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Page 1
Prevalence and parental origin of de novo RET mutations in multiple endocrine neoplasia type 2A and familial medullary thyroid carcinoma. Le Groupe d'Etude des Tumeurs a Calcitonine.
Schuffenecker I, Ginet N, Goldgar D, Eng C, Chambe B, Boneu A, Houdent C, Pallo D, Schlumberger M, Thivolet C, Lenoir GM. Schuffenecker I, et al. Among authors: houdent c. Am J Hum Genet. 1997 Jan;60(1):233-7. Am J Hum Genet. 1997. PMID: 8981969 Free PMC article. No abstract available.
Risk and penetrance of primary hyperparathyroidism in multiple endocrine neoplasia type 2A families with mutations at codon 634 of the RET proto-oncogene. Groupe D'etude des Tumeurs à Calcitonine.
Schuffenecker I, Virally-Monod M, Brohet R, Goldgar D, Conte-Devolx B, Leclerc L, Chabre O, Boneu A, Caron J, Houdent C, Modigliani E, Rohmer V, Schlumberger M, Eng C, Guillausseau PJ, Lenoir GM. Schuffenecker I, et al. Among authors: houdent c. J Clin Endocrinol Metab. 1998 Feb;83(2):487-91. doi: 10.1210/jcem.83.2.4529. J Clin Endocrinol Metab. 1998. PMID: 9467562
RET mutations in exons 13 and 14 of FMTC patients.
Bolino A, Schuffenecker I, Luo Y, Seri M, Silengo M, Tocco T, Chabrier G, Houdent C, Murat A, Schlumberger M, et al. Bolino A, et al. Among authors: houdent c. Oncogene. 1995 Jun 15;10(12):2415-9. Oncogene. 1995. PMID: 7784092
Primary hyperparathyroidism in multiple endocrine neoplasia type IIa: retrospective French multicentric study. Groupe d'Etude des Tumeurs á Calcitonine (GETC, French Calcitonin Tumors Study Group), French Association of Endocrine Surgeons.
Kraimps JL, Denizot A, Carnaille B, Henry JF, Proye C, Bacourt F, Sarfati E, Dupond JL, Maes B, Travagli JP, Boneu A, Roger P, Houdent C, Barbier J, Modigliani E. Kraimps JL, et al. Among authors: houdent c. World J Surg. 1996 Sep;20(7):808-12; discussion 812-3. doi: 10.1007/s002689900123. World J Surg. 1996. PMID: 8678955
[Coronary embolism in hyperthyroidism].
Kerleau JM, Lefebvre H, Houdent C, Wolf LM. Kerleau JM, et al. Among authors: houdent c. Presse Med. 1992 Dec 12;21(43):2107. Presse Med. 1992. PMID: 1297126 French. No abstract available.
Phaeochromocytoma in multiple endocrine neoplasia type 2 A: survey of 100 cases.
Casanova S, Rosenberg-Bourgin M, Farkas D, Calmettes C, Feingold N, Heshmati HM, Cohen R, Conte-Devolx B, Guillausseau PJ, Houdent C, et al. Casanova S, et al. Among authors: houdent c. Clin Endocrinol (Oxf). 1993 May;38(5):531-7. doi: 10.1111/j.1365-2265.1993.tb00350.x. Clin Endocrinol (Oxf). 1993. PMID: 8101147
[Postpartum definitive hypothyroidism. 7 cases].
Houdent C, Pellenc P, Carrara Balacheff O, Kuhn JM, Leclerc P, Cavelier B, Wolf LM. Houdent C, et al. Presse Med. 1985 Feb 9;14(5):257-61. Presse Med. 1985. PMID: 3157107 French.
47 results