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The Journal of Pathology|December 1, 1994
Recombination pattern of the TCR gamma locus in human peripheral T-cell lymphomasI Theodorou, M Raphaël, C Bigorgne, et al.
Annales D'Endocrinologie|January 1, 1996
[Hypercalcitoninemia in conditions other than medullary cancers of the thyroid]P Niccoli, B Conte-Devolx, P J Lejeune, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|December 5, 2023
Cytopathological analysis of salivary gland cancer: REFCOR recommendations by the formal consensus methodM Courtade-Saïdi, E Uro-Coste, S Vergez, et al.
Annales De Biologie Clinique|January 1, 1995
Comparison of the analytical and clinical performances of three thyrotropin immunoassay kitsA Minebois-Villégas, V Rohmer, F Rachédi, et al.
The Journal of Clinical Endocrinology and Metabolism|October 1, 1990
Diagnosis of medullary carcinoma of the thyroid (MCT) by calcitonin assay using monoclonal antibodies: criteria for the pentagastrin stimulation test in hereditary MCTD Guilloteau, R Perdrisot, C Calmettes, et al.
Human Genetics|November 1, 1989
Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytomaS A Narod, H Sobol, Y Nakamura, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1997
Interest of routine measurement of serum calcitonin: study in a large series of thyroidectomized patients. The French Medullary Study GroupP Niccoli, N Wion-Barbot, P Caron, et al.
European Journal of Endocrinology|November 27, 1999
Early or prophylactic thyroidectomy in MEN 2/FMTC gene carriers: results in 71 thyroidectomized patients. The French Calcitonin Tumours Study Group (GETC)P Niccoli-Sire, A Murat, E Baudin, et al.
Clinical Endocrinology|May 14, 1998
Prognostic factors for survival and for biochemical cure in medullary thyroid carcinoma: results in 899 patients. The GETC Study Group. Groupe d'étude des tumeurs à calcitonineE Modigliani, R Cohen, J M Campos, et al.
Human Pathology|August 19, 1999
Medullary thyroid microcarcinoma: a clinicopathologic retrospective study of 38 patients with no prior familial diseaseS Guyétant, F Dupre, J C Bigorgne, et al.
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