Zobrazeno 1 - 10
of 295
pro vyhledávání: '"Webb, S. M."'
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Webb, S. M, Valassi, Elena
Investigadores de l'Hospital de Sant Pau i el Germans Trias i Pujol han estudiat com la síndrome de Cushing afecta la qualitat de vida dels pacients. Tot i que el tractament funcioni, l'exposició continuada a quantitats elevades de cortisol suposa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1404::2d196c7c37504c9bfd8e2b6bc3850398
https://ddd.uab.cat/record/272581
https://ddd.uab.cat/record/272581
Autor:
Webb, S. M, Kristensen, Jette, Nordenström, Anna, Vitali, Diana, Amodru, Vincent, Wiehe, Lenja Katharina, Bolz-Johnson, Matt, Universitat Autònoma de Barcelona
Publikováno v:
Endocrine Connections
Endocrine Connections, 2022, 11 (12), ⟨10.1530/EC-22-0385⟩
Endocrine Connections, 2022, 11 (12), ⟨10.1530/EC-22-0385⟩
International audience; Patient journeys are instruments developed by EURORDIS, The Voice of Rare Disease Patients in Europe, to collect patients’ experiences; they may identify gaps and areas deserving improvement, as well as elements positively c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81b88b9693f85f3f052803bfc8317baf
https://hal-amu.archives-ouvertes.fr/hal-04039157/file/2049-3614-EC-22-0385.pdf
https://hal-amu.archives-ouvertes.fr/hal-04039157/file/2049-3614-EC-22-0385.pdf
Autor:
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., Webb, S. M., Dattani, M., Husebye, E., Zilaitiene, B., Gaztambide, S., Gatto, F., Ferone, D., Persani, L., Chiodini, I., Höybye, C., Meijer, O. C., Reincke, M., Vila, G., Perry, C., Heck, A., Stancampiano, M. R., van de Ven, A., Johannsson, G., Ragnarsson, O., Tóth, M.
Publikováno v:
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.
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.
Background Cushing’s syndrome (CS) is associated with an hypercoagulable state and an increased risk of venous thromboembolism (VTE). Evidence-based guidelines on thromboprophylaxis strategies in patients with CS are currently lacking. We aimed to
Publikováno v:
Science, 2014 Nov 01. 346(6210), 739-741.
Externí odkaz:
https://www.jstor.org/stable/24917792
Publikováno v:
Quality of Life Research, 2013 Dec 01. 22(10), 2941-2950.
Externí odkaz:
https://www.jstor.org/stable/24725635
Autor:
Wogelius, R. A., Manning, P. L., Barden, H. E., Edwards, N. P., Webb, S. M., Sellers, W. I., Taylor, K. G., Larson, P. L., Dodson, P., You, H., Da-qing, L., Bergmann, U.
Publikováno v:
Science, 2011 Sep . 333(6049), 1622-1626.
Externí odkaz:
http://dx.doi.org/10.1126/science.1205748
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.