293 related articles for article (PubMed ID: 2576938)
1. Hereditary medullary thyroid carcinoma: genetic annalysis of three related syndromes. Groupe d'Etude des Tumeurs a Calcitonine.
Sobol H; Narod SA; Schuffenecker I; Amos C; Ezekowitz RA; Lenoir GM
Henry Ford Hosp Med J; 1989; 37(3-4):109-11. PubMed ID: 2576938
[TBL] [Abstract][Full Text] [Related]
2. Early detection of hereditary medullary thyroid cancer with polymorphic DNA probes. Groupe d'Etude des Tumeurs a Calcitonine.
Narod SA; Sobol H; Schuffenecker I; Ezekowitz RA; Lenoir GM
Henry Ford Hosp Med J; 1989; 37(3-4):106-8. PubMed ID: 2576937
[TBL] [Abstract][Full Text] [Related]
3. Low incidence of loss of chromosome 10 in sporadic and hereditary human medullary thyroid carcinoma.
Nelkin BD; Nakamura Y; White RW; de Bustros AC; Herman J; Wells SA; Baylin SB
Cancer Res; 1989 Aug; 49(15):4114-9. PubMed ID: 2568166
[TBL] [Abstract][Full Text] [Related]
4. Familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2B map to the same region of chromosome 10 as multiple endocrine neoplasia type 2A.
Lairmore TC; Howe JR; Korte JA; Dilley WG; Aine L; Aine E; Wells SA; Donis-Keller H
Genomics; 1991 Jan; 9(1):181-92. PubMed ID: 1672289
[TBL] [Abstract][Full Text] [Related]
5. Statistical analysis of histomorphological findings in medullary thyroid carcinoma: distinction between the different familial forms of the disease. G.E.T.C. Groupe d'Etude des Tumeurs a Calcitonine.
Franc B; Rosenberg-Bourgin M; Auvert B; Caillou B; Dutrieux-Berger N; Floquet J; Houcke-Lecomte M; Justrabo E; Labat-Moleur F; Le Bodic MF
Henry Ford Hosp Med J; 1992; 40(3-4):261-3. PubMed ID: 1362419
[TBL] [Abstract][Full Text] [Related]
6. Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.
Moley JF; Brother MB; Fong CT; White PS; Baylin SB; Nelkin B; Wells SA; Brodeur GM
Cancer Res; 1992 Feb; 52(4):770-4. PubMed ID: 1346584
[TBL] [Abstract][Full Text] [Related]
7. Allele loss on chromosome 10 and point mutation of ras oncogenes are infrequent in tumors of MEN 2A.
Okazaki M; Miya A; Tanaka N; Miki T; Yamamoto M; Motomura K; Miyauchi A; Mori T; Takai S
Henry Ford Hosp Med J; 1989; 37(3-4):112-5. PubMed ID: 2576939
[TBL] [Abstract][Full Text] [Related]
8. Surgical treatment of medullary carcinoma of the thyroid.
Block MA
Otolaryngol Clin North Am; 1990 Jun; 23(3):453-73. PubMed ID: 1973281
[TBL] [Abstract][Full Text] [Related]
9. Mucosal neuroma, pheochromocytoma and medullary thyroid carcinoma: multiple endocrine neoplasia type 3.
Khairi MR; Dexter RN; Burzynski NJ; Johnston CC
Medicine (Baltimore); 1975 Mar; 54(2):89-112. PubMed ID: 1117836
[TBL] [Abstract][Full Text] [Related]
10. Changing concepts in the management of hereditary and sporadic medullary thyroid carcinoma.
Grauer A; Raue F; Gagel RF
Endocrinol Metab Clin North Am; 1990 Sep; 19(3):613-35. PubMed ID: 1979773
[TBL] [Abstract][Full Text] [Related]
11. Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.
Khosla S; Patel VM; Hay ID; Schaid DJ; Grant CS; van Heerden JA; Thibodeau SN
J Clin Invest; 1991 May; 87(5):1691-9. PubMed ID: 2022740
[TBL] [Abstract][Full Text] [Related]
12. Pheochromocytoma in multiple endocrine neoplasia type II: an example of the two-hit theory of neoplasia.
Cerny JC; Jackson CE; Talpos GB; Yott JB; Lee MW
Surgery; 1982 Nov; 92(5):849-52. PubMed ID: 6127813
[TBL] [Abstract][Full Text] [Related]
13. Medullary thyroid carcinoma: Australian experience with genetic testing.
Ward JL; Hyland VJ; Andrew DS; Marsh DJ; Robinson BG
Henry Ford Hosp Med J; 1992; 40(3-4):220-3. PubMed ID: 1362409
[TBL] [Abstract][Full Text] [Related]
14. Multiple endocrine neoplasia 2B (MEN 2B)/MEN 3.
Holloway KB; Flowers FP
Dermatol Clin; 1995 Jan; 13(1):99-103. PubMed ID: 7712657
[TBL] [Abstract][Full Text] [Related]
15. Mapping the inherited defects associated with multiple endocrine neoplasia type 2A, multiple endocrine neoplasia type 2B, and familial medullary thyroid carcinoma to chromosome 10 by linkage analysis.
Goodfellow PJ
Endocrinol Metab Clin North Am; 1994 Mar; 23(1):177-85. PubMed ID: 7913024
[No Abstract] [Full Text] [Related]
16. Genetic screening of endocrine tumour syndromes with DNA probes: the example of medullary thyroid carcinoma.
Sobol H; Narod SA; Assouline D; Lenoir GM
Horm Res; 1989; 32(1-3):34-40. PubMed ID: 2575577
[TBL] [Abstract][Full Text] [Related]
17. Hereditary medullary thyroid carcinoma.
Vasen HF; Vermey A
Cancer Detect Prev; 1995; 19(2):143-50. PubMed ID: 7750101
[TBL] [Abstract][Full Text] [Related]
18. Multiple endocrine neoplasia type 2A (MEN-2A): natural history, screening, and central registration.
Brouwers-Smalbraak GJ; Vasen HF; Struyvenberg A; Nieuwenhuijzen Kruseman AC; Helsloot MH; Lips CJ
Neth J Med; 1986; 29(4):111-7. PubMed ID: 2872602
[No Abstract] [Full Text] [Related]
19. Loss of genes on chromosome 22 in medullary thyroid carcinoma and pheochromocytoma.
Takai S; Tateishi H; Nishisho I; Miki T; Motomura K; Miyauchi A; Kato M; Ikeuchi T; Yamamoto K; Okazaki M
Jpn J Cancer Res; 1987 Sep; 78(9):894-8. PubMed ID: 2889715
[TBL] [Abstract][Full Text] [Related]
20. Characteristics of a family with the MEN-2A syndrome.
Haak HR; Nieuwenhuijzen Kruseman AC
Henry Ford Hosp Med J; 1987; 35(2-3):104-6. PubMed ID: 2891639
[No Abstract] [Full Text] [Related]
[Next] [New Search]
