Zobrazeno 1 - 10
of 3 531
pro vyhledávání: '"Claus, H."'
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
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:
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
Autor:
Huster, René J., Thunberg, Christina, Solbakk, Anne-Kristin, Gravholt, Claus H., Fjermestad, Krister
Publikováno v:
In NeuroImage: Clinical 2024 44
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 July 2024
Autor:
Stochholm, Kirstine, Holmgård, Camilla, Davis, Shanlee M., Gravholt, Claus H., Berglund, Agnethe
Publikováno v:
In Genetics in Medicine January 2024 26(1)
Publikováno v:
Endocrine Connections, Vol 12, Iss 5, Pp 1-13 (2023)
Context: Klinefelter syndrome (KS, 47,XXY) and 47,XYY syndrome are genetic conditions characterized by a supernumerary sex chromosome. The conditions share many traits, but considerable phenotypic differences are seen between the two. Focusing on mor
Externí odkaz:
https://doaj.org/article/c4c445c1f0684e1f917e3b462dbbc0f8