Zobrazeno 1 - 10
of 3 655
pro vyhledávání: '"CLAUS, H"'
Autor:
Agnethe Berglund, Emma B. Johannsen, Anne Skakkebæk, Simon Chang, Julia Rohayem, Sandra Laurentino, Arne Hørlyck, Simon O. Drue, Ebbe Norskov Bak, Jens Fedder, Frank Tüttelmann, Jörg Gromoll, Jesper Just, Claus H. Gravholt
Publikováno v:
Biology of Sex Differences, Vol 15, Iss 1, Pp 1-16 (2024)
Abstract Background 46,XX testicular disorder/difference of sex development (46,XX DSD) is a rare congenital condition, characterized by a combination of the typical female sex chromosome constitution, 46,XX, and a variable male phenotype. In the maj
Externí odkaz:
https://doaj.org/article/a87274221bac47398901277a729c969e
Publikováno v:
Large-scale Assessments in Education, Vol 12, Iss 1, Pp 1-11 (2024)
Abstract This editorial introduces a special issue of Large-Scale Assessments in Education (LSAE) that addresses key challenges in analyzing longitudinal data from large-scale studies. These challenges include ensuring fair measurement across time, d
Externí odkaz:
https://doaj.org/article/ddbd40eba9d74952aed1e99886ada2f5
Autor:
Cagla Margit Øzdemir, Mette Mølby Nielsen, Jani Liimatta, Clarissa D Voegel, Rawda Naamneh Elzenaty, Victor S Wasehuus, Marie Lind-Holst, Marie Juul Ornstrup, Stine Bjørn Gram, Lilian Bomme Ousager, Christa E Flück, Claus H Gravholt
Publikováno v:
Endocrinology, Diabetes & Metabolism Case Reports, Vol 1, Iss 1, Pp 1-8 (2024)
Congenital adrenal hyperplasia (CAH) is one of the most common inherited rare endocrine disorders. This case report presents two female siblings with delayed diagnosis of non-classical CAH 3β-hydroxysteroid dehydrogenase type 2 (3βHSD2D/HSD3B2) des
Externí odkaz:
https://doaj.org/article/fa243a86ff684261b55f0ddbd54c03c6
Autor:
Sørensen, Anders Lindholm, Skov, Vibe, Kjær, Lasse, Bjørn, Mads Emil, Eickhardt-Dalbøge, Christina Schjellerup, Larsen, Morten Kranker, Nielsen, Claus H, Thomsen, Carsten, Rahbek Gjerdrum, Lise Mette, Knudsen, Trine Alma, Ellervik, Christina, Overgaard, Ulrik Malthe, Andersen, Christen Lykkegaard, Hasselbalch, Hans
Publikováno v:
In Blood Advances 22 October 2024 8(20):5416-5425
Publikováno v:
In Ceramics International 1 October 2024 50(19) Part B:35855-35868
Autor:
Christoffer S. Graven-Nielsen, Ida.V. Vittrup, Anna J. Kragh, Fredrik Lund, Sofie Bliddal, MD, PhD, Kristian Kofoed, MD, PhD, Salome Kristensen, MD, PhD, Allan Stensballe, PhD, Claus H. Nielsen, MD, MsC, PhD, Ulla Feldt-Rasmussen, MD, DMSc, René Cordtz, MD, PhD, Lene Dreyer, MD, PhD
Publikováno v:
JAAD International, Vol 13, Iss , Pp 126-133 (2023)
Background: Polyautoimmunity is defined as having 2 or more autoimmune diseases. Little is known about polyautoimmunity in patients with cutaneous lupus erythematosus (CLE). Objectives: To estimate prevalence and 5-year incidence of non–lupus eryth
Externí odkaz:
https://doaj.org/article/02948dcf6c9742618464fe8f946ad005
Autor:
Stochholm, Kirstine, Holmgård, Camilla, Davis, Shanlee M., Gravholt, Claus H., Berglund, Agnethe
Publikováno v:
In Genetics in Medicine January 2024 26(1)
Autor:
Huster, René J., Thunberg, Christina, Solbakk, Anne-Kristin, Gravholt, Claus H., Fjermestad, Krister
Publikováno v:
In NeuroImage: Clinical 2024 44
Autor:
Helene Bandsholm Leere Tallaksen, Emma B Johannsen, Jesper Just, Mette Hansen Viuff, Claus H Gravholt, Anne Skakkebæk
Publikováno v:
Endocrine Connections, Vol 12, Iss 9, Pp 1-12 (2023)
Sex chromosome abnormalities (SCAs) are chromosomal disorders with either a complete or partial loss or gain of sex chromosomes. The most frequent SCAs include Turner syndrome (45,X), Klinefelter syndrome (47,XXY), Trisomy X syndrome (47,XXX), and Do
Externí odkaz:
https://doaj.org/article/df1b9f29e43849e39c614076585dcdff