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

Detaylı Bibliyografya
Asıl Yazarlar:	Charmandari, E, Pincus, S, Matthews, DR, Johnston, A, Brook, C, Hindmarsh, P
Materyal Türü:	Journal article
Dil:	English
Baskı/Yayın Bilgisi:	2003

Oral hydrocortisone administration in children with classic 21-hydroxylase deficiency leads to more synchronous joint GH and cortisol secretion.
Yazar:: Charmandari, E, ve diğerleri
Baskı/Yayın Bilgisi: (2002)

Serum cortisol and 17-hydroxyprogesterone interrelation in classic 21-hydroxylase deficiency: is current replacement therapy satisfactory?
Yazar:: Charmandari, E, ve diğerleri
Baskı/Yayın Bilgisi: (2001)

A sexually dimorphic pattern of growth hormone secretion in the elderly.
Yazar:: Hindmarsh, P, ve diğerleri
Baskı/Yayın Bilgisi: (1999)

Joint growth hormone and cortisol spontaneous secretion is more asynchronous in older females than in their male counterparts.
Yazar:: Charmandari, E, ve diğerleri
Baskı/Yayın Bilgisi: (2001)

Current and future perspectives on clinical management of classic 21-hydroxylase deficiency
Yazar:: Analia Yogi, ve diğerleri
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Variation in serum adrenal hormones in female 21-hydroxylase deficient patients
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21-Hydroxylase deficiency in Brazil
Yazar:: T.A.S.S. Bachega, ve diğerleri
Baskı/Yayın Bilgisi: (2000-10-01)

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Adrenal adenoma secreting 17-hydroxyprogesterone mimicking non-classical 21-hydroxylase deficiency
Yazar:: Beata Woźniak, ve diğerleri
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Miscarriages in families with an offspring that have classic congenital adrenal hyperplasia and 21-hydroxylase deficiency
Yazar:: Helmuth G. Dörr, ve diğerleri
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Mortality in children with classic congenital adrenal hyperplasia and 21-hydroxylase deficiency (CAH) in Germany
Yazar:: Helmuth G. Dörr, ve diğerleri
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NON CLASSIC 21 HYDROXYLASE DEFICIENT ADRENAL HYPERPLASIA IN PATIENTS WITH ISOLATED PRECOCIOUS PUBARCHE
Yazar:: H. Moayeri, ve diğerleri
Baskı/Yayın Bilgisi: (2003-09-01)

NON CLASSIC 21 HYDROXYLASE DEFICIENT ADRENAL HYPERPLASIA IN PATIENTS WITH ISOLATED PRECOCIOUS PUBARCHE
Yazar:: H. Moayeri, ve diğerleri
Baskı/Yayın Bilgisi: (2003-07-01)

Deconvolution analysis of 24-h serum cortisol profiles informs the amount and distribution of hydrocortisone replacement therapy.
Yazar:: Peters, C, ve diğerleri
Baskı/Yayın Bilgisi: (2013)

Adrenal Morphology as an Indicator of Long-Term Disease Control in Adults with Classic 21-Hydroxylase Deficiency
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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
Yazar:: M Emre Atabek, ve diğerleri
Baskı/Yayın Bilgisi: (2005-04-01)

Comparison of different glucocorticoid regimens in the management of classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Yazar:: T P Ajish, ve diğerleri
Baskı/Yayın Bilgisi: (2014-01-01)

The effect of repeated administration of hexarelin, a growth hormone releasing peptide, and growth hormone releasing hormone on growth hormone responsivity.
Yazar:: Massoud, A, ve diğerleri
Baskı/Yayın Bilgisi: (1996)

Best Practice for Identification of Classical 21-Hydroxylase Deficiency Should Include 21 Deoxycortisol Analysis with Appropriate Isomeric Steroid Separation
Yazar:: Ronda F. Greaves, ve diğerleri
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Genotype–phenotype correlation study and mutational and hormonal analysis in a Chinese cohort with 21‐hydroxylase deficiency
Yazar:: Chao Xu, ve diğerleri
Baskı/Yayın Bilgisi: (2019-06-01)

Sexual dimorphism in cortisol metabolism throughout pubertal development: a longitudinal study
Yazar:: Britt J van Keulen, ve diğerleri
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Peg3 Deficiency Results in Sexually Dimorphic Losses and Gains in the Normal Repertoire of Placental Hormones
Yazar:: Simon J. Tunster, ve diğerleri
Baskı/Yayın Bilgisi: (2018-09-01)

Clinical characteristics and treatment during preconception and perinatal period of infertile women with non-classical 21-hydroxylase deficiency
Yazar:: Xuejiao Cui, ve diğerleri
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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.
Yazar:: Ricardo P P Moreira, ve diğerleri
Baskı/Yayın Bilgisi: (2012-01-01)

Non-Classical 21-Hydroxylase Deficiency: Analysis of a Mutant Gene in a Uyghur Family and Literature Review
Yazar:: Maimaitiming J, ve diğerleri
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Long-Term Health Outcomes of Korean Adults With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Yazar:: Seung Gyun Lim, ve diğerleri
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Two Adults with Adrenal Myelolipoma and 21-Hydroxylase Deficiency
Yazar:: Ingrid Nermoen, ve diğerleri
Baskı/Yayın Bilgisi: (2009-01-01)

Monitoring treatment in pediatric patients with 21-hydroxylase deficiency
Yazar:: Tomoyo Itonaga, ve diğerleri
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Genotype-phenotype correlation in patients with 21-hydroxylase deficiency
Yazar:: Peng Tang, ve diğerleri
Baskı/Yayın Bilgisi: (2023-03-01)

Growth hormone secretion in children determined by time series analysis.
Yazar:: Hindmarsh, P, ve diğerleri
Baskı/Yayın Bilgisi: (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
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Non-classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency: laboratory criteria for the diagnosis and control of treatment efficacy
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Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
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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.
Yazar:: Crowley, S, ve diğerleri
Baskı/Yayın Bilgisi: (1995)

The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population
Yazar:: Katja K. Dumic, ve diğerleri
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Sexual dimorphism in the synchrony of joint growth hormone and cortisol dynamics in children with classic 21-hydroxylase deficiency.

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