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Acromegaly management in the Nordic countries: A Delphi consensus survey.
Arlien-Søborg MC, Dal J, Heck A, Stochholm K, Husted E, Feltoft CL, Rasmussen ÅK, Feldt-Rasmussen U, Andreassen M, Klose MC, Nielsen TL, Andersen MS, Christensen LL, Krogh J, Jarlov A, Bollerslev J, Nermoen I, Oksnes M, Dahlqvist P, Olsson T, Berinder K, Hoybye C, Petersson M, Akerman AK, Wahlberg J, Ekman B, Engstrom BE, Johannsson G, Ragnarsson O, Olsson D, Sigurjónsdóttir HÁ, Fougner SL, Matikainen N, Vehkavaara S, Metso S, Jaatinen P, Hämäläinen P, Rintamäki R, Yliaska I, Immonen H, Mäkimattila S, Cederberg-Tamminen H, Viukari M, Nevalainen P, Nuutila P, Schalin-Jäntti C, Burman P, Jørgensen JOL. Arlien-Søborg MC, et al. Among authors: olsson t, olsson d. Clin Endocrinol (Oxf). 2024 Sep;101(3):263-273. doi: 10.1111/cen.15095. Epub 2024 Jun 12. Clin Endocrinol (Oxf). 2024. PMID: 38865284
Cytokine Autoantibody Screening in the Swedish Addison Registry Identifies Patients With Undiagnosed APS1.
Eriksson D, Dalin F, Eriksson GN, Landegren N, Bianchi M, Hallgren Å, Dahlqvist P, Wahlberg J, Ekwall O, Winqvist O, Catrina SB, Rönnelid J; Swedish Addison Registry Study Group; Hulting AL, Lindblad-Toh K, Alimohammadi M, Husebye ES, Knappskog PM, Rosengren Pielberg G, Bensing S, Kämpe O. Eriksson D, et al. J Clin Endocrinol Metab. 2018 Jan 1;103(1):179-186. doi: 10.1210/jc.2017-01957. J Clin Endocrinol Metab. 2018. PMID: 29069385
Relation between HLA and copy number variation of steroid 21-hydroxylase in a Swedish cohort of patients with autoimmune Addison's disease.
Lundtoft C, Eriksson D, Bianchi M, Aranda-Guillén M, Landegren N, Rantapää-Dahlqvist S, Söderkvist P, Meadows JRS; DISSECT Consortium; ImmunoArray Consortium; Swedish Addison Registry Study Group; Bensing S, Pielberg GR, Lindblad-Toh K, Rönnblom L, Kämpe O. Lundtoft C, et al. Eur J Endocrinol. 2023 Aug 2;189(2):235-241. doi: 10.1093/ejendo/lvad102. Eur J Endocrinol. 2023. PMID: 37553728 Free article.
Corroborating written history with ancient DNA: The case of the Well-man described in an Old Norse saga.
Ellegaard MR, Ebenesersdóttir SS, Moore KHS, Petersén A, Vågene ÅJ, Bieker VC, Denham SD, Cavalleri GL, Gilbert E, Werge T, Hansen TF, Kockum I, Alfredsson L, Olsson T, Hovig E, Gilbert MTP, Stefánsson K, Stenøien HK, Helgason A, Martin MD. Ellegaard MR, et al. Among authors: olsson t. iScience. 2024 Oct 25;27(11):111076. doi: 10.1016/j.isci.2024.111076. eCollection 2024 Nov 15. iScience. 2024. PMID: 39620136 Free PMC article.
Exploring the relationship between polycystic ovarian syndrome, testosterone, and multiple sclerosis in women: A nationwide cohort study and genome-wide cross-trait analysis.
Jiang Y, Cesta CE, Liu Q, Kingwell E, Stridh P, Shchetynsky K, Olsson T, Kockum I, Stener-Victorin E, Jiang X, Manouchehrinia A. Jiang Y, et al. Among authors: olsson t. Mult Scler. 2024 Dec;30(14):1765-1774. doi: 10.1177/13524585241292802. Epub 2024 Nov 6. Mult Scler. 2024. PMID: 39503308 Free PMC article.
Digital voice analysis as a biomarker of acromegaly.
Vouzouneraki K, Nylén F, Holmberg J, Olsson T, Berinder K, Höybye C, Petersson M, Bensing S, Åkerman AK, Borg H, Ekman B, Robért J, Engström BE, Ragnarsson O, Burman P, Dahlqvist P. Vouzouneraki K, et al. Among authors: olsson t. J Clin Endocrinol Metab. 2024 Oct 4:dgae689. doi: 10.1210/clinem/dgae689. Online ahead of print. J Clin Endocrinol Metab. 2024. PMID: 39363748
Pharmacogenomics of clinical response to Natalizumab in multiple sclerosis: a genome-wide multi-centric association study.
Clarelli F, Corona A, Pääkkönen K, Sorosina M, Zollo A, Piehl F, Olsson T, Stridh P, Jagodic M, Hemmer B, Gasperi C, Harroud A, Shchetynsky K, Mingione A, Mascia E, Misra K, Giordano A, Mazzieri MLT, Priori A, Saarela J, Kockum I, Filippi M, Esposito F, Boneschi FGM. Clarelli F, et al. Among authors: olsson t. J Neurol. 2024 Nov;271(11):7250-7263. doi: 10.1007/s00415-024-12608-6. Epub 2024 Sep 12. J Neurol. 2024. PMID: 39264442 Free PMC article.
1,246 results