1. A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X‐Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo‐Epiphyseal Dysplasia. Issue 12 (14th September 2015) Authors: Zanni, Ginevra; Kalscheuer, Vera M.; Friedrich, Andreas; Barresi, Sabina; Alfieri, Paolo; Di Capua, Matteo; Haas, Stefan A.; Piccini, Giorgia; Karl, Thomas; Klauck, Sabine M.; Bellacchio, Emanuele; Emma, Francesco; Cappa, Marco; Bertini, Enrico; Breitenbach‐Koller, Lore Journal: Human mutation Issue: Volume 36:Issue 12(2015:Dec.) Page Start: 1155 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Aetiology, course and treatment of acute tubulointerstitial nephritis in paediatric patients: a cross-sectional web-based survey. Issue 5 (28th May 2021) Authors: Wente-Schulz, Sarah; Aksenova, Marina; Awan, Atif; Ambarsari, Cahyani Gita; Becherucci, Francesca; Emma, Francesco; Fila, Marc; Francisco, Telma; Gokce, Ibrahim; Gülhan, Bora; Hansen, Matthias; Jahnukainen, Timo; Kallash, Mahmoud; Kamperis, Konstantinos; Mason, Sherene; Mastrangelo, Antonio; Menc... Other Names: author non-byline.; Boyer Olivia author non-byline.; Buder Kathrin author non-byline.; Bulut İpek Kaplan author non-byline.; Cornelissen Elisabeth AM author non-byline.; Hernández Maria del Mar Espino author non-byline.; Hooman Nakysa author non-byline.; Kemper Markus author non-byline.; Maquet ... Journal: BMJ open Issue: Volume 11:Issue 5(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Anterior Ischemic Optical Neuropathy in Children on Chronic Peritoneal Dialysis: Report of 7 Cases. Issue 2 (March 2015) Authors: Di Zazzo, Giacomo; Guzzo, Isabella; De Galasso, Lara; Fortunato, Michele; Leozappa, Giovanna; Peruzzi, Licia; Vidal, Enrico; Corrado, Ciro; Verrina, Enrico; Picca, Stefano; Emma, Francesco Journal: Peritoneal dialysis international Issue: Volume 35:Issue 2(2015) Page Start: 135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome. (March 2016) Authors: Iatropoulos, Paraskevas; Noris, Marina; Mele, Caterina; Piras, Rossella; Valoti, Elisabetta; Bresin, Elena; Curreri, Manuela; Mondo, Elena; Zito, Anna; Gamba, Sara; Bettoni, Serena; Murer, Luisa; Fremeaux-Bacchi, Veronique; Vivarelli, Marina; Emma, Francesco; Daina, Erica; Remuzzi, Giuseppe Journal: Molecular immunology Issue: Volume 71(2016:Mar.) Page Start: 131 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Complement gene variants determine the risk of immunoglobulin-associated MPGN and C3 glomerulopathy and predict long-term renal outcome. (March 2016) Authors: Iatropoulos, Paraskevas; Noris, Marina; Mele, Caterina; Piras, Rossella; Valoti, Elisabetta; Bresin, Elena; Curreri, Manuela; Mondo, Elena; Zito, Anna; Gamba, Sara; Bettoni, Serena; Murer, Luisa; Fremeaux-Bacchi, Veronique; Vivarelli, Marina; Emma, Francesco; Daina, Erica; Remuzzi, Giuseppe Journal: Molecular immunology Issue: Volume 71(2016:Mar.) Page Start: 131 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Distal renal tubular acidosis: ERKNet/ESPN clinical practice points. Issue 9 (29th April 2021) Authors: Trepiccione, Francesco; Walsh, Steven B; Ariceta, Gema; Boyer, Olivia; Emma, Francesco; Camilla, Roberta; Ferraro, Pietro Manuel; Haffner, Dieter; Konrad, Martin; Levtchenko, Elena; Lopez-Garcia, Sergio Camilo; Santos, Fernando; Stabouli, Stella; Szczepanska, Maria; Tasic, Velibor; Topaloglu, Rez... Journal: Nephrology dialysis transplantation Issue: Volume 36:Issue 9(2021) Page Start: 1585 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. FC 131OFATUMUMAB OR RITUXIMAB FOR CHILDREN WITH STEROID-DEPENDENT NEPHROTIC SYNDROME. A RANDOMIZED CONTROLLED TRIAL. (29th May 2021) Authors: Ravani, Pietro; Colucci, Manuela; Bruschi, Maurizio; Vivarelli, Marina; Cioni, Michela; Di Donato, Armando; Cravedi, Paolo; Lugani, Francesca; Emma, Francesco; Angeletti, Andrea; Ghiggeri, Gian Marco Journal: Nephrology dialysis transplantation Issue: Volume 36(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. GP56 Severe hypercalcemic crisis in an infant with idiopathic infantile hypercalcemia caused by mutation in CYP24A1 gene. (June 2019) Authors: Rácz, Orsolya-Adrienn; Emma, Francesco; Konrad, Martin; Fufezan, Otilia; Bulată, Bogdan; Bungardi, Adriana; Căinap, Simona Journal: Archives of disease in childhood Issue: Volume 104:(2019)Supplement 3 Page Start: A52 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. How I Treat Steroid-Sensitive Nephrotic Syndrome in Children. Issue 11 (November 2022) Authors: Vivarelli, Marina; Emma, Francesco Journal: Clinical journal of the American Society of Nephrology Issue: Volume 17:Issue 11(2022) Page Start: 1685 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Impaired urinary concentration ability is a sensitive predictor of renal disease progression in Joubert syndrome. Issue 7 (6th November 2018) Authors: Nuovo, Sara; Fuiano, Laura; Micalizzi, Alessia; Battini, Roberta; Bertini, Enrico; Borgatti, Renato; Caridi, Gianluca; D'Arrigo, Stefano; Fazzi, Elisa; Fischetto, Rita; Ghiggeri, Gian Marco; Giordano, Lucio; Leuzzi, Vincenzo; Romaniello, Romina; Signorini, Sabrina; Stringini, Gilda; Zanni, Ginevr... Journal: Nephrology dialysis transplantation Issue: Volume 35:Issue 7(2020) Page Start: 1195 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗