Phebe N Adama van Scheltema
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Explore the profile of Phebe N Adama van Scheltema including associated specialties, affiliations and a list of published articles.
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10
Citations
84
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Recent Articles
1.
Koene S, Peeters-Scholte C, Knijnenburg J, de Vries L, van Scheltema P, Meuwissen M, et al.
Am J Med Genet A
. 2020 Nov;
185(2):571-574.
PMID: 33247988
Intracerebral hemorrhage is rare in term born neonates. Besides several non-genetic risk factors, pathogenic variants in COL4A1 and COL4A2 have been described to play a role in the pathophysiology of...
2.
Duin L, Fontanella F, Groen H, van Scheltema P, Cohen-Overbeek T, Pajkrt E, et al.
Prenat Diagn
. 2019 Oct;
39(13):1235-1241.
PMID: 31659787
Objective: To develop a prediction model of postnatal renal function in fetuses with lower urinary tract obstruction (LUTO) based on fetal ultrasound parameters and amniotic fluid volume. Methods: Retrospective nationwide...
3.
de Koning M, Haak M, van Scheltema P, Peeters-Scholte C, Koopmann T, Nibbeling E, et al.
Genet Med
. 2019 Mar;
21(10):2303-2310.
PMID: 30918357
Purpose: Exome sequencing (ES) is an efficient tool to diagnose genetic disorders postnatally. Recent studies show that it may have a considerable diagnostic yield in fetuses with structural anomalies on...
4.
Fontanella F, Duin L, van Scheltema P, Cohen-Overbeek T, Pajkrt E, Bekker M, et al.
Fetal Diagn Ther
. 2018 May;
45(3):155-161.
PMID: 29772579
Objective: To investigate the best criteria for discriminating fetuses with isolated posterior urethral valves from those theoretically not eligible for fetal treatment because of complex megacystis, high chance of spontaneous...
5.
Peeters-Scholte C, van Scheltema P, Klumper F, Everwijn S, Koopmans M, Hoffer M, et al.
Brain
. 2017 Oct;
140(11):e66.
PMID: 29053797
No abstract available.
6.
Lap C, Brizot M, Pistorius L, Kramer W, Teeuwen I, Eijkemans M, et al.
Early Hum Dev
. 2016 Nov;
103:209-218.
PMID: 27825040
Objective: To determine outcome of children born with isolated gastroschisis (no extra-gastrointestinal congenital abnormalities). Study Design: International cohort study and meta-analysis. Primary Outcome: time to full enteral feeding (TFEF); secondary...
7.
van Scheltema P, Zhang A, Ball L, Steggerda S, van Wijk R, Fransen van de Putte D, et al.
Clin Case Rep
. 2015 Oct;
3(10):862-5.
PMID: 26509025
Hemolytic anemia due to GPI deficiency can be severe and life threatening during fetal life. When parents decline invasive testing, ultrasound monitoring of fetuses at risk is feasible. Intrauterine transfusion...
8.
van den Oever J, Balkassmi S, Johansson L, van Scheltema P, Suijkerbuijk R, Hoffer M, et al.
Clin Chem
. 2013 Jan;
59(4):705-9.
PMID: 23315481
Background: Noninvasive trisomy 21 detection performed by use of massively parallel sequencing is achievable with high diagnostic sensitivity and low false-positive rates. Detection of fetal trisomy 18 and 13 has...
9.
van den Oever J, Balkassmi S, Verweij E, van Iterson M, van Scheltema P, Oepkes D, et al.
Clin Chem
. 2012 Jan;
58(4):699-706.
PMID: 22278607
Background: Noninvasive fetal aneuploidy detection by use of free DNA from maternal plasma has recently been shown to be achievable by whole genome shotgun sequencing. The high-throughput next-generation sequencing platforms...
10.
Chockalingam P, Jaeggi E, Rammeloo L, Haak M, van Scheltema P, Breur J, et al.
J Rheumatol
. 2011 Nov;
38(12):2682-5.
PMID: 22089457
Objective: To study the clinical course and outcome of fetal sinus bradycardia (SB) due to maternal antibody-induced sinus node dysfunction. Methods: We reviewed the maternal, prenatal, and postnatal findings of...