Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lene Bjerring, Gede"'
Autor:
Anne Marie Jelsig, Thomas van Overeem Hansen, Lene Bjerring Gede, Niels Qvist, Lise‐Lotte Christensen, Charlotte Kvist Lautrup, Jane Hübertz Frederiksen, Lone Sunde, Lilian Bomme Ousager, Ken Ljungmann, Birgitte Bertelsen, John Gásdal Karstensen
Publikováno v:
Jelsig, A M, van Overeem Hansen, T, Gede, L B, Qvist, N, Christensen, L-L, Lautrup, C K, Frederiksen, J H, Sunde, L, Ousager, L B, Ljungmann, K, Bertelsen, B & Karstensen, J G 2023, ' Survival, surveillance, and genetics in patients with Peutz-Jeghers syndrome : A nationwide study ', Clinical Genetics . https://doi.org/10.1111/cge.14337
Jelsig, A M, van Overeem Hansen, T, Gede, L B, Qvist, N, Christensen, L-L, Lautrup, C K, Frederiksen, J H, Sunde, L, Ousager, L B, Ljungmann, K, Bertelsen, B & Karstensen, J G 2023, ' Survival, surveillance, and genetics in patients with Peutz-Jeghers syndrome : A nationwide study ', Clinical Genetics, vol. 104, no. 1, pp. 81-89 . https://doi.org/10.1111/cge.14337
Jelsig, A M, van Overeem Hansen, T, Gede, L B, Qvist, N, Christensen, L-L, Lautrup, C K, Frederiksen, J H, Sunde, L, Ousager, L B, Ljungmann, K, Bertelsen, B & Karstensen, J G 2023, ' Survival, surveillance, and genetics in patients with Peutz-Jeghers syndrome : A nationwide study ', Clinical Genetics, vol. 104, no. 1, pp. 81-89 . https://doi.org/10.1111/cge.14337
Peutz-Jeghers syndrome (PJS) is an autosomal dominant hereditary polyposis syndrome causing increased morbidity and mortality due to complications of polyposis and the development of cancer. STK11 is the only gene known to be associated with PJS, alt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a0e28f39122f77623ae3f092734b4e7
https://vbn.aau.dk/da/publications/0767f777-bece-440f-9cc9-d9e53d80de93
https://vbn.aau.dk/da/publications/0767f777-bece-440f-9cc9-d9e53d80de93
Autor:
Anne Cathrine Bomann, Betina Elfving, Sune Bo, Erik B. Simonsen, Lene Bjerring Gede, Martin Balslev Jørgensen, Marianne Nielsen
Publikováno v:
Personality and Mental Health. 11:91-100
Background Social deficits and emotional dysregulation have been suggested as explanations for the relational difficulties experienced by patients with borderline personality disorder (BPD). The neuropeptide oxytocin (OXT) is a possible neurobiologic
Autor:
Jana Sachwitz, Julia Angélica López-Hernández, Karen Grønskov, Lene Bjerring Gede, Irène Netchine, Zeynep Tümer, Miriam Elbracht, Thomas Eggermann, Johan T. den Dunnen
Publikováno v:
Human mutation. 39(3)
Silver-Russell syndrome (SRS) is a clinically and molecularly heterogeneous disorder involving prenatal and postnatal growth retardation, and the term SRS-like is broadly used to describe individuals with clinical features resembling SRS. The main mo
Autor:
Anne Cathrine, Bomann, Martin Balslev, Jørgensen, Sune, Bo, Marianne, Nielsen, Lene Bjerring, Gede, Betina, Elfving, Erik, Simonsen
Publikováno v:
Personality and mental health. 11(2)
Social deficits and emotional dysregulation have been suggested as explanations for the relational difficulties experienced by patients with borderline personality disorder (BPD). The neuropeptide oxytocin (OXT) is a possible neurobiological underpin
Autor:
Lene Bjerring, Gede, Johanne M D, Hahnemann, Zeynep, Tümer, Karen, Brøndum-Nielsen, Karen, Grønskov
Publikováno v:
Prenatal diagnosis. 36(1)
Autor:
Niklas Rye Jørgensen, Lene Bjerring Gede, Derya Aslan, Mille Dahl Andersen, Tine Kellemann de Franca, Peter Schwarz, Sara Rubek Jørgensen
Publikováno v:
Scandinavian journal of clinical and laboratory investigation. 72(1)
Intermittent low-dose treatment with parathyroid hormone (PTH) analogues has become widely used in the treatment of severe osteoporosis. During normal physiological conditions, PTH stimulates both bone formation and resorption, and in patients with p