Pages that link to "Q43852912"
Jump to navigation
Jump to search
The following pages link to Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene (Q43852912):
Displaying 35 items.
- Androgen insensitivity syndrome (Q26850843) (← links)
- Anti-müllerian hormone: a valuable addition to the toolbox of the pediatric endocrinologist (Q28661014) (← links)
- New facets of androgen replacement therapy during childhood and adolescence (Q30437366) (← links)
- Neonatal amygdala lesions alter basal cortisol levels in infant rhesus monkeys (Q30437681) (← links)
- The androgen receptor is selectively involved in organization of sexually dimorphic social behaviors in mice (Q30439036) (← links)
- Androgen receptor mutations associated with androgen insensitivity syndrome: a high content analysis approach leading to personalized medicine (Q33518450) (← links)
- Is there any clinical relevant difference between non mosaic Klinefelter Syndrome patients with or without Androgen Receptor variations? (Q33793955) (← links)
- Mutational Analysis of Androgen Receptor Gene in Two Families with Androgen Insensitivity (Q33815483) (← links)
- Associations of Maternal and Infant Testosterone and Cortisol Levels With Maternal Depressive Symptoms and Infant Socioemotional Problems (Q33880230) (← links)
- Effects of perinatal testosterone on infant health, mother-infant interactions, and infant development (Q33894369) (← links)
- Diagnosis of diseases of steroid hormone production, metabolism and action. (Q34161154) (← links)
- Evidence that obesity and androgens have independent and opposing effects on gonadotropin production from puberty to maturity (Q34354008) (← links)
- The differential role of androgens in early human sex development (Q34783437) (← links)
- UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Q35094148) (← links)
- Mini puberty and its interpretation (Q35712677) (← links)
- Can Hypertrophy of the Contralateral Testis Predict the Absence of a Viable Testis in Infancy with Cryptorchidism: A Prospective Analysis (Q35962570) (← links)
- Familial forms of disorders of sex development may be common if infertility is considered a comorbidity (Q36207081) (← links)
- 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. (Q36225738) (← links)
- Complete androgen insensitivity syndrome caused by a deep intronic pseudoexon-activating mutation in the androgen receptor gene (Q37243611) (← links)
- The Long-Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor Gene (Q37393257) (← links)
- Molecular biology of androgen insensitivity (Q37922886) (← links)
- Complete Androgen Insensitivity Syndrome in Three Generations of Indian Pedigree (Q41651115) (← links)
- An infertile man with gynecomastia caused by a novel mutation of the androgen receptor gene (Q42555848) (← links)
- Society for Endocrinology UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Revised 2015). (Q42837374) (← links)
- Transient isolated scrotal hair development in infancy (Q44782716) (← links)
- AR and SRD5A2 gene mutations in a series of 51 Turkish 46,XY DSD children with a clinical diagnosis of androgen insensitivity (Q45151685) (← links)
- Early contributions to infants' mental rotation abilities. (Q46018051) (← links)
- Up-To-Date Review About Minipuberty and Overview on Hypothalamic-Pituitary-Gonadal Axis Activation in Fetal and Neonatal Life (Q57175032) (← links)
- Two Korean girls with complete androgen insensitivity syndrome diagnosed in infancy (Q60923380) (← links)
- Partial androgen insensitivity syndrome presenting as pubertal gynecomastia: clinical and hormonal findings and a novel mutation in the androgen receptor gene (Q60927469) (← links)
- Androgen Insensitivity Syndrome: Clinical Phenotype and Molecular Analysis in a Single Tertiary Center Cohort (Q64235840) (← links)
- [Genetic anomalies of the androgen receptor and sexual ambiguity with normal testicular function at birth] (Q81909602) (← links)
- A clinical algorithm to diagnose differences of sex development (Q91902349) (← links)
- Ontogeny of Hypothalamus-Pituitary Gonadal Axis and Minipuberty: An Ongoing Debate? (Q92132517) (← links)
- Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients (Q94450909) (← links)