Incidence and prevalence of multiple endocrine neoplasia 2A in Denmark 1901–2014: a nationwide study

Autor: Mathiesen JS, Kroustrup JP, Vestergaard P, Stochholm K, Poulsen PL, Rasmussen ÅK, Feldt-Rasmussen U, Schytte S, Pedersen HB, Hahn CH, Bentzen J, Möller S, Gaustadnes M, Rossing M, Nielsen FC, Brixen K, Frederiksen AL, Godballe C

Publikováno v: Clinical Epidemiology, Vol Volume 10, Pp 1479-1487 (2018)

Jes Sloth Mathiesen,1,2 Jens Peter Kroustrup,3 Peter Vestergaard,3,4 Kirstine Stochholm,5,6 Per Løgstrup Poulsen,5 Åse Krogh Rasmussen,7 Ulla Feldt-Rasmussen,7 Sten Schytte,8 Henrik Baymler Pedersen,9 Christoffer Holst Hahn,10 Jens Bentzen,11 Söre

Externí odkaz: https://doaj.org/article/b4054e2db5514b81a0e12ed245a2de1c

Evaluation of ICD-10 algorithms to identify hypopituitary patients in the Danish National Patient Registry

Autor: Berglund A, Olsen M, Andersen M, Nielsen EH, Feldt-Rasmussen U, Kistorp C, Gravholt CH, Stochholm K

Publikováno v: Clinical Epidemiology, Vol Volume 9, Pp 75-82 (2017)

Agnethe Berglund,1 Morten Olsen,2 Marianne Andersen,3 Eigil Husted Nielsen,4 Ulla Feldt-Rasmussen,5 Caroline Kistorp,6 Claus Højbjerg Gravholt,1,7 Kirstine Stochhholm1,8 1Department of Endocrinology and Internal Medicine, 2Department of Clinical Epi

Externí odkaz: https://doaj.org/article/cb2360a707124b6e96ec26281308238e

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)

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.

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

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fa3db872260fe058a14d59181ff089d
http://www.scopus.com/inward/record.url?scp=85129997291&partnerID=8YFLogxK

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A Rare Case of Embryonal Carcinoma in a Patient with Turner Syndrome without Y Chromosomal Material but Mutations in KIT, AKT1, and ZNF358 Demonstrated Using Exome Sequencing

Autor: Gravholt, CH, Dollerup, OL, Duval, L, Mejlgaard, E, Stribolt, K, Vang, S, Laursen, BE, Knudsen, M, Thorsen, K, Hersmus, Remko, Looijenga, LHJ (Leendert), Stochholm, K

Publikováno v: Gravholt, C H, Dollerup, O L, Duval, L, Mejlgaard, E, Stribolt, K, Vang, S, Laursen, B E, Knudsen, M, Thorsen, K, Hersmus, R, Looijenga, L H J & Stochholm, K 2018, ' A Rare Case of Embryonal Carcinoma in a Patient with Turner Syndrome without Y Chromosomal Material but Mutations in KIT, AKT1, and ZNF358 Demonstrated Using Exome Sequencing ', Sexual Development, vol. 11, no. 5-6, pp. 262-268 . https://doi.org/10.1159/000484398
Sexual Development, 11(5-6), 262-268. Karger

Gonadoblastoma and malignant transformations thereof can occur in females with Turner syndrome (TS) and Y chromosomal material. However, in females with TS and no Y chromosomal material, this is rarely seen. We report a female with an apparent 45,X k

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::c9c494ea23c95206047eae6fc22e6d2e
https://pure.au.dk/portal/da/publications/a-rare-case-of-embryonal-carcinoma-in-a-patient-with-turner-syndrome-without-y-chromosomal-material-but-mutations-in-kit-akt1-and-znf358-demonstrated-using-exome-sequencing(7b3c71bc-7276-498e-b462-d3e22639b770).html