C. Noordam

发表

Calcaneal Ultrasound Imaging in Healthy Children and Adolescents: Relation of the Ultrasound Parameters BUA and SOS to Age, Body Weight, Height, Foot Dimensions and Pubertal Stage

J. V. D. van den Bergh, C. Noordam, A. Özyılmaz, 2000, Osteoporosis International.

First‐year growth in children with Noonan syndrome: Associated with feeding problems?

N. Roeleveld, C. Noordam, J. Draaisma, 2018, American journal of medical genetics. Part A.

Normal height and weight in a series of ambulant Duchenne muscular dystrophy patients using the 10day on/10day off prednisone regimen

N. Alfen, L. Sie, C. Noordam, 2012, Neuromuscular Disorders.

Ocular findings in Noonan syndrome: a retrospective cohort study of 105 patients

J. Cruysberg, C. Noordam, J. Draaisma, 2018, European Journal of Pediatrics.

Noonan Syndrome: Comparing Mutation-Positive with Mutation-Negative Dutch Patients

H. Scheffer, W. Nillesen, H. Yntema, 2013, Molecular Syndromology.

Long-term GH treatment improves adult height in children with Noonan syndrome with and without mutations in protein tyrosine phosphatase, non-receptor-type 11.

C. Noordam, B. Otten, J. De Schepper, 2008, European journal of endocrinology.

Treatment of tall stature in boys with somatostatin analogue 201-995: effect on final height.

C. Noordam, B. Otten, S. V. van Daalen, 2006, European journal of endocrinology.

Bone Mineral Density and Body Composition in Noonan's Syndrome: Effects of Growth Hormone Treatment

R. V. van Rijn, C. Noordam, B. Otten, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Prader–Willi Syndrome and Hypogonadism: A Review Article

C. Höybye, U. Eiholzer, C. Noordam, 2021, International journal of molecular sciences.

Inactivating PAPSS2 mutations in a patient with premature pubarche.

N. Hanley, J. Smeitink, R. Smeets, 2009, The New England journal of medicine.

Adult height in short children born SGA treated with growth hormone and gonadotropin releasing hormone analog: results of a randomized, dose-response GH trial.

A. Hokken-Koelega, R. Odink, M. D. de Ridder, 2012, The Journal of clinical endocrinology and metabolism.

Reduced levels of GH during GnRH analogue treatment in pubertal short girls born small for gestational age (SGA)

A. Hokken-Koelega, C. Noordam, D. van der Kaay, 2009, Clinical endocrinology.

Effects of Growth Hormone Treatment on Left Ventricular Dimensions in Children with Noonan’s Syndrome

C. Noordam, B. Otten, I. van der Burgt, 2002, Hormone Research in Paediatrics.

Short stature associated with a novel heterozygous mutation in the insulin-like growth factor 1 gene.

J. Wade, C. Ruivenkamp, H. V. van Duyvenvoorde, 2010, The Journal of clinical endocrinology and metabolism.

Het Bloom-syndroom

J. Loeffen, C. Noordam, B. Otten, 2013 .

Klinefelter’s Syndrome and Prader-Willi Syndrome: A Rare Combination

B. D. de Vries, S. Tuinier, W. Verhoeven, 2007, Psychopathology.

Gonadal Hormone Substitution in People with Prader-Labhart-Willi Syndrome: An International Prader-Willi Syndrome Organisation Survey

U. Eiholzer, C. Noordam, Chris Fritz, 2021, Hormone Research in Paediatrics.

Growth hormone (GH) secretion in children with Noonan syndrome: frequently abnormal without consequences for growth or response to GH treatment

C. Sweep, H. Delemarre-van de Waal, R. Sengers, 2001, Clinical endocrinology.

An Adolescent with Food-Dependent Cushing's Syndrome Secondary to Ectopic Expression of GIP Receptor in Unilateral Adrenal Adenoma

C. Sweep, A. Lacroix, C. Noordam, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

Are ECG abnormalities in Noonan syndrome characteristic for the syndrome?

C. Noordam, J. Draaisma, J. Noonan, 2008, European Journal of Pediatrics.

Impaired Sertoli Cell Function in Males Diagnosed with Noonan Syndrome

C. Sweep, C. Noordam, K. Marcus, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Response to Growth Hormone Treatment and Final Height in Noonan Syndrome in a Large Cohort of Patients in the KIGS Database

J. Gregory, C. Noordam, B. Otten, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations.

P. Donohoue, M. Fassnacht, L. Dunkel, 2005, The Journal of clinical endocrinology and metabolism.

Growth, Endocrine Features, and Growth Hormone Treatment in Noonan Syndrome

C. Noordam, J. Dahlgren, 2022, Journal of clinical medicine.

Homozygous and heterozygous expression of a novel mutation of the acid-labile subunit.

M. Kempers, H. V. van Duyvenvoorde, M. Losekoot, 2008, European journal of endocrinology.

Hepatocyte nuclear factor‐1 beta mutations cause neonatal diabetes and intrauterine growth retardation: support for a critical role of HNF‐1β in human pancreatic development

S. Ellard, C. Noordam, A. S. Slingerland, 2006, Diabetic medicine : a journal of the British Diabetic Association.

Motor performance in children with Noonan syndrome

C. Noordam, J. Draaisma, I. van der Burgt, 2017, American journal of medical genetics. Part A.

Mitochondrial dysfunction and organic aciduria in five patients carrying mutations in the Ras-MAPK pathway

Saskia B Wortmann, Eva Morava, Martin Lammens, 2011, European Journal of Human Genetics.

Copy number variants in patients with short stature

J. Baron, J. Lui, C. Ruivenkamp, 2013, European Journal of Human Genetics.

Growth in Noonan Syndrome

C. Noordam, B. Otten, Cees Noordam, 2009, Hormone Research in Paediatrics.

Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial

R. Sengers, C. Noordam, B. Otten, 2001, Acta paediatrica.

Growth before and during growth hormone treatment in children operated for craniopharyngioma.

C. Noordam, B. Otten, G. Massa, 1997, Hormone research.

Can GnRH Agonist Treatment Cause Slipped Capital Femoral Epiphysis?

C. Noordam, B. Otten, C. Rouwé, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

From Bone Biology to Bone Analysis

Z. Hochberg, N. Crabtree, E. Schoenau, 2004, Hormone Research in Paediatrics.

The severe short stature in two siblings with a heterozygous IGF1 mutation is not caused by a dominant negative effect of the putative truncated protein.

J. Wade, C. Ruivenkamp, H. V. van Duyvenvoorde, 2011, Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society.

I-cell disease presenting with severe hypophosphatemia and cardiomyopathy.

R. Wevers, J. Smeitink, C. Noordam, 2000, Neuropediatrics.

Measuring Skeletal Changes with Calcaneal Ultrasound Imaging in Healthy Children and Adults: The Influence of Size and Location of the Region of Interest

J. V. D. van den Bergh, C. Noordam, A. Smals, 2001, Osteoporosis International.

Metabolic Health in Short Children Born Small for Gestational Age Treated With Growth Hormone and Gonadotropin-Releasing Hormone Analog: Results of a Randomized, Dose-Response Trial.

A. Hokken-Koelega, R. Odink, C. Noordam, 2015, The Journal of clinical endocrinology and metabolism.

Genetic Analysis of Short Children with Apparent Growth Hormone Insensitivity

H. Delemarre-van de Waal, C. Ruivenkamp, H. V. van Duyvenvoorde, 2012, Hormone Research in Paediatrics.

Newborn screening for congenital adrenal hyperplasia in the Netherlands.

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

Long-term GH treatment improves adult height in children with Noonan syndrome with and without mutations in protein tyrosine phosphatase, non-receptor-type 11.

C. Noordam, J. Schepper, Petronella G. M. Peer, 2008, European journal of endocrinology.

Growth Hormone and the Heart in Noonan Syndrome

C. Noordam, 2009, Hormone Research in Paediatrics.

Gonadal Hormone Substitution in People with Prader-Labhart-Willi Syndrome: An International Prader-Willi Syndrome Organisation Survey

U. Eiholzer, C. Noordam, Chris Fritz, 2021, Hormone Research in Paediatrics.