Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Kristian J. Fougner"'
Autor:
Eirik Bratland, Daniel Eriksson, Ileana Ruxandra Botusan, Eystein S. Husebye, Alberto Falorni, Bergithe E. Oftedal, Stefan Johansson, Ellen C. Røyrvik, Haydee Artaza Alvarez, Per Dahlqvist, Anna-Lena Hulting, Jeanette Wahlberg Hughes, Åsa Hallgren, Lars Breivik, Nils Landegren, Olov Ekwall, Maribel Aranda Guillen, Anette S. B. Wolff, Anders Palmstrøm Jørgensen, Øyvind Helgeland, Sophie Bensing, Johan Svartberg, Olle Kämpe, Mark Vaudel, Amund Holte Berger, Sara Ström, Bjørn G. Nedrebø, Marianne Aardal Grytaas, Per M. Knappskog, Kristian J. Fougner
Publikováno v:
Journal of the Endocrine Society. 5:A167-A168
Autoimmune Addison’s disease is the predominant cause of primary adrenal failure, and is highly heritable. The genetic background has remained poorly understood due to the low prevalence and complex inheritance of the disease. We performed a genome
Autor:
Anne Grethe Myhre, Mihaela Cuida Marthinussen, Kristian J. Fougner, Nils Landegren, Olle Kämpe, Anette S. B. Wolff, Eystein S. Husebye, Eirik Bratland, Johan Svartberg, Kristian Løvås, Åsne Bakke, Bjørn G. Nedrebø, Bjarne Mella, Lars Breivik, Øyvind Bruserud, Per M. Knappskog, Martina M. Erichsen, Bergithe E. Oftedal, Anders Palmstrøm Jørgensen, Kari Lima, Marte K. Viken
Publikováno v:
Journal of Clinical Endocrinology and Metabolism
The Journal of Clinical Endocrinology and Metabolism
The Journal of Clinical Endocrinology and Metabolism
Context: Autoimmune polyendocrine syndrome type 1 (APS1) is a childhood-onset monogenic disease defined by the presence of two of the three major components: hypoparathyroidism, primary adrenocortical insufficiency, and chronic mucocutaneous candidia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de3f2d36c854ad1968c3437e44bf14a
https://hdl.handle.net/10037/10560
https://hdl.handle.net/10037/10560
Autor:
Kristian J. Fougner, Erik Fink Eriksen, Synnove Emblem Holte, Kristian Løvås, Johan Svartberg, Eystein S. Husebye, Bjørn G. Nedrebø, Ragnar B. Moe, Johan Arild Evang, Kari Lima, E. Helen Kemp, Marianne Catharina Astor, Anne Grethe Myhre, Aleksandra Debowska, Christian Fossum
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Objective: The epidemiology of hypoparathyroidism (HP) is largely unknown. We aimed to determine prevalence, etiologies, health related quality of life (HRQOL) and treatment pattern of HP. Methods: Patients with HP and 22q11 deletion syndrome (DiGeor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0459dc105210058e5203bb6e9acf4954
https://hdl.handle.net/10037/10438
https://hdl.handle.net/10037/10438
Autor:
Kristian J. Fougner, Kristian Løvås, Marianne Øksnes, Ingeborg Brønstad, Johan Svartberg, Eystein S. Husebye, Ingrid Nermoen
Publikováno v:
European Journal of Endocrinology. 167:507-516
ObjectiveThe aim of this study was to determine the genetic, anthropometric and metabolic features in an unselected population of adult Norwegian patients with 21-hydroxylase deficiency (21OHD).Patients, methods and designSixty-four 21OHD patients pa
Publikováno v:
International Journal of Clinical Practice. 66:741-747
Summary Objective: To assess whether 4 week’s use of a continuous glucose monitoring (CGM) system improves glucose control, treatment satisfaction or health status, as compared to intensified conventional finger-prick measurements (ICFM) in patient
Autor:
Pia Burman, Ola Gudmundsen, Thor Ueland, Thomas Schreiner, A. P. Jorgensen, Kristian J. Fougner, Jens Bollerslev
Publikováno v:
Growth Hormone & IGF Research. 21:69-75
Objective: The goal of growth hormone (GH) replacement is to improve quality of life (QoL) and prevent the long-term complications of GH deficiency (GHD). Thirty-nine patients with adult-onset GH deficiency (AOGHD) who had originally participated in
Autor:
Thor Ueland, Kristin Godang, Kristian J. Fougner, Jens Bollerslev, Pål Aukrust, Anders Palmstrøm Jørgensen, Pia Burman
Publikováno v:
Clinical Endocrinology. 74:60-66
Objective: We examined the effect of GH substitution on adipose tissue derived hormones and cytokines and sought to identify predictors for changes in body composition during therapy. Long-standing adult-onset GH deficiency (AO-GHD) is associated wit
Autor:
Beate Skinningsrud, Joyce Carlson, Eystein S. Husebye, Kristian Løvås, Dag E. Undlien, Henry A. Erlich, Kristian J. Fougner, Tore Julsrud Berg, Jens Bollerslev, Martina M. Erichsen, Bjarne Mella, Anette S. B. Wolff, Johan Svartberg
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 94:4882-4890
Primary adrenal insufficiency [Addison's disease (AD)] is rare, and systematic studies are few, mostly conducted on small patient samples. We aimed to determine the clinical, immunological, and genetic features of a national registry-based cohort.Pat
Publikováno v:
Journal of Internal Medicine. 248:492-500
Autor:
Thor Ueland, Anders Palmstrøm Jørgensen, Jens Bollerslev, Thomas Schreiner, Ragnhild Wergeland, Kristian J. Fougner, Pia Burman
Publikováno v:
European Journal of Endocrinology. 154:537-543
Objective: GH deficiency is associated with an increased cardiovascular mortality. Fifty-five patients with adult-onset GH deficiency (AO-GHD) (24 female, 31 male, mean age 49 years) were enrolled in a placebo-controlled double-blind crossover study