Added value of buccal cell FISH analysis in the diagnosis and management of Turner syndrome von Graff, A., Donadille, B., Morel, H., Villy, M. C., Bourcigaux, N., Vatier, C., Borgel, A., Khodawardi, A., Siffroi, J. P., Christin-Maitre, S.

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MEN1 Disease Occurring Before 21 Years Old: A 160-Patient Cohort Study From the Groupe d'étude des Tumeurs Endocrines von Goudet, P, Dalac, A, Le Bras, M, Cardot-Bauters, C, Niccoli, P, Lévy-Bohbot, N, du Boullay, H, Bertagna, X, Ruszniewski, P, Borson-Chazot, F, Vergès, B, Sadoul, J. L, Ménégaux, F, Tabarin, A, Kühn, J. M, d'Anella, P, Chabre, O, Christin-Maitre, S, Cadiot, G, Binquet, C, Delemer, B

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Computed tomography findings of pulmonary venoocclusive disease in scleroderma patients presenting with precapillary pulmonary hypertension von Günther, S., Jaïs, X., Maitre, S., Bérezné, A., Dorfmüller, P., Seferian, A., Savale, L., Mercier, O., Fadel, E., Sitbon, O., Mouthon, L., Simonneau, G., Humbert, M., Montani, D.

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A comparative randomized multicentric study comparing the step‐up versus step‐down protocol in polycystic ovary syndrome von Christin‐Maitre, S., Hugues, J.N.

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Impact on testicular function of a single ablative activity of 3.7 GBq radioactive iodine for differentiated thyroid carcinoma von Bourcigaux, N, Rubino, C, Berthaud, I, Toubert, M E, Donadille, B, Leenhardt, L, Petrot-Keller, I, Brailly-Tabard, S, Fromigué, J, de Vathaire, F, Simon, T, Siffroi, J P, Schlumberger, M, Bouchard, P, Christin-Maitre, S

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X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood von Fiot, Elodie, Zénaty, Delphine, Boizeau, Priscilla, Haignere, Jérémie, Dos Santos, Sophie, Léger, Juliane

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Significant prevalence of NR3C1 mutations in incidentally discovered bilateral adrenal hyperplasia: results of the French MUTA-GR Study von Vitellius, Géraldine, Trabado, Séverine, Hoeffel, Christine, Bouligand, Jérôme, Bennet, Antoine, Castinetti, Frederic, Decoudier, Bénédicte, Guiochon-Mantel, Anne, Lombes, Marc, Delemer, Brigitte

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Dunnigan lipodystrophy syndrome: French National Diagnosis and Care Protocol (PNDS; Protocole National de Diagnostic et de Soins) von Mosbah, H, Donadille, B, Vatier, C, Janmaat, S, Atlan, M, Badens, C, Barat, P, Béliard, S, Beltrand, J, Ben Yaou, R, Bismuth, E, Boccara, F, Cariou, B, Chaouat, M, Charriot, G, Christin-Maitre, S, De Kerdanet, M, Delemer, B, Disse, E, Dubois, N, Eymard, B, Fève, B, Lascols, O, Mathurin, P, Nobécourt, E, Poujol-Robert, A, Prevost, G, Richard, P, Sellam, J, Tauveron, I, Treboz, D, Vergès, B, Vermot-Desroches, V, Wahbi, K, Jéru, I, Vantyghem, M C, Vigouroux, C

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Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency von Hyon, C, Mansour-Hendili, L, Chantot-Bastaraud, S, Donadille, B, Kerlan, V, Dodé, C, Jonard, S, Delemer, B, Gompel, A, Reznik, Y, Touraine, P, Siffroi, J. P, Christin-Maitre, S

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Comparison of a 24-day and a 21-day pill regimen for the novel combined oral contraceptive, nomegestrol acetate and 17β-estradiol (NOMAC/E2): a double-blind, randomized study von Christin-Maitre, S., Serfaty, D., Chabbert-Buffet, N., Ochsenbein, E., Chassard, D., Thomas, J.-L.

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Unraveling the intrafamilial correlations and heritability of tumor types in MEN1: a Groupe d'étude des Tumeurs Endocrines study von Thevenon, J, Bourredjem, A, Faivre, L, Cardot-Bauters, C, Calender, A, Le Bras, M, Giraud, S, Niccoli, P, Odou, M F, Borson-Chazot, F, Barlier, A, Lombard-Bohas, C, Clauser, E, Tabarin, A, Pasmant, E, Chabre, O, Castermans, E, Ruszniewski, P, Bertherat, J, Delemer, B, Christin-Maitre, S, Beckers, A, Guilhem, I, Rohmer, V, Goichot, B, Caron, P, Baudin, E, Chanson, P, Groussin, L, Du Boullay, H, Weryha, G, Lecomte, P, Schillo, F, Bihan, H, Archambeaud, F, Kerlan, V, Bourcigaux, N, Kuhn, J M, Vergès, B, Rodier, M, Renard, M, Sadoul, J L, Binquet, C, Goudet, P

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A New Clinical Condition Linked to a Novel Mutation in Lamins A and C with Generalized Lipoatrophy, Insulin-Resistant Diabetes, Disseminated Leukomelanodermic Papules, Liver Steato... von Caux, F., Dubosclard, E., Lascols, O., Buendia, B., Chazouillères, O., Cohen, A., Courvalin, J.-C., Laroche, L., Capeau, J., Vigouroux, C., Christin-Maitre, S.

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An arterio-venous malformation related to a uterine scar defect, an unusual association von Lebreton, C., Deffieux, X., Vieillefosse, S., Maitre, S., Vivanti, A.J.

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Birth after TESE–ICSI in a man with hypogonadotropic hypogonadism and congenital adrenal hypoplasia linked to a DAX-1 (NR0B1) mutation von Frapsauce, C., Ravel, C., Legendre, M., Sibony, M., Mandelbaum, J., Donadille, B., Achermann, J.C., Siffroi, J.-P., Christin-Maitre, S.

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Automatic referral of patients after thoracic surgery to the pain team von Soni, S., Maitre, S., Thomas, S., Koertzen, M.

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Volvulus of the sigmoid colon is associated with hypotrophy of the left lateral segment of the liver and the absence of sigmoid diverticulum von Barral, M., Lassalle, L., Dautry, R., Eveno, C., De Laveaucoupet, J., Maitre, S., Dohan, A., Pocard, M., Soyer, P.

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Ovarian hyperthecosis on grayscale and color Doppler ultrasound von Rousset, P., Gompel, A., Christin‐Maitre, S., Pugeat, M., Hugol, D., Ghossain, M. A., Buy, J.‐N.

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Genome-wide association study and premature ovarian failure von Christin-Maitre, S, Tachdjian, G

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Transient Elastography and Combination of Fibrotest® and Transient Elastography for Diagnosis of Advanced Fibrosis and Cirrhosis in Patients with Alcoholic Liver Disease: A Prospec... von Voican, C.S, Louvet, A, Trabut, J.-B, Njiké-Nakseu, M, Dharancy, S, Sanchez, A, Corouge, M, Lamouri, K, Lebrun, A, Balian, A, Prévot, S, Lachgar, M, Maitre, S, Agostini, H, Mathurin, P, Perlemuter, G, Naveau, S

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A new LH receptor splice mutation responsible for male hypogonadism with subnormal sperm production in the propositus, and infertility with regular cycles in an affected sister von Bruysters, M., Christin-Maitre, S., Verhoef-Post, M., Sultan, C., Auger, J., Faugeron, I., Larue, L., Lumbroso, S., Themmen, A.P.N., Bouchard, P.

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