1. Analysis of therapy monitoring in the International Congenital Adrenal Hyperplasia Registry. (11th July 2022) Authors: Lawrence, Neil; Bacila, Irina; Dawson, Jeremy; Bryce, Jillian; Ali, Salma R.; van den Akker, Erica L. T.; Bachega, Tânia A. S. S.; Baronio, Federico; Birkebæk, Niels H.; Bonfig, Walter; van der Grinten, Hedi C.; Costa, Eduardo C.; de Vries, Liat; Elsedfy, Heba; Güven, Ayla; Hannema, Sabine; Iotov... Journal: Clinical endocrinology Issue: Volume 97:Number 5(2022) Page Start: 551 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Gonadectomy in conditions affecting sex development: a registry-based cohort study. Issue 6 (4th May 2021) Authors: Lucas-Herald, Angela K; Bryce, Jillian; Kyriakou, Andreas; Ljubicic, Marie Lindhardt; Arlt, Wiebke; Audi, Laura; Balsamo, Antonio; Baronio, Federico; Bertelloni, Silvano; Bettendorf, Markus; Brooke, Antonia; Claahsen van der Grinten, Hedi L; Davies, Justin H; Hermann, Gloria; de Vries, Liat; Hugh... Journal: European journal of endocrinology Issue: Volume 184:Issue 6(2021) Page Start: 791 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Growth, puberty and testicular function in boys born small for gestational age with a nonspecific disorder of sex development. (20th October 2021) Authors: Tack, Lloyd J. W.; van der Straaten, Saskia; Riedl, Stefan; Springer, Alexander; Holterhus, Paul‐Martin; Hornig, Nadine C.; Kolesinska, Zofia; Niedziela, Marek; Baronio, Federico; Balsamo, Antonio; Hannema, Sabine E.; Nordenström, Anna; Poyrazoglu, Sukran; Darendeliler, Fatma F.; Grinspon, Romina... Journal: Clinical endocrinology Issue: Volume 96:Number 2(2022) Page Start: 165 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Hereditary multiple exostoses and solitary osteochondroma associated with growth hormone deficiency: to treat or not to treat?. Issue 1 (December 2015) Authors: Bozzola, Mauro; Gertosio, Chiara; Gnoli, Maria; Baronio, Federico; Pedrini, Elena; Meazza, Cristina; Sangiorgi, Luca Journal: Italian journal of pediatrics Issue: Volume 41:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Long-term renal outcome in children with OCRL mutations: retrospective analysis of a large international cohort. Issue 1 (5th October 2016) Authors: Zaniew, Marcin; Bökenkamp, Arend; Kołbuc, Marcin; La Scola, Claudio; Baronio, Federico; Niemirska, Anna; Szczepańska, Maria; Bürger, Julia; La Manna, Angela; Miklaszewska, Monika; Rogowska-Kalisz, Anna; Gellermann, Jutta; Zampetoglou, Argyroula; Wasilewska, Anna; Roszak, Magdalena; Moczko, Jerzy;... Journal: Nephrology dialysis transplantation Issue: Volume 33:Issue 1(2018) Page Start: 85 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Medium-Chain Acyl-CoA Deficiency: Outlines from Newborn Screening, In Silico Predictions, and Molecular Studies. (31st October 2013) Authors: Catarzi, Serena; Caciotti, Anna; Thusberg, Janita; Tonin, Rodolfo; Malvagia, Sabrina; la Marca, Giancarlo; Pasquini, Elisabetta; Cavicchi, Catia; Ferri, Lorenzo; Donati, Maria A.; Baronio, Federico; Guerrini, Renzo; Mooney, Sean D.; Morrone, Amelia Other Names: Briassoulis G. Academic Editor.; Gorodischer R. Academic Editor. Journal: TheScientificWorldjournal Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Phenotypic diversity, disease progression, and pathogenicity of MVK missense variants in mevalonic aciduria. Issue 5 (28th June 2021) Authors: Brennenstuhl, Heiko; Nashawi, Mohammed; Schröter, Julian; Baronio, Federico; Beedgen, Lars; Gleich, Florian; Jeltsch, Kathrin; von Landenberg, Christina; Martini, Silvia; Simon, Anna; Thiel, Christian; Tsiakas, Konstantinos; Opladen, Thomas; Kölker, Stefan; Hoffmann, Georg F.; Haas, Dorothea Journal: Journal of inherited metabolic disease Issue: Volume 44:Issue 5(2021) Page Start: 1272 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Prenatal dexamethasone treatment for classic 21-hydroxylase deficiency in Europe. Issue 5 (23rd March 2022) Authors: Nowotny, Hanna; Neumann, Uta; Tardy-Guidollet, Véronique; Ahmed, S Faisal; Baronio, Federico; Battelino, Tadej; Bertherat, Jérôme; Blankenstein, Oliver; Bonomi, Marco; Bouvattier, Claire; Brac de la Perrière, Aude; Brucker, Sara; Cappa, Marco; Chanson, Philippe; Claahsen-van der Grinten, Hedi L; ... Journal: European journal of endocrinology Issue: Volume 186:Issue 5(2022) Page Start: K17 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. The genetic diagnosis of rare endocrine disorders of sex development and maturation: a survey among Endo-ERN centres. Issue 12 (14th November 2022) Authors: 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, Claud... Journal: Endocrine connections Issue: Volume 11:Issue 12(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗