Rhiem K - Search Results

1

Validation of the Manchester scoring system for predicting BRCA1/2 mutations in 9,390 families suspected of having hereditary breast and ovarian cancer.

Kast K, Schmutzler RK, Rhiem K, Kiechle M, Fischer C, Niederacher D, Arnold N, Grimm T, Speiser D, Schlegelberger B, Varga D, Horvath J, Beer M, Briest S, Meindl A, Engel C. Kast K, et al. Among authors: rhiem k. Int J Cancer. 2014 Nov 15;135(10):2352-61. doi: 10.1002/ijc.28875. Epub 2014 Apr 25. Int J Cancer. 2014. PMID: 24700448

2

Familial ovarian dysgerminomas (Swyer syndrome) in females associated with 46 XY-karyotype.

Kempe A, Engels H, Schubert R, Meindl A, van der Ven K, Plath H, Rhiem K, Schwanitz G, Schmutzler RK. Kempe A, et al. Among authors: rhiem k. Gynecol Endocrinol. 2002 Apr;16(2):107-11. Gynecol Endocrinol. 2002. PMID: 12012620

3

Chromosomal region 15q21.1 is a frequent target of allelic imbalance in advanced breast carcinomas.

Rhiem K, Klein A, Münch M, Kreutzfeld R, Ramser J, Wardelmann E, Schackert G, Von Deimling A, Wiestler OD, Schmutzler RK. Rhiem K, et al. Int J Cancer. 2003 Aug 10;106(1):74-7. doi: 10.1002/ijc.11169. Int J Cancer. 2003. PMID: 12794759

4

Limited relevance of the CHEK2 gene in hereditary breast cancer.

Dufault MR, Betz B, Wappenschmidt B, Hofmann W, Bandick K, Golla A, Pietschmann A, Nestle-Krämling C, Rhiem K, Hüttner C, von Lindern C, Dall P, Kiechle M, Untch M, Jonat W, Meindl A, Scherneck S, Niederacher D, Schmutzler RK, Arnold N. Dufault MR, et al. Among authors: rhiem k. Int J Cancer. 2004 Jun 20;110(3):320-5. doi: 10.1002/ijc.20073. Int J Cancer. 2004. PMID: 15095295

5

Systematic identification and molecular characterization of genes differentially expressed in breast and ovarian cancer.

Dahl E, Sadr-Nabavi A, Klopocki E, Betz B, Grube S, Kreutzfeld R, Himmelfarb M, An HX, Gelling S, Klaman I, Hinzmann B, Kristiansen G, Grützmann R, Kuner R, Petschke B, Rhiem K, Wiechen K, Sers C, Wiestler O, Schneider A, Höfler H, Nährig J, Dietel M, Schäfer R, Rosenthal A, Schmutzler R, Dürst M, Meindl A, Niederacher D. Dahl E, et al. Among authors: rhiem k. J Pathol. 2005 Jan;205(1):21-8. doi: 10.1002/path.1687. J Pathol. 2005. PMID: 15586368

6

Strong evidence that the common variant S384F in BRCA2 has no pathogenic relevance in hereditary breast cancer.

Wappenschmidt B, Fimmers R, Rhiem K, Brosig M, Wardelmann E, Meindl A, Arnold N, Mallmann P, Schmutzler RK. Wappenschmidt B, et al. Among authors: rhiem k. Breast Cancer Res. 2005;7(5):R775-9. doi: 10.1186/bcr1291. Epub 2005 Jul 27. Breast Cancer Res. 2005. PMID: 16168123 Free PMC article.

7

BRCA1-associated breast carcinomas frequently present with benign sonographic features.

Rhiem K, Flucke U, Schmutzler RK. Rhiem K, et al. AJR Am J Roentgenol. 2006 May;186(5):E11-2; author reply E12-3. doi: 10.2214/AJR.06.5041. AJR Am J Roentgenol. 2006. PMID: 16632699 No abstract available.

8

Screening for ovarian cancer by transvaginal ultrasound and serum CA125 measurement in women with a familial predisposition: a prospective cohort study.

Bosse K, Rhiem K, Wappenschmidt B, Hellmich M, Madeja M, Ortmann M, Mallmann P, Schmutzler R. Bosse K, et al. Among authors: rhiem k. Gynecol Oncol. 2006 Dec;103(3):1077-82. doi: 10.1016/j.ygyno.2006.06.032. Epub 2006 Aug 9. Gynecol Oncol. 2006. PMID: 16904167

9

Outcome of a structured surveillance programme in women with a familial predisposition for breast cancer.

Schmutzler RK, Rhiem K, Breuer P, Wardelmann E, Lehnert M, Coburger S, Wappenschmidt B. Schmutzler RK, et al. Among authors: rhiem k. Eur J Cancer Prev. 2006 Dec;15(6):483-9. doi: 10.1097/01.cej.0000220624.70234.14. Eur J Cancer Prev. 2006. PMID: 17106326

10

Association of the BRCA1 missense variant R1699W with a malignant phyllodes tumor of the breast.

Rhiem K, Flucke U, Engel C, Wappenschmidt B, Reinecke-Lüthge A, Büttner R, Schmutzler RK. Rhiem K, et al. Cancer Genet Cytogenet. 2007 Jul 1;176(1):76-9. doi: 10.1016/j.cancergencyto.2007.03.006. Cancer Genet Cytogenet. 2007. PMID: 17574969

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