Insensitivity Syndrome
10.1016/j.jsbmb.2019.105420

Features of the fetal gonad in androgen synthesis in the postpubertal testis are preserved in complete androgen insensitivity syndrome due to a novel genetic splice site donor variant in androgen receptor gene intron 1


Insensitivity Syndrome
10.1007/978-3-030-05683-4_3

Biology of Gender Identity and Gender Incongruence


Insensitivity Syndrome
10.1016/j.steroids.2019.02.007

Severe forms of complete androgen insensitivity syndrome caused by a p.Q65X novel mutation in androgen receptor: Clinical manifestations, imaging findings and molecular genetics


Insensitivity Syndrome
10.1016/J.JPEDSURG.2018.12.011

Postnatal germ cell development during first 18 months of life in testes from boys with non-syndromic cryptorchidism and complete or partial androgen insensitivity syndrome.


Insensitivity Syndrome
10.1515/jpem-2018-0323

Sex assignment practice in disorders of sexual differentiation: survey results from paediatric endocrinologists in the Arab region


Insensitivity Syndrome
10.1159/000509812

Spectrum of Pathogenic Variants in SRD5A2 in Indian Children with 46,XY Disorders of Sex Development and Clinically Suspected Steroid 5α-Reductase 2 Deficiency


Insensitivity Syndrome
10.18597/rcog.3177

[SAFETY AND EFFICACY OF VECCHIETTI VAGINOPLASTY IN VAGINAL AGENESIS: COHORT STUDY. MEDELLÍN, COLOMBIA 2007-2012].


Insensitivity Syndrome
10.1080/08941939.2019.1602690

Genetic Analysis Reveals Complete Androgen Insensitivity Syndrome in Female Children Surgically Treated for Inguinal Hernia.


Insensitivity Syndrome
10.1159/000502644

Gonadal Tissue Cryopreservation for Children with Differences of Sex Development


Insensitivity Syndrome
10.1016/j.jpag.2019.08.001

Novel Androgen Receptor gene variant containing a premature termination codon in a patient with androgen insensitivity syndrome.


Insensitivity Syndrome
10.1016/j.jpag.2019.06.005

A Management Protocol for Gonad Preservation in Patients with Androgen Insensitivity Syndrome.


Insensitivity Syndrome
10.1210/JS.2019-SAT-205

SAT-205 ESR1 Q375H and R394H Mutants Associated with Estrogen Insensitivity Syndrome Mediate Genome-Wide Genetic and Epigenetic Aberrances


Insensitivity Syndrome
10.3760/cma.j.issn.1003-9406.2019.04.017

[Analysis of AR gene variant in an infant with complete androgen insensitivity syndrome].


Insensitivity Syndrome
10.14341/PROBL10166

[Somatic mutations in the androgen receptor gene as the cause of androgen insensitivity syndrome].


Insensitivity Syndrome
10.1210/js.2019-00306

Next-Generation Sequencing Reveals Novel Genetic Variants (SRY, DMRT1, NR5A1, DHH, DHX37) in Adults With 46,XY DSD


Insensitivity Syndrome
10.1530/ERC-19-0132

Non-canonical dimerization of the androgen receptor and other nuclear receptors: implications for human disease.


Insensitivity Syndrome
10.7322/jhgd.v29.9418

Complete Androgen Insensitivity Syndrome and Literature Review


Insensitivity Syndrome
10.1186/s13256-019-2166-9

Diagnosis of female 17α-hydroxylase deficiency after gonadectomy: a case report


Insensitivity Syndrome
10.1210/JS.2019-SUN-018

SUN-018 Epigenetic Loss of the PIWI/piRNA Machinery in Gonadal Tumors in Androgen Insensitivity Syndrome


Insensitivity Syndrome
10.1080/01443615.2018.1554634

A novel missense mutation in the androgen receptor gene causes the complete androgen insensitivity syndrome


Insensitivity Syndrome
10.1002/mgg3.906

Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique


Insensitivity Syndrome
10.4103/ijem.IJEM_271_19

Disorders of Sex Development: A 10 Years Experience with 73 Cases from the Kashmir Valley


Insensitivity Syndrome
10.1002/uog.20585

OC23.05: Effect of maternal BMI on ultrasound image quality at the routine anatomy scan


Insensitivity Syndrome
10.1093/humrep/dez004

Gonadoblastoma Y locus genes expressed in germ cells of individuals with dysgenetic gonads and a Y chromosome in their karyotypes include DDX3Y and TSPY


Insensitivity Syndrome
10.4103/jdrntruhs.jdrntruhs_101_18

Complete androgen insensitivity syndrome: A case report


Insensitivity Syndrome
10.1242/dmm.039297

Genome-wide analysis of androgen receptor binding and transcriptomic analysis in mesenchymal subsets during prostate development


Insensitivity Syndrome
10.1507/endocrj.EJ18-0494

Dihydrotestosterone induces minor transcriptional alterations in genital skin fibroblasts of children with and without androgen insensitivity.


Insensitivity Syndrome
10.4103/jhrs.jhrs_151_18

Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy


Insensitivity Syndrome
10.15562/bmj.v8i2.1380

Testicular carcinoma in a female with 46-XY karyotype: a case report


Insensitivity Syndrome
10.1007/7854_2018_70

The Sexual Differentiation of the Human Brain: Role of Sex Hormones Versus Sex Chromosomes.


Insensitivity Syndrome
10.1016/j.sempedsurg.2019.150841

Clinical management in mixed gonadal dysgenesis with chromosomal mosaicism: Considerations in newborns and adolescents.


Insensitivity Syndrome
10.1080/24694193.2019.1691677

The XY Female: Exploring Care for Adolescent Girls with Complete Androgen Insensitivity Syndrome


Insensitivity Syndrome
10.3389/fendo.2019.00906

Hypogonadism and Cryptorchidism


Insensitivity Syndrome
10.1002/uog.20586

OC23.06: Significant variation in practice for first trimester anatomy assessment: results from a nationwide survey


Insensitivity Syndrome
10.1530/EJE-19-0383

Bone mineral density, body composition and metabolic profiles in adult women with complete androgen insensitivity syndrome and removed gonads using oral or transdermal estrogens.


Insensitivity Syndrome
10.1210/jc.2019-00144

Mobile DNA in Endocrinology: LINE-1 retrotransposon causing Partial Androgen Insensitivity Syndrome.


Insensitivity Syndrome
10.1016/j.jmig.2019.02.025

Novel Minimally Invasive Technique of Neovaginoplasty Using An Absorbable Adhesion Barrier.


Insensitivity Syndrome
10.3760/CMA.J.ISSN.0253-3006.2019.04.011

Efficacy of urethroplasty for disorders of sex development with concurrent severe hypospadias


Insensitivity Syndrome
10.7326/AITC201907020

Care of the Transgender Patient


Insensitivity Syndrome
10.1080/19396368.2018.1549619

Molecular diagnostics of disorders of sexual development: an Indian survey and systems biology perspective


Insensitivity Syndrome
10.1016/j.steroids.2019.108489

Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome


Insensitivity Syndrome
10.1136/archdischild-2019-epa.572

P222 Analysis of medical help organisation for intersex-people in Russian federation. the study was formed by the leading clinicians and doctors of the St. petersburg state pediatric medical university


Insensitivity Syndrome
10.12816/EJHM.2019.63574

Disorders of Sexual Development in Proximal Hypospadias in Children


Insensitivity Syndrome
10.3760/cma.j.issn.0578-1310.2019.06.007

[Gender selection and postoperative follow-up analysis in 85 children with 46, XY disorders of sex development].


Insensitivity Syndrome
10.31729/JNMA.4206

Malignant Leydig Cell Tumor in Elderly Complete Androgen Insensitivity Patient: A Case Report.


Insensitivity Syndrome
10.1210/JS.2019-SAT-213

SAT-213 Late Diagnosis of Complete Androgen Insensitivity


Insensitivity Syndrome
10.1007/s12325-019-01021-5

Evaluation of Safety and Efficacy of Growth Hormone Therapy by IGF-1 Z Score in Children with Short Stature


Insensitivity Syndrome
10.1080/09513590.2018.1529160

New mutation causing androgen insensitivity syndrome – a case report and review of literature


Insensitivity Syndrome
10.1210/js.2019-00023

Gonadal Tissue Cryopreservation for a Girl With Partial Androgen Insensitivity Syndrome


Insensitivity Syndrome
10.3390/ijerph16071268

Different Clinical Presentations and Management in Complete Androgen Insensitivity Syndrome (CAIS)


Insensitivity Syndrome
10.1007/978-1-60327-161-5_10

Androgen Insensitivity Syndrome


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