Belloni DR - Search Results

1

Tampon samplings with longer cervicovaginal cell exposures are equivalent to two consecutive swabs for the detection of high-risk human papillomavirus.

Harper DM, Raymond M, Noll WW, Belloni DR, Duncan LT, Cole BF. Harper DM, et al. Among authors: belloni dr. Sex Transm Dis. 2002 Nov;29(11):628-36. doi: 10.1097/00007435-200211000-00003. Sex Transm Dis. 2002. PMID: 12438897 Clinical Trial.

2

Randomized clinical trial of PCR-determined human papillomavirus detection methods: self-sampling versus clinician-directed--biologic concordance and women's preferences.

Harper DM, Noll WW, Belloni DR, Cole BF. Harper DM, et al. Among authors: belloni dr. Am J Obstet Gynecol. 2002 Mar;186(3):365-73. doi: 10.1067/mob.2002.121076. Am J Obstet Gynecol. 2002. PMID: 11904593 Clinical Trial.

3

Factors affecting the detection rate of human papillomavirus.

Harper DM, Longacre MR, Noll WW, Belloni DR, Cole BF. Harper DM, et al. Among authors: belloni dr. Ann Fam Med. 2003 Nov-Dec;1(4):221-7. doi: 10.1370/afm.90. Ann Fam Med. 2003. PMID: 15055412 Free PMC article. Clinical Trial.

4

Multiple endocrine neoplasia 2A due to a unique C609S RET mutation presents with pheochromocytoma and reduced penetrance of medullary thyroid carcinoma.

Kinlaw WB, Scott SM, Maue RA, Memoli VA, Harris RD, Daniels GH, Porter DM, Belloni DR, Spooner ET, Ernesti MM, Noll WW. Kinlaw WB, et al. Among authors: belloni dr. Clin Endocrinol (Oxf). 2005 Dec;63(6):676-82. doi: 10.1111/j.1365-2265.2005.02400.x. Clin Endocrinol (Oxf). 2005. PMID: 16343103

5

Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2).

Park JP, Moeschler JB, Hani VH, Hawk AB, Belloni DR, Noll WW, Mohandas TK. Park JP, et al. Among authors: belloni dr. Am J Med Genet. 1998 Jun 30;78(2):134-9. Am J Med Genet. 1998. PMID: 9674903

6

Loss of heterozygosity on chromosome 11q22-23 in melanoma is associated with retention of the insertion polymorphism in the matrix metalloproteinase-1 promoter.

Noll WW, Belloni DR, Rutter JL, Storm CA, Schned AR, Titus-Ernstoff L, Ernstoff MS, Brinckerhoff CE. Noll WW, et al. Among authors: belloni dr. Am J Pathol. 2001 Feb;158(2):691-7. doi: 10.1016/S0002-9440(10)64011-4. Am J Pathol. 2001. PMID: 11159206 Free PMC article.

7

Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.

Mohandas TK, Park JP, Spellman RA, Filiano JJ, Mamourian AC, Hawk AB, Belloni DR, Noll WW, Moeschler JB. Mohandas TK, et al. Among authors: belloni dr. Am J Med Genet. 1999 Feb 12;82(4):294-300. Am J Med Genet. 1999. PMID: 10051161

8

Polymorphism in intron 4 of HFE does not compromise haemochromatosis mutation results.

Noll WW, Belloni DR, Stenzel TT, Grody WW. Noll WW, et al. Among authors: belloni dr. Nat Genet. 1999 Nov;23(3):271-2. doi: 10.1038/15722. Nat Genet. 1999. PMID: 10610176 No abstract available.

9

Increased brain activation during working memory in cognitively intact adults with the APOE epsilon4 allele.

Wishart HA, Saykin AJ, Rabin LA, Santulli RB, Flashman LA, Guerin SJ, Mamourian AC, Belloni DR, Rhodes CH, McAllister TW. Wishart HA, et al. Among authors: belloni dr. Am J Psychiatry. 2006 Sep;163(9):1603-10. doi: 10.1176/ajp.2006.163.9.1603. Am J Psychiatry. 2006. PMID: 16946187

10

Detection of the C282Y and H63D polymorphisms associated with hereditary hemochromatosis using the ABI 7500 fast real time PCR platform.

Tafe LJ, Belloni DR, Tsongalis GJ. Tafe LJ, et al. Among authors: belloni dr. Diagn Mol Pathol. 2007 Jun;16(2):112-5. doi: 10.1097/PDM.0b013e3180310489. Diagn Mol Pathol. 2007. PMID: 17525682

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