Zobrazeno 1 - 10
of 175
pro vyhledávání: '"Anna, Nordenström"'
Autor:
Tim Cheetham, Sukran Poyrazoglu, Justin H Davies, S Faisal Ahmed, Jillian Bryce, Anna Nordenström, Angela K Lucas-Herald, Paul-Martin Holterhus, Marcio Lopes Miranda, Stuart O’Toole, Eduardo Corrêa Costa, Kathryn Scougall, Federico Baronio, Rachel L Boal, Jose Roberto Castera, Sebastián Castro, Feyza Darendeliler, Mirjam Dirlewanger, Gabriella Gazdagh, Evgenia Globa, Gil Guerra-Junior, Tulay Guran, Gloria Herrmann, Ahsen Karagözlü Akgül, Renata Markosyan, Kenneth McElreavey, Gianni Russo, Valerie Schwitzgebel, Marianna Stancampiano, Michael Steigert
Publikováno v:
World Journal of Pediatric Surgery, Vol 6, Iss 4 (2023)
Background Complications are frequently reported after hypospadias repair and there is a need to understand the factors that influence their occurrence.Methods Data from boys with hypospadias born between 2000 and 2020 were obtained from the Internat
Externí odkaz:
https://doaj.org/article/b2a11fe3b8a642f185956951b5a23a49
Autor:
Susan M Webb, Jette Kristensen, Anna Nordenström, Diana Vitali, Vincent Amodru, Lenja Katharina Wiehe, Matt Bolz-Johnson
Publikováno v:
Endocrine Connections, Vol 11, Iss 12, Pp 1-9 (2022)
Patient journeys are instruments developed by EURORDIS, The Voice of Rare Disease Patients in Europe, to collect patients’ experiences; they may identify gaps and areas deserving improvement, as well as elements positively considere d by affected p
Externí odkaz:
https://doaj.org/article/a90c659a37464c79a80cb0e258b0cefd
Publikováno v:
Endocrinology and Metabolism, Vol 37, Iss 4, Pp 587-598 (2022)
A plethora of negative long-term outcomes have been associated with congenital adrenal hyperplasia (CAH). The causes are multiple and involve supra-physiological gluco- and mineralocorticoid replacement, excess adrenal androgens both intrauterine and
Externí odkaz:
https://doaj.org/article/6cde7943b78b4620946152ada56b50ff
Autor:
Anna Nordenström, Henrik Falhammar
Publikováno v:
The Lancet Regional Health. Europe, Vol 28, Iss , Pp 100616- (2023)
Externí odkaz:
https://doaj.org/article/06e69b18c8e04e0e88f74b516e5483e0
Autor:
David Olsson, Michela Barbaro, Charlotte Haglind, Maria Halldin, Svetlana Lajic, Sara Tucci, Rolf H. Zetterström, Anna Nordenström
Publikováno v:
JIMD Reports, Vol 63, Iss 2, Pp 181-190 (2022)
Abstract Very long‐chain acyl‐CoA dehydrogenase deficiency (VLCADD) is a recessive disorder of fatty acid beta‐oxidation with variable phenotype. Patients may present during the neonatal period with lethal multi‐organ failure or during adulth
Externí odkaz:
https://doaj.org/article/8328a7b424524de6862a3d3efb445668
Autor:
Rasmus Stenlid, David Olsson, Jing Cen, Hannes Manell, Charlotte Haglind, Azazul Islam Chowdhury, Peter Bergsten, Anna Nordenström, Maria Halldin
Publikováno v:
Clinical and Translational Science, Vol 15, Iss 1, Pp 182-194 (2022)
Abstract Inborn errors of mitochondrial fatty acid oxidation (FAO), such as medium‐chain acyl‐CoA dehydrogenase deficiency (MCAD) and very long‐chain acyl‐CoA dehydrogenase deficiency (VLCAD) affects cellular function and whole‐body metabol
Externí odkaz:
https://doaj.org/article/db6476faf15045b5b713c69b949a33a7
Autor:
Hanna Björlin Avdic, Agnieszka Butwicka, Anna Nordenström, Catarina Almqvist, Agneta Nordenskjöld, Hedvig Engberg, Louise Frisén
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-9 (2021)
Abstract Background Turner syndrome is the result of the partial or complete absence of an X chromosome in phenotypic girls. This can cause an array of medical and developmental difficulties. The intelligence quotient in females with Turner syndrome
Externí odkaz:
https://doaj.org/article/405e4349ed4a461ca509a155cf522178
Publikováno v:
Endocrine Practice. 29:266-271
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:
Marion Rapp, Esther Mueller-Godeffroy, Peter Lee, Robert Roehle, Baudewijntje P. C. Kreukels, Birgit Köhler, Anna Nordenström, Claire Bouvattier, Ute Thyen, on behalf of the dsd-LIFE group
Publikováno v:
Health and Quality of Life Outcomes, Vol 16, Iss 1, Pp 1-13 (2018)
Abstract Background Previous studies in quality of life (QOL) in individuals with disorders/differences of sex development (DSD) have been restricted to subpopulations of the condition. We describe QOL in adult persons with DSD compared to country sp
Externí odkaz:
https://doaj.org/article/4303d0e6c2af44deb15efdb8c5c7b7f8