Iris A L M van Rooij
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Explore the profile of Iris A L M van Rooij including associated specialties, affiliations and a list of published articles.
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86
Citations
1223
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Recent Articles
1.
Ishorst N, Holzel S, Greve C, Yilmaz O, Lindenberg T, Lambertz J, et al.
Eur J Hum Genet
. 2024 Dec;
PMID: 39702590
Orofacial clefting (OFC) is a frequent congenital anomaly and can occur either in the context of underlying syndromes or in isolation (nonsyndromic). The two common OFC phenotypes are cleft lip...
2.
Haghshenas S, Karimi K, Stevenson R, Levy M, Relator R, Kerkhof J, et al.
Am J Hum Genet
. 2024 Aug;
111(8):1643-1655.
PMID: 39089258
The term "recurrent constellations of embryonic malformations" (RCEM) is used to describe a number of multiple malformation associations that affect three or more body structures. The causes of these disorders...
3.
Hageman I, Midrio P, van der Steeg H, Jenetzky E, Iacobelli B, Morandi A, et al.
Br J Surg
. 2024 Feb;
111(2).
PMID: 38364059
No abstract available.
4.
Groen In t Woud S, van Gelder M, van Rooij I, Feitz W, Roeleveld N, Schreuder M, et al.
Nephrol Dial Transplant
. 2023 Sep;
39(3):463-472.
PMID: 37738450
Background: Congenital solitary functioning kidney (CSFK) is an anomaly predisposing to hypertension, albuminuria and chronic kidney disease. Its aetiology is complex and includes genetic and environmental factors. The role of...
5.
Bouwman F, Verhaak C, de Blaauw I, Schultze Kool L, Loo D, van Rooij I, et al.
Eur J Pediatr
. 2023 Sep;
182(11):5067-5077.
PMID: 37665335
Conclusions: Overall median HRQOL was reasonable and not significantly different from the norm sample. Parental ratings were significantly lower than their children's ratings. A quarter of the patients had an...
6.
de Beaufort C, Gorter R, Iacobelli B, Midrio P, Sloots C, Samuk I, et al.
Pediatr Surg Int
. 2023 Jul;
39(1):242.
PMID: 37507508
Purpose: To assess the number, characteristics, and functional short-, and midterm outcomes of patients with rectal atresia (RA) and stenosis (RS) in the ARM-Net registry. Methods: Patients with RA/RS were...
7.
van der Zanden L, Groen In t Woud S, van Rooij I, Quaedackers J, Steffens M, de Wall L, et al.
Front Pediatr
. 2023 May;
11:1110117.
PMID: 37187579
Introduction: Posterior urethral valves (PUV) is a congenital disorder causing an obstruction of the lower urinary tract that affects approximately 1 in 4,000 male live births. PUV is considered a...
8.
Hageman I, van Rooij I, de Blaauw I, Trajanovska M, King S
Orphanet J Rare Dis
. 2023 May;
18(1):106.
PMID: 37147718
Patient registries serve to overcome the research limitations inherent in the study of rare diseases, where patient numbers are typically small. Despite the value of real-world data collected through registries,...
9.
Hageman I, van der Steeg H, Jenetzky E, Trajanovska M, King S, de Blaauw I, et al.
J Pediatr Surg
. 2023 Apr;
58(10):1921-1928.
PMID: 37045715
Background: Registries are important in rare disease research. The Anorectal Malformation Network (ARM-Net) registry is a well-established European patient registry collecting demographic, clinical, and functional outcome data. We assessed the...
10.
Groen In t Woud S, Roeleveld N, van Rooij I, Feitz W, Schreuder M, van der Zanden L
Pediatr Nephrol
. 2023 Feb;
38(8):2631-2641.
PMID: 36808305
Background: The etiology of congenital solitary functioning kidney (CSFK) is largely unknown but likely includes various risk factors. We performed a case-control study to compare exposure to environmental and parental...