Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Nils P. Krone"'
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Treatment of congenital adrenal hyperplasia in children aged 0-3 years
Autor: Uta Neumann, Annelieke van der Linde, Ruth E Krone, Nils P Krone, Ayla Güven, Tülay Güran, Heba Elsedfy, Sukran Poyrazoglu, Feyza Darendeliler, Tania A S S Bachega, Antonio Balsamo, Sabine E Hannema, Niels Birkebaek, Ana Vieites, Ajay Thankamony, Martine Cools, Tatjana Milenkovic, Walter Bonfig, Eduardo Correa Costa, Navoda Atapattu, Liat de Vries, Guilherme Guaragna-Filho, Marta Korbonits, Klaus Mohnike, Jillian Bryce, S Faisal Ahmed, Bernard Voet, Oliver Blankenstein, Hedi L Claahsen-van der Grinten
Publikováno v: Neumann, U, van der Linde, A, Krone, R E, Krone, N P, Güven, A, Güran, T, Elsedfy, H, Poyrazoglu, S, Darendeliler, F, Bachega, T A, Balsamo, A, Hannema, S E, Birkebæk, N, Vieites, A, Thankamony, A, Cools, M, Milenkovic, T, Bonfig, W, Costa, E C, Atapattu, N, de Vries, L, Guaragna-Filho, G, Korbonits, M, Mohnike, K, Bryce, J, Ahmed, S F, Voet, B, Blankenstein, O & Claahsen-van der Grinten, H L 2022, ' Treatment of congenital adrenal hyperplasia in children aged 0-3 years : A retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure ', European Journal of Endocrinology, vol. 187, no. 2, pp. 587-596 . https://doi.org/10.1530/EJE-21-1085
European Journal of Endocrinology, 187(2), 587-596. BioScientifica Ltd.
Neumann, U, van der Linde, A, Krone, R E, Krone, N P, Güven, A, Güran, T, Elsedfy, H, Poyrazoglu, S, Darendeliler, F, Bachega, T A S S, Balsamo, A, Hannema, S E, Birkebaek, N, Vieites, A, Thankamony, A, Cools, M, Milenkovic, T, Bonfig, W, Costa, E C, Atapattu, N, de Vries, L, Guaragna-Filho, G, Korbonits, M, Mohnike, K, Bryce, J, Ahmed, S F, Voet, B, Blankenstein, O & Claahsen-van der Grinten, H L 2022, ' Treatment of congenital adrenal hyperplasia in children aged 0-3 years : a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure ', European Journal of Endocrinology, vol. 186, no. 5, pp. 587-596 . https://doi.org/10.1530/EJE-21-1085
EUROPEAN JOURNAL OF ENDOCRINOLOGY
European Journal of Endocrinology, 186(5), 587-596. Bioscientifica Ltd
European Journal of Endocrinology, 186, 587-596
European Journal of Endocrinology, 186, 5, pp. 587-596
Objectives International guidelines recommend additional salt supplementation during infancy in classic congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency. The influence of corticoid medication and growth has not been assessed. Aim
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::441ad2130e4f0b1b276b3c55b7ed5d97
http://www.scopus.com/inward/record.url?scp=85128487416&partnerID=8YFLogxK
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3
Management of Acute Adrenal Insufficiency-Related Adverse Events in Children with Congenital Adrenal Hyperplasia: Results of an International Survey of Specialist Centres
Autor: Salma Rashid Ali, Jillian Bryce, Nils P. Krone, Hedi L. Claahsen-van der Grinten, S.Faisal Ahmed
Publikováno v: Hormone Research in Paediatrics, 95, 363-373
Hormone Research in Paediatrics, 95, 4, pp. 363-373
Introduction: There is wide variation in reported rates of acute adrenal insufficiency (AI)-related adverse events (sick day episodes and adrenal crises) between centres. This study aimed to evaluate the level of consensus on criteria considered esse
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff0755afd4f76f591473d05d600e4dc9
https://doi.org/10.1159/000525075
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5
Adrenal insufficiency
Autor: Eystein S Husebye, Simon H Pearce, Nils P Krone, Olle Kämpe
Publikováno v: The Lancet. 397:613-629
Adrenal insufficiency can arise from a primary adrenal disorder, secondary to adrenocorticotropic hormone deficiency, or by suppression of adrenocorticotropic hormone by exogenous glucocorticoid or opioid medications. Hallmark clinical features are u
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a43e81589de823724865f0fff85b739
https://doi.org/10.1016/s0140-6736(21)00136-7
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6
Genetics of Congenital Adrenal Hyperplasia
Autor: Nils P. Krone
Congenital adrenal hyperplasia (CAH) comprises a group of autosomal recessive disorders causing impaired cortisol biosynthesis. The phenotypic expression of different CAH forms depends on the underlying enzyme deficiency. Steroid 21-hydroxylase (CYP2
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2d9c4b147e8505dee045f5a74a68fc85
https://doi.org/10.1093/med/9780198870197.003.0104
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7
Congenital adrenal hyperplasia
Autor: Nils P. Krone, Ieuan A. Hughes
Congenital adrenal hyperplasia (CAH) results from enzymatic defects in the pathways of adrenal steroidogenesis, with over 90% of cases being due to 21-hydroxylase deficiency caused by autosomal recessive mutations in the CYP21A2 gene. Management requ
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2ce5aea799a0b1fe146a80e49f57c872
https://doi.org/10.1093/med/9780198746690.003.0250
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