA2 mutation carriers. J Natl Cancer Inst. 1999;91:1310Y1316.
-
(1999)
J. Natl. Cancer Inst.
, vol.91
, pp. 1310-1316
-
-
-
84
-
-
0035099690
-
The rate of the 6174delT founder Jewish mutation in BRCA2 in patients with non-colonic gastrointestinal tract tumours in israel
-
Figer A, Irmin L, Geva R, et al. The rate of the 6174delT founder Jewish mutation in BRCA2 in patients with non-colonic gastrointestinal tract tumours in Israel. Br J Cancer. 2001;84:478Y481.
-
(2001)
Br. J. Cancer
, vol.84
, pp. 478-481
-
-
Figer, A.1
Irmin, L.2
Geva, R.3
-
85
-
-
0037037332
-
BRCA2 gene mutations in families with aggregations of breast and stomach cancers
-
Jakubowska A, Nej K, Huzarski T, et al. BRCA2 gene mutations in families with aggregations of breast and stomach cancers. Br J Cancer. 2002;87:888Y891.
-
(2002)
Br. J. Cancer
, vol.87
, pp. 888-891
-
-
Jakubowska, A.1
Nej, K.2
Huzarski, T.3
-
86
-
-
0346656816
-
A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer
-
Jakubowska A, Scott R, Menkiszak J, et al. A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer. Eur J Hum Genet. 2003;11:955Y958.
-
(2003)
Eur. J. Hum. Genet
, vol.11
, pp. 955-958
-
-
Jakubowska, A.1
Scott, R.2
Menkiszak, J.3
-
87
-
-
0032794999
-
Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers
-
Johannsson O, Loman N, Moller T, et al. Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers. Eur J Cancer. 1999;35:1248Y1257.
-
(1999)
Eur. J. Cancer
, vol.35
, pp. 1248-1257
-
-
Johannsson, O.1
Loman, N.2
Moller, T.3
-
88
-
-
10944255106
-
Risk of cancer at sites other than the breast in swedish families eligible for BRCA1 or BRCA2 mutation testing
-
Lorenzo B, Hemminki K. Risk of cancer at sites other than the breast in Swedish families eligible for BRCA1 or BRCA2 mutation testing. Ann Oncol. 2004;15:1834Y1841.
-
(2004)
Ann. Oncol.
, vol.15
, pp. 1834-1841
-
-
Lorenzo, B.1
Hemminki, K.2
-
89
-
-
0037130889
-
Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program
-
Brose MS, Rebbeck TR, Calzone KA, et al. Cancer risk estimates for BRCA1 mutation carriers identified in a risk evaluation program. J Natl Cancer Inst. 2002;94:1365Y1372.
-
(2002)
J. Natl. Cancer Inst.
, vol.94
, pp. 1365-1372
-
-
Brose, M.S.1
Rebbeck, T.R.2
Calzone, K.A.3
-
90
-
-
0035098503
-
Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer
-
Risch H, McLaughlin J, Cole D, et al. Prevalence and penetrance of germline BRCA1 and BRCA2 mutations in a population series of 649 women with ovarian cancer. Am J Hum Genet. 2001;68:700Y710.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 700-710
-
-
Risch, H.1
McLaughlin, J.2
Cole, D.3
-
91
-
-
25144445294
-
BRCA1 and BRCA2 pathways and the risk of cancers other than breast or ovarian
-
Friedenson B. BRCA1 and BRCA2 pathways and the risk of cancers other than breast or ovarian. MedGenMed. 2005;7:60.
-
(2005)
Med. Gen. Med.
, vol.7
, pp. 60
-
-
Friedenson, B.1
-
92
-
-
40749125350
-
Gastric adenocarcinoma arising from fundic gland polyps in a patient with familial adenomatous polyposis syndrome
-
Garrean S, Hering J, Saied A, et al. Gastric adenocarcinoma arising from fundic gland polyps in a patient with familial adenomatous polyposis syndrome. Am Surg. 2008;74:79Y83.
-
(2008)
Am. Surg.
, vol.74
, pp. 79-83
-
-
Garrean, S.1
Hering, J.2
Saied, A.3
-
93
-
-
0026537747
-
The risk of upper gastrointestinal cancer in familial adenomatous polyposis
-
Offerhaus GJ, Giardiello FM, Krush AJ, et al. The risk of upper gastrointestinal cancer in familial adenomatous polyposis. Gastroenterology. 1992;102:1980Y1982.
-
(1992)
Gastroenterology
, vol.102
, pp. 1980-1982
-
-
Offerhaus, G.J.1
Giardiello, F.M.2
Krush, A.J.3
-
94
-
-
0242406863
-
Gastric fundic gland polyps
-
Burt RW. Gastric fundic gland polyps. Gastroenterology. 2003;125: 1462Y1469.
-
(2003)
Gastroenterology
, vol.125
, pp. 1462-1469
-
-
Burt, R.W.1
-
95
-
-
78650200253
-
FAP gastric cancer and genetic counseling featuring children and young adults: A family study and review
-
Lynch HT, Snyder C, Davies JM, et al. FAP, gastric cancer, and genetic counseling featuring children and young adults: a family study and review. Fam Cancer. 2010;9:581Y588.
-
(2010)
Fam. Cancer
, vol.9
, pp. 581-588
-
-
Lynch, H.T.1
Snyder, C.2
Davies, J.M.3
-
96
-
-
0028823186
-
Attenuated familial adenomatous polyposis AFAP a phenotypically and genotypically distinctive variant of FAP
-
Lynch HT, Smyrk T, McGinn T, et al. Attenuated familial adenomatous polyposis (AFAP). A phenotypically and genotypically distinctive variant of FAP. Cancer. 1995;76:2427Y2433.
-
(1995)
Cancer
, vol.76
, pp. 2427-2433
-
-
Lynch, H.T.1
Smyrk, T.2
McGinn, T.3
-
97
-
-
0034495101
-
Fundic gland polyps in familial adenomatous polyposis: Neoplasms with frequent somatic adenomatous polyposis coli gene alterations
-
Abraham SC, Nobukawa B, Giardiello FM, et al. Fundic gland polyps in familial adenomatous polyposis: neoplasms with frequent somatic adenomatous polyposis coli gene alterations. Am J Pathol. 2000;157: 747Y754.
-
(2000)
Am. J. Pathol.
, vol.157
, pp. 747-754
-
-
Abraham, S.C.1
Nobukawa, B.2
Giardiello, F.M.3
-
98
-
-
38649110440
-
Fundic gland polyp dysplasia is common in familial adenomatous polyposis
-
Bianchi LK, Burke CA, Bennett AE, et al. Fundic gland polyp dysplasia is common in familial adenomatous polyposis. Clin Gastroenterol Hepatol. 2008;6:180Y185.
-
(2008)
Clin. Gastroenterol. Hepatol.
, vol.6
, pp. 180-185
-
-
Bianchi, L.K.1
Burke, C.A.2
Bennett, A.E.3
-
99
-
-
49049098513
-
Total gastrectomy for gastric dysplasia in a patient with attenuated familial adenomatous polyposis syndrome
-
Dunn K, Chey W, Gibbs J. Total gastrectomy for gastric dysplasia in a patient with attenuated familial adenomatous polyposis syndrome. J Clin Oncol. 2008;26:3641Y3642.
-
(2008)
J. Clin. Oncol.
, vol.26
, pp. 3641-3642
-
-
Dunn, K.1
Chey, W.2
Gibbs, J.3
-
100
-
-
0142157701
-
Li-Fraumeni and related syndromes: Correlation between tumor type family structure and TP53 genotype
-
Olivier M, Goldgar DE, Sodha N, et al. Li-Fraumeni and related syndromes: correlation between tumor type, family structure, and TP53 genotype. Cancer Res. 2003;63:6643Y6650.
-
(2003)
Cancer Res.
, vol.63
, pp. 6643-6650
-
-
Olivier, M.1
Goldgar, D.E.2
Sodha, N.3
-
101
-
-
0014587529
-
Soft-tissue sarcomas breast cancer and other neoplasms a familial syndrome
-
Li F, Fraumeni JJ. Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome? Ann Intern Med. 1969;71:747Y752.
-
(1969)
Ann. Intern. Med.
, vol.71
, pp. 747-752
-
-
Li, F.1
Fraumeni, J.J.2
-
102
-
-
0025633582
-
Germ line p53 mutations in a familial syndrome of breast cancer sarcomas and other neoplasms
-
Malkin D, Li F, Strong L, et al. Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science. 1990;250:1233Y1238.
-
(1990)
Science
, vol.250
, pp. 1233-1238
-
-
Malkin, D.1
Li, F.2
Strong, L.3
-
103
-
-
33748060942
-
Joint effects of germ-line p53 mutation and sex on cancer risk in li-fraumeni syndrome
-
Wu CC, Shete S, Amos CI, et al. Joint effects of germ-line p53 mutation and sex on cancer risk in Li-Fraumeni syndrome. Cancer Res. 2006; 66:8287Y8292.
-
(2006)
Cancer Res.
, vol.66
, pp. 8287-8292
-
-
Wu, C.C.1
Shete, S.2
Amos, C.I.3
-
104
-
-
0032522623
-
Multiple primary cancers in families with li-fraumeni syndrome
-
Hisada M, Garber J, Fung C, et al. Multiple primary cancers in families with Li-Fraumeni syndrome. J Natl Cancer Inst. 1998;90:606Y611.
-
(1998)
J. Natl. Cancer Inst.
, vol.90
, pp. 606-611
-
-
Hisada, M.1
Garber, J.2
Fung, C.3
-
105
-
-
70349705753
-
High frequency of de novo mutations in Li-fraumeni syndrome
-
Gonzalez K, Buzin C, Noltner K, et al. High frequency of de novo mutations in Li-Fraumeni syndrome. J Med Genet. 2009;46:689Y693.
-
(2009)
J. Med. Genet.
, vol.46
, pp. 689-693
-
-
Gonzalez, K.1
Buzin, C.2
Noltner, K.3
-
107
-
-
79960845375
-
Gastric cancer in individuals with li-fraumeni syndrome
-
Masciari S, Dewanwala A, Stoffel EM, et al. Gastric cancer in individuals with Li-Fraumeni syndrome. Genet Med. 2011;13:651Y657.
-
(2011)
Genet. Med.
, vol.13
, pp. 651-657
-
-
Masciari, S.1
Dewanwala, A.2
Stoffel, E.M.3
-
108
-
-
77953718900
-
TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: Mutation detection rate and relative frequency of cancers in different familial phenotypes
-
Ruijs MW, Verhoef S, Rookus MA, et al. TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes. J Med Genet. 2010;47:421Y428.
-
(2010)
J. Med. Genet.
, vol.47
, pp. 421-428
-
-
Ruijs, M.W.1
Verhoef, S.2
Rookus, M.A.3
-
109
-
-
0000043603
-
Very remarkable case of familial polyposis of mucous membrane of intestinal tract and nasopharynx accompanied by peculiar pigmentations of skin and mucous membrane
-
Peutz J. Very remarkable case of familial polyposis of mucous membrane of intestinal tract and nasopharynx accompanied by peculiar pigmentations of skin and mucous membrane. Nederl Maandschr Geneesk. 1921;10:134Y146.
-
(1921)
Nederl. Maandschr. Geneesk
, vol.10
, pp. 134-146
-
-
Peutz, J.1
-
110
-
-
0000152018
-
Generalized intestinal polyposis and melanin spots of the oral mucosa lips and digits a syndrome of diagnostic significance
-
Jeghers H, Mc KV, Katz KH. Generalized intestinal polyposis and melanin spots of the oral mucosa, lips and digits; a syndrome of diagnostic significance. N Engl J Med. 1949;241:1031Y1036.
-
(1949)
N. Engl. J. Med.
, vol.241
, pp. 1031-1036
-
-
Jeghers, H.1
Mc, K.V.2
Katz, K.H.3
-
112
-
-
2942527434
-
Relative frequency and morphology of cancers in STK11 mutation carriers
-
LimW, Olschwang S,Keller JJ, et al. Relative frequency and morphology of cancers in STK11 mutation carriers. Gastroenterology. 2004;126: 1788Y1794.
-
(2004)
Gastroenterology
, vol.126
, pp. 1788-1794
-
-
Lim, W.1
Olschwang, S.2
Keller, J.J.3
-
113
-
-
0034464147
-
Very high risk of cancer in familial peutz-jeghers syndrome
-
Giardiello F, Brensinger J, Tersmette A, et al. Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology. 2000;119: 1447Y1453.
-
(2000)
Gastroenterology
, vol.119
, pp. 1447-1453
-
-
Giardiello, F.1
Brensinger, J.2
Tersmette, A.3
-
114
-
-
77953230425
-
High cancer risk in peutz-jeghers syndrome: A systematic review and surveillance recommendations
-
van Lier MG,Wagner A, Mathus-Vliegen EM, et al. High cancer risk in Peutz-Jeghers syndrome: a systematic review and surveillance recommendations. Am J Gastroenterol. 2010;105:1258Y1264.
-
(2010)
Am. J. Gastroenterol.
, vol.105
, pp. 1258-1264
-
-
Van Lier, M.G.1
Wagner, A.2
Mathus-Vliegen, E.M.3
-
115
-
-
78651095553
-
High cancer risk and increased mortality in patients with peutz-jeghers syndrome
-
van Lier MG, Westerman AM, Wagner A, et al. High cancer risk and increased mortality in patients with Peutz-Jeghers syndrome. Gut. 2011;60:141Y147.
-
(2011)
Gut.
, vol.60
, pp. 141-147
-
-
Van Lier, M.G.1
Westerman, A.M.2
Wagner, A.3
-
116
-
-
0032403068
-
Pathogenesis of adenocarcinoma in peutz-jeghers syndrome
-
Gruber SB, Entius MM, Petersen GM, et al. Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome. Cancer Res. 1998;58:5267Y5270.
-
(1998)
Cancer Res.
, vol.58
, pp. 5267-5270
-
-
Gruber, S.B.1
Entius, M.M.2
Petersen, G.M.3
-
117
-
-
0043234584
-
Hereditary polyposis syndromes and hereditary non-polyposis colorectal cancer
-
Allen BA, Terdiman JP. Hereditary polyposis syndromes and hereditary non-polyposis colorectal cancer. Best Pract Res Clin Gastroenterol. 2003;17:237Y258.
-
(2003)
Best Pract. Res. Clin. Gastroenterol.
, vol.17
, pp. 237-258
-
-
Allen, B.A.1
Terdiman, J.P.2
-
118
-
-
0024400328
-
Gastrointestinal polyposis syndromes
-
Finan MC, Ray MK. Gastrointestinal polyposis syndromes. Dermatol Clin. 1989;7:419Y434.
-
(1989)
Dermatol. Clin.
, vol.7
, pp. 419-434
-
-
Finan, M.C.1
Ray, M.K.2
-
119
-
-
0032528265
-
The concise handbook of family cancer syndromes
-
Mayo Familial Cancer Program
-
Lindor NM, Greene MH. The concise handbook of family cancer syndromes. Mayo Familial Cancer Program. J Natl Cancer Inst. 1998;90: 1039Y1071.
-
(1998)
J. Natl. Cancer Inst.
, vol.90
, pp. 1039-1071
-
-
Lindor, N.M.1
Greene, M.H.2
-
120
-
-
0016611185
-
Peutz-jeghers syndrome: Its natural course and management
-
Johns Hopkins
-
Utsunomiya J, Gocho H, Miyanaga T, et al. Peutz-Jeghers syndrome: its natural course and management. Johns Hopkins Med J. 1975;136:71Y82.
-
(1975)
Med. J.
, vol.136
, pp. 71-82
-
-
Utsunomiya, J.1
Gocho, H.2
Miyanaga, T.3
-
121
-
-
3142746721
-
The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2 BMPR1B and ACVR1 mutations
-
Howe JR, Sayed MG, Ahmed AF, et al. The prevalence of MADH4 and BMPR1A mutations in juvenile polyposis and absence of BMPR2, BMPR1B, and ACVR1 mutations. J Med Genet. 2004;41:484Y491.
-
(2004)
J. Med. Genet.
, vol.41
, pp. 484-491
-
-
Howe, J.R.1
Sayed, M.G.2
Ahmed, A.F.3
-
122
-
-
0036842005
-
Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis
-
SayedMG, Ahmed AF, Ringold JR, et al. Germline SMAD4 or BMPR1A mutations and phenotype of juvenile polyposis. Ann Surg Oncol. 2002;9:901Y906.
-
(2002)
Ann. Surg. Oncol.
, vol.9
, pp. 901-906
-
-
Sayed, M.G.1
Ahmed, A.F.2
Ringold, J.R.3
-
123
-
-
33749260421
-
SMAD4 mutations found in unselected HHT patients
-
Gallione C, Richards J, Letteboer T, et al. SMAD4 mutations found in unselected HHT patients. J Med Genet. 2006;43:793Y797.
-
(2006)
J. Med. Genet.
, vol.43
, pp. 793-797
-
-
Gallione, C.1
Richards, J.2
Letteboer, T.3
|