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The Journal of Clinical Psychiatry|June 29, 2002
Effects of antidepressant treatment on the quality of daily life: an experience sampling studyDaniela Q C M Barge-Schaapveld, Nancy A Nicolson
American Journal of Medical Genetics. Part A|April 6, 2011
The atypical 16p11.2 deletion: a not so atypical microdeletion syndrome?Daniela Q C M Barge-Schaapveld, Saskia M Maas, Abeltje Polstra, et al.
European Heart Journal. Case Reports|May 1, 2023
Genetic variant in the <i>BRAF</i> gene compatible with Noonan spectrum disorders in an adult Fontan patient with refractory protein losing enteropathy: a follow-up reportMarieke Nederend, J Lauran Stoger, Anastasia D Egorova, et al.
Journal of Cardiovascular Development and Disease|March 6, 2021
Characterization of Degenerative Mitral Valve Disease: Differences between Fibroelastic Deficiency and Barlow's DiseaseAniek L van Wijngaarden, Boudewijn P T Kruithof, Tommaso Vinella, et al.
American Journal of Medical Genetics. Part A|April 5, 2013
Intellectual disability and hemizygous GPD2 mutationDaniela Q C M Barge-Schaapveld, Rob Ofman, Alida C Knegt, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|November 18, 2018
Possible hints and pitfalls in diagnosing Peutz-Jeghers syndromeJudith S Renes, Jeroen Knijnenburg, Sharmila Chitoe-Ramawadhdoebe, et al.
Pediatric Neurology|March 15, 2011
Beare-Stevenson syndrome: two Dutch patients with cerebral abnormalitiesDaniela Q C M Barge-Schaapveld, Alice S Brooks, Maarten H Lequin, et al.
The Journal of Clinical Endocrinology and Metabolism|July 6, 2026
Bone phenotype of patients with genetic forms of lipodystrophy: a systematic review of literatureElif Kusgozoglu, Daniela Q C M Barge-Schaapveld, Patrick C N Rensen, et al.
Clinical Case Reports|March 31, 2025
A <i>PDLIM7</i> Variant in Familial Mitral Valve Prolapse: A Case SeriesAniek L van Wijngaarden, Tamara T Koopmann, Claudia A L Ruivenkamp, et al.
Molecular Genetics & Genomic Medicine|November 29, 2018
Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variantEline Overwater, Rifka Efrat, Daniela Q C M Barge-Schaapveld, et al.
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