Cummings T - Search Results

1

The clinical and screening age-at-onset distribution for the MEN-2 syndrome.

Easton DF, Ponder MA, Cummings T, Gagel RF, Hansen HH, Reichlin S, Tashjian AH Jr, Telenius-Berg M, Ponder BA. Easton DF, et al. Among authors: cummings t. Am J Hum Genet. 1989 Feb;44(2):208-15. Am J Hum Genet. 1989. PMID: 2563193 Free PMC article.

2

High-sensitivity serum calcitonin assays applied to screening for thyroid C-cell disease in multiple endocrine neoplasia type 2A.

Kaplan MM, Stall GM, Cummings T, MacAulay A, Motté P, Wolfe HJ, Reichlin S, Tashjian AH Jr. Kaplan MM, et al. Among authors: cummings t. Henry Ford Hosp Med J. 1992;40(3-4):227-31. Henry Ford Hosp Med J. 1992. PMID: 1362411 Free article.

3

The clinical outcome of prospective screening for multiple endocrine neoplasia type 2a. An 18-year experience.

Gagel RF, Tashjian AH Jr, Cummings T, Papathanasopoulos N, Kaplan MM, DeLellis RA, Wolfe HJ, Reichlin S. Gagel RF, et al. Among authors: cummings t. N Engl J Med. 1988 Feb 25;318(8):478-84. doi: 10.1056/NEJM198802253180804. N Engl J Med. 1988. PMID: 2893259

4

Impact of prospective screening for multiple endocrine neoplasia type 2.

Gagel RF, Tashjian AH Jr, Cummings T, Papathanasopoulos N, Reichlin S. Gagel RF, et al. Among authors: cummings t. Henry Ford Hosp Med J. 1987;35(2-3):94-8. Henry Ford Hosp Med J. 1987. PMID: 2891654 Free article. No abstract available.

5

Clinical use of molecular information in the management of multiple endocrine neoplasia type 2A.

Gagel RF, Cote GJ, Martins Bugalho MJ, Boyd AE 3rd, Cummings T, Goepfert H, Evans DB, Cangir A, Khorana S, Schultz PN. Gagel RF, et al. Among authors: cummings t. J Intern Med. 1995 Oct;238(4):333-41. doi: 10.1111/j.1365-2796.1995.tb01207.x. J Intern Med. 1995. PMID: 7595169

6

Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2.

Gardner E, Papi L, Easton DF, Cummings T, Jackson CE, Kaplan M, Love DR, Mole SE, Moore JK, Mulligan LM, et al. Gardner E, et al. Among authors: cummings t. Hum Mol Genet. 1993 Mar;2(3):241-6. doi: 10.1093/hmg/2.3.241. Hum Mol Genet. 1993. PMID: 8098977

7

Early markers for the multiple endocrine neoplasia syndromes.

Snow KJ, Cummings T, Boyd AE 3rd. Snow KJ, et al. Among authors: cummings t. Contemp Intern Med. 1994 Nov;6(11):9-11, 15-9. Contemp Intern Med. 1994. PMID: 10150295 No abstract available.

8

Hereditary benign intraepithelial dyskeratosis: an evaluation of diagnostic cytology.

Cummings TJ, Dodd LG, Eedes CR, Klintworth GK. Cummings TJ, et al. Arch Pathol Lab Med. 2008 Aug;132(8):1325-8. doi: 10.5858/2008-132-1325-HBIDAE. Arch Pathol Lab Med. 2008. PMID: 18684035 Free article.

9

Loss of chromosome 13 in a case of soft tissue perineurioma.

Mott RT, Goodman BK, Burchette JL, Cummings TJ. Mott RT, et al. Among authors: cummings tj. Clin Neuropathol. 2005 Mar-Apr;24(2):69-76. Clin Neuropathol. 2005. PMID: 15803806 Review.

10

Biphasic malignant meningioma: a comparative genomic hybridization study.

Heimberger AB, Wiltshire RN, Bronec R, McLendon RE, Cummings TJ. Heimberger AB, et al. Among authors: cummings tj. Clin Neuropathol. 2002 Nov-Dec;21(6):258-64. Clin Neuropathol. 2002. PMID: 12489674

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