Laparoscopic transabdominal pre-peritoneal hernia repair with bilateral orchidectomy in partial androgen insensitivity syndrome.

Genetic variants, clinical characteristics, and surgical treatments of 46 children with androgen insensitivity syndrome.

Case Report: Laparoscopic vaginoplasty in a case of partial androgen insensitivity syndrome and a literature review of 16 cases in China.

Partial Androgen Insensitivity Syndrome and Congenital Adrenal Hyperplasia-A Case Report of the Coexistence of Two Rare Diseases in One Patient.

Familial novel androgen receptor gene variant associated with bilateral cryptorchidism and severe male infertility: A case report.

Genital masculinizing reconstruction for untreated intersex individuals in adulthood: a case report.

Gynecomastia and Its Management In Boys With Partial Androgen Insensitivity Syndrome.

Recommendations for 46,XY Disorders/Differences of Sex Development Across Two Decades: Insights from North American Pediatric Endocrinologists and Urologists.

A 10-YEAR STUDY OF CHILDREN WITH GONADAL TUMORS AND DISORDERS OF SEX DIFFERENTIATION, IN ROMANIA.

Clinical, Hormonal, and Genetic Spectrum of 46 XY Disorders of Sexual Development (DSD) Patients.

The role of pre- and postnatal investigations in suspected isolated hypospadias.

MYRF mutation leads to a single manifestation of sexual development and mimics partial androgen insensitivity syndrome: a case report and literature review.

A case of mild partial androgen insensitivity syndrome in a juvenile boy.

Adult Outcome After Partial Androgen Insensitivity Syndrome: Diagnosed and Assigned Female in Infancy.

Urethral reconstruction using amniotic membrane allograft in hereditary androgen insensitivity syndrome: a case series.

Serum steroid metabolite profiling by LC-MS/MS in two phenotypic male patients with HSD17B3 deficiency: Implications for hormonal diagnosis.

A Case Report on Ambiguous Genitalia: A Diagnostic, Therapeutic, and Cosmetic Challenge.

Pubertal and Gonadal Outcomes in 46,XY Individuals with Partial Androgen Insensitivity Syndrome Raised as Girls.

Case report: Identification of a frameshift mutation in GC enrichment and the GCC repeat region of the androgen insensitivity receptor (AR) gene in a patient with complete androgen insensitivity syndrome by whole-exome sequencing (WES) combined with specific PCR and deep sequencing.

Clinical characteristics, AR gene variants, and functional domains in 64 patients with androgen insensitivity syndrome.

Total corpora mobilization for penile reconstruction.

Leydig and Sertoli cell function in individuals with genital ambiguity, 46,XY karyotype, palpable gonads and normal testosterone secretion: a case-control study.

Ventral clitoroplasty preserves dorsal nerves in case of partial androgen insensitivity syndrome: 4 years follow-up.

Identification of Potential Genes in Pathogenesis and Diagnostic Value Analysis of Partial Androgen Insensitivity Syndrome Using Bioinformatics Analysis.

Clinical, Biochemical, and Molecular Characterization of Indian Children with Clinically Suspected Androgen Insensitivity Syndrome.

One hundred twelve cases of 46, XY DSD patients after initial gender assignment: a short-term survey of gender role and gender dysphoria.

One-stage sex reassignment surgery at the delayed presentation in a patient with partial androgen insensitivity syndrome: A case report.

Late Diagnosis of Partial Androgen Insensitivity Syndrome in a Peruvian Child.

[Feminizing genitoplasty for prepubertal children and teenagers female].

Disorders of sex development and female reproductive capacity: A literature review.

Masculinizing surgery in disorders/differences of sex development: clinician- and participant-evaluated appearance and function.

Gender identity disorder (GID) in adolescents and adults with differences of sex development (DSD): A systematic review and meta-analysis.

The FKBP4 Gene, Encoding a Regulator of the Androgen Receptor Signaling Pathway, Is a Novel Candidate Gene for Androgen Insensitivity Syndrome.

The LH/FSH ratio is not a sex-dimorphic marker after infancy: data from 6417 healthy individuals and 125 patients with Differences of Sex Development.

Post-operative complications following feminizing genitoplasty in moderate to severe genital atypia: Results from a multicenter, observational prospective cohort study.

Generation of human induced pluripotent stem cell (SKLRMi001-A) from a patient with partial androgen insensitivity syndrome (PAIS).

"Idiopathic" partial androgen insensitivity syndrome in 11 grandsons of women treated by diethylstilbestrol during gestation: a multi-generational impact of endocrine disruptor contamination?

Community perspectives on difference of sex development (DSD) diagnoses: A crowdsourced survey.

Clinical, hormonal and genetic characteristics of androgen insensitivity syndrome in 39 Chinese patients.

Complete Androgen Insensitivity Syndrome: Dilemmas for Further Management after Gonadectomy.

Hypogonadism and Cryptorchidism.

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

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

Gonadal Tissue Cryopreservation for Children with Differences of Sex Development.

Mobile DNA in Endocrinology: LINE-1 Retrotransposon Causing Partial Androgen Insensitivity Syndrome.

Initial assessment of a child with suspected disorder of sex development.

Gonadal Tissue Cryopreservation for a Girl With Partial Androgen Insensitivity Syndrome.

Establishing reproductive potential and advances in fertility preservation techniques for XY individuals with differences in sex development.

Partial androgen insensitivity syndrome in a 68-year-old patient.

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

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.

Partial androgen insensitivity syndrome presenting as pubertal gynecomastia: clinical and hormonal findings and a novel mutation in the androgen receptor gene.

Long-term Healthcare of People with Disorders of Sex Development: Predictors of Pubertal Outcomes of Partial Androgen Insensitivity Syndrome - Authors' Reply.

Long-term healthcare of people with disorders of sex development: Predictors of pubertal outcomes of partial androgen insensitivity syndrome.

Management of Gonads in Adults with Androgen Insensitivity: An International Survey.

Predicting puberty in partial androgen insensitivity syndrome: Use of clinical and functional androgen receptor indices.

Growth Hormone Deficiency Causing Micropenis: Lessons Learned From a Well-Adjusted Adult.

Partial androgen insensitivity syndrome caused by a deep intronic mutation creating an alternative splice acceptor site of the AR gene.

Comparison between two inhibin B ELISA assays in 46,XY testicular disorders of sex development (DSD) with normal testosterone secretion.

Partial androgen insensitivity syndrome due to somatic mosaicism of the androgen receptor.

Identification of the Underlying Androgen Receptor Defect in the Dallas Reifenstein Family.

Another Look at Hereditary Partial Androgen Insensitivity Syndrome in an Indigenous Community in the Northern Territory of Australia.

Re: Topical Dihydrotestosterone to Treat Micropenis Secondary to Partial Androgen Insensitivity Syndrome (PAIS) before, during, and after Puberty-A Case Series.

Creation of a Neovagina by Laparoscopic Modified Davydov Vaginoplasty in Patients with Partial Androgen Insensitivity Syndrome.

Controversies of Sex Re-assignment in Genetic Males with Congenital Inadequacy of the Penis.

AR mutations in 28 patients with androgen insensitivity syndrome (Prader grade 0-3).

Heterozygous Nonsense Mutation in the Androgen Receptor Gene Associated with Partial Androgen Insensitivity Syndrome in an Individual with 47,XXY Karyotype.

Efficacy and Safety of Continuous Subcutaneous Infusion of Recombinant Human Gonadotropins for Congenital Micropenis during Early Infancy
.

Novel mutations of the SRD5A2 and AR genes in Thai patients with 46, XY disorders of sex development.

Identification of an AR Mutation-Negative Class of Androgen Insensitivity by Determining Endogenous AR Activity.

The Long-Term Outcome of Boys With Partial Androgen Insensitivity Syndrome and a Mutation in the Androgen Receptor Gene.

Gender identity and gender of rearing in 46 XY disorders of sexual development.

46,XY disorder of sex development (DSD) due to 17β-hydroxysteroid dehydrogenase type 3 deficiency.

A Novel Mutation in Human Androgen Receptor Gene Causing Partial Androgen Insensitivity Syndrome in a Patient Presenting with Gynecomastia at Puberty.

Sigmoid vaginoplasty in testicular feminising syndrome: surgical technique, outcome and review of the literature.

Endocrine and molecular investigations in a cohort of 25 adolescent males with prominent/persistent pubertal gynecomastia.

Gonadal malignancy in 202 female patients with disorders of sex development containing Y-chromosome material.

Topical dihydrotestosterone to treat micropenis secondary to partial androgen insensitivity syndrome (PAIS) before, during, and after puberty - a case series.

Partial androgen insensitivity syndrome with persistent müllerian remnants. A case report.

Invasive Ductal Carcinoma in a 46,XY Partial Androgen Insensitivity Syndrome Patient on Hormone Therapy.

Subjective need for psychological support (PsySupp) in parents of children and adolescents with disorders of sex development (dsd).

Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review.

Screening for mutations in 17β-hydroxysteroid dehydrogenase and androgen receptor in women presenting with partially virilised 46,XY disorders of sex development.