Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Renate Zeevaert"'
Publikováno v:
Vaccine: X, Vol 15, Iss , Pp 100397- (2023)
In this systematic review with meta-analysis, the efficacy, effectiveness, and safety of the new GSK recombinant zoster vaccine (RZV) were assessed.Twenty three publications reporting on 14 studies were selected, including 2 pivotal RCTs in older imm
Externí odkaz:
https://doaj.org/article/0cf711738a5c4322811da829722b55d5
Autor:
Wouter M.A. Franssen, Charly Keytsman, Nastasia Marinus, Kenneth Verboven, Bert O. Eijnde, Lisa van Ryckeghem, Paul Dendale, Renate Zeevaert, Guy Massa, Dominique Hansen
Publikováno v:
Journal of Sport and Health Science, Vol 12, Iss 2, Pp 194-201 (2023)
Background: Adults with obesity may display disturbed cardiac chronotropic responses during cardiopulmonary exercise testing, which relates to poor cardiometabolic health and an increased risk for adverse cardiovascular events. It is unknown whether
Externí odkaz:
https://doaj.org/article/3ee83f3bc4e44323ad6576138e011e50
Autor:
Paul Dendale, Guy Massa, Dominique Hansen, Bert O. Eijnde, Wouter M. A. Franssen, Lisa Van Ryckeghem, Charly Keytsman, Renate Zeevaert, Kenneth Verboven, Nastasia Marinus
Publikováno v:
J Sport Health Sci
BACKGROUND: Adults with obesity may display disturbed cardiac chronotropic responses during cardiopulmonary exercise testing, which relates to poor cardiometabolic health and an increased risk for adverse cardiovascular events. It is unknown whether
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5257033af063f413c6dbf594cce808ac
https://pubmed.ncbi.nlm.nih.gov/33529767
https://pubmed.ncbi.nlm.nih.gov/33529767
Autor:
Peter Declercq, Anniek Op 't Eyndt, Anne Wijnands, Renate Zeevaert, Guy Massa, Esmiralda Bevilacqua, Inge Gys
Publikováno v:
Hormone Research in Paediatrics. 89:189-199
Background/Aims: The FreeStyle® Libre Flash Glucose Monitoring System (FGM, Abbott) measures glucose concentrations in the interstitial fluid for up to 14 days. It has been approved for use in children aged > 4 years in January 2016. Experience in c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::516005241b87f530a73c502d9c59f9be
https://doi.org/10.1159/000487361
https://doi.org/10.1159/000487361
Publikováno v:
Diabetes research and clinical practice. 152
In 2016 intermittently scanned continuous glucose monitoring (isCGM) became the first reimbursed CGM system in Belgium. Many children with type 1 diabetes (T1D) treated with multiple daily injections as well as with continuous subcutaneous insulin in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09e6a0a35cbbd5e833b87c5a7da28242
https://pubmed.ncbi.nlm.nih.gov/31121275
https://pubmed.ncbi.nlm.nih.gov/31121275
Autor:
Tomas Honzik, Antonio F. Martinez, Federic Tort, David Cassiman, Joana Correia, Christian Thiel, Simone Funke, Mari Anne Vals, Carlota Pascoal, Hossein Moravej, Katrin Õunap, Rita Barone, Marlen Hutter, Małgorzata Seroczyńska, Hudson H. Freeze, Ruqaiah Altassan, María Eugenia de la Morena-Barrio, Anna Cechova, Kimiyo Raymond, Dulce Quelhas, Carlos Ferreira, Matthijs Gert, Delphine Borgel, Trinidad Hernández-Caselles, David Coman, Romain Péanne, Paula A. Videira, Renate Zeevaert, Dorinda Marques-da-Silva, Stephanie Grunewald, Nathalie Seta, Javier Corral, Muad Bidet, Rita Francisco, Mercedes Serrano, Jaak Jaeken, Peter Witters, Manuel Schiff, Thatjana Gardeitchik, Joy Lee, Peymaneh Sarkhail, Christina Lam, Agata Fiumara, Pascale de Lonlay, Tiffany Pascreau, Sandra Brasil, Muriel Girad, Eva Morava, Dirk Lefeber, Marc C. Patterson, Marisa Giros, Donna M. Krasnewich, Jolanta Sykut-Cegielska, Vanessa dos Reis
Publikováno v:
JOURNAL OF INHERITED METABOLIC DISEASE
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Journal of Inherited Metabolic Disease, 42, 5-28
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Journal of Inherited Metabolic Disease, 42, 1, pp. 5-28
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Journal of Inherited Metabolic Disease, 42, 5-28
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Journal of Inherited Metabolic Disease, 42, 1, pp. 5-28
Contains fulltext : 203022.pdf (Publisher’s version ) (Closed access) Phosphomannomutase 2 (PMM2-CDG) is the most common congenital disorder of N-glycosylation and is caused by a deficient PMM2 activity. The clinical presentation and the onset of P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae285ac9e00a9e5f1fe580c5329ea2ab
http://hdl.handle.net/20.500.11769/360623
http://hdl.handle.net/20.500.11769/360623
Autor:
Romain Péanne, David Cassiman, Dulce Quelhas, Trinidad Hernández-Caselles, Vanessa dos Reis Ferreira, Javier Corral, Anna Cechova, Stephanie Grunewald, Dirk Lefeber, Małgorzata Seroczyńska, Marisa Giros, Matthijs Gert, Rita Barone, Joy Lee, Thatjana Gardeitchik, Christina Lam, Hossein Moravej, Donna M. Krasnewich, David Coman, Peymaneh Sarkhail, Jolanta Sykut-Cegielska, Tomas Honzik, Renate Zeevaert, Agata Fiumara, Katrin Õunap, Tiffany Pascreau, Antonio F. Martinez, Joana Correia, Simone Funke, Muad Bidet, Marlen Hutter, Muriel Girad, Eva Morava, Marc C. Patterson, Dorinda Marques-da-Silva, Ruqaiah Altassan, Carlota Pascoal, Nathalie Seta, Carlos Ferreira, Manuel Schiff, Jaak Jaeken, Pascale de Lonlay, Delphine Borgel, Mari-Anne Vals, Peter Witters, Mercedes Serrano, Paula A. Videira, María Eugenia de la Morena-Barrio, Rita Francisco, Kimiyo Raymond, Hudson H. Freeze, Federic Tort, Christian Thiel, Sandra Brasil
Publikováno v:
Journal of Inherited Metabolic Disease. 42:577-577
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f267db3dedcc3beb7e0dc6eaa122aed
https://doi.org/10.1002/jimd.12082
https://doi.org/10.1002/jimd.12082
Autor:
Jean De Schepper, Carine de Beaufort, Jaak Jaeken, Emmanuel Scalais, Renate Zeevaert, Linda De Meirleir, Laura Muino Mosquera, Michael Witsch
Publikováno v:
Acta clinica Belgica. 71(6)
OBJECTIVE AND IMPORTANCE: Phosphoglucomutase 1 (PGM1) deficiency, first described as a glycogenosis (type XIV) is also a congenital disorder of glycosylation (CDG). We want to illustrate the wide clinical spectrum of PGM1 deficiency and in particular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca598b24e46bf7a8727d28944cebc20b
https://pubmed.ncbi.nlm.nih.gov/27351072
https://pubmed.ncbi.nlm.nih.gov/27351072
Autor:
Pierre Morsomme, Mustapha Amyere, Valerie Race, Dominique Legrand, W. Annaert, Hudson H. Freeze, Jaak Jaeken, Neil R. M. Buist, Didier Demaegd, Riet Bammens, Emile Van Schaftingen, Els Schollen, Renate Zeevaert, Claire Rosnoblet, David Cheillan, Gert Matthijs, François Foulquier, Miikka Vikkula, Willy Morelle, Nathalie Guffon
Publikováno v:
The American Journal of Human Genetics. 91(1):15-26
Protein glycosylation is a complex process that depends not only on the activities of several enzymes and transporters but also on a subtle balance between vesicular Golgi trafficking, compartmental pH, and ion homeostasis. Through a combination of a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f23a40b3ffa5832f0fe301ee5f7dabc
Autor:
David Cassiman, Paul P. Van Veldhoven, Jaak Jaeken, Philippe Demaerel, Sofie Huybrechts, Marc Fransen, Rita Vos, Marijke Brams, Renate Zeevaert, Ilse Hoffman
Publikováno v:
Journal of Medical Genetics. 45:376-383
Background: Peroxisome biogenesis disorders are a clinically and genetically heterogeneous group of very severe autosomal recessive disorders caused by impaired peroxisome biogenesis. The prototype of this group of disorders is the cerebro-hepato-ren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1371b61297159e4735f1ff8f3475cb4
https://doi.org/10.1136/jmg.2007.056697
https://doi.org/10.1136/jmg.2007.056697