Zobrazeno 1 - 10 of 239 pro vyhledávání: '"Helmuth Günther Dörr"'
1
Akademický článek
Hydrocortisone dosing in children with classic congenital adrenal hyperplasia: results of the German/Austrian registry
Autor: Heike Hoyer-Kuhn, Angela Huebner, Anette Richter-Unruh, Markus Bettendorf, Tilman Rohrer, Klaus Kapelari, Stefan Riedl, Klaus Mohnike, Helmuth-Günther Dörr, Friedrich-Wilhelm Roehl, Katharina Fink, Reinhard W Holl, Joachim Woelfle
Publikováno v: Endocrine Connections, Vol 10, Iss 5, Pp 561-569 (2021)
Objective: Treatment of classic congenital adrenal hyperplasia (CAH) is necessary to compensate for glucocorticoid/mineralocorticoid deficiencies and to suppress androgen excess. Hydrocortisone (HC) is preferred in growing children with classic CAH b
Externí odkaz: https://doaj.org/article/8df44d6c4b764632b81748064f355400
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2
Akademický článek
Psychometric properties of the quality of life in short statured youth (QoLISSY) questionnaire within the course of growth hormone treatment
Autor: Janika Bloemeke, Neuza Silva, Monika Bullinger, Stefanie Witt, Helmuth-Günther Dörr, Julia Quitmann
Publikováno v: Health and Quality of Life Outcomes, Vol 17, Iss 1, Pp 1-15 (2019)
Abstract Background The Quality of Life of Short Stature Youth (QoLISSY) questionnaire is a patient- and parent-reported outcome measure assessing health-related quality of life (HRQOL) in short stature youth. This study evaluates the psychometric pr
Externí odkaz: https://doaj.org/article/75bfc35abdbc40e584a8ec557045956b
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3
Akademický článek
Genotype/phenotype correlations in 538 congenital adrenal hyperplasia patients from Germany and Austria: discordances in milder genotypes and in screened versus prescreening patients
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
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4
Safety and Efficacy of Pediatric Growth Hormone Therapy
Autor: Mohamad Maghnie, Michael B Ranke, Mitchell E Geffner, Elpis Vlachopapadopoulou, Lourdes Ibáñez, Martin Carlsson, Wayne Cutfield, Raoul Rooman, Roy Gomez, Michael P Wajnrajch, Agnès Linglart, Renata Stawerska, Peter E Clayton, Feyza Darendeliler, Anita C S Hokken-Koelega, Reiko Horikawa, Toshiaki Tanaka, Helmuth-Günther Dörr, Kerstin Albertsson-Wikland, Michel Polak, Adda Grimberg
Publikováno v: Journal of Clinical Endocrinology and Metabolism, 107(12), 3287-3301. Endocrine Society
Maghnie, M, Ranke, M B, Geffner, M E, Vlachopapadopoulou, E, Ibáñez, L, Carlsson, M, Cutfield, W, Rooman, R, Gomez, R, Wajnrajch, M P, Linglart, A, Stawerska, R, Clayton, P E, Darendeliler, F, Hokken-Koelega, A C S, Horikawa, R, Tanaka, T, Dörr, H G, Albertsson-Wikland, K, Polak, M & Grimberg, A 2022, ' Safety and Efficacy of Pediatric Growth Hormone Therapy: Results From the Full KIGS Cohort ', The Journal of Clinical Endocrinology & Metabolism . https://doi.org/10.1210/clinem/dgac517
Context The Kabi/Pfizer International Growth Database (KIGS) is a large, international database (1987-2012) of children treated with recombinant human growth hormone (rhGH) in real-world settings. Objective This work aimed to evaluate the safety and
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc764b4cf7e8d0fa5017f08cc6f7406
https://doi.org/10.1210/clinem/dgac517
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5
Akademický článek
Quality of Life of Short-Statured Children Born Small for Gestational Age or Idiopathic Growth Hormone Deficiency Within 1 Year of Growth Hormone Treatment
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
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7
Caring for a Child with Congenital Adrenal Hyperplasia Diagnosed by Newborn Screening: Parental Health-Related Quality of Life, Coping Patterns, and Needs
Autor: Laura Rautmann, Stefanie Witt, Christoph Theiding, Birgit Odenwald, Uta Nennstiel-Ratzel, Helmuth-Günther Dörr, Julia Hannah Quitmann
Publikováno v: International Journal of Environmental Research and Public Health
Volume 20
Issue 5
Pages: 4493
Diagnosing a child by newborn screening with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency (CAH) causes multiple challenges for the affected parents and the whole family. We aimed to examine the health-related Quality of Lif
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6537b934bd611e2e692f9acca1dd92cc
https://doi.org/10.3390/ijerph20054493
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8
Medizinische Betreuung von jungen Frauen mit Ullrich-Turner-Syndrom in Deutschland
Autor: Martin Wabitsch, Heinrich Schmidt, Gerhard Binder, Klaus Mohnike, Berthold P. Hauffa, Markus Bettendorf, Paul-Martin Holterhus, Günter K. Stalla, Joachim Wölfle, Jürgen Brämswig, Helmuth-Günther Dörr
Publikováno v: DMW - Deutsche Medizinische Wochenschrift. 145:e18-e23
Zusammenfassung Hintergrund Für die medizinische Betreuung von Frauen mit Ullrich-Turner-Syndrom (UTS) nach dem Ende der kinderärztlichen Betreuung liegen zahlreiche Empfehlungen vor. Es gibt bisher keine Untersuchung, die die Betreuungssituation d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::47bf36b222b3b45359ce4c0df618c1ac
https://doi.org/10.1055/a-0923-4191
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9
Lebenssituation von jungen Frauen mit Ullrich-Turner-Syndrom nach dem Ende der Wachstumshormontherapie: Ergebnisse einer Umfrage in Deutschland
Autor: Jürgen Brämswig, Dornburg Geschäftsstelle: Am Bornstück, Paul-Martin Holterhus, Berthold P. Hauffa, Klaus Mohnike, Heinrich Schmidt, Helmuth-Günther Dörr, Martin Wabitsch, Gerhard Binder, Markus Bettendorf, Joachim Wölfle, Günter K. Stalla
Publikováno v: DMW - Deutsche Medizinische Wochenschrift. 144:e87-e93
Zusammenfassung Einleitung Bei Mädchen und Frauen mit Ullrich-Turner-Syndrom (UTS) werden psychosoziale Auffälligkeiten wie eine ängstliche Persönlichkeit, geringeres Selbstwertgefühl, spätes Lösen vom Elternhaus und/oder späte sexuelle Erfah
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e78f3670f4930e8b28918cf463edadf8
https://doi.org/10.1055/a-0841-9918
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10
Recombinant Human Growth Hormone Activates Neuroprotective Growth Factors in Hypoxic Brain Injury in Neonatal Mice
Autor: Klara Terörde, Helmuth-Günther Dörr, Regina Trollmann, Susan Jung
Publikováno v: Endocrinology. 162
Perinatal hypoxia severely disrupts cerebral metabolic and maturational programs beyond apoptotic cell death. Antiapoptotic treatments such as erythropoietin are suggested to improve outcomes in hypoxic brain injury; however, the results are controve
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dcf248eb23a060d842b2e7d29726d8d0
https://doi.org/10.1210/endocr/bqab008
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