Cargando…

THU207 11-oxygenated Androgens Are Strongly Associated With Treatment Quality In Children With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency

Disclosure: O. Abawi: None. T. Du Toit: None. G. Sommer: None. C.D. Vögel: None. M. Groessl: None. U. Halbsguth: None. S.E. Hannema: None. C. de Bruin: None. E. Charmandari: None. E.L. van den Akker: None. C.E. Flueck: None. Introduction: Treatment of children with Congenital Adrenal Hyperplasia (CA...

Descripción completa

Detalles Bibliográficos
Autores principales:	Abawi, Ozair, Du Toit, Therina, Sommer, Grit, Vögel, Clarissa D, Groessl, Michael, Halbsguth, Ulrike, Hannema, Sabine Elisabeth, de Bruin, Christiaan, Charmandari, Evangelia, van den Akker, Erica L T, Flueck, Christa E
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2023
Materias:	Pediatric Endocrinology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10553741/ http://dx.doi.org/10.1210/jendso/bvad114.1458

Ejemplares similares

THU208 Predicting Treatment Quality Assessment Of Children With Congenital Adrenal Hyperplasia Using 24h Urine Metabolomics Profiling And A Machine Learning-assisted Approach
por: Abawi, Ozair, et al.
Publicado: (2023)

FRI382 High Androgen And Progesterone Metabolite Concentrations In Naturally Matured Follicles Are Concurrent With High Serum Anti-Müllerian Hormone Concentrations
por: Du Toit, Therina, et al.
Publicado: (2023)

SUN-073 Urine Steroid Profile of Girls with Premature Adrenarche
por: Sommer, Grit, et al.
Publicado: (2020)

Characteristics of Growth in Children With Classic Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency During Adrenarche and Beyond
por: Troger, Tobias, et al.
Publicado: (2021)

Parallel targeted and non-targeted quantitative analysis of steroids in human serum and peritoneal fluid by liquid chromatography high-resolution mass spectrometry
por: Andrieu, Thomas, et al.
Publicado: (2022)

Androstenedione Is the Preferred Substrate for Cytochrome P450 11β-hydroxylase Leading to the Production of 11β-Hydroxyandrostenedione in the Adrenal Gland
por: Barbier, Inge Doney, et al.
Publicado: (2021)

SAT-207 Adrenocortical Carcinoma in Untreated Congenital Adrenal Hyperplasia
por: David, Julia, et al.
Publicado: (2020)

Development and function of the fetal adrenal
por: Pignatti, Emanuele, et al.
Publicado: (2022)

THU406 24-hydroxylase Deficiency, A Rare Cause Of Hypercalcemia
por: Hodge, Jordesha, et al.
Publicado: (2023)

Levels in $^{207}$Po populated in the decay of $^{207}$At
por: Jonson, B, et al.
Publicado: (1970)

Levels in $^{207}Po$ populated in the decay of $^{207}At$
por: Jonson, B, et al.
Publicado: (1971)

The decay $^{207}_{80}$Hg --> $^{207}_{81}$Tl
por: Jonson, B, et al.
Publicado: (1981)

At R207
Publicado: (1975)

At R207
Publicado: (1975)

SAT-742 Characterising the Metabolism, Glucuronidation and Sulfation of C11-oxy C(19) Steroids
por: Toit, Therina Du, et al.
Publicado: (2020)

THU187 Genotype-Phenotype Correlation, Clinical Presentation And Feminizing Surgery In Children With Congenital Adrenal Hyperplasia Due To 21-Hydroxylase Deficiency: A Nationwide Multi-Center Study
por: Lind-Holst, Marie, et al.
Publicado: (2023)

THU015 Unilateral Adrenal Hyperplasia Causing ACTH-independent Hypercortisolism
por: Mogar, Nikita, et al.
Publicado: (2023)

Gamma-ray transition in $^{207}$Bi following the decay of $^{207}$Po
por: Alpsten, M, et al.
Publicado: (1970)

Impact of BMI on Growth Hormone Stimulation Tests in Children and Adolescents: A Systematic Review and Meta-Analysis
por: Abawi, Ozair, et al.
Publicado: (2021)

THU398 Variants In The Vitamin D Receptor, 1alpha-hydroxylase Enzyme Genes In Cholecalciferol Therapy
por: Kalinchenko, Svetlana, et al.
Publicado: (2023)

Treatment and Outcome of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
por: Lee, Peter A., et al.
Publicado: (2010)

Genetic Disruption of 21-Hydroxylase in Zebrafish Causes Interrenal Hyperplasia
por: Eachus, Helen, et al.
Publicado: (2017)

The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
por: Pignatelli, Duarte, et al.
Publicado: (2019)

Optimizing the Timing of Highest Hydrocortisone Dose in Children and Adolescents With 21-Hydroxylase Deficiency
por: Schröder, Mariska A M, et al.
Publicado: (2021)

Expression of TMEM207 in Colorectal Cancer: Relation between TMEM207 and Intelectin-1
por: Maeda, Kenichi, et al.
Publicado: (2016)

SAT-019 Clinical Disorders and Diseases Marked by Elevated Adrenal C11-oxy C(21) and C11-oxy C(19) Steroid Levels
por: Du Toit, Therina, et al.
Publicado: (2019)

Memorandum 207: plans for 1985
por: Garreta, D
Publicado: (1984)

Another view of R207
Publicado: (1975)

Health Tract, No. 207: Inheritances
Publicado: (1864)

Health Tract, No. 207: Inheritances
Publicado: (1865)

Height augmentation in 11β-hydroxylase deficiency congenital adrenal hyperplasia
por: Nour, Munier A, et al.
Publicado: (2015)

Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia
por: Kolahdouz, Mahsa, et al.
Publicado: (2015)

Gender identity in congenital adrenal hyperplasia secondary to 11-hydroxylase deficiency
por: Bin-Abbas, Bassam S., et al.
Publicado: (2006)

Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
por: Pignatelli, Duarte, et al.
Publicado: (2020)

THU188 Clinical Conundrum: Salt Wasting Congenital Adrenal Hyperplasia With Paradoxical High Cortisol
por: Pillai, Chanthu
Publicado: (2023)

Adrenocortical tumor in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
por: Dung, Vu Chi, et al.
Publicado: (2015)

Phenotype of patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
por: Dung, Vu Chi, et al.
Publicado: (2015)

Birth Size in Neonates with Congenital Adrenal Hyperplasia due to 21-hydroxylase Deficiency
por: Dörr, Helmuth G., et al.
Publicado: (2019)

Sexuality in Males With Congenital Adrenal Hyperplasia Resulting From 21-Hydroxylase Deficiency
por: Gehrmann, Katharina, et al.
Publicado: (2019)

Molecular diagnosis of patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency
por: Espinosa Reyes, Tania Mayvel, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_a8iblg39r7e0m592058ml9bdur