Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Dag E Undlien"'
Autor:
Kristina Gervin, Magnus D Vigeland, Morten Mattingsdal, Martin Hammerø, Heidi Nygård, Anne O Olsen, Ingunn Brandt, Jennifer R Harris, Dag E Undlien, Robert Lyle
Publikováno v:
PLoS Genetics, Vol 8, Iss 1, p e1002454 (2012)
Monozygotic (MZ) twins do not show complete concordance for many complex diseases; for example, discordance rates for autoimmune diseases are 20%-80%. MZ discordance indicates a role for epigenetic or environmental factors in disease. We used MZ twin
Externí odkaz:
https://doaj.org/article/27716f2bb8584c238a4e5baf4779bd58
Autor:
Anette S. B. Wolff, Beate Skinningsrud, Klaus Badenhoop, Anna L. Mitchell, Gesine Meyer, Dag E. Undlien, Marissa Penna-Martinez, William Ollier, Eystein S. Husebye, Simon H. S. Pearce, Corrado Betterle, Alberto Falorni
Publikováno v:
European Journal of Endocrinology. 184:373-381
Objective While vitamin D regulates immune cells, little is known about it in autoimmune Addison’s disease (AAD). We investigated the vitamin D status in AAD patients from five European populations to assess its deficiency. In addition, we studied
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0afb307668f324cf62aeee512ec749d9
https://doi.org/10.1530/eje-20-0956
https://doi.org/10.1530/eje-20-0956
Autor:
Vibeke Moe, Dag E. Undlien, Christian M. Page, Marissa LeBlanc, Einar Heiervang, Ellen Wikenius, Lars Smith, Anne Margrethe Myhre
Publikováno v:
Nordic Journal of Psychiatry
Background: Prenatal maternal stress increases the risk of offspring developmental and psychological difficulties. The biological mechanisms behind these associations are mostly unknown. One explan...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5e03b1474de5b28396eacbfacf9cfbe
https://doi.org/10.1080/08039488.2019.1613446
https://doi.org/10.1080/08039488.2019.1613446
Publikováno v:
HLA. 98:3-4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb0aed0bd1504934f38391efcb766347
https://doi.org/10.1111/tan.14290
https://doi.org/10.1111/tan.14290
Autor:
Sigrid Aslaksen, Paal Methlie, Magnus D. Vigeland, Dag E. Jøssang, Anette B. Wolff, Ying Sheng, Bergithe E. Oftedal, Beate Skinningsrud, Dag E. Undlien, Kaja K. Selmer, Eystein S. Husebye, Eirik Bratland
Publikováno v:
Frontiers in Endocrinology
Frontiers in Endocrinology, Vol 10 (2019)
Frontiers in Endocrinology, Vol 10 (2019)
Background: Underlying causes of adrenal insufficiency include congenital adrenal hyperplasia (CAH) and autoimmune adrenocortical destruction leading to autoimmune Addison's disease (AAD). Here, we report a patient with a homozygous stop-gain mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f807061679f7fa5df5ef8dc10c412b9
http://europepmc.org/articles/PMC6776599
http://europepmc.org/articles/PMC6776599
Autor:
Eirik Bratland, Eystein S. Husebye, Dag E. Undlien, Bergithe E. Oftedal, Sigrid Aslaksen, Kaja Kristine Selmer, Haydee Artaza, Magnus Dehli Vigeland, Ying Sheng, Lars Breivik, Anette S. B. Wolff, Beate Skinningsrud
Publikováno v:
Journal of Translational Autoimmunity
Journal of Translational Autoimmunity, Vol 1, Iss, Pp-(2019)
Journal of Translational Autoimmunity, Vol 1, Iss, Pp-(2019)
Autoimmune Addison's disease (AAD) is a classic organ-specific autoimmune disease characterized by an immune-mediated attack on the adrenal cortex. As most autoimmune diseases, AAD is believed to be caused by a combination of genetic and environmenta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0047b47d5e2b3a280ab9eedab03e2d5e
https://pubmed.ncbi.nlm.nih.gov/32743495
https://pubmed.ncbi.nlm.nih.gov/32743495
Autor:
Roar Fjær, Marivi N. Moen, Ying Sheng, Dag E. Undlien, El Hassan Hamdani, Robin Johansen Menchini, Farrukh A. Chaudhry, Kaja Kristine Selmer, Mustafa A. Salih, Heba Y. El Khashab, Jon K. Laerdahl, Magnus Dehli Vigeland, Bjørnar Hassel
Publikováno v:
Brain. 139:3109-3120
Progressive myoclonus epilepsy is a heterogeneous group of disorders characterized by myoclonic and tonic-clonic seizures, ataxia and cognitive decline. We here present two affected brothers. At 9 months of age the elder brother developed ataxia and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9950ddaa5c201e021e850e758d76431
https://doi.org/10.1093/brain/aww244
https://doi.org/10.1093/brain/aww244
Autor:
Jan Norum, Eli Marie Grindedal, Sarah Louise Ariansen, Lovise Maehle, Dag E. Undlien, Ellen Schlichting, Inga Karsrud, Cecilie Heramb
Publikováno v:
BMC Cancer, Vol 17, Iss 1, Pp 1-13 (2017)
BMC Cancer
BMC Cancer
Background Identification of BRCA mutations in breast cancer (BC) patients influences treatment and survival and may be of importance for their relatives. Testing is often restricted to women fulfilling high-risk criteria. However, there is limited k
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e859d8edf897142a62580d087f417291
https://hdl.handle.net/10037/12161
https://hdl.handle.net/10037/12161
Autor:
Karin C. Lødrup Carlsen, Dag E. Undlien, Bettina Kulle Andreassen, Kai-Håkon Carlsen, Monica Cheng Munthe-Kaas, Hanne Sagsveen Hjorthaug, Kristina Gervin, Robert Lyle
Publikováno v:
Clinical Epigenetics
Background Several studies have reported age-associated changes in DNA methylation in the first few years of life and in adult populations, but the extent of such changes during childhood is less well studied. The goals of this study were to investig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fec578820d801076e633db021f7461f
https://doi.org/10.1186/s13148-016-0277-3
https://doi.org/10.1186/s13148-016-0277-3
Autor:
Truls Oppedal, Isabel Filges, Irene Hoesli, Peter Meyer, Ying Sheng, Dag E. Undlien, Petter Strømme, Stephanie Meier, Max Schubach, Kristin Brandal, Peter Miny, Kaja Kristine Selmer, Trine Rygvold Waage, Tjaart A. P. de Beer, Oddveig Røsby, Elisabeth Bruder, Sylvia Hoeller, Sevgi Tercanli, Sven M. Schulzke
Publikováno v:
Human mutation. 37(7)
Strømme syndrome was first described by Strømme et al. (1993) in siblings presenting with "apple peel" type intestinal atresia, ocular anomalies and microcephaly. The etiology remains unknown to date. We describe the long-term clinical follow-up da
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5eb4fb2d50c96c30b90bc83dcd36b07
https://pubmed.ncbi.nlm.nih.gov/26820108
https://pubmed.ncbi.nlm.nih.gov/26820108