Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Ulrike, Steuerwald"'
Autor:
Clara Amalie Gade Timmermann, Esben Budtz-Jørgensen, Tina Kold Jensen, Christa Elyse Osuna, Maria Skaalum Petersen, Ulrike Steuerwald, Flemming Nielsen, Lars K. Poulsen, Pál Weihe, Philippe Grandjean
Publikováno v:
Journal of Immunotoxicology, Vol 14, Iss 1, Pp 39-49 (2017)
Perfluoroalkyl substances (PFASs) are highly persistent chemicals that might be associated with asthma and allergy, but the associations remain unclear. Therefore, this study examined whether pre- and postnatal PFAS exposure was associated with child
Externí odkaz:
https://doaj.org/article/1a48f6585ddf4853a29ae8ca629ad74d
Autor:
Terry G. J. Derks MD, PhD, Antal Nemeth MD, PhD, Katrin Adrian MD, PhD, Henrik Arnell MD, PhD, Ann Bech Roskjær RD, Eva Beijer MD, Sebastiaan te Boekhorst BICT, Carina Heidenborg RD, Marcus Landgren MD ,PhD, Mikael Nilsson RD, Domniki Papadopoulou MD, Katalin Ross RD, Elisabeth Sjöqvist RD, U Stachelhaus-Theimer MD, Ulrike Steuerwald MD, Carl-Johan Törnhage MD, PhD, David A. Weinstein MD, PhD
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 5 (2017)
The third international meeting of the Scandinavian Association for Glycogen Storage Disease focused on hepatic glycogen storage disease and was organized for health-care professionals, patient representatives, and representatives from the industry.
Externí odkaz:
https://doaj.org/article/f081dbb83c644ac6b24016df1062e2d6
Autor:
Kieran Clarke, Jeroen A. L. Jeneson, Ulrike Steuerwald, Caroline J. van Der Schaaf, Irene J. Hoogeveen, Johannes H. van der Hoeven, Terry G J Derks, Riemer J K Vegter, Anita Sibeijn-Kuiper, M. Rebecca Heiner-Fokkema, Pete J. Cox, Foekje de Boer, Willemijn F. Boonstra
Publikováno v:
Journal of Inherited Metabolic Disease
Journal of Inherited Metabolic Disease, 44(1), 226-239. SPRINGER
Journal of Inherited Metabolic Disease, 44(1), 226-239. SPRINGER
Glycogen storage disease type IIIa (GSDIIIa) is an inborn error of carbohydrate metabolism caused by a debranching enzyme deficiency. A subgroup of GSDIIIa patients develops severe myopathy. The purpose of this study was to investigate whether acute
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d95f29e4a4f463ab5e8357e64fbea93
https://research.rug.nl/en/publications/bc84bb86-6b20-4e80-b93d-4a9c06728a65
https://research.rug.nl/en/publications/bc84bb86-6b20-4e80-b93d-4a9c06728a65
Autor:
Ulrike Steuerwald, Lars Køber, Olav W. Nielsen, Høgni D Joensen, Steen Holger Hansen, Allan M. Lund, Morten Duno, Jan Audun Rasmussen
Publikováno v:
Journal of Inherited Metabolic Disease. 43:290-296
Primary carnitine deficiency (PCD) affects fatty acid oxidation and is associated with cardiomyopathy and cardiac arrhythmia, but the risk of sudden death in PCD is unknown. The Faroe Islands have a high prevalence of PCD, 1:300. This study systemati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45a5d34e9f145a54bd9c2bd06a709f87
https://doi.org/10.1002/jimd.12158
https://doi.org/10.1002/jimd.12158
Autor:
Ulrike Steuerwald, Allan M. Lund, Jan Rasmussen, Nils Janzen, David M. Hougaard, Nicola Longo
Publikováno v:
International Journal of Neonatal Screening, Vol 3, Iss 1, p 1 (2017)
Primary carnitine deficiency is caused by the defective OCTN2 carnitine transporter encoded by the SLC22A5 gene. A lack of carnitine impairs fatty acid oxidation resulting in hypoketotic hypoglycemia, hepatic encephalopathy, skeletal and cardiac myop
Externí odkaz:
https://doaj.org/article/fee05de143f843f29c98e62a5d39bd24
Publikováno v:
Pediatric Clinics of North America. 65:247-265
Although hyperinsulinism is the predominant inherited cause of hypoglycemia in the newborn period, inborn errors of metabolism are the primary etiologies after 1 month of age. Disorders of carbohydrate metabolism often present with hypoglycemia when
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc5dce0d3ec084b8092dfbb3ee73f392
https://doi.org/10.1016/j.pcl.2017.11.005
https://doi.org/10.1016/j.pcl.2017.11.005
Autor:
Damaskini Valvi, Ulrike Steuerwald, Youssef Oulhote, Kristian S. Bjerve, Pal Weihe, Christine Dalgård, Philippe Grandjean
Publikováno v:
Environment International, Vol 107, Iss, Pp 205-215 (2017)
Valvi, D, Oulhote, Y, Weihe, P, Dalgård, C, Bjerve, K S, Steuerwald, U & Grandjean, P 2017, ' Gestational diabetes and offspring birth size at elevated environmental pollutant exposures ', Environment International, vol. 107, pp. 205-215 . https://doi.org/10.1016/j.envint.2017.07.016
Valvi, D, Oulhote, Y, Weihe, P, Dalgård, C, Bjerve, K S, Steuerwald, U & Grandjean, P 2017, ' Gestational diabetes and offspring birth size at elevated environmental pollutant exposures ', Environment International, vol. 107, pp. 205-215 . https://doi.org/10.1016/j.envint.2017.07.016
BACKGROUND: Gestational diabetes mellitus (GDM) is associated with increased availability of glucose and macronutrients in fetal circulation and macrosomia. Therefore, the role of GDM in the association between metabolism-disrupting chemicals and bir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f87a7271c74c75e5816d048dba71e3ab
https://doi.org/10.1016/j.envint.2017.07.016
https://doi.org/10.1016/j.envint.2017.07.016
Publikováno v:
Oulhote, Y, Steuerwald, U, Debes, F, Weihe, P & Grandjean, P 2016, ' Behavioral difficulties in 7-year old children in relation to developmental exposure to perfluorinated alkyl substances ', Environment International, vol. 97, pp. 237-245 . https://doi.org/10.1016/j.envint.2016.09.015
Environment International, Vol 97, Iss, Pp 237-245 (2016)
Environment International, Vol 97, Iss, Pp 237-245 (2016)
Background: Perfluorinated alkyl substances (PFAS) are suspected endocrine disruptors that are highly persistent and neurotoxic in animals. Human epidemiological studies of exposure-related deviations of children's behaviors are sparse. We assessed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cad78cf43e79b4954289ea5dfdbfc060
https://doi.org/10.1016/j.envint.2016.09.015
https://doi.org/10.1016/j.envint.2016.09.015
Publikováno v:
Pediatric clinics of North America. 65(2)
Although hyperinsulinism is the predominant inherited cause of hypoglycemia in the newborn period, inborn errors of metabolism are the primary etiologies after 1 month of age. Disorders of carbohydrate metabolism often present with hypoglycemia when
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9ad79047233a43c2d736f42c256504d3
https://pubmed.ncbi.nlm.nih.gov/29502912
https://pubmed.ncbi.nlm.nih.gov/29502912
Autor:
Daniela Zugna, John Penders, Lorenzo Richiardi, Claudia Galassi, Agnes M.M. Sonnenschein-van der Voort, Ulrike Steuerwald, Isabella Annesi-Maesano, Sofia Correia, Henrique Barros, Francesco Forastiere, Mikel Basterrechea, Nour Baïz, Pernille Stemann Larsen, Maria Skaalum Petersen, Jordi Sunyer, Martine Vrijheid, Maria Pia Fantini, Anne-Marie Nybo Andersen, Monique Mommers, Hazel Inskip, Ana Esplugues, Franca Rusconi, Daniela Porta, Mireia Gascon, Maties Torrent, Davide Gori, Katharine C. Pike, Liesbeth Duijts
Publikováno v:
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY
r-FISABIO. Repositorio Institucional de Producción Científica
instname
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
International Journal of Epidemiology, 44(1), 199-208. Oxford University Press
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
r-FISABIO. Repositorio Institucional de Producción Científica
instname
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
International Journal of Epidemiology, 44(1), 199-208. Oxford University Press
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Background: Evidence on the effect of maternal complications in pregnancy on wheezing in offspring is still insufficient. Methods: A pooled analysis was performed on individual participant data from fourteen European birth cohorts to assess the relat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ee6a6c9f6aa0b4b02b2aad0e4eb826d
https://doi.org/10.1093/ije/dyu260
https://doi.org/10.1093/ije/dyu260