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Advances in diagnostic practices affect thyroid cancer incidence in France.
Published in:
European Journal of Endocrinology, 2004, v. 150, n. 2, p. 0133, doi. 10.1530/eje.0.1500133
By:
- L Leenhardt;
- M O Bernier;
- M H Boin-Pineau;
- B Conte Devolx;
- R Marechaud;
- P Niccoli-Sire;
- M Nocaudie;
- J Orgiazzi;
- M Schlumberger;
- J L Wemeau;
- L Cherie-Challine;
- F De Vathaire
Publication type:
Article
Experience gained from operation of 103 adrenal incidentalomas.
Published in:
Langenbeck's Archives of Surgery, 1998, v. 383, n. 5, p. 330, doi. 10.1007/s004230050142
By:
- Proye, C.;
- Jafari Manjili, M.;
- Combemale, F.;
- Pattou, F.;
- Ernst, O.;
- Carnaille, B.;
- Wemeau, J. L.
Publication type:
Article
Modified-Release Recombinant Human TSH (MRrhTSH) Augments the Effect of <sup>131</sup>I Therapy in Benign Multinodular Goiter: Results from a Multicenter International, Randomized, Placebo-Controlled Study.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 5, p. 1368, doi. 10.1210/jc.2010-1193
By:
- Graf, H.;
- Fast, S.;
- Pacini, F.;
- Pinchera, A.;
- Leung, A.;
- Vaisman, M.;
- Reiners, C.;
- Wemeau, J. L.;
- Huysmans, D.;
- Harper, W.;
- Driedger, A.;
- de Souza, H. Noemberg;
- Castagna, M. G.;
- Antonangeli, L.;
- Braverman, L.;
- Corbo, R.;
- Düren, C.;
- Proust-Lemoine, E.;
- Edelbroek, M. A.;
- Marriott, C.
Publication type:
Article
Prognostic Factors of Disease-Free Survival after Thyroidectomy in 170 Young Patients with a RET Germline Mutation: A Multicenter Study of the Groupe Français d’Etude des Tumeurs Endocrines.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2011, v. 96, n. 3, p. E509, doi. 10.1210/jc.2010-1234
By:
- Rohmer, V.;
- Vidal-Trecan, G.;
- Bourdelot, A.;
- Niccoli, P.;
- Murat, A.;
- Wemeau, J. L.;
- Borson-Chazot, F.;
- Schvartz, C.;
- Tabarinc, A.;
- Chabre, O.;
- Chabrier, G.;
- Caron, P.;
- Rodien, P.;
- Schlumberger, M.;
- Baudin, E.
Publication type:
Article
Fertility and Obstetrical Complications in Women with LMNA-Related Familial Partial Lipodystrophy.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 6, p. 2223, doi. 10.1210/jc.2007-2521
By:
- Vantyghem, M. C.;
- Vincent-Desplanques, D.;
- Defrance-Faivre, F.;
- Capeau, J.;
- Fermon, C.;
- Valat, A. S.;
- Lascols, O.;
- Hecart, A. C.;
- Pigny, P.;
- Delemer, B.;
- Vigouroux, C.;
- Wemeau, J. L.
Publication type:
Article
Beneficial Effects of Propylthiouracil plus L-Thyroxine Treatment in a Patient with a Mutation in MCT8.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2008, v. 93, n. 6, p. 2084, doi. 10.1210/jc.2007-2719
By:
- Wémeau, J. L.;
- Pigeyre, M.;
- Proust-Lemoine, E.;
- d’Herbomez, M.;
- Gottrand, F.;
- Jansen, J.;
- Visser, T. J.;
- Ladsous, M.
Publication type:
Article
Clinical Characterization of Familial Isolated Pituitary Adenomas.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 9, p. 3316, doi. 10.1210/jc.2005-2671
By:
- Daly, A. F.;
- Jaffrain-Rea, M.-L.;
- Ciccarelli, A.;
- Valdes-Socin, H.;
- Rohmer, V.;
- Tamburrano, G.;
- Borson-Chazot, C.;
- Estour, B.;
- Ciccarelli, E.;
- Brue, T.;
- Ferolla, P.;
- Emy, P.;
- Colao, A.;
- Menis, E. De;
- Lecomte, P.;
- Penfornis, F.;
- Delemer, B.;
- Bertherat, J.;
- Wémeau, J. L.;
- Herder, W. De
Publication type:
Article
Octreotide (Long-Acting Release Formulation) Treatment in Patients with Graves’ Orbitopathy: Clinical Results of a Four-Month, Randomized, Placebo-Controlled, Double-Blind Study.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2005, v. 90, n. 2, p. 841, doi. 10.1210/jc.2004-1334
By:
- Wémeau, J. L.;
- Caron, P.;
- Beckers, A.;
- Rohmer, V.;
- Orgiazzi, J.;
- Borson-Chazot, F.;
- Nocaudie, M.;
- Perimenis, P.;
- Bisot-Locard, S.;
- Bourdeix, I.;
- Dejager, S.
Publication type:
Article
Patients with Familial Partial Lipodystrophy of the Dunnigan Type Due to a LMNA R482W Mutation Show Muscular and Cardiac Abnormalities.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 11, p. 5337, doi. 10.1210/jc.2003-031658
By:
- VANTYGHEM, M. C.;
- PIGNY, P.;
- MAURAGE, C. A.;
- ROUAIX-EMERY, N.;
- STOJKOVIC, T.;
- CUISSET, J. M.;
- MILLAIRE, A.;
- LASCOLS, O.;
- VERMERSCH, P.;
- WEMEAU, J. L.;
- CAPEAU, J.;
- VIGOUROUX, C.
Publication type:
Article
Phenotype-genotype correlation and follow-up in adult patients with hypokalaemia of renal origin suggesting Gitelman syndrome.
Published in:
European Journal of Endocrinology, 2011, v. 165, n. 4, p. 665, doi. 10.1530/EJE-11-0224
By:
- Balavoine, A. S.;
- Bataille, P.;
- Vanhille, P.;
- Azar, R.;
- Noël, C.;
- Asseman, P.;
- Soudan, B.;
- Wémeau, J. L.;
- Vantyghem, M. C.
Publication type:
Article
Treatment of carcinoid syndrome: a prospective crossover evaluation of lanreotide versus octreotide in terms of efficacy, patient acceptability, and tolerance.
Published in:
2000
By:
- O'Toole, D;
- Ducreux, M;
- Bommelaer, G;
- Wemeau, J L;
- Bouché, O;
- Catus, F;
- Blumberg, J;
- Ruszniewski, P
Publication type:
journal article
Quantitative Ultrasound of Bone and Markers of Bone Turnover in Cushing’s Syndrome.
Published in:
Osteoporosis International, 2001, v. 12, n. 2, p. 117, doi. 10.1007/s001980170143
By:
- Cortet, B.;
- Cortet, C.;
- Blanckaert, F.;
- d'Herbomez, M.;
- Marchandise, X.;
- Wémeau, J.-L.;
- Decoulx, M.;
- Dewailly, D.
Publication type:
Article
Thyroid Carcinomas Involving Follicular and Parafollicular C Cells: Seventeen Cases with Characterization of RET Oncogenic Activation.
Published in:
Thyroid, 2004, v. 14, n. 10, p. 842
By:
- M. C. Vantyghem;
- P. Pigny;
- E. Leteurtre;
- L. Leclerc;
- C. Bauters;
- C. Douillard;
- M. D'Herbomez;
- B. Carnaille;
- C. Proye;
- J. L. Wemeau;
- M. Lecomte-Houcke
Publication type:
Article
Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?
Published in:
Clinical Endocrinology, 2008, v. 69, n. 3, p. 506, doi. 10.1111/j.1365-2265.2008.03230.x
By:
- Cardot-Bauters, C.;
- Leteurtre, E.;
- Leclerc, L.;
- Vantyghem, M.-C.;
- Do cao, C.;
- Wemeau, J.-L.;
- d'Herbomez, M.;
- Carnaille, B.;
- Barbu, V.;
- Pinson, S.;
- Pigny, P.
Publication type:
Article
Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism.
Published in:
Clinical Endocrinology, 2007, v. 67, n. 2, p. 247, doi. 10.1111/j.1365-2265.2007.02870.x
By:
- Vantyghem, M. C.;
- Faivre-Defrance, F.;
- Marcelli-Tourvieille, S.;
- Fermon, C.;
- Evrard, A.;
- Bourdelle-Hego, M. F.;
- Vigouroux, C.;
- Defebvre, L.;
- Delemer, B.;
- Wemeau, J. L.
Publication type:
Article

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