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Megalobastic anemia, infantile leukemia, and immunodeficiency caused by a novel homozygous mutation in the DHFR gene.
Kuijpers TW, de Vries ACH, van Leeuwen EM, Ermens ATAM, de Pont S, Smith DEC, Wamelink MMC, Mensenkamp AR, Nelen MR, Lango Allen H, Pals ST, Beverloo BHB, Huidekoper HH, Wagner A. Kuijpers TW, et al. Among authors: de pont s. Blood Adv. 2022 Nov 22;6(22):5829-5834. doi: 10.1182/bloodadvances.2022007233. Blood Adv. 2022. PMID: 35977078 Free PMC article. No abstract available.
Uncovering risk factors for kidney injury in children with a solitary functioning kidney.
Groen In 't Woud S, Roeleveld N, Westland R, Renkema KY, Steffens MG, Gracchi V, Lilien MR, van Wijk JAE, Feitz WFJ, Schreuder MF, van der Zanden LFM; Solitary Functioning Kidney: Aetiology and Prognosis (SOFIA) study group. Groen In 't Woud S, et al. Kidney Int. 2023 Jan;103(1):156-165. doi: 10.1016/j.kint.2022.09.028. Epub 2022 Oct 28. Kidney Int. 2023. PMID: 36374825 Free article.
Genetic and environmental factors driving congenital solitary functioning kidney.
Groen In 't Woud S, van Gelder MMHJ, van Rooij IALM, Feitz WFJ, Roeleveld N, Schreuder MF, van der Zanden LFM; SOFIA study group. Groen In 't Woud S, et al. Nephrol Dial Transplant. 2024 Feb 28;39(3):463-472. doi: 10.1093/ndt/gfad202. Nephrol Dial Transplant. 2024. PMID: 37738450 Free PMC article.
Dependability of esophageal pH monitoring data on software.
Vandenplas Y, de Pont S, Vandemaele C, Troch E, Waterschoot S, Kaufman L, Blecker U. Vandenplas Y, et al. Among authors: de pont s. J Pediatr Gastroenterol Nutr. 1996 Aug;23(2):203-4. doi: 10.1097/00005176-199608000-00021. J Pediatr Gastroenterol Nutr. 1996. PMID: 8856593 Clinical Trial. No abstract available.
12 results