Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Susanne Fricke-Otto"'
Autor:
Cécile Carl, Lars Dinkelbach, Julia Mohr, Ruy Perez, Tobias Vera Lopez, Susanne Fricke-Otto, Tim Niehues
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2024)
We describe two female infants at the age of five and six months with urinary tract infections presenting with vomiting and reduced drinking behavior. On laboratory analysis, severe hyponatremia (106 mmol/L and 109 mmol/L) was seen with hyperkalemia
Externí odkaz:
https://doaj.org/article/dd644c32db814b299ae3d0dcc04d6ede
Autor:
Anna-Lisa Sorg, Leon Bergfeld, Marietta Jank, Victor Corman, Ilia Semmler, Anna Goertz, Andreas Beyerlein, Eva Verjans, Norbert Wagner, Horst Von Bernuth, Fabian Lander, Katharina Weil, Markus Hufnagel, Ute Spiekerkoetter, Cho-Ming Chao, Lutz Naehrlich, Ania Carolina Muntau, Ulf Schulze-Sturm, Gesine Hansen, Martin Wetzke, Anna-Maria Jung, Tim Niehues, Susanne Fricke-Otto, Ulrich Von Both, Johannes Huebner, Uta Behrends, Johannes G. Liese, Christian Schwerk, Christian Drosten, Ruediger Von Kries, Horst Schroten
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-9 (2022)
Children are less likely to be infected with SARS-CoV-2 and develop less severe disease than adults, which makes estimation of infection rates challenging. Here, the authors conduct seroprevalence surveys of children in Germany, describe changes in p
Externí odkaz:
https://doaj.org/article/155b66c56a5d4cee8aa6492ffb7809ef
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:
Julia Quitmann, Janika Bloemeke, Neuza Silva, Monika Bullinger, Stefanie Witt, Ilker Akkurt, Desiree Dunstheimer, Christian Vogel, Volker Böttcher, Ursula Kuhnle Krahl, Markus Bettendorf, Eckhard Schönau, Susanne Fricke-Otto, Alexandra Keller, Klaus Mohnike, Helmuth-Günther Dörr
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Aside from clinical endpoints like height gain, health-related quality of life has also become an important outcome indicator in the medical field. However, the data on short stature and health-related quality of life is inconsistent. Therefore, we e
Externí odkaz:
https://doaj.org/article/cb362cac78f54cf7a52805cc392c3141
Autor:
Julia Thomann, Sascha R. Tittel, Egbert Voss, Rudolf Oeverink, Katja Palm, Susanne Fricke-Otto, Klaus Kapelari, Reinhard W. Holl, Joachim Woelfle, Markus Bettendorf
Publikováno v:
International Journal of Neonatal Screening, Vol 7, Iss 1, p 10 (2021)
Neonatal screening for congenital primary hypothyroidism (CH) is mandatory in Germany but medical care thereafter remains inconsistent. Therefore, the registry HypoDok of the German Society of Pediatric Endocrinology and Diabetology (DGKED) was analy
Externí odkaz:
https://doaj.org/article/c56d350f3e6c4f06b11e06020d8aa134
Autor:
Antonino Montalbano, Lonny Juergensen, Ralph Roeth, Birgit Weiss, Maki Fukami, Susanne Fricke‐Otto, Gerhard Binder, Tsutomu Ogata, Eva Decker, Gudrun Nuernberg, David Hassel, Gudrun A Rappold
Publikováno v:
EMBO Molecular Medicine, Vol 8, Iss 12, Pp 1455-1469 (2016)
Abstract Mutations in the homeobox gene SHOX cause SHOX deficiency, a condition with clinical manifestations ranging from short stature without dysmorphic signs to severe mesomelic skeletal dysplasia. In rare cases, individuals with SHOX deficiency a
Externí odkaz:
https://doaj.org/article/58e159e9c09d4bc3a1633d55a5311edb
Autor:
Johanna Hammersen, Markus Bettendorf, Walter Bonfig, Eckhard Schönau, Katharina Warncke, Alexander J. Eckert, Susanne Fricke-Otto, Katja Palm, Reinhard W. Holl, Joachim Woelfle
Publikováno v:
Medizinische Genetik. 34:29-40
Congenital primary hypothyroidism (CH) and congenital adrenal hyperplasia (CAH) are targeted by the German and Austrian newborn screening. For both diseases, there are registries for quality improvement, based on standardized observational data from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca5efcaf71cee73a0beb5f8f7207e976
https://doi.org/10.1515/medgen-2022-2114
https://doi.org/10.1515/medgen-2022-2114
Autor:
Herman L Müller, Imke Gätjen, Aniko Krumbholz, Susanne Fricke-Otto, Erwin Lankes, Bettina Gohlke, Felix Reschke, Elke Müller-Rossberg, Klaus Mohnike, Berthold P. Hauffa, Sabine Kliesch, Norbert Jorch, Désirée Dunstheimer, Johannes Weigel, Julia Rohayem, Jürgen Brämswig, Annette Richter-Unruh, Claus Jourdan, Michael Zitzmann, Lena Maria Bäumer
Objective To study the impact of the quality of therapeutic control on fertility and on the prevalence of testicular adrenal rest tumours (TART) in young males with congenital adrenal hyperplasia (CAH). Design Combined cross-sectional and retrospecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::228bbecaefd3c02ab467bdf8d0af8728
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/83504
https://opus.bibliothek.uni-augsburg.de/opus4/frontdoor/index/index/docId/83504
Autor:
Anna-Lisa Sorg, Leon Bergfekd, Marietta Jank, Victor M. Corman, Ilia Semmler, Anna Görtz, Andreas Beyerlein, Eva Verjans, Norbert Wagner, Horst von Bernuth, Fabian Lander, Katharina Weil, Markus Hufnagel, Ute Spiekerkoetter, Chao Cho-Ming, Lutz Nährlich, Ania C. Muntau, Ulf Schulze-Sturm, Gesine Hansen, Martin Wetzke, Anna-Maria Jung, Tim Niehues, Susanne Fricke-Otto, Ulrich von Both, Johannes Hübner, Uta Behrends, Johannes G. Liese, Christian Schwerk, Christian Drosten, Rüdiger von Kries, Horst Schroten
Publikováno v:
SSRN Electronic Journal.
Background: Investigating the role of children in the COVID-19 pandemic is pivotal to prevent the virus spreading. In most cases, children infected with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) develop non-specific symptoms or are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::370a95954bdb1e1debdf381c0da0e9e2
https://doi.org/10.2139/ssrn.3965378
https://doi.org/10.2139/ssrn.3965378
Autor:
Neuza Silva, Helmuth-Günther Dörr, Ilker Akkurt, Stefanie Witt, Markus Bettendorf, Eckhard Schönau, Janika Bloemeke, Julia Quitmann, Klaus Mohnike, Alexandra Keller, Desiree Dunstheimer, Ursula Kuhnle Krahl, Christian Vogel, Susanne Fricke-Otto, Volker Böttcher, Monika Bullinger
Publikováno v:
Frontiers in Pediatrics, Vol 7 (2019)
Frontiers in Pediatrics
Frontiers in Pediatrics
Aside from clinical endpoints like height gain, health-related quality of life has also become an important outcome indicator in the medical field. However, the data on short stature and health-related quality of life is inconsistent. Therefore, we e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::949d70ab4093d53975560a10b602d48d
https://www.frontiersin.org/article/10.3389/fped.2019.00164/full
https://www.frontiersin.org/article/10.3389/fped.2019.00164/full