Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.
about
Anti-müllerian hormone: a valuable addition to the toolbox of the pediatric endocrinologistNew facets of androgen replacement therapy during childhood and adolescence.Neonatal amygdala lesions alter basal cortisol levels in infant rhesus monkeys.The androgen receptor is selectively involved in organization of sexually dimorphic social behaviors in mice.Androgen receptor mutations associated with androgen insensitivity syndrome: a high content analysis approach leading to personalized medicineIs there any clinical relevant difference between non mosaic Klinefelter Syndrome patients with or without Androgen Receptor variations?Mutational Analysis of Androgen Receptor Gene in Two Families with Androgen InsensitivityAssociations of Maternal and Infant Testosterone and Cortisol Levels With Maternal Depressive Symptoms and Infant Socioemotional Problems.Effects of perinatal testosterone on infant health, mother-infant interactions, and infant development.Diagnosis of diseases of steroid hormone production, metabolism and action.Evidence that obesity and androgens have independent and opposing effects on gonadotropin production from puberty to maturity.The differential role of androgens in early human sex development.UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex developmentMini puberty and its interpretationCan Hypertrophy of the Contralateral Testis Predict the Absence of a Viable Testis in Infancy with Cryptorchidism: A Prospective AnalysisFamilial forms of disorders of sex development may be common if infertility is considered a comorbidity.The in vivo role of androgen receptor SUMOylation as revealed by androgen insensitivity syndrome and prostate cancer mutations targeting the proline/glycine residues of synergy control motifs.Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor geneThe Long-Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor GeneComplete Androgen Insensitivity Syndrome in Three Generations of Indian Pedigree.An infertile man with gynecomastia caused by a novel mutation of the androgen receptor gene.Society for Endocrinology UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Revised 2015).Transient isolated scrotal hair development in infancy.AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity.Early contributions to infants' mental rotation abilities.Up-To-Date Review About Minipuberty and Overview on Hypothalamic-Pituitary-Gonadal Axis Activation in Fetal and Neonatal Life
P2860
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P2860
Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
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2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
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2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.
@en
Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.
@nl
type
label
Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.
@en
Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.
@nl
prefLabel
Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.
@en
Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.
@nl
P2093
P356
P1476
Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene.
@en
P2093
Albert David
Anne-Marie Bertrand
Charles Sultan
Claire Bouvattier
Claudine Lecointre
Jean-Claude Carel
Jean-Louis Chaussain
Yves Morel
P356
10.1210/JCEM.87.1.7923
P407
P577
2002-01-01T00:00:00Z