Zobrazeno 1 - 10
of 3 403
pro vyhledávání: '"Skakkebæk, A."'
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
Autor:
Clara Lundetoft Clausen, Trine Holm Johannsen, Niels Erik Skakkebæk, Hanne Frederiksen, Anders Juul, Thomas Benfield
Publikováno v:
Endocrine Connections, Vol 13, Iss 8, Pp 1-7 (2024)
In the context of severe coronavirus disease 2019 (COVID-19) illness, we examined endogenous glucocorticoid concentrations, steroidogenic enzyme activity, and their correlation with inflammation and patient outcomes. This observational study included
Externí odkaz:
https://doaj.org/article/f7fa1a2206224364a1b11b5c31db2124
Autor:
Sofia B. Winge, Niels E. Skakkebaek, Lise Aksglaede, Gülizar Saritaş, Ewa Rajpert-De Meyts, Ellen Goossens, Anders Juul, Kristian Almstrup
Publikováno v:
Cell Death and Disease, Vol 15, Iss 6, Pp 1-9 (2024)
Abstract Klinefelter syndrome (47,XXY) causes infertility with a testicular histology comprising two types of Sertoli cell-only tubules, representing mature and immature-like Sertoli cells, and occasionally focal spermatogenesis. Here, we show that t
Externí odkaz:
https://doaj.org/article/213b1e601e994cd09253e3f58a93d4b8
Publikováno v:
Basic and Clinical Andrology, Vol 33, Iss 1, Pp 1-13 (2023)
Abstract Background Structural abnormalities as well as minor variations of the Y chromosome may cause disorders of sex differentiation or, more frequently, azoospermia. This study aimed to determine the prevalence of loss of Y chromosome material wi
Externí odkaz:
https://doaj.org/article/abb72dc977e14464865bd4c0efbddd2c
Autor:
Stine A. Holmboe, Astrid L. Beck, Anna-Maria Andersson, Katharina M. Main, Niels Jørgensen, Niels E. Skakkebæk, Lærke Priskorn
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
Congenital cryptorchidism, also known as undescended testis, is the condition where one or both testes are not in place in the scrotum at birth and is one of the most common birth defects in boys. Temporal trends and geographic variation in the preva
Externí odkaz:
https://doaj.org/article/1cb2cf55fe634d91ac90f8244576eb3f
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:
Anne Skakkebæk, Kasper Kjær-Sørensen, Vladimir V. Matchkov, Lise-Lotte Christensen, Jesper Just, Cagla Cömert, Niels Holmark Andersen, Claus Oxvig, Claus Højbjerg Gravholt
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract The genetic architecture of the QT interval, defined as the period from onset of depolarisation to completion of repolarisation of the ventricular myocardium, is incompletely understood. Only a minor part of the QT interval variation in the
Externí odkaz:
https://doaj.org/article/6353e4e709f04d6b8c35f814a8fad646
Akademický článek
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Akademický článek
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Autor:
Mette Viuff, Anne Skakkebæk, Emma B. Johannsen, Simon Chang, Steen Bønlykke Pedersen, Katrine Meyer Lauritsen, Mette Glavind Bülow Pedersen, Christian Trolle, Jesper Just, Claus H. Gravholt
Publikováno v:
Genome Medicine, Vol 15, Iss 1, Pp 1-19 (2023)
Abstract Background Sex chromosome aneuploidies (SCAs) give rise to a broad range of phenotypic traits and diseases. Previous studies based on peripheral blood samples have suggested the presence of ripple effects, caused by altered X chromosome numb
Externí odkaz:
https://doaj.org/article/db4f75ab2f61487782271ccbb0b67421