Madlensky L - Search Results

1

Hereditary and familial ovarian cancer in southern Ontario.

Narod SA, Madlensky L, Bradley L, Cole D, Tonin P, Rosen B, Risch HA. Narod SA, et al. Among authors: madlensky l. Cancer. 1994 Oct 15;74(8):2341-6. doi: 10.1002/1097-0142(19941015)74:8<2341::aid-cncr2820740819>3.0.co;2-z. Cancer. 1994. PMID: 7922985

2

Mismatch repair gene defects contribute to the genetic basis of double primary cancers of the colorectum and endometrium.

Millar AL, Pal T, Madlensky L, Sherman C, Temple L, Mitri A, Cheng H, Marcus V, Gallinger S, Redston M, Bapat B, Narod S. Millar AL, et al. Among authors: madlensky l. Hum Mol Genet. 1999 May;8(5):823-9. doi: 10.1093/hmg/8.5.823. Hum Mol Genet. 1999. PMID: 10196371

3

The genetic basis of Muir-Torre syndrome includes the hMLH1 locus.

Bapat B, Xia L, Madlensky L, Mitri A, Tonin P, Narod SA, Gallinger S. Bapat B, et al. Among authors: madlensky l. Am J Hum Genet. 1996 Sep;59(3):736-9. Am J Hum Genet. 1996. PMID: 8751876 Free PMC article. No abstract available.

4

Immunohistochemistry for hMLH1 and hMSH2: a practical test for DNA mismatch repair-deficient tumors.

Marcus VA, Madlensky L, Gryfe R, Kim H, So K, Millar A, Temple LK, Hsieh E, Hiruki T, Narod S, Bapat BV, Gallinger S, Redston M. Marcus VA, et al. Among authors: madlensky l. Am J Surg Pathol. 1999 Oct;23(10):1248-55. doi: 10.1097/00000478-199910000-00010. Am J Surg Pathol. 1999. PMID: 10524526

5

Confirmation of FWT1 as a Wilms' tumour susceptibility gene and phenotypic characteristics of Wilms' tumour attributable to FWT1.

Rahman N, Abidi F, Ford D, Arbour L, Rapley E, Tonin P, Barton D, Batcup G, Berry J, Cotter F, Davison V, Gerrard M, Gray E, Grundy R, Hanafy M, King D, Lewis I, Ridolfi Luethy A, Madlensky L, Mann J, O'Meara A, Oakhill T, Skolnick M, Strong L, Stratton MR, et al. Rahman N, et al. Among authors: madlensky l. Hum Genet. 1998 Nov;103(5):547-56. doi: 10.1007/pl00008708. Hum Genet. 1998. PMID: 9860296

6

A truncated hMSH2 transcript occurs as a common variant in the population: implications for genetic diagnosis.

Xia L, Shen W, Ritacca F, Mitri A, Madlensky L, Berk T, Cohen Z, Gallinger S, Bapat B. Xia L, et al. Among authors: madlensky l. Cancer Res. 1996 May 15;56(10):2289-92. Cancer Res. 1996. PMID: 8625301

7

A comparison of self-reported colorectal cancer screening with medical records.

Madlensky L, McLaughlin J, Goel V. Madlensky L, et al. Cancer Epidemiol Biomarkers Prev. 2003 Jul;12(7):656-9. Cancer Epidemiol Biomarkers Prev. 2003. PMID: 12869407

8

Assessing the evidence for organised cancer screening programmes.

Madlensky L, Goel V, Polzer J, Ashbury FD. Madlensky L, et al. Eur J Cancer. 2003 Aug;39(12):1648-53. doi: 10.1016/s0959-8049(03)00315-0. Eur J Cancer. 2003. PMID: 12888358 Review.

9

Characteristics of small bowel carcinoma in hereditary nonpolyposis colorectal carcinoma. International Collaborative Group on HNPCC.

Rodriguez-Bigas MA, Vasen HF, Lynch HT, Watson P, Myrhøj T, Järvinen HJ, Mecklin JP, Macrae F, St John DJ, Bertario L, Fidalgo P, Madlensky L, Rozen P. Rodriguez-Bigas MA, et al. Among authors: madlensky l. Cancer. 1998 Jul 15;83(2):240-4. doi: 10.1002/(sici)1097-0142(19980715)83:2<240::aid-cncr6>3.0.co;2-u. Cancer. 1998. PMID: 9669805

10

The clinical features of ovarian cancer in hereditary nonpolyposis colorectal cancer.

Watson P, Bützow R, Lynch HT, Mecklin JP, Järvinen HJ, Vasen HF, Madlensky L, Fidalgo P, Bernstein I; International Collaborative Group on HNPCC. Watson P, et al. Among authors: madlensky l. Gynecol Oncol. 2001 Aug;82(2):223-8. doi: 10.1006/gyno.2001.6279. Gynecol Oncol. 2001. PMID: 11531271

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