Barto J. Otten - Publications

Long-term follow-up of children with classic congenital adrenal hyperplasia: suggestions for age dependent treatment in childhood and puberty.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: January 04, 2019

A delayed diagnosis of salt-wasting congenital adrenal hyperplasia.

Journal: Clinical endocrinology

Published: May 21, 2016

Growth hormone therapy, muscle thickness, and motor development in Prader-Willi syndrome: an RCT.

Journal: Pediatrics

Published: November 26, 2014

Karyotype-specific ear and hearing problems in young adults with Turner syndrome and the effect of oxandrolone treatment.

Journal: Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology

Published: August 19, 2014

Salivary morning androstenedione and 17α-OH progesterone levels in childhood and puberty in patients with classic congenital adrenal hyperplasia.

Journal: Clinical chemistry and laboratory medicine

Published: April 06, 2014

Long-term effects of oxandrolone treatment in childhood on neurocognition, quality of life and social-emotional functioning in young adults with Turner syndrome.

Journal: Hormones and behavior

Published: December 06, 2013

Comparison of body surface area versus weight-based growth hormone dosing for girls with Turner syndrome.

Journal: Hormone research in paediatrics

Published: October 18, 2013

Safety and efficacy of oxandrolone in growth hormone-treated girls with Turner syndrome: evidence from recent studies and recommendations for use.

Journal: Hormone research in paediatrics

Published: July 23, 2013

Splice site mutations in GH1 detected in previously (Genetically) undiagnosed families with congenital isolated growth hormone deficiency type II.

Journal: Hormone research in paediatrics

Published: March 19, 2013

Growth hormone combined with child-specific motor training improves motor development in infants with Prader-Willi syndrome: a randomized controlled trial.

Journal: Research in developmental disabilities

Published: January 25, 2013

Buccal cell FISH and blood PCR-Y detect high rates of X chromosomal mosaicism and Y chromosomal derivatives in patients with Turner syndrome.

Journal: European journal of medical genetics

Published: November 04, 2012

Objective evaluation of muscle strength in infants with hypotonia and muscle weakness.

Journal: Research in developmental disabilities

Published: October 25, 2012