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pro vyhledávání: '"P. Niccoli-Sire"'
Autor:
P. Niccoli-Sire, P. Ruszniewski
Publikováno v:
Oncologie. 10:398-405
Le reseau RENATEN se propose de structurer l’offre de soins pour les patients atteints de tumeurs endocrines, sporadiques ou hereditaires, sur le territoire francais. Apres avoir rappele les objectifs et les finalites du reseau, cet article precise
Autor:
B. Conte-Devolx, P. Niccoli-Sire
Publikováno v:
Annales d'Endocrinologie. 68:317-324
Multiple endocrine neoplasia type 2 (MEN2) is an hereditary disease with a prevalence of 1/5000. Three phenotypic variants have been identified: MEN2A associates medullary thyroid carcinoma (MTC) to pheochromocytoma in about 20–50% of cases and to
Autor:
P Niccoli-Sire, B Conte-Devolx
Publikováno v:
Annales d'Endocrinologie. 68:325-331
Medullary thyroid carcinoma (MTC) is developed from thyroid C cells that secrete calcitonin (CT). MTC represents 5-10% of thyroid cancers with a 1-2% incidence in nodular thyroid diseases. Diagnosis is usually made by a solitary nodule often associat
Autor:
B. Conte-Devolx, P. Niccoli-Sire
Publikováno v:
Annales d'Endocrinologie. 66:168-175
Autor:
P Niccoli-Sire, B Conte-Devolx
Publikováno v:
Immuno-analyse & Biologie Spécialisée. 18:320-328
Resume La neoplasie endocrinienne multiple de type 2 (NEM2) est une affection multiglandulaire hereditaire, autosomique dominante, associant un cancer medullaire de la thyroide, un pheochromocytome et une hyperparathyroidie, phenotype lie a une anoma
Autor:
S. Franc, P. Niccoli-Sire, R. Cohen, S. Bardet, B. Maes, A. Murat, A. Krivitzky, E. Modigliani, The French Medullary Study Group getc
Publikováno v:
Clinical Endocrinology. 55:403-409
BACKGROUND Medullary thyroid carcinoma is a rare tumour derived from the thyroid parafollicular calcitonin-secreting cells. Calcitonin is a very specific marker of this cancer that allows preoperative diagnosis. Serum calcitonin assay is particularly
Autor:
P Niccoli-Sire
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
Review on RET (Rearranged during transfection), with data on DNA, on the protein encoded, and where the gene is implicated.
Autor:
P. Niccoli-Sire, M. Giovannini
Publikováno v:
Tumeurs endocrines thoraciques et digestives ISBN: 9782287355738
Les TE gastro-entero-pancreatiques sont difficiles a localiser car elles sont souvent de petite taille. Elles sont suspectees sur des signes cliniques et biologiques. De plus jusqu’a une epoque recente, le diagnostic etait oriente de facon tres imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e7ab92e3e423ec7b88fa9b1ba18235c
https://doi.org/10.1007/978-2-287-35574-5_9
https://doi.org/10.1007/978-2-287-35574-5_9
Autor:
P, Niccoli-Sire, B, Conte-Devolx
Publikováno v:
Annales d'endocrinologie. 68(5)
Multiple endocrine neoplasia type 2 (MEN2) is an hereditary disease with a prevalence of 1/5000. Three phenotypic variants have been identified: MEN2A associates medullary thyroid carcinoma (MTC) to pheochromocytoma in about 20-50% of cases and to pr
Autor:
P, Niccoli-Sire, B, Conte-Devolx
Publikováno v:
Annales d'endocrinologie. 68(5)
Medullary thyroid carcinoma (MTC) is developed from thyroid C cells that secrete calcitonin (CT). MTC represents 5-10% of thyroid cancers with a 1-2% incidence in nodular thyroid diseases. Diagnosis is usually made by a solitary nodule often associat