Zobrazeno 1 - 10
of 455
pro vyhledávání: '"Annette Richter"'
Autor:
Sabine Wiegmann, Ralph Schilling, Mirja Winter, Martina Ernst, Katja Wechsung, Ute Kalender, Barbara Stöckigt, Annette Richter-Unruh, Olaf Hiort, Ulla Döhnert, Louise Marshall, Julia Rohayem, Klaus-Peter Liesenkötter, Martin Wabitsch, Gloria Herrmann, Gundula Ernst, Stephanie Roll, Thomas Keil, Uta Neumann
Publikováno v:
PEC Innovation, Vol 5, Iss , Pp 100321- (2024)
Objective: Evaluation of the participant satisfaction with a newly developed interdisciplinary, modular education program for children, adolescents, and young adults with differences of sex development (DSD) and their parents. Methods: The two-day pr
Externí odkaz:
https://doaj.org/article/f4aeea3d5bf343b8916af0c2026eb7af
Autor:
Lisanne Brueck, Sascha Roocke, Veronika Matschke, Annette Richter-Unruh, Katrin Marcus-Alic, Carsten Theiss, Sarah Stahlke
Publikováno v:
Cells, Vol 13, Iss 18, p 1515 (2024)
Our study investigates the impact of FGF23 overexpression on SaOS-2 cells to elucidate its role in cellular stress and morphology, contributing to the understanding of skeletal pathologies like X-linked hypophosphatemia (XLH). Using transmission elec
Externí odkaz:
https://doaj.org/article/0ba2d1a10db546899059638b78d0a225
Autor:
Sebastian Franik, Kathrin Fleischer, Barbara Kortmann, Nike M Stikkelbroeck, Kathleen D’Hauwers, Claire Bouvattier, Jolanta Slowikowska-Hilczer, Solange Grunenwald, Tim van de Grift, Audrey Cartault, Annette Richter-Unruh, Nicole Reisch, Ute Thyen, Joanna IntHout, Hedi L Claahsen-van der Grinten
Publikováno v:
Endocrine Connections, Vol 12, Iss 10, Pp 1-11 (2023)
Background: Klinefelter syndrome (KS) is associated with an increased risk of lower socioeconomic status and a higher risk for morbidity and mortal ity, which may have a significant impact on quality of life (QOL). The objective of this study is to i
Externí odkaz:
https://doaj.org/article/2fdf5a44260d45bb8b376133ed4665d5
Autor:
Sabine Wiegmann, Martina Ernst, Loretta Ihme, Katja Wechsung, Ute Kalender, Barbara Stöckigt, Annette Richter-Unruh, Sander Vögler, Olaf Hiort, Martina Jürgensen, Louise Marshall, Ingo Menrath, Julia Schneidewind, Isabel Wagner, Julia Rohayem, Klaus-Peter Liesenkötter, Martin Wabitsch, Malaika Fuchs, Gloria Herrmann, Henriette Lutter, Gundula Ernst, Christine Lehmann, Martina Haase, Stephanie Roll, Ralph Schilling, Thomas Keil, Uta Neumann
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-13 (2022)
Abstract Background Differences in sexual development (DSD) are rare diseases, which affect the chromosomal, anatomical or gonadal sex differentiation. Although patient education is recommended as essential in a holistic care approach, standardised p
Externí odkaz:
https://doaj.org/article/665174da0b424cea88160122ba0dfe0a
Autor:
Sebastian Franik, Kathrin Fleischer, Barbara Kortmann, Nike M Stikkelbroeck, Kathleen D’Hauwers, Claire Bouvattier, Jolanta Slowikowska-Hilczer, Solange Grunenwald, Tim van de Grift, Audrey Cartault, Annette Richter-Unruh, Nicole Reisch, Ute Thyen, Joanna IntHout, Hedi L Claahsen-van der Grinten
Publikováno v:
Endocrine Connections, Vol 11, Iss 7, Pp 1-11 (2022)
Klinefelter syndrome (KS) is associated with an increased risk of neuropsychological morbidity, such as learning disabilities, which may have a significant impact on socioeconomic status (SES). The objective of this study was to investigate the SES i
Externí odkaz:
https://doaj.org/article/e9a9983507f94fe08975119b3bc9e33d
Autor:
Stefan Riedl, Friedrich-Wilhelm Röhl, Walter Bonfig, Jürgen Brämswig, Annette Richter-Unruh, Susanne Fricke-Otto, Markus Bettendorf, Felix Riepe, Gernot Kriegshäuser, Eckhard Schönau, Gertrud Even, Berthold Hauffa, Helmuth-Günther Dörr, Reinhard W Holl, Klaus Mohnike
Publikováno v:
Endocrine Connections, Vol 8, Iss 2, Pp 86-94 (2019)
Congenital adrenal hyperplasia (CAH) due to CYP21A2 gene mutations is associated with a variety of clinical phenotypes (salt wasting, SW; simple virilizing, SV; nonclassical, NC) depending on residual 21-hydroxylase activity. Phenotypes and genotypes
Externí odkaz:
https://doaj.org/article/68ef31c9b5c04841b2e269eae98fe5ce
Autor:
Myrthe J. M. Verhees, Manon Engels, Paul N. Span, Fred C. G. J. Sweep, Antonius E. van Herwaarden, Henrik Falhammar, Anna Nordenström, Emma A. Webb, Annette Richter-Unruh, Claire Bouvattier, Aude Brac de la Perrière, Wiebke Arlt, Nicole Reisch, Birgit Köhler, Marion Rapp, Nike M. M. L. Stikkelbroeck, Nel Roeleveld, Hedi L. Claahsen-van der Grinten
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency (21OHD) is a disorder of adrenal steroid biosynthesis, leading to hypocortisolism, hypoaldosteronism, and hyperandrogenism. Impaired quality of life (QoL) has been demonstrated in
Externí odkaz:
https://doaj.org/article/139af0e0c1a84096aae75811337fa356
Autor:
Iris D. Noordman, Janiëlle AEM. van der Velden, Henri JLM. Timmers, Nicole Reisch, Annette Richter-Unruh, Catherine Pienkowksi, Nel Roeleveld, Hedi L. Claahsen-van der Grinten
Publikováno v:
Comprehensive Psychoneuroendocrinology, Vol 5, Iss , Pp 100030- (2021)
Background: Turner syndrome (TS) is a genetic condition with a broad phenotypic spectrum. In contrast to the medical conditions, socioeconomic factors are not well understood. Our goal was to evaluate the socioeconomic status (SES) among women with T
Externí odkaz:
https://doaj.org/article/28d13b5fd8d942cf9fd69336e1971772
Publikováno v:
PLoS Medicine, Vol 5, Iss 4, p e88 (2008)
Male pseudohermaphroditism, or Leydig cell hypoplasia (LCH), is an autosomal recessive disorder in individuals with a 46,XY karyotype, characterized by a predominantly female phenotype, a blind-ending vagina, absence of breast development, primary am
Externí odkaz:
https://doaj.org/article/395bd7ae7d8649e2a52319f64c596630
This look at the field of ichnology is “an excellent compendium and a timely piece on a rapidly expanding and changing area of research” (Quarterly Review of Biology).The latest advances in dinosaur ichnology are showcased in this comprehensive a