Health-related quality of life and binge eating among adolescent girls with PCOS by Lidaka, Lasma, Lazdane, Gunta, Kivite-Urtane, Anda, Gailite, Linda, Dzivite-Krisane, Iveta, Stokenberga, Ieva

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Children’s rights in healthcare: The influence of age on involvement by Popeiko, Polina, Pukite, Ieva, Davidsone, Zane, Dzivite-Krisane, Iveta, Visnevska, Inta, Gardovska, Dace

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Role of Single Nucleotide Variants in the YAP1 Gene in Adolescents with Polycystic Ovary Syndrome by Lidaka, Lasma, Bekere, Laine, Lazdane, Gunta, Lazovska, Marija, Dzivite-Krisane, Iveta, Gailite, Linda

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Prominent seasonality of 25(OH)D vitamin deficiency in Latvia: Age and gender-related variations and testing regimen by Nikulshin, Sergey, Osite, Jana, Lapina, Stella, Krisane, Anda, Dzivite-Krisane, Iveta, Gardovska, Dace

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Non-Classical Congenital Adrenal Hyperplasia-Causing Alleles in Adolescent Girls with PCOS and in Risk Group for PCOS Development by Lidaka, Lasma, Bekere, Laine, Lazdane, Gunta, Dzivite-Krisane, Iveta, Kivite-Urtane, Anda, Gailite, Linda

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Graves’ disease as a manifestation of immune reconstitution inflammatory syndrome in an HIV-1-infected adolescent patient: A case report by Kornete, Liga, Terauda, Ruta, Sausa, Sintija, Dzivite-Krisane, Iveta, Melderis, Ivars, Sitkare, Valentina, Rozentale, Baiba, Zakis, Davis Rudolfs

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Role of Single Nucleotide Variants in FSHR , GNRHR , ESR2 and LHCGR Genes in Adolescents with Polycystic Ovary Syndrome by Lidaka, Lasma, Bekere, Laine, Rota, Adele, Isakova, Jekaterina, Lazdane, Gunta, Kivite-Urtane, Anda, Dzivite-Krisane, Iveta, Kempa, Inga, Dobele, Zane, Gailite, Linda

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Two Cases of Leigh Syndrome in One Family: Diagnostic Challenges and Clinical Management Experience in Latvia by Katkevica, Arta, Kreile, Madara, Grinfelde, Ieva, Taurina, Gita, Micule, Ieva, Dzivite-Krisane, Iveta, Smite-Laguna, Arta, Malniece, Ieva

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The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres by Persani, Luca, Cools, Martine, Ioakim, Stamatina, Faisal Ahmed, S, Andonova, Silvia, Avbelj-Stefanija, Magdalena, Baronio, Federico, Bouligand, Jerome, Bruggenwirth, Hennie T, Davies, Justin H, De Baere, Elfride, Dzivite-Krisane, Iveta, Fernandez-Alvarez, Paula, Gheldof, Alexander, Giavoli, Claudia, Gravholt, Claus H, Hiort, Olaf, Holterhus, Paul-Martin, Juul, Anders, Krausz, Csilla, Lagerstedt-Robinson, Kristina, McGowan, Ruth, Neumann, Uta, Novelli, Antonio, Peyrassol, Xavier, Phylactou, Leonidas A, Rohayem, Julia, Touraine, Philippe, Westra, Dineke, Vezzoli, Valeria, Rossetti, Raffaella

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Can a mother's polycystic ovary syndrome (PCOS)-related symptoms be used to predict the future clinical profile of PCOS in her adolescent daughter? A pilot study by Lidaka, Lasma, Grasmane, Adele, Lazdane, Gunta, Dzivite-Krisane, Iveta, Gailite, Linda, Viberga, Ilze

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Short-Term Predictors for Weight Correction Success of the First Paediatric Weight Correction Programme in Children's Clinical University Hospital in Riga by Gailite, Jurgita, Apela, Dana, Dzīvīte-Krišāne, Iveta, Gardovska, Dace

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Insulin pump therapy in children with type 1 diabetes: analysis of data from the SWEET registry by Szypowska, Agnieszka, Schwandt, Anke, Svensson, Jannet, Shalitin, Shlomit, Cardona-Hernandez, Roque, Forsander, Gun, Sundberg, Frida, De Beaufort, Carine, Maahs, David, Maffeis, Claudio, O'Riordan, Stephen M.P., Krisane, Iveta Dzivite, Scharf, Mauro, Castro, Sofia, Konstantinova, Maia, Obermannova, Barbora, Casteels, Kristina, Gökşen, Damla, Galhardo, Júlia, Kanaka-Gantenbein, Christina, Rami-Merhar, Birgit, Madacsy, Laszlo

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Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN) by Eggermann, Thomas, Elbracht, Miriam, Kurth, Ingo, Juul, Anders, Johannsen, Trine Holm, Netchine, Irène, Mastorakos, George, Johannsson, Gudmundur, Musholt, Thomas J, Zenker, Martin, Prawitt, Dirk, Pereira, Alberto M, Hiort, Olaf, Riedl, Stefan, Vila, Greisa, Baumgartner-Parzner, Sabina, Heinrichs, Claudine, Maiter, Dominique, Gies, Inge, Cools, Martine, Casteels, Kristina, Beckers, Albert, Zacharieva, Sabina, Iotova, Violeta, Rahelic, Dario, Neocleous, Vassos, Phylactou, Leonidas, Krsek, Michal, Lebl, Jan, Gravholt, Claus, Tillmann, Vallo, Volke, Vallo, Ebeling, Tapani, Brue, Thierry, Bertherat, Jérôme, Bernert, Christine Poitou, Touraine, Philippe, Chanson, Philippe, Polak, Michel, Tauber, Maithe, Spranger, Joachim, Fuhrer, Dagmar, Danne, Thomas, Mohnike, Klaus, Reisch, Nicole, Reincke, Martin, Rohayem, Julia, Fassnacht, Martin, Tóth, Miklós, Cassio, Alessandra, Toni, Sonia, Piccini, Barbara, Ferone, Diego, Russo, Gianni, Persani, Luca, Colao, Annamaria, Salerno, Mariacarolina, Boscaro, Marco, Scaroni, Carla, Santini, Ferruccio, Ceccarini, Giovanni, Ghigo, Ezio, Dzivite - Krisane, Iveta, Rovite, Vita, Janozola, Lauma, Verkauskiene, Rasa, Witsch, Michael, Clark, James, Romijn, Johannes, Links, Thera, Biermasz, Nienke, Hannema, Sabine, Havekes, Bas, der Grinten, Hedi Claahsen-van, Timmers, Henri, Peeters, Robin, Valk, Gerlof, Stuart, A. A. Verrijn, Husebye, Eystein, Bollerslev, Jens, Jarzab, Barbara, Szypowska, Agnieszka, Raposo, João-Filipe, Craiu, Dana, Piciu, Doina, Kostalova, Ludmila, Vojtková, Jarmila, Battelino, Tadej, Cardona-Hernandez, Roque, Yeste, Diego, Gaztambide, Sonia, Nordenström, Anna, Gittoes, Neil, Cole, Trevor, Ahmed, Faisal, Didi, Mohammed, Korbonits, Marta, Dattani, Mehul, Clayton, Peter, Davies, Justin

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A description of clinician reported diagnosis of type 2 diabetes and other non-type 1 diabetes included in a large international multicentered pediatric diabetes registry (SWEET) by Pacaud, Danièle, Schwandt, Anke, de Beaufort, Carine, Casteels, Kristina, Beltrand, Jacques, Birkebaek, Niels H., Campagnoli, Myrna, Bratina, Natasa, Limbert, Catarina, MP O'Riordan, Stephen, Ribeiro, Rogério, Gerasimidi-Vazeou, Andriani, Petruzelkova, Lenka, Verkauskiene, Rasa, Krisane, Iveta Dzivite

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Adult growth hormone deficiency in CEE region: Heterogeneity of the patient pathway by Shimon, Ilan, Badiu, Corin, Bossowski, Artur, Doknic, Mirjana, Dzivite-Krisane, Iveta, Hána, Václav, Kollerova, Jana, Natchev, Emil, Pfeifer, Marija, Szũcs, Nikolette, Hey-Hadavi, Juliana, Gomez, Roy

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The European registry for rare bone and mineral conditions (EuRR-Bone): results of a survey on osteogenesis imperfecta and fibrous dysplasia McCune-Albright syndrome by Zurita, Ana Luisa Priego, Danila, Oana O., Allgrove, Jeremy, Brandi, Maria Luisa, Bryce, Jillian, Chapurlat, Roland, Dzivite-Krisane, Iveta, Grasemann, Corinna, Högler, Wolfgang, Javaid, M. Kassim, McDevitt, Helen, Montero-Lopez, Rodrigo, Mortier, Geert, Oheim, Ralf, Riancho, Jose A., de Sanctis, Luisa, Verrijn Stuart, Annemarie A., Tessaris, Daniele, Ahmed, S. Faisal, Appelman-Dijkstra, Natasha

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Evaluation of Prenatal and Postnatal Risk Factors of Obesity in Obese and Normal Weight Children and Adolescents by Gailīte, Jurgita, Siliņa, Ieva, Petrošina, Eva, Dzīvīte-Krišāne, Iveta, Dace Gardovska

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Two Cases of Leigh Syndrome in One Family: Diagnostic Challenges and Clinical Management Experience in Latvia by Katkevica, Arta, Kreile, Madara, Grinfelde, Ieva, Taurina, Gita, Micule, Ieva, Dzivite-Krisane, Iveta, Smite-Laguna, Arta, Malniece, Ieva

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