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Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression.
Published in:
European Journal of Pediatrics, 2012, v. 171, n. 3, p. 447, doi. 10.1007/s00431-011-1557-8
By:
- Bruyn, Gwendolyn;
- Casaer, Alexandra;
- Devolder, Katrien;
- Acker, Geert;
- Logghe, Hilde;
- Devriendt, Koen;
- Cornette, Luc
Publication type:
Article
Introduction of Hypothermia for Neonates with Perinatal Asphyxia in the Netherlands and Flanders.
Published in:
Neonatology (16617800), 2013, v. 104, n. 1, p. 15, doi. 10.1159/000348823
By:
- Groenendaal, Floris;
- Casaer, alexandra;
- Dijkman, Koen P.;
- Gavilanes, antonio W.D.;
- de Haan, Timo R.;
- ter Horst, Henk J.;
- Laroche, Sabine;
- Naulaers, Gunnar;
- Rijken, Monique;
- van Straaten, Henrica L.M.;
- Steiner, Katerina;
- Swarte, Renate M.C.;
- Zecic, alexandra;
- Zonnenberg, Inge a.
Publication type:
Article
Cranial ultrasound and MRI: complementary or not in the diagnostic assessment of children with congenital CMV infection?
Published in:
European Journal of Pediatrics, 2022, v. 181, n. 3, p. 911, doi. 10.1007/s00431-021-04273-y
By:
- Keymeulen, Annelies;
- De Leenheer, Els;
- Casaer, Alexandra;
- Cossey, Veerle;
- Herregods, Nele;
- Laroche, Sabine;
- Mahieu, Ludo;
- Van Mol, Christine;
- Vanhaesebrouck, Sophie;
- Walle, Caroline Vande;
- Smets, Koenraad
Publication type:
Article
Clinical presentation and spectrum of neuroimaging findings in newborn infants with incontinentia pigmenti.
Published in:
2016
By:
- Soltirovska Salamon, Aneta;
- Lichtenbelt, Klaske;
- Cowan, Frances M;
- Casaer, Alexandra;
- Dudink, Jeroen;
- Dereymaeker, Anneleen;
- Paro-Panjan, Darja;
- Groenendaal, Floris;
- Vries, Linda S;
- de Vries, Linda S
Publication type:
journal article
Diagnosing Autism Spectrum Disorder in Toddlers Born Very Preterm: Estimated Prevalence and Usefulness of Screeners and the Autism Diagnostic Observation Schedule (ADOS).
Published in:
Journal of Autism & Developmental Disorders, 2021, v. 51, n. 5, p. 1508, doi. 10.1007/s10803-020-04573-6
By:
- Vermeirsch, Julie;
- Verhaeghe, Liedewij;
- Casaer, Alexandra;
- Faes, Fran;
- Oostra, Ann;
- Roeyers, Herbert
Publication type:
Article

Found: 5

Hydrops fetalis and pulmonary lymphangiectasia due to FOXC2 mutation: an autosomal dominant hereditary lymphedema syndrome with variable expression.

Introduction of Hypothermia for Neonates with Perinatal Asphyxia in the Netherlands and Flanders.

Cranial ultrasound and MRI: complementary or not in the diagnostic assessment of children with congenital CMV infection?

Clinical presentation and spectrum of neuroimaging findings in newborn infants with incontinentia pigmenti.

Diagnosing Autism Spectrum Disorder in Toddlers Born Very Preterm: Estimated Prevalence and Usefulness of Screeners and the Autism Diagnostic Observation Schedule (ADOS).