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A step-by-step, multidisciplinary strategy to maximize the yield of genetic testing in pediatric patients with chronic kidney diseases.
Pediatr Nephrol. 2024 Feb 6. doi: 10.1007/s00467-024-06299-4. Online ahead of print.
Pediatr Nephrol. 2024.
PMID: 38316682
Severe parental phenotype associates with hypertension in children with ADPKD.
Demoulin N, Van Regemorter E, Dahan K, Hougardy C, Morelle J, Gillion V, Ranguelov N, Godefroid N.
Demoulin N, et al. Among authors: hougardy c.
Pediatr Nephrol. 2023 Aug;38(8):2733-2740. doi: 10.1007/s00467-022-05870-1. Epub 2023 Jan 16.
Pediatr Nephrol. 2023.
PMID: 36645493
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PKD1 mosaicism associated with severe renal, hepatic, and vascular phenotype.
Van Regemorter E, Dahan K, Hougardy C, Ciccarelli O, Kanaan N, Pirson Y, Demoulin N.
Van Regemorter E, et al. Among authors: hougardy c.
Clin Nephrol. 2022 Dec;98(6):296-300. doi: 10.5414/CN110704.
Clin Nephrol. 2022.
PMID: 36278297
Review.
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Erythritol Availability in Bovine, Murine and Human Models Highlights a Potential Role for the Host Aldose Reductase during Brucella Infection.
Barbier T, Machelart A, Zúñiga-Ripa A, Plovier H, Hougardy C, Lobet E, Willemart K, Muraille E, De Bolle X, Van Schaftingen E, Moriyón I, Letesson JJ.
Barbier T, et al. Among authors: hougardy c.
Front Microbiol. 2017 Jun 13;8:1088. doi: 10.3389/fmicb.2017.01088. eCollection 2017.
Front Microbiol. 2017.
PMID: 28659902
Free PMC article.
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