Orphanet Journal of Rare Diseases, 17, 1 Endo-ERN Cushing and Thrombosis study group 2022, ' Current clinical practice for thromboprophylaxis management in patients with Cushing’s syndrome across reference centers of the European Reference Network on Rare Endocrine Conditions (Endo-ERN) ', Orphanet Journal of Rare Diseases, vol. 17, no. 1, 178 . https://doi.org/10.1186/s13023-022-02320-x Endo-ERN Cushing and Thrombosis study group 2022, ' Current clinical practice for thromboprophylaxis management in patients with Cushing’s syndrome across reference centers of the European Reference Network on Rare Endocrine Conditions (Endo-ERN) ', Orphanet Journal of Rare Diseases, vol. 17, 178 . https://doi.org/10.1186/s13023-022-02320-x Orphanet Journal of Rare Diseases, 17 van Haalen, F M, Kaya, M, Pelsma, I C M, Dekkers, O M, Biermasz, N R, Cannegieter, S C, Huisman, M V, van Vlijmen, B J M, Feelders, R, Klok, F A, Pereira, A M, Stochholm, K, Fliers, E, Castinetti, F, Brue, T, Bertherat, J, Scaroni, C, Colao, A, Giordano, R, Druce, M R, Beckers, A, Spranger, J, Driessens, N, Maiter, D, Feldt-Rasmussen, U, Feelders, R, Webb, S M, Dattani, M, Husebye, E, Zilaitiene, B, Gaztambide, S, Gatto, F, Ferone, D, Persani, L, Chiodini, I, Höybye, C, Pereira, A M, Biermasz, N R, Klok, F A, Meijer, O C, Reincke, M, Vila, G, Perry, C, Heck, A, Stancampiano, M R, van de Ven, A, Johannsson, G, Ragnarsson, O, Tóth, M & Endo-ERN Cushing and Thrombosis study group 2022, ' Current clinical practice for thromboprophylaxis management in patients with Cushing’s syndrome across reference centers of the European Reference Network on Rare Endocrine Conditions (Endo-ERN) ', Orphanet Journal of Rare Diseases, vol. 17, no. 1, 178 . https://doi.org/10.1186/s13023-022-02320-x Orphanet Journal of Rare Diseases, 17. BMC Orphanet journal of rare diseases, 17(1):178. BMC Orphanet journal of rare diseases, 17(1):178. BioMed Central Orphanet journal of rare diseases, Vol. 17, no.1, p. 178 [1-12] (2022) Orphanet Journal of Rare Diseases, 17(1):178. BioMed Central Orphanet Journal of Rare Diseases, 17(1):178. BioMed Central Ltd.