Hospital Universitario La Paz

Frequency and characteristics of axial involvement in psoriatic arthritis: results from the International Multicentre AXIS Study (2026) Torgutalp M, Almodovar R, Azevedo VF, Baraliakos X, Bosch FVd, Braun J, Chandran V, et al. Journal article Addressing unmet needs in pregnancy and family planning of people living with rare and low-prevalence diseases: results of the “ERN transversal working group on pregnancy and family planning” survey (2025) Fulvio G, Marinello D, Zucchi D, Aguilera S, Benachi A, Biller R, Blanco I, et al. Journal article Quality indicators for breast reconstruction following cancer - an international Delphi consensus study supported by the European Society of Plastic, Reconstructive and Aesthetic Surgery (2025) Hansson E, Moellhoff N, Ahlstedt Karlsson S, Uusimäki A, Kaartinen I, Rosenkrantz Hölmich L, Zic R, et al. Journal article Pregnancy-related issues in rare and low-prevalence diseases: results of ERN transversal working group on pregnancy and family planning survey (2025) Zucchi D, Marinello D, Tani C, Fulvio G, Aguilera S, Benachi A, Biller R, et al. Journal article In-Depth Characterization of L1CAM+ Extracellular Vesicles as Potential Biomarkers for Anti-CD20 Therapy Response in Relapsing–Remitting Multiple Sclerosis (2025) Anandan S, Maciak K, Breinbauer R, Otero-Ortega L, Feliciello G, Stojanović Gužvić N, Torkildsen O, Myhr KM Journal article DNA methylation episignature and comparative epigenomic profiling for Pitt-Hopkins syndrome caused by TCF4 variants (2024) van der Laan L, Lauffer P, Rooney K, Silva A, Haghshenas S, Relator R, Levy MA, et al. Journal article Spliceosome malfunction causes neurodevelopmental disorders with overlapping features (2024) Li D, Wang Q, Bayat A, Battig MR, Zhou Y, Bosch DG, van Haaften G, et al. Journal article Pediatric kidney transplantation in Europe, a clinical snapshot pilot (2024) Oomen L, Bootsma-Robroeks CM, Bouts AH, Carbonell Pradas M, Gander R, Kienzl-Wagner K, König P, et al. Journal article Deleterious ZNRF3 germline variants cause neurodevelopmental disorders with mirror brain phenotypes via domain-specific effects on Wnt/β-catenin signaling (2024) Boonsawat P, Asadollahi R, Niedrist D, Steindl K, Begemann A, Joset P, Bhoj EJ, et al. Journal article 2023 EULAR recommendations on imaging in diagnosis and management of crystal-induced arthropathies in clinical practice (2024) Mandl P, D'Agostino MA, Navarro-Compán V, Geßl I, Sakellariou G, Abhishek A, Becce F, et al. Journal article