Università degli Studi di Napoli Federico II

Screening and management of hypertensive patients with chronic kidney disease referred to Hypertension Excellence Centres among 27 countries. A pilot survey based on questionnaire (2024) Halimi JM, Sarafidis P, Azizi M, Bilo G, Burkard T, Bursztyn M, Camafort M, et al. Journal article Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome (2024) Rots D, Bouman A, Yamada A, Levy M, Dingemans AJ, de Vries BB, Ruiterkamp-Versteeg M, et al. Journal article PragmaticTrial Design to Compare Real-world Effectiveness of DifferentTreatments for Inflammatory Bowel Diseases:The PRACTICE-IBD European Consensus (2024) Fantini MC, Fiorino G, Colli A, Laharie D, Armuzzi A, Caprioli FA, Gisbert JP, et al. Journal article Did You Note My Palette? Unveiling Synthetic Images Through Color Statistics (2024) Uhlenbrock L, Cozzolino D, Moussa D, Verdoliva L, Riess C Conference contribution, Conference Contribution Genetic landscape of pediatric acute liver failure of indeterminate origin. (2024) Lenz D, Schlieben LD, Shimura M, Bianzano A, Smirnov D, Kopajtich R, Berutti R, et al. Journal article, Original article [con Alfredo Troiano] Un manoscritto da Santa Croce: Venezia, Biblioteca Nazionale Marciana, ms. It. Z. 10 (= 4741) (2024) Bürgel SM, Troiano A Book chapter / Article in edited volumes Greening Regional Airports: A Vision for Carbon Neutral Infrastructure (2024) Meindl M, de Ruiter C, Marciello V, Di Stasio M, Saavedra-Rubio K, Laurent A, Ruocco M, März M Book chapter / Article in edited volumes ECCO Guidelines on Therapeutics in Crohn's Disease: Medical Treatment. (2024) Gordon H, Minozzi S, Kopylov U, Verstockt B, Chaparro M, Buskens C, Warusavitarne J, et al. Journal article ARID1B-related disorder in 87 adults: Natural history and self-sustainability (2024) van der Sluijs PJ, Gösgens M, Dingemans AJ, Striano P, Riva A, Mignot C, Faudet A, et al. Journal article Dominantly acting variants in ATP6V1C1 and ATP6V1B2 cause a multisystem phenotypic spectrum by altering lysosomal and/or autophagosome function. (2024) Carpentieri G, Cecchetti S, Bocchinfuso G, Radio FC, Leoni C, Onesimo R, Calligari P, et al. Journal article