Kohlmann WK - Search Results

1

Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome.

Kratz CP, Achatz MI, Brugières L, Frebourg T, Garber JE, Greer MC, Hansford JR, Janeway KA, Kohlmann WK, McGee R, Mullighan CG, Onel K, Pajtler KW, Pfister SM, Savage SA, Schiffman JD, Schneider KA, Strong LC, Evans DGR, Wasserman JD, Villani A, Malkin D. Kratz CP, et al. Among authors: kohlmann wk. Clin Cancer Res. 2017 Jun 1;23(11):e38-e45. doi: 10.1158/1078-0432.CCR-17-0408. Clin Cancer Res. 2017. PMID: 28572266 Review.

2

Malignant triton tumor in a patient with Li-Fraumeni syndrome and a novel TP53 mutation.

Chao MM, Levine JE, Ruiz RE, Kohlmann WK, Bower MA, Petty EM, Mody RJ. Chao MM, et al. Among authors: kohlmann wk. Pediatr Blood Cancer. 2007 Dec;49(7):1000-4. doi: 10.1002/pbc.20700. Pediatr Blood Cancer. 2007. PMID: 16333835

3

Identification and screening of individuals at increased risk for pancreatic cancer with emphasis on known environmental and genetic factors and hereditary syndromes.

Chu D, Kohlmann W, Adler DG. Chu D, et al. JOP. 2010 May 5;11(3):203-12. JOP. 2010. PMID: 20442513 Free article. Review.

4

Genetic/familial high-risk assessment: breast and ovarian.

Daly MB, Axilbund JE, Buys S, Crawford B, Farrell CD, Friedman S, Garber JE, Goorha S, Gruber SB, Hampel H, Kaklamani V, Kohlmann W, Kurian A, Litton J, Marcom PK, Nussbaum R, Offit K, Pal T, Pasche B, Pilarski R, Reiser G, Shannon KM, Smith JR, Swisher E, Weitzel JN; National Comprehensive Cancer Network. Daly MB, et al. J Natl Compr Canc Netw. 2010 May;8(5):562-94. doi: 10.6004/jnccn.2010.0043. J Natl Compr Canc Netw. 2010. PMID: 20495085 No abstract available.

5

Complex genotype sarcomas display familial inheritance independent of known cancer predisposition syndromes.

Jones KB, Schiffman JD, Kohlmann W, Randall RL, Lessnick SL, Cannon-Albright LA. Jones KB, et al. Cancer Epidemiol Biomarkers Prev. 2011 May;20(5):751-7. doi: 10.1158/1055-9965.EPI-10-1174. Epub 2011 Jan 17. Cancer Epidemiol Biomarkers Prev. 2011. PMID: 21242332 Free PMC article.

6

Melanoma mimic: a case of multiple pagetoid Spitz nevi.

Harris K, Florell SR, Papenfuss J, Kohlmann W, Jahromi M, Schiffman JD, Quackenbush J, Cassidy P, Leachman S. Harris K, et al. Arch Dermatol. 2012 Mar;148(3):370-4. doi: 10.1001/archdermatol.2011.356. Epub 2011 Nov 21. Arch Dermatol. 2012. PMID: 22105811

7

Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome.

Yurgelun MB, Mercado R, Rosenblatt M, Dandapani M, Kohlmann W, Conrad P, Blanco A, Shannon KM, Chung DC, Terdiman J, Gruber SB, Garber JE, Syngal S, Stoffel EM. Yurgelun MB, et al. Gynecol Oncol. 2012 Dec;127(3):544-51. doi: 10.1016/j.ygyno.2012.08.031. Epub 2012 Aug 29. Gynecol Oncol. 2012. PMID: 22940489 Free PMC article.

8

Familial risk of childhood cancer and tumors in the Li-Fraumeni spectrum in the Utah Population Database: implications for genetic evaluation in pediatric practice.

Curtin K, Smith KR, Fraser A, Pimentel R, Kohlmann W, Schiffman JD. Curtin K, et al. Int J Cancer. 2013 Nov 15;133(10):2444-53. doi: 10.1002/ijc.28266. Epub 2013 Jun 12. Int J Cancer. 2013. PMID: 23661176 Free PMC article.

9

Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families.

Jasperson KW, Kohlmann W, Gammon A, Slack H, Buchmann L, Hunt J, Kirchhoff AC, Baskin H, Shaaban A, Schiffman JD. Jasperson KW, et al. Fam Cancer. 2014 Jun;13(2):257-65. doi: 10.1007/s10689-013-9639-6. Fam Cancer. 2014. PMID: 23934599

10

Identification, management, and evaluation of children with cancer-predisposition syndromes.

Knapke S, Zelley K, Nichols KE, Kohlmann W, Schiffman JD. Knapke S, et al. Am Soc Clin Oncol Educ Book. 2012:576-84. doi: 10.14694/EdBook_AM.2012.32.8. Am Soc Clin Oncol Educ Book. 2012. PMID: 24451799 Free article.

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