Search Results - "Wemeau, L."

2013 European Thyroid Association Guidelines for the Diagnosis and Treatment of Thyrotropin-Secreting Pituitary Tumors by Beck-Peccoz, P., Lania, A., Beckers, A., Chatterjee, K., Wemeau, J.-L.

“…Hyperthyroidism is mainly due to autoimmune thyroid disorders or toxic goiter, and very rarely to the presence of thyrotropin (TSH)-secreting pituitary…”
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Beneficial Effects of Propylthiouracil plus l-Thyroxine Treatment in a Patient with a Mutation in MCT8 by Wémeau, J. L., Pigeyre, M., Proust-Lemoine, E., d'Herbomez, M., Gottrand, F., Jansen, J., Visser, T. J., Ladsous, M.

“…Context: Mutations of the monocarboxylate transporter 8 (MCT8) gene determine a distinct X-linked phenotype of severe psychomotor retardation and consistently…”
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Clinical Characterization of Familial Isolated Pituitary Adenomas 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., De Menis, E., Lecomte, P., Penfornis, F., Delemer, B., Bertherat, J., Wémeau, J. L., De Herder, W., Archambeaud, F., Stevenaert, A., Calender, A., Murat, A., Cavagnini, F., Beckers, A.

“…Context: Familial pituitary adenomas occur rarely in the absence of multiple endocrine neoplasia type 1 (MEN1) and Carney complex (CNC). Objective: Our…”
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Iodine 131 in the treatment of large goiters by Béron, A., Wémeau, J.-L.

“…The treatment of large, complicated goiters with iodine 131 constitutes an interesting alternative to surgery. It is minimally invasive, safe, and effective in…”
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Long-term effects of pulmonary rehabilitation on daily life physical activity of patients with stage IV sarcoidosis: A randomized controlled trial by Wallaert, B., Kyheng, M., Labreuche, J., Stelianides, S., Wemeau, L., Grosbois, J.M.

“…Pulmonary rehabilitation (PR) is known to improve exercise tolerance, mood, and quality of life in patients with chronic respiratory diseases. The aim of this…”
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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 by Rohmer, V, Vidal-Trecan, G, Bourdelot, A, Niccoli, P, Murat, A, Wemeau, J. L, Borson-Chazot, F, Schvartz, C, Tabarin, A, Chabre, O, Chabrier, G, Caron, P, Rodien, P, Schlumberger, M, Baudin, E, for the Groupe Français des Tumeurs Endocrines

“…Medullary thyroid carcinoma diameter and N1 are associated with disease free survival, whereas preoperative basal CT > 10 or 30 ng/liter, age > 10, and class D…”
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Octreotide (Long-Acting Release Formulation) Treatment in Patients with Graves’ Orbitopathy: Clinical Results of a Four-Month, Randomized, Placebo-Controlled, Double-Blind Study 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.

“…There are few effective, safe modalities for the management of Graves’ ophthalmopathy (GO), a cell-mediated immune comorbidity of thyroid disease. Somatostatin…”
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Spectrum of Pulmonary Aspergillosis in Hyper-IgE Syndrome with Autosomal-Dominant STAT3 Deficiency by Duréault, Amélie, Tcherakian, Colas, Poiree, Sylvain, Catherinot, Emilie, Danion, François, Jouvion, Grégory, Bougnoux, Marie Elisabeth, Mahlaoui, Nizar, Givel, Claire, Castelle, Martin, Picard, Capucine, Chansdesris, Marie Olivia, Lortholary, Olivier, Lanternier, Fanny, Coignard, H., Amazzough, K., Suarez, F., Blanche, S., Sendid, B., Cornu, M., Bervar, J.F., Deschildre, A., Wemeau, L., Fieschi, C., Alanio, A., Menetrey, C., Senechal, A., Ader, F., Tattevin, P., Pison, C., Grandiere-Perez, L., Garcia-Hermoso, D., Botterel-Chartier, F.

“…Autosomal-dominant signal transducer and activator of transcription 3 (STAT3) deficiency predisposes to recurrent bacterial pneumonia, complicated by…”
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Fertility and Obstetrical Complications in Women with LMNA-Related Familial Partial Lipodystrophy 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.

“…Objective: Familial partial lipodystrophy due to LMNA (lamin A/C) mutations is a rare disorder characterized by a selective loss of adipose tissue and insulin…”
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Advances in diagnostic practices affect thyroid cancer incidence in France by Leenhardt, L, Bernier, MO, Boin-Pineau, MH, Conte Devolx, B, Marechaud, R, Niccoli-Sire, P, Nocaudie, M, Orgiazzi, J, Schlumberger, M, Wemeau, JL, Cherie-Challine, L, De Vathaire, F

“…OBJECTIVE: To analyse trends in diagnostic practices of thyroid diseases and to relate them to the increase in thyroid cancer incidence in France over time…”
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The 1-minute sit-to-stand test to evaluate quadriceps muscle strength in patients with interstitial lung disease by Wallaert, B., Briand, J., Behal, H., Perez, T., Wemeau, L., Chenivesse, C.

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Patients with Familial Partial Lipodystrophy of the Dunnigan Type Due to a LMNA R482W Mutation Show Muscular and Cardiac Abnormalities 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.

“…Diseases due to mutations in the lamin A/C gene (LMNA) are highly heterogeneous, including neuromuscular and cardiac dystrophies, lipodystrophies, and…”
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Six-minute stepper test to assess effort intolerance in interstitial lung diseases by Delourme, J, Stervinou-Wemeau, L, Salleron, J, Grosbois, J M, Wallaert, B

“…The six-minute stepper test (6MST) is a new test for evaluating exercise tolerance. Unlike the six-minute walk test (6MWT) it can be carried out in a limited…”
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Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma? 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.

“…Summary Objective  The RET (rearranged during transfection) proto‐oncogene G691S variant is over‐represented in the germline of patients with sporadic…”
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Quantitative ultrasound of bone and markers of bone turnover in Cushing's syndrome by CORTET, B, CORTET, C, BLANCKAERT, F, D'HERBOMEZ, M, MARCHANDISE, X, WEMEAU, J.-L, DECOULX, M, DEWAILLY, D

“…Quantitative ultrasound (QUS) of bone is a valuable tool in the assessment of postmenopausal osteoporosis. QUS and new markers of bone turnover have been…”
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Treatment of carcinoid syndrome : A prospective crossover evaluation of lanreotide versus octreotide in terms of efficacy, patient acceptability, and tolerance by O'TOOLE, D, DUCREUX, M, BOMMELAER, G, WEMEAU, J.-L, BOUCHE, O, CATUS, F, BLUMBERG, J, RUSZNIEWSKI, P

“…The somatostatin analogues lanreotide and octreotide have previously been shown to be effective in controlling flushing and diarrhea in patients with carcinoid…”
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Hypercalcitonemia revealing a somatostatinoma by Do Cao, C, Mekinian, A, Ladsous, M, Aubert, S, D’Herbomez, M, Pattou, F, Bourdelle-Hego, M.-F, Wémeau, J.-L

“…Résumé Les somatostatinomes sont des tumeurs très rares, développées aux dépens de cellules endocrines duodénales ou pancréatiques. En général bien…”
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Do have patients with "Hashimoto disease" to be operated on? A critical reading of The Norvegian Trial Surgery Study, a prospective randomized investigation published in Annals of Internal Medicine (2019) by Wémeau, J-L

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Good practice guide for cervical ultrasound scan and echo-guided techniques in treating differentiated thyroid cancer of vesicular origin by Leenhardt, L, Borson-Chazot, F, Calzada, M, Carnaille, B, Charrié, A, Cochand-Priollet, B, Cao, C.D, Leboulleux, S, Le Clech, G, Mansour, G, Menegaux, F, Monpeyssen, H, Orgiazzi, J, Rouxel, A, Sadoul, J.L, Schlumberger, M, Tramalloni, J, Tranquart, F, Wemeau, J.L

“…Résumé Des recommandations américaines, européennes et françaises pour la prise en charge des cancers thyroïdiens différenciés de souche vésiculaire ont été…”
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Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronism 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.

“…Summary Objective  To describe new data about the wide phenotypic variability of diseases due to mutations in the lamin A/C gene (LMNA). Design  We report a…”
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