Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Maria Halldin"'
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:
Rasmus Stenlid, Hannes Manell, Rikard Seth, Sara Y. Cerenius, Azazul Chowdhury, Camilla Roa Cortés, Isabelle Nyqvist, Thomas Lundqvist, Maria Halldin, Peter Bergsten
Publikováno v:
Metabolites, Vol 13, Iss 7, p 780 (2023)
(1) Background: Deficiencies of mitochondrial fatty acid oxidation (FAO) define a subgroup of inborn errors of metabolism, with medium-chain acyl-CoA dehydrogenase deficiency (MCAD) and very long-chain acyl-CoA dehydrogenase deficiency (VLCAD) being
Externí odkaz:
https://doaj.org/article/cdf4d614c37a4ae19b2cf545f02add49
Autor:
Bergsten, Rasmus Stenlid, Hannes Manell, Rikard Seth, Sara Y. Cerenius, Azazul Chowdhury, Camilla Roa Cortés, Isabelle Nyqvist, Thomas Lundqvist, Maria Halldin, Peter
Publikováno v:
Metabolites; Volume 13; Issue 7; Pages: 780
(1) Background: Deficiencies of mitochondrial fatty acid oxidation (FAO) define a subgroup of inborn errors of metabolism, with medium-chain acyl-CoA dehydrogenase deficiency (MCAD) and very long-chain acyl-CoA dehydrogenase deficiency (VLCAD) being
Autor:
Georgios Karamanis, Thomas Frisell, Mats Holmberg, Maria Halldin, Sara Sylvén, Alkistis Skalkidou, Fotios C. Papadopoulos
Publikováno v:
JAMA Pediatrics.
This cohort study examines the incidence of idiopathic intracranial hypertension (IHH) among individuals in Sweden undergoing gonadotropin-releasing hormone analogue (GnRHa) treatment for gender dysphoria.
Autor:
Peter Bergsten, Charlotte Bieneck Haglind, Rasmus Stenlid, Maria Halldin, Azazul Islam Chowdhury, Jing Cen, Anna Nordenström, Hannes Manell, David Olsson
Publikováno v:
Clinical and Translational Science, Vol 15, Iss 1, Pp 182-194 (2022)
Clinical and Translational Science
Clinical and Translational Science
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 metabolism. Carnitine upta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::525120b00a089b5d702dc61a07eecb01
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-468646
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-468646
Autor:
David Olsson, Michela Barbaro, Charlotte Haglind, Maria Halldin, Svetlana Lajic, Sara Tucci, Rolf H. Zetterström, Anna Nordenström
Publikováno v:
JIMD reports. 63(2)
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 adulthood with a myopat
Autor:
Kristina Teär Fahnehjelm, Ying Liu, Charlotte Bieneck Haglind, Gerd Holmström, Anna Nordenström, Sten Andréasson, Maria Halldin, Urban Amrén, David Olsson
Publikováno v:
Acta Paediatrica. 105:1451-1460
Aim: There have been few studies on long-term electroretinographic findings in patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). This study correlated long-term electroretinographic findings with age, metabolic control and
Autor:
Jovanna Dahlgren, Nils-Östen Nilsson, Ralph Decker, Maria Halldin, Kerstin Albertsson-Wikland, Berit Kriström, Jan Gustafsson
Publikováno v:
The Journal of clinical endocrinology and metabolism. 104(3)
Context GH responsiveness guides GH dosing during the catch-up growth (CUG) period; however, little is known regarding GH dosing during the prepubertal maintenance treatment period. Objective To evaluate whether SD score (SDS) channel parallel growth
Autor:
Rasmus Stenlid, Joel Kullberg, Hannes Manell, Katharina Paulmichl, Håkan Ahlström, Anders Forslund, Peter Bergsten, Levon Manukyan, Daniel Weghuber, Fanni Zsoldos, Maria Halldin
Publikováno v:
The Journal of clinical endocrinology and metabolism. 103(8)
Context Dipeptidyl peptidase 4 (DPP-4) metabolizes glucagon-like peptide-1 (GLP-1), and increased DPP4 levels are associated with obesity and visceral adiposity in adults. Objective Investigating DPP-4 levels in adolescents and their association with