Nocturnal Glucose Control with an Artificial Pancreas at a Diabetes Camp von Phillip, Moshe, Battelino, Tadej, Atlas, Eran, Kordonouri, Olga, Bratina, Natasa, Miller, Shahar, Biester, Torben, Avbelj Stefanija, Magdalena, Muller, Ido, Nimri, Revital, Danne, Thomas

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Multifocal gastric adenocarcinoma in a patient with LRBA deficiency von Bratanič, Nina, Kovač, Jernej, Pohar, Katka, Trebušak Podkrajšek, Katarina, Ihan, Alojz, Battelino, Tadej, Avbelj Stefanija, Magdalena

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Case Report: Multiple prolactinomas in a young man with Kallmann syndrome and familial hypocalciuric hypercalcemia von Jensterle, Mojca, Janež, Andrej, Vipotnik Vesnaver, Tina, Debeljak, Maruša, Breznik, Nika, Trebušak Podkrajšek, Katarina, Herman, Rok, Fliers, Eric, Battelino, Tadej, Avbelj Stefanija, Magdalena

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Genetic and clinical characteristics including occurrence of testicular adrenal rest tumors in Slovak and Slovenian patients with congenital adrenal hyperplasia due to 21-hydroxyla... von Saho, Robert, Dolzan, Vita, Zerjav Tansek, Mojca, Pastorakova, Andrea, Petrovic, Robert, Knapkova, Maria, Trebusak Podkrajsek, Katarina, Suput Omladic, Jasna, Bertok, Sara, Avbelj Stefanija, Magdalena, Kotnik, Primoz, Battelino, Tadej, Pribilincova, Zuzana, Groselj, Urh

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GNRHR-related central hypogonadism with spontaneous recovery – case report von Šmigoc Schweiger, Darja, Davidović Povše, Maja, Trebušak Podkrajšek, Katarina, Battelino, Tadej, Avbelj Stefanija, Magdalena

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Genetic Overlap in Kallmann Syndrome, Combined Pituitary Hormone Deficiency, and Septo-Optic Dysplasia von Raivio, Taneli, Avbelj, Magdalena, McCabe, Mark J, Romero, Christopher J, Dwyer, Andrew A, Tommiska, Johanna, Sykiotis, Gerasimos P, Gregory, Louise C, Diaczok, Daniel, Tziaferi, Vaitsa, Elting, Mariet W, Padidela, Raja, Plummer, Lacey, Martin, Cecilia, Feng, Bihua, Zhang, Chengkang, Zhou, Qun-Yong, Chen, Huaibin, Mohammadi, Moosa, Quinton, Richard, Sidis, Yisrael, Radovick, Sally, Dattani, Mehul T, Pitteloud, Nelly

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Acute Hyperglycemia and Spatial Working Memory in Adolescents With Type 1 Diabetes von Šuput Omladič, Jasna, Slana Ozimič, Anka, Vovk, Andrej, Šuput, Dušan, Repovš, Grega, Dovc, Klemen, Bratina, Nataša, Avbelj Stefanija, Magdalena, Battelino, Tadej

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Congenital Idiopathic Hypogonadotropic Hypogonadism: Evidence of Defects in the Hypothalamus, Pituitary, and Testes von Sykiotis, Gerasimos P., Hoang, Xuan-Huong, Avbelj, Magdalena, Hayes, Frances J., Thambundit, Apisadaporn, Dwyer, Andrew, Au, Margaret, Plummer, Lacey, Crowley, William F., Pitteloud, Nelly

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Hypercholesterolemia in Two Siblings with Resistance to Thyroid Hormones Due to Disease-Causing Variant in Thyroid Hormone Receptor ( THRB ) Gene von Pajek, Maja, Avbelj Stefanija, Magdalena, Trebusak Podkrajsek, Katarina, Suput Omladic, Jasna, Zerjav Tansek, Mojca, Battelino, Tadej, Groselj, Urh

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Central TSH Dysregulation in a Patient with Familial Non-Autoimmune Autosomal Dominant Hyperthyroidism Due to a Novel Thyroid-Stimulating Hormone Receptor Disease-Causing Variant von Suput Omladic, Jasna, Pajek, Maja, Groselj, Urh, Trebusak Podkrajsek, Katarina, Avbelj Stefanija, Magdalena, Zerjav Tansek, Mojca, Kotnik, Primoz, Battelino, Tadej, Smigoc Schweiger, Darja

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Anthropometry and bone mineral density in treated and untreated hyperphenylalaninemia von Zerjav Tansek, Mojca, Bertoncel, Ana, Sebez, Brina, Zibert, Janez, Groselj, Urh, Battelino, Tadej, Avbelj Stefanija, Magdalena

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MD‐Logic overnight type 1 diabetes control in home settings: A multicentre, multinational, single blind randomized trial von Nimri, Revital, Bratina, Natasa, Kordonouri, Olga, Avbelj Stefanija, Magdalena, Fath, Maryam, Biester, Torben, Muller, Ido, Atlas, Eran, Miller, Shahar, Fogel, Aviel, Phillip, Moshe, Danne, Thomas, Battelino, Tadej

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Precocious puberty in a girl with 3-methylglutaconic aciduria type 1 (3-MGA-I) due to a novel AUH gene mutation von Bizjak, Neli, Zerjav Tansek, Mojca, Avbelj Stefanija, Magdalena, Repic Lampret, Barbka, Mezek, Ajda, Drole Torkar, Ana, Battelino, Tadej, Groselj, Urh

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Medium-chain acyl-CoA dehydrogenase deficiency: Two novel ACADM mutations identified in a retrospective screening von Smon, Andraz, Groselj, Urh, Debeljak, Marusa, Zerjav Tansek, Mojca, Bertok, Sara, Avbelj Stefanija, Magdalena, Trebusak Podkrajsek, Katarina, Battelino, Tadej, Repic Lampret, Barbka

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PERSISTENT HYPOGLYCAEMIA IN A NEWBORN – CASE REPORT OF A GIRL WITH BECKWITH-WIEDEMANN SYNDROME von Kavčič, Mojca, Lozar Krivec, Jana, Avbelj Stefanija, Magdalena

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Final adult height in children with central precocious puberty - a retrospective study von Knific, Taja, Lazarevič, Melisa, Žibert, Janez, Obolnar, Nika, Aleksovska, Nataša, Šuput Omladič, Jasna, Battelino, Tadej, Avbelj Stefanija, Magdalena

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Two Cases With an Early Presented Proopiomelanocortin Deficiency-A Long-Term Follow-Up and Systematic Literature Review von Gregoric, Nadan, Groselj, Urh, Bratina, Natasa, Debeljak, Marusa, Zerjav Tansek, Mojca, Suput Omladic, Jasna, Kovac, Jernej, Battelino, Tadej, Kotnik, Primoz, Avbelj Stefanija, Magdalena

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An Adolescent Boy with Klinefelter Syndrome and 47,XXY/46,XX Mosaicism: Case Report and Review of Literature von Hovnik, Tinka, Zitnik, Eva, Avbelj Stefanija, Magdalena, Bertok, Sara, Sedej, Katarina, Bancic Silva, Vesna, Battelino, Tadej, Groselj, Urh

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Long-Term Follow-Up of Three Family Members with a Novel NNT Pathogenic Variant Causing Primary Adrenal Insufficiency von Krasovec, Tjasa, Sikonja, Jaka, Zerjav Tansek, Mojca, Debeljak, Marusa, Ilovar, Sasa, Trebusak Podkrajsek, Katarina, Bertok, Sara, Tesovnik, Tine, Kovac, Jernej, Suput Omladic, Jasna, Hartmann, Michaela F, Wudy, Stefan A, Avbelj Stefanija, Magdalena, Battelino, Tadej, Kotnik, Primoz, Groselj, Urh

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A Novel Splice-Site Deletion in the POU1F1 Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees von Hassan, Samar S, Abdullah, Mohamed, Trebusak Podkrajsek, Katarina, Musa, Salwa, Ibrahim, Areej, Babiker, Omer, Kovac, Jernej, Battelino, Tadej, Avbelj Stefanija, Magdalena

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