Correction to: Editorial pediatric endocrinology series european journal of pediatrics “New developments and therapies in pediatric endocrinology” von Gevers, Evelien F., de Winter, J Peter

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Dominant-negative STAT5B mutations cause growth hormone insensitivity with short stature and mild immune dysregulation von Klammt, Jürgen, Neumann, David, Gevers, Evelien F., Andrew, Shayne F., Schwartz, I. David, Rockstroh, Denise, Colombo, Roberto, Sanchez, Marco A., Vokurkova, Doris, Kowalczyk, Julia, Metherell, Louise A., Rosenfeld, Ron G., Pfäffle, Roland, Dattani, Mehul T., Dauber, Andrew, Hwa, Vivian

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New developments and therapies in pediatric endocrinology von Gevers, Evelien F, de Winter, J Peter

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Frequency and clinical characteristics of children and young people with type 2 diabetes at diagnosis from five world regions between 2012 and 2021: data from the SWEET Registry von Gesuita, Rosaria, Eckert, Alexander J., Besançon, Stéphane, Crimmins, Nancy A., Cavallo, Fred, Kim, Jaehyun, Jefferies, Craig, Gevers, Evelien F., Vamvakis, Anastasios, Shah, Sejal, Amed, Shazhan, Cherubini, Valentino

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A Mutation in the Thyroid Hormone Receptor Alpha Gene von Bochukova, Elena, Schoenmakers, Nadia, Schoenmakers, Erik, Agostini, Maura, Rajanayagam, Odelia, Keogh, Julia M, Henning, Elana, Reinemund, Jana, Gevers, Evelien, Sarri, Margarita, Downes, Kate, Offiah, Amaka, Albanese, Assunta, Halsall, David, Schwabe, John W.R, Bain, Murray, Lindley, Keith, Muntoni, Francesco, Khadem, Faraneh Vargha, Dattani, Mehul, Farooqi, I. Sadaf, Gurnell, Mark, Chatterjee, Krishna

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Mutation in human selenocysteine transfer RNA selectively disrupts selenoprotein synthesis von Schoenmakers, Erik, Carlson, Bradley, Agostini, Maura, Moran, Carla, Rajanayagam, Odelia, Bochukova, Elena, Tobe, Ryuta, Peat, Rachel, Gevers, Evelien, Muntoni, Francesco, Guicheney, Pascale, Schoenmakers, Nadia, Farooqi, Sadaf, Lyons, Greta, Hatfield, Dolph, Chatterjee, Krishna

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Arid1b haploinsufficient mice reveal neuropsychiatric phenotypes and reversible causes of growth impairment von Celen, Cemre, Chuang, Jen-Chieh, Luo, Xin, Nijem, Nadine, Walker, Angela K, Chen, Fei, Zhang, Shuyuan, Chung, Andrew S, Nguyen, Liem H, Nassour, Ibrahim, Budhipramono, Albert, Sun, Xuxu, Bok, Levinus A, McEntagart, Meriel, Gevers, Evelien F, Birnbaum, Shari G, Eisch, Amelia J, Powell, Craig M, Ge, Woo-Ping, Santen, Gijs We, Chahrour, Maria, Zhu, Hao

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132-OR: Ten-Year Evaluation of Diabetes Categories in Youth Shows a Continuous Increase in Frequency of Newly Diagnosed Type 2 Diabetes—Results from the Worldwide SWEET Registry von CHERUBINI, VALENTINO, ECKERT, ALEXANDER J., AMED, SHAZHAN, BESANÇON, STÉPHANE, CAVALLO AITA, FRED, CRIMMINS, NANCY A., GEVERS, EVELIEN F., JEFFERIES, CRAIG A., KIM, JAEHYUN, SHAH, SEJAL, VAMVAKIS, ANASTASIOS, GESUITA, ROSARIA, BEHALF OF THE SWEET STUDY GROUP, ON

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PTH Infusion for Seizures in Autosomal Dominant Hypocalcemia Type 1 von Sastre, Ana, Valentino, Kevin, Hannan, Fadil M, Lines, Kate E, Gluck, Anna K, Stevenson, Mark, Ryalls, Michael, Gorrigan, Rebecca J, Pullen, Debbie, Buck, Jackie, Sankaranarayanan, Sailesh, Allgrove, Jeremy, Thakker, Rajesh V, Gevers, Evelien F

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Insertional Gene Activation by Lentiviral and Gammaretroviral Vectors von BOKHOVEN, Marieke, STEPHEN, Sam L, KNIGHT, Sean, GEVERS, Evelien F, ROBINSON, Iain C, TAKEUCHI, Yasuhiro, COLLINS, Mary K

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Exploring the Surge in Paediatric Type 2 Diabetes in an Inner-City London Centre-A Decade-Long Analysis of Incidence, Outcomes, and Transition von Abdelhameed, Farah, Giuffrida, Anna, Thorp, Ben, Moorthy, Myuri K, Gevers, Evelien F

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Proportion of Basal to Total Insulin Dose Is Associated with Metabolic Control, Body Mass Index, and Treatment Modality in Children with Type 1 Diabetes—A Cross-Sectional Study wit... von Rasmussen, Vinni Faber, Vestergaard, Esben Thyssen, Schwandt, Anke, Beltrand, Jacques, Rami-Merhar, Birgit, O'Riordan, Stephen M.P., Jarosz-Chobot, Przemyslawa, Castro-Correia, Cintia, Gevers, Evelien F., Birkebæk, Niels H.

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Activating mutations in BRAF disrupt the hypothalamo-pituitary axis leading to hypopituitarism in mice and humans von Gualtieri, Angelica, Kyprianou, Nikolina, Gregory, Louise C., Vignola, Maria Lillina, Nicholson, James G., Tan, Rachael, Inoue, Shin-ichi, Scagliotti, Valeria, Casado, Pedro, Blackburn, James, Abollo-Jimenez, Fernando, Marinelli, Eugenia, Besser, Rachael E. J., Högler, Wolfgang, Karen Temple, I., Davies, Justin H., Gagunashvili, Andrey, Robinson, Iain C.A.F., Camper, Sally A., Davis, Shannon W., Cutillas, Pedro R., Gevers, Evelien F., Aoki, Yoko, Dattani, Mehul T., Gaston-Massuet, Carles

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Diabetic Ketoacidosis Severity at Diagnosis and Glycaemic Control in the First Year of Childhood Onset Type 1 Diabetes-A Longitudinal Cohort Study von Khanolkar, Amal R, Amin, Rakesh, Taylor-Robinson, David, Viner, Russell M, Warner, Justin, Gevers, Evelien F, Stephenson, Terence

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Paediatric pancreatic neuroendocrine tumours in von Hippel–Lindau disease von O’Toole, Samuel M, Sahdev, Anju, Bhattacharya, Satya, Feakins, Roger, Gevers, Evelien F, Drake, William M

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Structural Pituitary Abnormalities Associated With CHARGE Syndrome von Gregory, Louise C, Gevers, Evelien F, Baker, Joanne, Kasia, Tessa, Chong, Kling, Josifova, Dragana J, Caimari, Maria, Bilan, Frederic, McCabe, Mark J, Dattani, Mehul T

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Behavioral changes in patients with Prader-Willi syndrome receiving diazoxide choline extended-release tablets compared to the PATH for PWS natural history study von Strong, Theresa V, Miller, Jennifer L, McCandless, Shawn E, Gevers, Evelien, Yanovski, Jack A, Matesevac, Lisa, Bohonowych, Jessica, Ballal, Shaila, Yen, Kristen, Hirano, Patricia, Cowen, Neil M, Bhatnagar, Anish

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Factors predicting poor glycemic control in the first two years of childhood onset type 1 diabetes in a cohort from East London, UK: Analyses using mixed effects fractional polynom... von Mazarello Paes, Veena, Barrett, Jessica K., Dunger, David B., Gevers, Evelien F., Taylor‐Robinson, David C., Viner, Russell M., Stephenson, Terence J.

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An Infant with Pseudohyperkalemia, Hemolysis, and Seizures: Cation-Leaky GLUT1-Deficiency Syndrome due to a SLC2A1 Mutation von Bawazir, Waleed M, Gevers, Evelien F, Flatt, Joanna F, Ang, Ai Leen, Jacobs, Benjamin, Oren, Caroline, Grunewald, Stephanie, Dattani, Mehul, Bruce, Lesley J, Stewart, Gordon W

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Modeling Congenital Adrenal Hyperplasia and Testing Interventions for Adrenal Insufficiency Using Donor-Specific Reprogrammed Cells von Ruiz-Babot, Gerard, Balyura, Mariya, Hadjidemetriou, Irene, Ajodha, Sharon J., Taylor, David R., Ghataore, Lea, Taylor, Norman F., Schubert, Undine, Ziegler, Christian G., Storr, Helen L., Druce, Maralyn R., Gevers, Evelien F., Drake, William M., Srirangalingam, Umasuthan, Conway, Gerard S., King, Peter J., Metherell, Louise A., Bornstein, Stefan R., Guasti, Leonardo

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