Early malignant progression of hereditary medullary thyroid cancer
- Author
- MACHENS, Andreas1 ; NICCOLI-SIRE, Patricia2 ; DRALLE, Henning1 ; HOEGEL, Josef3 ; FRANK-RAUE, Karin4 ; VAN VROONHOVEN, Theo J5 ; ROEHER, Hans-Dietrich6 ; WAHL, Robert A7 ; LAMESCH, Peter8 ; RAUE, Friedhelm4 ; CONTE-DEVOLX, Bernard2
[1] Klinik für Allgemein-, Viszeral-, und Gefässchirurgie, Martin-Luther-Universität Halle-Wittenberg, Halle (Saale), Germany
[2] Centre Hospitalier Régional et Universitaire de Marseille, Service d'Endocrinologie et Maladies Métaboliques, Marseilles, France
[3] Abteilung Biometrie und Medizinische Dokumentation, Universitat Ulm, Ulm, Germany
[4] Endokrinologische Gemeinschaftspraxis, Heidelberg, Germany
[5] Department of Surgery, University Hospital Utrecht, Utrecht, Netherlands
[6] Klinik für Allgemeine und Unfallchirurgie, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany
[7] Chirurgische Klinik, Bürgerhospital Frankfurt am Main, Frankfurt am Main, Germany
[8] Chirurgische Klinik und Poliklinik für Abdominal-, Transplantations-, und Gefässchirurgie, Universität Leipzig, Leipzig, Germany
European Multiple Endocrine Neoplasia (EUROMEN) Study Group, Europe - Source
The New England journal of medicine. 2003, Vol 349, Num 16, pp 1517-1525, 9 p ; ref : 40 ref
- CODEN
- NEJMAG
- ISSN
- 0028-4793
- Scientific domain
- General medicine general surgery
- Publisher
- Massachusetts Medical Society, Boston, MA
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Asymptomatique Carcinome médullaire Etude multicentrique Gène Homme Héréditaire Mutation Progression carcinogenèse Précoce Thyroïde Endocrinopathie Maladie héréditaire Thyroïde pathologie Tumeur maligne
- Keyword (en)
- Asymptomatic Medullary carcinoma Multicenter study Gene Human Hereditary Mutation Tumor progression Early Thyroid gland Endocrinopathy Genetic disease Thyroid diseases Malignant tumor
- Keyword (es)
- Asintomático Carcinoma medular Estudio multicéntrico Gen Hombre Hereditario Mutación Progresión carcinogénesis Precoz Tiroides Endocrinopatía Enfermedad hereditaria Tiroides patología Tumor maligno
- Classification
- Pascal
- 002 Biological and medical sciences / 002B Medical sciences / 002B21 Endocrinopathies / 002B21C Thyroid. Thyroid axis (diseases) / 002B21C02 Malignant tumors
- Discipline
- Endocrinopathies
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 15207832
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1056/NEJMoa012915 
https://dx.doi.org/10.1056/NEJMoa012915
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