Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Natascha van der Werf-Grohmann"'
Autor:
Sarah C. Grünert, Uta Matysiak, Franka Hodde, Gunda Ruzaike, Ekkehart Lausch, Anke Schumann, Natascha van der Werf-Grohmann, Ute Spiekerkoetter, Miriam Schmidts
Publikováno v:
Diagnostics, Vol 11, Iss 5, p 749 (2021)
Hypomethylation of H19 and IGF2 can cause Silver–Russell syndrome (SRS), a clinically and genetically heterogeneous condition characterized by intrauterine growth restriction, poor postnatal growth, relative macrocephaly, craniofacial abnormalities
Externí odkaz:
https://doaj.org/article/84dc88eb5cec4a3f8fd53f21847b48ce
Autor:
Corinna Melanie Held, Karl Otfried Schwab, Michael Wurm, Natascha van der Werf-Grohmann, Ekkehart Lausch, Anic Guebelin, Jörn Oliver Sass, Andreas Krebs
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEMReferences. 35(2)
Objectives Patients with childhood hypophosphatasia (HPP) often have unspecific symptoms. It was our aim to identify patients with mild forms of HPP by laboratory data screening for decreased alkaline phosphatase (AP) within a pediatric population. M
Autor:
Karl Otfried Schwab, Jochen Grohmann, Klaus-Georg Kunz, Brigitte Stiller, Natascha van der Werf-Grohmann, Rouven Kubicki
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 33(11)
Background The thyroid gland of patients with congenital heart disease may be exposed to large doses of iodine from various sources. We assessed the thyroid response after iodine exposure during conventional angiography in cardiac catheterization and
Autor:
Hans-Willi Clement, Andreas Krebs, Michael Wurm, Eberhard Schulz, Karl Otfried Schwab, Jürgen Doerfer, Natascha van der Werf-Grohmann, Corinna Brichta, Jutta Zimmerer
Publikováno v:
Experimental and Clinical Endocrinology & Diabetes. 127:289-294
Objective We evaluated percutaneous penetration of topical testosterone and subsequent transfer to subcutaneous tissue, blood and saliva. Methods This microdialysis trial involved eight healthy male volunteers. Five participants received a single dos
Autor:
Andreas Krebs, Natascha van der Werf-Grohmann, Franka Hodde, Michael Wurm, Karl Otfried Schwab, Alexandra Krause, Thomas Kratzin, Jürgen Doerfer, Corinna Brichta
Publikováno v:
Repetitorium Kinder-und Jugendmedizin ISBN: 9783662567890
In dem Kapitel „Diabetologie und Endokrinologie“ werden die Besonderheiten der padiatrischen Diabetologie und Endokrinologie erortert. Hierzu gehoren, u. a. der Diabetes mellitus, Wachstumsstorungen, Storungen im Zusammenhang mit der Pubertat sow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::49cf0552c737d69406fbdffeaf00bdb5
https://doi.org/10.1007/978-3-662-56790-6_4
https://doi.org/10.1007/978-3-662-56790-6_4
Start low, go slowly - mental abnormalities in young prolactinoma patients under cabergoline therapy
Autor:
Corinna Brichta, Andreas Krebs, Michael Wurm, Natascha van der Werf-Grohmann, Karl Otfried Schwab
Publikováno v:
Journal of pediatric endocrinologymetabolism : JPEM. 32(9)
Background Prolactin-secreting pituitary adenomas in childhood and adolescence are rare. First-line therapy consists of dopamine agonists (DAs) like cabergoline. Experience in treating prolactinomas in paediatric and adolescent patients is limited. M
Autor:
Ludwig Schwering, Michael Vohrer, Lars Peterson, Peter C. Kreuz, Natascha van der Werf-Grohmann
Publikováno v:
The American Journal of Sports Medicine. 41:1621-1628
Background:Until now, no study has been published about the electromyographic changes in the extensor apparatus after the Green procedure for proximal realignment in young patients with recurrent patellar dislocations. This electromyographic study wa
Autor:
Elena Neumann, Natascha van der Werf-Grohmann, Jochen Grohmann, Markus-Johann Dechant, Brigitte Stiller, Ute Spiekerkoetter
Publikováno v:
International journal of cardiology. 223
Background Cardiac catheterisation requiring the use of contrast medium is increasingly utilised in infants with congenital heart disease. Thyroid function in infants is potentially vulnerable to relatively high doses of iodine. Methods Single-centre
Autor:
Olaf Hiort, Stefan A. Wudy, Karl Otfried Schwab, Andrea Superti-Furga, Alexander Frankenschmidt, Frederike B Kienzle, Natascha van der Werf-Grohmann, Kerstin N. Walter
Publikováno v:
Hormone Research in Paediatrics. 74:67-71
Background/Aims: Steroid 5α-reductase deficiency (MIM*607306) caused by mutations in the SRD5A2 gene is characterized by a predominantly female phenotype at birth and significant virilization at puberty. The undermasculinization at birth results fro
Autor:
Jochen Grohmann, Johannes Kroll, Ute Spiekerkoetter, Judith Mayer, Natascha van der Werf-Grohmann, Brigitte Stiller
Publikováno v:
World Journal of Cardiology
Aberrant right subclavian artery (arteria lusoria) is the most common congenital root anomaly, remaining asymptomatic in most cases. Nevertheless, some of the 20%-40% of those affected present tracheo-esophageal symptoms. We report on a 6-year-old pr