H. J. van der Kamp

发表

Cutoff levels of 17-alpha-hydroxyprogesterone in neonatal screening for congenital adrenal hyperplasia should be based on gestational age rather than on birth weight.

J. Wit, B. Otten, P. Verkerk, 2005, The Journal of clinical endocrinology and metabolism.

The Efficacy, Safety, and Side Effects of Intrapericardial Triamcinolone Treatment in Children with Post-surgical Pericardial Effusion: A Case Series

J. Breur, H. J. van der Kamp, Manon H. van der Werff, 2021, Pediatric Cardiology.

The jumping SHOX gene--crossover in the pseudoautosomal region resulting in unusual inheritance of Leri-Weill dyschondrosteosis.

G. Rappold, E. Bakker, M. Losekoot, 2011, The Journal of clinical endocrinology and metabolism.

Leptin receptor deficiency: a systematic literature review and prevalence estimation based on population genetics.

H. Meijers-Heijboer, E. V. van Rossum, M. Alders, 2020, European journal of endocrinology.

International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia - data from the I-CAH registry.

M. Korbonits, S. Poyrazoglu, F. Darendeliler, 2021, European journal of endocrinology.

Effects of total-body irradiation on growth, thyroid and pituitary gland in rhesus monkeys.

J. J. Broerse, J. Wit, J. Broerse, 1999, Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology.

Rapid early increase in BMI is associated with impaired longitudinal growth in children with cystic fibrosis

H. Arets, C. van der Ent, H. J. van der Kamp, 2019, Pediatric pulmonology.

Pseudoisodicentric Xp Chromosome [46,X,psu idic(X)(q21.1)] and Its Effect on Growth and Pubertal Development

C. Ruivenkamp, S. Kant, W. Oostdijk, 2014, Hormone Research in Paediatrics.

Long-range conserved non-coding SHOX sequences regulate expression in developing chicken limb and are associated with short stature phenotypes in human patients.

C. Tickle, J. Kapeller, G. Rappold, 2006, Human molecular genetics.

GnRH-deficient phenotypes in humans and mice with heterozygous variants in KISS1/Kiss1.

R. Schiffmann, S. Kirsch, R. Quinton, 2011, The Journal of clinical endocrinology and metabolism.

Phenotypic characterization of patients with deletions in the 3’-flanking SHOX region

E. V. van Zwet, E. Bakker, M. Losekoot, 2013, PeerJ.

Neonatal screening for congenital adrenal hyperplasia.

J. Wit, H. J. van der Kamp, 2004, European journal of endocrinology.

Real-World Estimates of Adrenal Insufficiency–Related Adverse Events in Children With Congenital Adrenal Hyperplasia

J. Lewsey, M. Korbonits, S. Poyrazoglu, 2020, The Journal of clinical endocrinology and metabolism.

Evaluation of the Dutch neonatal screening for congenital adrenal hyperplasia

M. Finken, A. Boelen, R. Odink, 2019, Archives of Disease in Childhood.

Newborn screening for congenital adrenal hyperplasia in the Netherlands.

C. Noordam, B. Otten, K. Noordam, 2001, Pediatrics.

Optimizing the Timing of Highest Hydrocortisone Dose in Children and Adolescents With 21-Hydroxylase Deficiency

P. Span, F. Sweep, A. V. van Herwaarden, 2021, Journal of Clinical Endocrinology and Metabolism.

Second-tier testing for 21-hydroxylase deficiency in the Netherlands; a newborn screening pilot study.

A. Heijboer, M. Finken, M. Ackermans, 2021, The Journal of clinical endocrinology and metabolism.

Longitudinal analysis of growth and puberty in 21-hydroxylase deficiency patients

M. Jansen, B. Otten, S. de Muinck Keizer-Schrama, 2002, Archives of disease in childhood.

The Predictive Value of the Individual Components of the Metabolic Syndrome for Insulin Resistance in Obese Children

H. Pijl, J. Wit, R. Vos, 2011, Hormone Research in Paediatrics.

A variable degree of intrauterine and postnatal growth retardation in a family with a missense mutation in the insulin-like growth factor I receptor.

J. Romijn, H. V. van Duyvenvoorde, J. Wit, 2006, The Journal of clinical endocrinology and metabolism.

Evaluation of young women with congenital adrenal hyperplasia: a pilot study.

F. Slijper, S. Drop, S. de Muinck Keizer-Schrama, 1992, Hormone research.

Influence of peritoneal loss of GHBP, IGF-I and IGFBP-3 on serum levels in children with ESRD.

C. Sweep, L. Monnens, B. Otten, 1999, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Neonatal screening for congenital adrenal hyperplasia.

J. Wit, H. J. van der Kamp, 2004, European journal of endocrinology.