Consensus statement on management of intersex disorders - Wikidata - wikimedia - TriplyDB

Consensus statement on management of intersex disorders

Consensus statement on management of intersex disorders

http://www.wikidata.org/entity/Q24675420

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Gadd45g is essential for primary sex determination, male fertility and testis development Ovaries and female phenotype in a girl with 46,XY karyotype and mutations in the CBX2 gene Sex and gender issues in competitive sports: investigation of a historical case leads to a new viewpoint Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline Male sex determination: insights into molecular mechanisms Was "variations of reproductive development" considered?Congenital Adrenal Hyperplasia: Review from a Surgeon's Perspective in the Beginning of the Twenty-First Century Management of adolescents with congenital adrenal hyperplasia We used to call them hermaphrodites Sex-related variation in human behavior and the brain A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development The novel p.Cys65Tyr mutation in NR5A1 gene in three 46,XY siblings with normal testosterone levels and their mother with primary ovarian insufficiency Anogenital distance as a marker of androgen exposure in humans.Otoacoustic emissions, auditory evoked potentials and self-reported gender in people affected by disorders of sex development (DSD)Intrinsic androgen-dependent gene expression patterns revealed by comparison of genital fibroblasts from normal males and individuals with complete and partial androgen insensitivity syndrome.Clinical evaluation study of the German network of disorders of sex development (DSD)/intersexuality: study design, description of the study population, and data quality.A novel SRY missense mutation affecting nuclear import in a 46,XY female patient with bilateral gonadoblastoma.FSH Injections and Ultrasonography Determine Presence of Ovarian Components in the Evaluation of Ovotesticular Disorders of Sex Development Steroid hormone analysis in diagnosis and treatment of DSD: position paper of EU COST Action BM 1303 'DSDnet'.Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management".Holistic management of DSD.Utilization of health care services and satisfaction with care in adults affected by disorders of sex development (DSD).Tumors of bilateral streak gonads in patients with disorders of sex development containing y chromosome material.Mutation analysis of NR5A1 encoding steroidogenic factor 1 in 77 patients with 46, XY disorders of sex development (DSD) including hypospadias 46,XY female sex reversal syndrome with bilateral gonadoblastoma and dysgerminoma.Xenografting of human fetal testis tissue: a new approach to study fetal testis development and germ cell differentiation.Delayed Recognition of Disorders of Sex Development (DSD): A Missed Opportunity for Early Diagnosis of Malignant Germ Cell Tumors.Prenatal endocrine influences on sexual orientation and on sexually differentiated childhood behavior.New technologies for the identification of novel genetic markers of disorders of sex development (DSD).Normal intelligence in female and male patients with congenital adrenal hyperplasia How do Individuals with Complete Androgen Insensitivity Syndrome, Mayer-Rokitansky-Küster-Hauser Syndrome or Polycystic Ovary Syndrome Experience Contact to Other Affected Persons?The dilemma of the gender assignment in a Portuguese adolescent with disorder of sex development due to 17β-hydroxysteroid-dehydrogenase type 3 enzyme deficiency Disorders of sex development: new genes, new concepts.Disorders of sex development: a genetic study of patients in a multidisciplinary clinic.Prevalence of c-KIT mutations in gonadoblastoma and dysgerminomas of patients with disorders of sex development (DSD) and ovarian dysgerminomas.Classifying Intersex in DSM-5: Critical Reflections on Gender Dysphoria.Clinical Presentation of Klinefelter's Syndrome: Differences According to Age.Long-Term Follow-Up of Patients with 46,XY Partial Gonadal Dysgenesis Reared as Males.Normal sex differences in prenatal growth and abnormal prenatal growth retardation associated with 46,XY disorders of sex development are absent in newborns with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development

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P2860

Consensus statement on management of intersex disorders

http://www.wikidata.org/entity/Q24675420

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2006 nî lūn-bûn

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Consensus statement on management of intersex disorders

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Consensus statement on management of intersex disorders

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Consensus statement on management of intersex disorders

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Consensus statement on management of intersex disorders

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Consensus statement on management of intersex disorders

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Consensus statement on management of intersex disorders

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Consensus statement on management of intersex disorders

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Intersexuality and gender identity differentiation

Feminizing genitoplasty for congenital adrenal hyperplasia: what happens at puberty?

Phenotypic features, androgen receptor binding, and mutational analysis in 278 clinical cases reported as androgen insensitivity syndrome

Consensus statement on 21-hydroxylase deficiency from the European Society for Paediatric Endocrinology and the Lawson Wilkins Pediatric Endocrine Society

The role of maternal stimulation in the development of sexual behavior and its neural basis

Cognitive theories of early gender development

Carcinoma of the neovagina: case report and review of the literature

Aetiological diagnosis of male sex ambiguity: a collaborative study

Ambiguous genitalia with perineoscrotal hypospadias in 46,XY individuals: long-term medical, surgical, and psychosexual outcome

Female genital appearance: "normality" unfolds

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