Laura C. G. de Graaff

<i>PROP1, HESX1, POU1F1, LHX3 </i>and<i> LHX4</i> Mutation and Deletion Screening and <i>GH1 </i>P89L and IVS3+1/+2 Mutation Screening in a Dutch Nationwide Cohort of Patients with Combined Pituitary Hormone Deficiency

Laura C. G. de Graaff, Jesús Argente, Danielle Veenma et al. · Hormone Research in Paediatrics · 2010 · 34 citations · Full text

GH receptor <i>d3</i> polymorphism in Dutch patients with MPHD and IGHD born small or appropriate for gestational age

Laura C. G. de Graaff, Silke Meyer, Charl Els et al. · Clinical Endocrinology · 2007 · 26 citations

Genetic screening of a Dutch population with isolated GH deficiency (IGHD)

Laura C. G. de Graaff, Jesús Argente, Danielle Veenma et al. · Clinical Endocrinology · 2008 · 26 citations

Antipituitary Antibodies in Dutch Patients with Idiopathic Hypopituitarism

Laura C. G. de Graaff, Annamaria De Bellis, Antonio Bellastella et al. · Hormone Research in Paediatrics · 2008 · 19 citations

Understanding the impact of tuberous sclerosis complex: development and validation of the TSC-PROM

Annelieke R. Müller, Michiel A. J. Luijten, Lotte Haverman et al. · BMC Medicine · 2023 · 18 citations · Full text