Kiviniemi H - Search Results

1

Application of fine-needle aspiration to the demonstration of ERBB2 and MYC expression by in situ hybridization in breast carcinoma.

Soini Y, Mannermaa A, Winqvist R, Kamel D, Poikonen K, Kiviniemi H, Pääkkö P. Soini Y, et al. Among authors: kiviniemi h. J Histochem Cytochem. 1994 Jun;42(6):795-803. doi: 10.1177/42.6.7910618. J Histochem Cytochem. 1994. PMID: 7910618

2

Human familial and sporadic breast cancer: analysis of the coding regions of the 17 beta-hydroxysteroid dehydrogenase 2 gene (EDH17B2) using a single-strand conformation polymorphism assay.

Mannermaa A, Peltoketo H, Winqvist R, Ponder BA, Kiviniemi H, Easton DF, Poutanen M, Isomaa V, Vihko R. Mannermaa A, et al. Among authors: kiviniemi h. Hum Genet. 1994 Mar;93(3):319-24. doi: 10.1007/BF00212030. Hum Genet. 1994. PMID: 8125484

3

Refinement of regional loss of heterozygosity for chromosome 11p15.5 in human breast tumors.

Winqvist R, Mannermaa A, Alavaikko M, Blanco G, Taskinen PJ, Kiviniemi H, Newsham I, Cavenee W. Winqvist R, et al. Among authors: kiviniemi h. Cancer Res. 1993 Oct 1;53(19):4486-8. Cancer Res. 1993. PMID: 8402619

4

Wire-guided excision of non-palpable breast cancer: determinants and correlations between radiologic and histologic margins and residual disease in re-excisions.

Saarela AO, Rissanen TJ, Lähteenmäki KM, Soini Y, Haukipuro K, Kaarela O, Kiviniemi HO. Saarela AO, et al. Among authors: kiviniemi ho. Breast. 2001 Feb;10(1):28-34. doi: 10.1054/brst.2000.0174. Breast. 2001. PMID: 14965555

5

Loss of heterozygosity in sporadic human breast carcinoma: a common region between 11q22 and 11q23.3.

Hampton GM, Mannermaa A, Winqvist R, Alavaikko M, Blanco G, Taskinen PJ, Kiviniemi H, Newsham I, Cavenee WK, Evans GA. Hampton GM, et al. Among authors: kiviniemi h. Cancer Res. 1994 Sep 1;54(17):4586-9. Cancer Res. 1994. PMID: 8062246

6

Nonpalpable breast lesions: pathologic correlation of ultrasonographically guided fine-needle aspiration biopsy.

Saarela AO, Kiviniemi HO, Rissanen TJ, Paloneva TK. Saarela AO, et al. Among authors: kiviniemi ho. J Ultrasound Med. 1996 Aug;15(8):549-53; quiz 555-6. doi: 10.7863/jum.1996.15.8.549. J Ultrasound Med. 1996. PMID: 8839401

7

Loss of heterozygosity for chromosome 11 in primary human breast tumors is associated with poor survival after metastasis.

Winqvist R, Hampton GM, Mannermaa A, Blanco G, Alavaikko M, Kiviniemi H, Taskinen PJ, Evans GA, Wright FA, Newsham I, et al. Winqvist R, et al. Among authors: kiviniemi h. Cancer Res. 1995 Jun 15;55(12):2660-4. Cancer Res. 1995. PMID: 7780982

8

Evidence of founder mutations in Finnish BRCA1 and BRCA2 families.

Huusko P, Pääkkönen K, Launonen V, Pöyhönen M, Blanco G, Kauppila A, Puistola U, Kiviniemi H, Kujala M, Leisti J, Winqvist R. Huusko P, et al. Among authors: kiviniemi h. Am J Hum Genet. 1998 Jun;62(6):1544-8. doi: 10.1086/301880. Am J Hum Genet. 1998. PMID: 9585608 Free PMC article. No abstract available.

9

Ultrasonographically guided wire localization of nonpalpable breast lesions.

Rissanen TJ, Mäkäräinen HP, Kiviniemi HO, Suramo II. Rissanen TJ, et al. Among authors: kiviniemi ho. J Ultrasound Med. 1994 Mar;13(3):183-8. doi: 10.7863/jum.1994.13.3.183. J Ultrasound Med. 1994. PMID: 7932975

10

Radiography of the male breast in gynecomastia.

Rissanen TJ, Mäkäräinen HP, Kallioinen MJ, Kiviniemi HO, Salmela PI. Rissanen TJ, et al. Among authors: kiviniemi ho. Acta Radiol. 1992 Mar;33(2):110-4. Acta Radiol. 1992. PMID: 1562400

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