Accuracy, satisfaction and usability of a flash glucose monitoring system among children and adolescents with type 1 diabetes attending a summer camp von Hansen, Erik A., Klee, Philippe, Dirlewanger, Mirjam, Bouthors, Thérèse, Elowe‐Gruau, Eglantine, Stoppa‐Vaucher, Sophie, Phan‐Hug, Franziska, Antoniou, Maria‐Christina, Pasquier, Jérôme, Dwyer, Andrew A., Pitteloud, Nelly, Hauschild, Michael

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Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures von Cassatella, Daniele, Howard, Sasha R, Acierno, James S, Xu, Cheng, Papadakis, Georgios E, Santoni, Federico A, Dwyer, Andrew A, Santini, Sara, Sykiotis, Gerasimos P, Chambion, Caroline, Meylan, Jenny, Marino, Laura, Favre, Lucie, Li, Jiankang, Liu, Xuanzhu, Zhang, Jianguo, Bouloux, Pierre-Marc, Geyter, Christian De, Paepe, Anne De, Dhillo, Waljit S, Ferrara, Jean-Marc, Hauschild, Michael, Lang-Muritano, Mariarosaria, Lemke, Johannes R, Flück, Christa, Nemeth, Attila, Phan-Hug, Franziska, Pignatelli, Duarte, Popovic, Vera, Pekic, Sandra, Quinton, Richard, Szinnai, Gabor, l’Allemand, Dagmar, Konrad, Daniel, Sharif, Saba, Iyidir, Özlem Turhan, Stevenson, Brian J, Yang, Huanming, Dunkel, Leo, Pitteloud, Nelly

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Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosis von Tommiska, Johanna, Känsäkoski, Johanna, Skibsbye, Lasse, Vaaralahti, Kirsi, Liu, Xiaonan, Lodge, Emily J., Tang, Chuyi, Yuan, Lei, Fagerholm, Rainer, Kanters, Jørgen K., Lahermo, Päivi, Kaunisto, Mari, Keski-Filppula, Riikka, Vuoristo, Sanna, Pulli, Kristiina, Ebeling, Tapani, Valanne, Leena, Sankila, Eeva-Marja, Kivirikko, Sirpa, Lääperi, Mitja, Casoni, Filippo, Giacobini, Paolo, Phan-Hug, Franziska, Buki, Tal, Tena-Sempere, Manuel, Pitteloud, Nelly, Veijola, Riitta, Lipsanen-Nyman, Marita, Kaunisto, Kari, Mollard, Patrice, Andoniadou, Cynthia L., Hirsch, Joel A., Varjosalo, Markku, Jespersen, Thomas, Raivio, Taneli

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Testosterone-induced increase in libido in a patient with a loss-of-function mutation in the AR gene von Marino, Laura, Messina, Andrea, S Acierno, James, Phan-Hug, Franziska, J Niederländer, Nicolas, Santoni, Federico, La Rosa, Stefano, Pitteloud, Nelly

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Impact of videogame playing on glucose metabolism in children with type 1 diabetes von Phan-Hug, Franziska, Thurneysen, Esther, Theintz, Gerald, Ruffieux, Christiane, Grouzmann, Eric

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Diabetes and immune thrombocytopenic purpura: a new association with good response to anti-CD20 therapy von von Laer Tschudin, Letizia, Schwitzgebel, Valérie M., von Scheven-Gête, Annette, Blouin, Jean-Louis, Hofer, Michael, Hauschild, Michael, Ansari, Marc, Stoppa-Vaucher, Sophie, Phan-Hug, Franziska

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A novel CHD7 mutation in an adolescent presenting with growth and pubertal delay von Antoniou, Maria-Christina, Bouthors, Thérèse, Xu, Cheng, Phan-Hug, Franziska, Elowe-Gruau, Eglantine, Stoppa-Vaucher, Sophie, Sloot, Almer van der, Acierno, James, Cassatella, Daniele, Richard, Celine, Dwyer, Andrew, Pitteloud, Nelly, Hauschild, Michael

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Genetic testing facilitates prepubertal diagnosis of congenital hypogonadotropic hypogonadism von Xu, C., Lang‐Muritano, M., Phan‐Hug, F., Dwyer, A.A., Sykiotis, G.P., Cassatella, D., Acierno, J., Mohammadi, M., Pitteloud, N.

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TRANSITION IN ENDOCRINOLOGY: Hypogonadism in adolescence von Dwyer, Andrew A, Phan-Hug, Franziska, Hauschild, Michael, Elowe-Gruau, Eglantine, Pitteloud, Nelly

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DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development von Bouilly, Justine, Messina, Andrea, Papadakis, Georgios, Cassatella, Daniele, Xu, Cheng, Acierno, James S, Tata, Brooke, Sykiotis, Gerasimos, Santini, Sara, Sidis, Yisrael, Elowe-Gruau, Eglantine, Phan-Hug, Franziska, Hauschild, Michael, Bouloux, Pierre-Marc, Quinton, Richard, Lang-Muritano, Mariarosaria, Favre, Lucie, Marino, Laura, Giacobini, Paolo, Dwyer, Andrew A, Niederländer, Nicolas J, Pitteloud, Nelly

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Améliorer les pratiques de soins pour les personnes présentant une variation du développement du sexe en Suisse. L’École de Lausanne (depuis 2005) von Cynthia Kraus, Franziska Phan-Hug, François Ansermet, Blaise Julien Meyrat

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Congenital hypogonadotropic hypogonadism with split hand/foot malformation: a clinical entity with a high frequency of FGFR1 mutations von Villanueva, Carine, Jacobson-Dickman, Elka, Xu, Cheng, Manouvrier, Sylvie, Dwyer, Andrew A., Sykiotis, Gerasimos P., Beenken, Andrew, Liu, Yang, Tommiska, Johanna, Hu, Youli, Tiosano, Dov, Gerard, Marion, Leger, Juliane, Drouin-Garraud, Valérie, Lefebvre, Hervé, Polak, Michel, Carel, Jean-Claude, Phan-Hug, Franziska, Hauschild, Michael, Plummer, Lacey, Rey, Jean-Pierre, Raivio, Taneli, Bouloux, Pierre, Sidis, Yisrael, Mohammadi, Moosa, de Roux, Nicolas, Pitteloud, Nelly

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Developing and evaluating rare disease educational materials co-created by expert clinicians and patients: the paradigm of congenital hypogonadotropic hypogonadism von Badiu, Corin, Bonomi, Marco, Borshchevsky, Ivan, Cools, Martine, Craen, Margarita, Ghervan, Cristina, Hauschild, Michael, Hershkovitz, Eli, Hrabovszky, Erik, Juul, Anders, Kim, Soo-Hyun, Kumanov, Phillip, Lecumberri, Beatriz, Lemos, Manuel C, Neocleous, Vassos, Niedziela, Marek, Djurdjevic, Sandra Pekic, Persani, Luca, Phan-Hug, Franziska, Pignatelli, Duarte, Pitteloud, Nelly, Popovic, Vera, Quinton, Richard, Skordis, Nicos, Smith, Neil, Stefanija, Magdalena Avbelj, Xu, Cheng, Young, Jacques, Dwyer, Andrew A

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DCC/NTN1 complex mutations in patients with congenital hypogonadotropic hypogonadism impair GnRH neuron development von Bouilly, Justine, Messina, Andrea, Papadakis, Georgios, Cassatella, Daniele, Xu, Cheng, Acierno, James S, Tata, Brooke, Sykiotis, Gerasimos, Santini, Sara, Sidis, Yisrael, Elowe-Gruau, Eglantine, Phan-Hug, Franziska, Hauschild, Michael, Bouloux, Pierre-Marc, Quinton, Richard, Lang-Muritano, Mariarosaria, Favre, Lucie, Marino, Laura, Giacobini, Paolo, Dwyer, Andrew A, Niederländer, Nicolas J, Pitteloud, Nelly

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Congenital hypogonadotropic hypogonadism and constitutional delay of growth and puberty have distinct genetic architectures von Cassatella, Daniele, Howard, Sasha R, Acierno, James S, Xu, Cheng, Papadakis, Georgios E, Santoni, Federico A, Dwyer, Andrew A, Santini, Sara, Sykiotis, Gerasimos P, Chambion, Caroline, Meylan, Jenny, Marino, Laura, Favre, Lucie, Li, Jiankang, Liu, Xuanzhu, Zhang, Jianguo, Bouloux, Pierre-Marc, De Geyter, Christian, De Paepe, Anne, Dhillo, Waljit S, Ferrara, Jean-Marc, Hauschild, Michael, Lang-Muritano, Mariarosaria, Lemke, Johannes R, Flück, Christa, Nemeth, Attila, Phan-Hug, Franziska, Pignatelli, Duarte, Popovic, Vera, Pekic, Sandra, Konrad, Daniel

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Temporal Trends in Acute Adrenal Insufficiency Events in Children With Congenital Adrenal Hyperplasia During 2019-2022 von Tseretopoulou, Xanthippi, Ali, Salma R, Bryce, Jillian, Amin, Nadia, Atapattu, Navoda, Bachega, Tania A S S, Baronio, Federico, Ortolano, Rita, Birkebaek, Niels H, Bonfig, Walter, Cools, Martine, Davies, Justin H, Thomas, Tessy, de Vries, Liat, Elsedfy, Heba, Amr, Nermine H, Flueck, Christa E, Globa, Evgenia, Guran, Tulay, Yavas-Abali, Zehra, Guven, Ayla, Hannema, Sabine E, Iotova, Violeta, Konrad, Daniel, Lenherr-Taube, Nina, Krone, Nils P, Leka-Emiri, Sofia, Vlachopapadopoulou, Elpis, Lichiardopol, Corina, Marginean, Otilia, Markosyan, Renata, Neumann, Uta, Niedziela, Marek, Banaszak-Ziemska, Magdalena, Phan-Hug, Franziska, Poyrazoglu, Sukran, Probst-Scheidegger, Ursina, Randell, Tabitha, Russo, Gianni, Salerno, Mariacarolina, Seneviratne, Sumudu, Shnorhavorian, Margarett, Thankamony, Ajay, Tadokoro-Curraro, Rieko, van den Akker, Erica, van Eck, Judith, Vieites, Ana, Wasniewska, Malgorzata, Ahmed, S Faisal

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Natural History of Growth Hormone Deficiency in a Pediatric Cohort von Deillon, Eva, Hauschild, Michael, Faouzi, Mohamed, Stoppa-Vaucher, Sophie, Elowe-Gruau, Eglantine, Dwyer, Andrew, Theintz, Gerald E., Dubuis, Jean-Michel, Mullis, Primus E., Pitteloud, Nelly, Phan-Hug, Franziska

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Améliorer les pratiques de soins pour les personnes présentant une variation du développement du sexe en Suisse. L’École de Lausanne (depuis 2005) von Kraus, Cynthia, Phan-Hug, Franziska, Ansermet, François, Meyrat, Blaise Julien

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SOX11 variants cause a neurodevelopmental disorder with infrequent ocular malformations and hypogonadotropic hypogonadism and with distinct DNA methylation profile von Al-Jawahiri, Reem, Foroutan, Aidin, Kerkhof, Jennifer, McConkey, Haley, Levy, Michael, Haghshenas, Sadegheh, Rooney, Kathleen, Turner, Jasmin, Shears, Debbie, Holder, Muriel, Lefroy, Henrietta, Castle, Bruce, Reis, Linda M, Semina, V. Elena, Lachlan, Katherine, Chandler, Kate, Wright, Thomas, Clayton-Smith, Jill, Hug, Franziska Phan, Pitteloud, Nelly, Bartoloni, Lucia, Hoffjan, Sabine, Park, Soo-Mi, Thankamony, Ajay, Lees, Melissa, Wakeling, Emma, Naik, Swati, Hanker, Britta, Girisha, Katta M, Agolini, Emanuele, Giuseppe, Zampino, Alban, Ziegler, Tessarech, Marine, Keren, Ziegler Boris, Afenjar, Alexandra, Zweier, Christiane, Reis, Andre, Smol, Thomas, Tsurusaki, Yoshinori, Nobuhiko, Okamoto, Sekiguchi, Futoshi, Tsuchida, Naomi, Matsumoto, Naomichi, Kou, Ikuyo, Yonezawa, Yoshiro, Ikegawa, Shiro, Callewaert, Bert, Freeth, Megan, Kleinendorst, Lotte, Donaldson, Alan, Alders, Marielle, De Paepe, Anne, Sadikovic, Bekim, McNeill, Alisdair

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The aldosterone/renin ratio as a diagnostic tool for the diagnosis of primary hypoaldosteronism in newborns and infants von Ruecker, Beate, Lang-Muritano, Mariarosaria, Spanaus, Katharina, Welzel, Maik, l'Allemand, Dagmar, Phan-Hug, Franziska, Katschnig, Claudia, Konrad, Daniel, Holterhus, Paul-Martin, Schoenle, Eugen J

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