Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Maria Van Dyck"'
Autor:
Evelien Snauwaert, Stefanie De Buyser, An Desloovere, Wim Van Biesen, Ann Raes, Griet Glorieux, Laure Collard, Koen Van Hoeck, Maria Van Dyck, Nathalie Godefroid, Johan Vande Walle, Sunny Eloot
Publikováno v:
Toxins, Vol 16, Iss 8, p 349 (2024)
To promote improved trial design in upcoming randomized clinical trials in childhood chronic kidney disease (CKD), insight in the within- and inter-patient variability of uremic toxins with its nutritional, treatment- and patient-related confounding
Externí odkaz:
https://doaj.org/article/0bfac0465d854f04b277e2546986042d
Autor:
Amina El Amouri, Evelien Snauwaert, Aurélie Foulon, Charlotte Vande Moortel, Maria Van Dyck, Koen Van Hoeck, Nathalie Godefroid, Griet Glorieux, Wim Van Biesen, Johan Vande Walle, Ann Raes, Sunny Eloot
Publikováno v:
Toxins, Vol 13, Iss 3, p 225 (2021)
Imbalanced colonic microbial metabolism plays a pivotal role in generating protein-bound uraemic toxins (PBUTs), which accumulate with deteriorating kidney function and contribute to the uraemic burden of children with chronic kidney disease (CKD). D
Externí odkaz:
https://doaj.org/article/088ebab6d0c94d5ea0db448af99f9a28
Autor:
Evelien Snauwaert, Els Holvoet, Wim Van Biesen, Ann Raes, Griet Glorieux, Johan Vande Walle, Sanne Roels, Raymond Vanholder, Varvara Askiti, Karolis Azukaitis, Aysun Bayazit, Nur Canpolat, Michel Fischbach, Nathalie Godefroid, Saoussen Krid, Mieczyslaw Litwin, Lukasz Obrycki, Fabio Paglialonga, Bruno Ranchin, Charlotte Samaille, Franz Schaefer, Claus Peter Schmitt, Brankica Spasojevic, Constantinos J. Stefanidis, Maria Van Dyck, Koen Van Hoeck, Laure Collard, Sunny Eloot, Rukshana Shroff
Publikováno v:
Toxins, Vol 11, Iss 4, p 235 (2019)
Protein-bound uremic toxins (PBUTs) play a role in the multisystem disease that children on hemodialysis (HD) are facing, but little is known about their levels and protein binding (%PB). In this study, we evaluated the levels and %PB of six PBUTs cr
Externí odkaz:
https://doaj.org/article/49bdd5457df04f20994d3eb31259d206
De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in females
Autor:
Eugênia Ribeiro Valadares, Kaitlyn M Shen, Sérgio D.J. Pena, Alanna Strong, Dong Li, Natália D. Linhares, David Cassiman, Elaine H. Zackai, Deindl Philipp, Penny Chow, Arupa Ganguly, Jaak Jaeken, Samantha A. Schrier Vergano, Maria Van Dyck, Tatjana Bierhals, Tiancheng Wang, Elizabeth J. Bhoj, Hakon Hakonarson, Anne Hing, Tasja Scholz
Publikováno v:
Genetics in Medicine. 23:637-644
Purpose Hardikar syndrome (MIM 612726) is a rare multiple congenital anomaly syndrome characterized by facial clefting, pigmentary retinopathy, biliary anomalies, and intestinal malrotation, but with preserved cognition. Only four patients have been
Autor:
Ilona Zagozdzon, Nina Battelino, Jaap W. Groothoff, Thomas Neuhaus, Heather Maxwell, Polina Miteva, Maria Van Dyck, Lars Pape, Rezan Topaloglu, Maria S. Molchanova, Marjolein Bonthuis, Karlien Cransberg, Gabriel Kolvek, Ana Rita Sandes, Anna Bjerre, Elisa Ylinen, Sergey Baiko, Gema Ariceta, György Reusz, Jérôme Harambat, Caroline Rousset-Rouviere, Kitty J. Jager
Publikováno v:
Transplantation, 104(1), 137-144. Lippincott Williams and Wilkins
Transplantation
Transplantation, Lippincott, Williams & Wilkins, 2020, 104 (1), pp.137-144. ⟨10.1097/tp.0000000000002726⟩
Transplantation, 104, 137-144. Lippincott Williams & Wilkins
Transplantation
Transplantation, Lippincott, Williams & Wilkins, 2020, 104 (1), pp.137-144. ⟨10.1097/tp.0000000000002726⟩
Transplantation, 104, 137-144. Lippincott Williams & Wilkins
BACKGROUND: Improved management of growth impairment might have resulted in less growth retardation after pediatric kidney transplantation (KT) over time. We aimed to analyze recent longitudinal growth data after KT in comparison to previous eras, it
Autor:
Marleen Renard, Gert De Hertogh, Lambertus P. van den Heuvel, Maria Van Dyck, Mohamed A. Elmonem, Koenraad Veys, Fanny Oliveira Arcolino, Elena Levtchenko, Francesca Diomedi-Camassei, Maria Chiara Benedetti
Publikováno v:
American Journal of Transplantation, 18, 11, pp. 2823-2828
American Journal of Transplantation, 18, 2823-2828
American Journal of Transplantation, 18, 2823-2828
Cystinosis is an autosomal recessive lysosomal storage disorder characterized by the defective transport of the amino acid cystine out of the lysosome due to a deficiency of cystinosin, the lysosomal cystine transporter. Patients have lysosomal cysti
Autor:
Griet Glorieux, Sunny Eloot, Wim Van Biesen, Aurélie Foulon, Maria Van Dyck, Koen Van Hoeck, Evelien Snauwaert, Charlotte Vande Moortel, Johan Vande Walle, Ann Raes, Amina El Amouri, Nathalie Godefroid
Publikováno v:
Toxins
Volume 13
Issue 3
Toxins, Vol. 13, no.3, p. 225 (2021)
Toxins, Vol 13, Iss 225, p 225 (2021)
TOXINS
Volume 13
Issue 3
Toxins, Vol. 13, no.3, p. 225 (2021)
Toxins, Vol 13, Iss 225, p 225 (2021)
TOXINS
Imbalanced colonic microbial metabolism plays a pivotal role in generating protein-bound uraemic toxins (PBUTs), which accumulate with deteriorating kidney function and contribute to the uraemic burden of children with chronic kidney disease (CKD). D
De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in females
Autor:
Dong, Li, Alanna, Strong, Kaitlyn M, Shen, David, Cassiman, Maria, Van Dyck, Natalia Duarte, Linhares, Eugenia Ribeiro, Valadares, Tiancheng, Wang, Sergio D J, Pena, Jaak, Jaeken, Samantha, Vergano, Elaine, Zackai, Anne, Hing, Penny, Chow, Arupa, Ganguly, Tasja, Scholz, Tatjana, Bierhals, Deindl, Philipp, Hakon, Hakonarson, Elizabeth, Bhoj
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 23(4)
Hardikar syndrome (MIM 612726) is a rare multiple congenital anomaly syndrome characterized by facial clefting, pigmentary retinopathy, biliary anomalies, and intestinal malrotation, but with preserved cognition. Only four patients have been reported
Autor:
Aurélie Foulon, Johan Vande Walle, Evelien Snauwaert, Amina El Amouri, Griet Glorieux, Sunny Eloot, Nathalie Godefroid, Charlotte Vande Moortel, Wim Van Biesen, Maria Van Dyck, Koen Van Hoeck, Ann Raes
Publikováno v:
Pediatric nephrology, Vol. 36, no. 6, p. 1589-1595 (2021)
Pediatric nephrology
Pediatric nephrology
Background Chronic kidney disease (CKD) in children is a pro-inflammatory condition leading to a high morbidity and mortality. Accumulation of organic metabolic waste products, coined as uraemic toxins, parallels kidney function decline. Several of t
Autor:
Mirian C. H. Janssen, Elena Levtchenko, Giusi Prencipe, Lambertus P. van den Heuvel, Maria Van Dyck, Koenraad Veys, Mohamed A. Elmonem, Elisabeth A.M. Cornelissen, Katharina Hohenfellner
Publikováno v:
Journal of the American Society of Nephrology, 31, 1092-1106
J Am Soc Nephrol
Journal of the American Society of Nephrology, 31, 5, pp. 1092-1106
J Am Soc Nephrol
Journal of the American Society of Nephrology, 31, 5, pp. 1092-1106
BACKGROUND: Nephropathic cystinosis, a hereditary lysosomal storage disorder caused by dysfunction of the lysosomal cotransporter cystinosin, leads to cystine accumulation and cellular damage in various organs, particularly in the kidney. Close thera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfb6a54d8e9ae7730953eacb0fb961dd
http://hdl.handle.net/2066/219535
http://hdl.handle.net/2066/219535