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Hormone Research in Paediatrics|April 30, 2014
Safety and efficacy of oxandrolone in growth hormone-treated girls with Turner syndrome: evidence from recent studies and recommendations for useT C J Sas, E J Gault, M Zeger Bardsley, et al.
Journal of Voice : Official Journal of the Voice Foundation|October 26, 2010
The effect of oxandrolone on voice frequency in growth hormone-treated girls with Turner syndromeLeonie A Menke, Theo C J Sas, Sophie H L van Koningsbrugge, et al.
Hormone Research in Paediatrics|April 30, 2014
Comparison of body surface area versus weight-based growth hormone dosing for girls with Turner syndromeLenneke Schrier, Marieke L de Kam, Rachel McKinnon, et al.
Pediatric Neurology|April 16, 2025
Glycosylphosphatidylinositol Biosynthesis Defect Due To Novel Biallelic Pathogenic Variants in PIGWNazim Rabouhi, Smrithi Salian, Hind Benkerroum, et al.
Hormones and Behavior|January 7, 2015
Long-term effects of oxandrolone treatment in childhood on neurocognition, quality of life and social-emotional functioning in young adults with Turner syndromeK Freriks, C M Verhaak, T C J Sas, et al.
American Journal of Medical Genetics. Part A|November 16, 2022
Growth charts for Marfan syndrome in the Netherlands and analysis of genotype-phenotype relationshipsPeter Lauffer, Gerard Pals, Aeilko H Zwinderman, et al.
Clinical Genetics|January 4, 2020
Phenotypic spectrum of TGFB3 disease-causing variants in a Dutch-French cohort and first report of a homozygous patientLuisa Marsili, Eline Overwater, Nadine Hanna, et al.
American Journal of Medical Genetics. Part A|February 21, 2018
Further delineation of an entity caused by CREBBP and EP300 mutations but not resembling Rubinstein-Taybi syndromeLeonie A Menke, , Thatjana Gardeitchik, et al.
Human Mutation|June 17, 2018
Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disordersEline Overwater, Luisa Marsili, Marieke J H Baars, et al.
American Journal of Medical Genetics. Part A|June 18, 2016
CREBBP mutations in individuals without Rubinstein-Taybi syndrome phenotypeLeonie A Menke, Martine J van Belzen, Marielle Alders, et al.
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