Zobrazeno 1 - 10
of 798
pro vyhledávání: '"Wim, Van Hul"'
Autor:
Neus Roca-Ayats, Iago Maceda, Carlos David Bruque, Núria Martínez-Gil, Natàlia Garcia-Giralt, Mónica Cozar, Leonardo Mellibovsky, Wim Van Hul, Oscar Lao, Daniel Grinberg, Susanna Balcells
Publikováno v:
Human Genomics, Vol 18, Iss 1, Pp 1-13 (2024)
Abstract Background The human lineage has undergone a postcranial skeleton gracilization (i.e. lower bone mass and strength relative to body size) compared to other primates and archaic populations such as the Neanderthals. This gracilization has bee
Externí odkaz:
https://doaj.org/article/2a5c385622cf4df6aa552691ff00a630
Autor:
Evelien Van Dijck, Sara Diels, Erik Fransen, Tycho Canter Cremers, An Verrijken, Eveline Dirinck, Alexander Hoischen, Geert Vandeweyer, Wim Vanden Berghe, Luc Van Gaal, Sven Francque, Wim Van Hul
Publikováno v:
Antioxidants, Vol 13, Iss 9, p 1051 (2024)
The paraoxonase (PON) gene family (including PON1, PON2, and PON3), is known for its anti-oxidative and anti-inflammatory properties, protecting against metabolic diseases such as obesity and metabolic dysfunction-associated steatotic liver disease (
Externí odkaz:
https://doaj.org/article/3610f4d5206345fe9f8499759c900757
Autor:
Claudia Theys, Tineke Vanderhaeghen, Evelien Van Dijck, Cedric Peleman, Anne Scheepers, Joe Ibrahim, Ligia Mateiu, Steven Timmermans, Tom Vanden Berghe, Sven M. Francque, Wim Van Hul, Claude Libert, Wim Vanden Berghe
Publikováno v:
Frontiers in Molecular Medicine, Vol 3 (2024)
Metabolic Dysfunction Associated Steatotic Liver Disease (MASLD) is a growing epidemic with an estimated prevalence of 20%–30% in Europe and the most common cause of chronic liver disease worldwide. The onset and progression of MASLD are orchestrat
Externí odkaz:
https://doaj.org/article/949581703c6a48e18ffca39d01ec79c1
Autor:
Liza Das, DM, Vandana Dhiman, PhD, Pinaki Dutta, DM, Ashwani Sood, DNB, Mahesh Prakash, MD, Simran Kaur, MSc, Ellen Steenackers, BSc, Gretl Hendrickx, PhD, Devi Dayal, MD, Wim Van Hul, PhD, Sanjay Kumar Bhadada, DM
Publikováno v:
AACE Clinical Case Reports, Vol 8, Iss 2, Pp 58-64 (2022)
Background: Camurati-Engelmann disease (CED) is a rare bone dysplasia characterized by diffuse diaphyseal osteosclerosis. Skull base involvement in CED can result in hypopituitarism but is seldom reported. Our objective was to report a patient with a
Externí odkaz:
https://doaj.org/article/f3ebae3857834778b4b43c7af47b0c1d
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/8dda9061f9b5434ab98d1e877d513719
Publikováno v:
Frontiers in Endocrinology, Vol 13 (2022)
Externí odkaz:
https://doaj.org/article/b770f0607bb64987a2cb29c0f3da1b47
Autor:
Yentl Huybrechts, Pieter Evenepoel, Mathias Haarhaus, Etienne Cavalier, Geert Dams, Wim Van Hul, Patrick C. D’Haese, Anja Verhulst
Publikováno v:
Nutrients, Vol 15, Iss 3, p 598 (2023)
Renal osteodystrophy (ROD) is a complex and serious complication of chronic kidney disease (CKD), a major global health problem caused by loss of renal function. Currently, the gold standard to accurately diagnose ROD is based on quantitative histomo
Externí odkaz:
https://doaj.org/article/b344f9a6c8094da4b9ed635386fd590f
Autor:
Martina Rauner, Ines Foessl, Melissa M. Formosa, Erika Kague, Vid Prijatelj, Nerea Alonso Lopez, Bodhisattwa Banerjee, Dylan Bergen, Björn Busse, Ângelo Calado, Eleni Douni, Yankel Gabet, Natalia García Giralt, Daniel Grinberg, Nika M. Lovsin, Xavier Nogues Solan, Barbara Ostanek, Nathan J. Pavlos, Fernando Rivadeneira, Ivan Soldatovic, Jeroen van de Peppel, Bram van der Eerden, Wim van Hul, Susanna Balcells, Janja Marc, Sjur Reppe, Kent Søe, David Karasik
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
The availability of large human datasets for genome-wide association studies (GWAS) and the advancement of sequencing technologies have boosted the identification of genetic variants in complex and rare diseases in the skeletal field. Yet, interpreti
Externí odkaz:
https://doaj.org/article/ab5cda7f24e346b4a98b3e682c545407
Autor:
Melissa M. Formosa, Dylan J. M. Bergen, Celia L. Gregson, Antonio Maurizi, Anders Kämpe, Natalia Garcia-Giralt, Wei Zhou, Daniel Grinberg, Diana Ovejero Crespo, M. Carola Zillikens, Graham R. Williams, J. H. Duncan Bassett, Maria Luisa Brandi, Luca Sangiorgi, Susanna Balcells, Wolfgang Högler, Wim Van Hul, Outi Mäkitie
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Genetic disorders of the skeleton encompass a diverse group of bone diseases differing in clinical characteristics, severity, incidence and molecular etiology. Of particular interest are the monogenic rare bone mass disorders, with the underlying gen
Externí odkaz:
https://doaj.org/article/c40099a1d4c14c6b8b27c337b7001312
Autor:
Sara Diels, Sander Huybreghts, Kim Van Hoorenbeeck, Guy Massa, An Verrijken, Stijn L. Verhulst, Luc F. Van Gaal, Wim Van Hul
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100656- (2020)
Genome-wide copy number surveys associated chromosome 11q11 with obesity. As this is an olfactory receptor-rich region, we hypothesize that genetic variation in olfactory receptor genes might be implicated in the pathogenesis of obesity. Multiplex Am
Externí odkaz:
https://doaj.org/article/b49b7fab0d3d4189954827a4d3cd3bb6