Sexual dimorphism in the synchrony of joint growth hormone and cortisol dynamics in children with classic 21-hydroxylase deficiency.

Sexual dimorphism in the synchrony of joint growth hormone and cortisol dynamics in children with classic 21-hydroxylase deficiency.

In humans, growth hormone (GH) and cortisol are secreted in a pulsatile fashion and a mutual bidirectional interaction between the GH/insulin-like growth factor (IGF)-I axis and hypothalamic-pituitary-adrenal (HPA) axis has been established. Classic congenital adrenal hyperplasia (CAH) is characteri...

Descripció completa

Dades bibliogràfiques
Autors principals:	Charmandari, E, Pincus, S, Matthews, DR, Johnston, A, Brook, C, Hindmarsh, P
Format:	Journal article
Idioma:	English
Publicat:	2003

Ítems similars

Oral hydrocortisone administration in children with classic 21-hydroxylase deficiency leads to more synchronous joint GH and cortisol secretion.
per: Charmandari, E, et al.
Publicat: (2002)

Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?
per: Charmandari, E, et al.
Publicat: (2001)

A sexually dimorphic pattern of growth hormone secretion in the elderly.
per: Hindmarsh, P, et al.
Publicat: (1999)

Joint growth hormone and cortisol spontaneous secretion is more asynchronous in older females than in their male counterparts.
per: Charmandari, E, et al.
Publicat: (2001)

Current and future perspectives on clinical management of classic 21-hydroxylase deficiency
per: Analia Yogi, et al.
Publicat: (2023-10-01)

Variation in serum adrenal hormones in female 21-hydroxylase deficient patients
per: Ditte Sofie Dahl Sørensen, et al.
Publicat: (2022-06-01)

21-Hydroxylase deficiency in Brazil
per: T.A.S.S. Bachega, et al.
Publicat: (2000-10-01)

Clinical and Hormonal Profile of Classical 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia: Experience from a Tertiary Centre In India
per: Harshitha Boyareddy, et al.
Publicat: (2024-08-01)

Adrenal adenoma secreting 17-hydroxyprogesterone mimicking non-classical 21-hydroxylase deficiency
per: Beata Woźniak, et al.
Publicat: (2024-11-01)

Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
per: Helmuth G. Dörr, et al.
Publicat: (2018-11-01)

Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
per: Helmuth G. Dörr, et al.
Publicat: (2018-06-01)

NON CLASSIC 21 HYDROXYLASE DEFICIENT ADRENAL HYPERPLASIA IN PATIENTS WITH ISOLATED PRECOCIOUS PUBARCHE
per: H. Moayeri, et al.
Publicat: (2003-09-01)

NON CLASSIC 21 HYDROXYLASE DEFICIENT ADRENAL HYPERPLASIA IN PATIENTS WITH ISOLATED PRECOCIOUS PUBARCHE
per: H. Moayeri, et al.
Publicat: (2003-07-01)

Deconvolution analysis of 24-h serum cortisol profiles informs the amount and distribution of hydrocortisone replacement therapy.
per: Peters, C, et al.
Publicat: (2013)

Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency
per: Taek Min Kim, et al.
Publicat: (2022-02-01)

Clinical Profile, Predictors of Death and Anthropometric Follow up in Neonates with Classical 21-Hydroxylase Deficiency
per: Usha Devi Rajendran, et al.
Publicat: (2018-05-01)

Obesity and Cardiometabolic Risk Factors in Children and Young Adults With Non-classical 21-Hydroxylase Deficiency
per: Liat de Vries, et al.
Publicat: (2019-10-01)

Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome
per: M Emre Atabek, et al.
Publicat: (2005-04-01)

Comparison of different glucocorticoid regimens in the management of classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
per: T P Ajish, et al.
Publicat: (2014-01-01)

The effect of repeated administration of hexarelin, a growth hormone releasing peptide, and growth hormone releasing hormone on growth hormone responsivity.
per: Massoud, A, et al.
Publicat: (1996)

Best Practice for Identification of Classical 21-Hydroxylase Deficiency Should Include 21 Deoxycortisol Analysis with Appropriate Isomeric Steroid Separation
per: Ronda F. Greaves, et al.
Publicat: (2023-10-01)

Genotype–phenotype correlation study and mutational and hormonal analysis in a Chinese cohort with 21‐hydroxylase deficiency
per: Chao Xu, et al.
Publicat: (2019-06-01)

Sexual dimorphism in cortisol metabolism throughout pubertal development: a longitudinal study
per: Britt J van Keulen, et al.
Publicat: (2020-06-01)

Peg3 Deficiency Results in Sexually Dimorphic Losses and Gains in the Normal Repertoire of Placental Hormones
per: Simon J. Tunster, et al.
Publicat: (2018-09-01)

Clinical characteristics and treatment during preconception and perinatal period of infertile women with non-classical 21-hydroxylase deficiency
per: Xuejiao Cui, et al.
Publicat: (2024-10-01)

Impact of glucocorticoid receptor gene polymorphisms on the metabolic profile of adult patients with the classical form of 21-hydroxylase deficiency.
per: Ricardo P P Moreira, et al.
Publicat: (2012-01-01)

Non-Classical 21-Hydroxylase Deficiency: Analysis of a Mutant Gene in a Uyghur Family and Literature Review
per: Maimaitiming J, et al.
Publicat: (2021-04-01)

Long-Term Health Outcomes of Korean Adults With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
per: Seung Gyun Lim, et al.
Publicat: (2021-10-01)

Two Adults with Adrenal Myelolipoma and 21-Hydroxylase Deficiency
per: Ingrid Nermoen, et al.
Publicat: (2009-01-01)

Monitoring treatment in pediatric patients with 21-hydroxylase deficiency
per: Tomoyo Itonaga, et al.
Publicat: (2023-02-01)

Genotype-phenotype correlation in patients with 21-hydroxylase deficiency
per: Peng Tang, et al.
Publicat: (2023-03-01)

Growth hormone secretion in children determined by time series analysis.
per: Hindmarsh, P, et al.
Publicat: (1988)

A recent overview of non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: pathophysiology, recognition, and management
per: Rafał Podgórski, et al.
Publicat: (2023-12-01)

NON-CLASSIC 21 HYDROXYLASE DEFICIENCY CAUSED BY NEW COMPOUND HETEROZYGOUS MUTATIONS: A CASE REPORT AND LITERATURE REVIEW
per: QI Mengmeng, WANG Xuemei, LIU Yunting, WANG Qian, XIN Qianyu, LIN Hua, LYU Wenshan, YANG Lili
Publicat: (2023-12-01)

Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: laboratory criteria for the diagnosis and control of treatment efficacy
per: O.V. Rykova
Publicat: (2019-09-01)

Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: laboratory criteria for the diagnosis and control of treatment efficacy
per: O.V. Rykova
Publicat: (2019-08-01)

Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
per: David Q Stoye, et al.
Publicat: (2020-11-01)

Sexual dimorphism in the effects of maternal adipose tissue growth hormone receptor deficiency on offspring metabolic health
per: Liyuan Ran, et al.
Publicat: (2024-12-01)

Growth and the growth hormone axis in prepubertal children with asthma.
per: Crowley, S, et al.
Publicat: (1995)

The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population
per: Katja K. Dumic, et al.
Publicat: (2023-05-01)