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

ग्रंथसूची विवरण
मुख्य लेखकों:	Charmandari, E, Pincus, S, Matthews, DR, Johnston, A, Brook, C, Hindmarsh, P
स्वरूप:	Journal article
भाषा:	English
प्रकाशित:	2003

Oral hydrocortisone administration in children with classic 21-hydroxylase deficiency leads to more synchronous joint GH and cortisol secretion.
द्वारा: Charmandari, E, और अन्य
प्रकाशित: (2002)

Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?
द्वारा: Charmandari, E, और अन्य
प्रकाशित: (2001)

A sexually dimorphic pattern of growth hormone secretion in the elderly.
द्वारा: Hindmarsh, P, और अन्य
प्रकाशित: (1999)

Joint growth hormone and cortisol spontaneous secretion is more asynchronous in older females than in their male counterparts.
द्वारा: Charmandari, E, और अन्य
प्रकाशित: (2001)

Current and future perspectives on clinical management of classic 21-hydroxylase deficiency
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Variation in serum adrenal hormones in female 21-hydroxylase deficient patients
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21-Hydroxylase deficiency in Brazil
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Clinical and Hormonal Profile of Classical 21-Hydroxylase Deficiency Congenital Adrenal Hyperplasia: Experience from a Tertiary Centre In India
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Adrenal adenoma secreting 17-hydroxyprogesterone mimicking non-classical 21-hydroxylase deficiency
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Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
द्वारा: Helmuth G. Dörr, और अन्य
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Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
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NON CLASSIC 21 HYDROXYLASE DEFICIENT ADRENAL HYPERPLASIA IN PATIENTS WITH ISOLATED PRECOCIOUS PUBARCHE
द्वारा: H. Moayeri, और अन्य
प्रकाशित: (2003-09-01)

NON CLASSIC 21 HYDROXYLASE DEFICIENT ADRENAL HYPERPLASIA IN PATIENTS WITH ISOLATED PRECOCIOUS PUBARCHE
द्वारा: H. Moayeri, और अन्य
प्रकाशित: (2003-07-01)

Deconvolution analysis of 24-h serum cortisol profiles informs the amount and distribution of hydrocortisone replacement therapy.
द्वारा: Peters, C, और अन्य
प्रकाशित: (2013)

Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency
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प्रकाशित: (2022-02-01)

Clinical Profile, Predictors of Death and Anthropometric Follow up in Neonates with Classical 21-Hydroxylase Deficiency
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Obesity and Cardiometabolic Risk Factors in Children and Young Adults With Non-classical 21-Hydroxylase Deficiency
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Female pseudohermaphroditism due to classical 21-hydroxylase deficiency and insulin resistance in a girl with Turner syndrome
द्वारा: M Emre Atabek, और अन्य
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Comparison of different glucocorticoid regimens in the management of classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
द्वारा: T P Ajish, और अन्य
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The effect of repeated administration of hexarelin, a growth hormone releasing peptide, and growth hormone releasing hormone on growth hormone responsivity.
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प्रकाशित: (1996)

Best Practice for Identification of Classical 21-Hydroxylase Deficiency Should Include 21 Deoxycortisol Analysis with Appropriate Isomeric Steroid Separation
द्वारा: Ronda F. Greaves, और अन्य
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Genotype–phenotype correlation study and mutational and hormonal analysis in a Chinese cohort with 21‐hydroxylase deficiency
द्वारा: Chao Xu, और अन्य
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Sexual dimorphism in cortisol metabolism throughout pubertal development: a longitudinal study
द्वारा: Britt J van Keulen, और अन्य
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Peg3 Deficiency Results in Sexually Dimorphic Losses and Gains in the Normal Repertoire of Placental Hormones
द्वारा: Simon J. Tunster, और अन्य
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Clinical characteristics and treatment during preconception and perinatal period of infertile women with non-classical 21-hydroxylase deficiency
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Impact of glucocorticoid receptor gene polymorphisms on the metabolic profile of adult patients with the classical form of 21-hydroxylase deficiency.
द्वारा: Ricardo P P Moreira, और अन्य
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Non-Classical 21-Hydroxylase Deficiency: Analysis of a Mutant Gene in a Uyghur Family and Literature Review
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Long-Term Health Outcomes of Korean Adults With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
द्वारा: Seung Gyun Lim, और अन्य
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Two Adults with Adrenal Myelolipoma and 21-Hydroxylase Deficiency
द्वारा: Ingrid Nermoen, और अन्य
प्रकाशित: (2009-01-01)

Monitoring treatment in pediatric patients with 21-hydroxylase deficiency
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Genotype-phenotype correlation in patients with 21-hydroxylase deficiency
द्वारा: Peng Tang, और अन्य
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Growth hormone secretion in children determined by time series analysis.
द्वारा: Hindmarsh, P, और अन्य
प्रकाशित: (1988)

A recent overview of non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: pathophysiology, recognition, and management
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NON-CLASSIC 21 HYDROXYLASE DEFICIENCY CAUSED BY NEW COMPOUND HETEROZYGOUS MUTATIONS: A CASE REPORT AND LITERATURE REVIEW
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Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: laboratory criteria for the diagnosis and control of treatment efficacy
द्वारा: O.V. Rykova
प्रकाशित: (2019-09-01)

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

Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
द्वारा: David Q Stoye, और अन्य
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Sexual dimorphism in the effects of maternal adipose tissue growth hormone receptor deficiency on offspring metabolic health
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Growth and the growth hormone axis in prepubertal children with asthma.
द्वारा: Crowley, S, और अन्य
प्रकाशित: (1995)

The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population
द्वारा: Katja K. Dumic, और अन्य
प्रकाशित: (2023-05-01)

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

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