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Research 91–120 of 532
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- The involvement of androgens in human hair growth
- Dermoscopy: not just for dermatologists
- Out/Performing Our Selves: Invitation for Dialogue
- Diagnosis and treatments of hirsutism: where are we?
- Testosterone therapy for transgender men
- The dihydrotestosterone (DHT) hypothesis of prostate cancer and its therapeutic implications
- Acquired scalp alopecia. Part II: A review
- Estimating the Contribution of the Prostate to Blood Dihydrotestosterone
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- A case study on hair fall, PCOS, and metabolic correction through homeopathy
- Beyond the Surface: Exploring the Mind-Skin Dynamics of Psychodermatology
- Menopause in Women, Andropause in Men: Myth, Reality, and Management
- Clinical Management in Psychodermatology
- Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report
- An Adult With Hair Loss! a Rare Case of Non-Classical 3β Hydroxysteroid Dehydrogenase (3β HSD) Deficiency
- Clinical biochemistry of dihydrotestosterone
- Hormonal Therapies for Individuals with Intersex Conditions
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Identification of two additional novel mutations in the AR gene associated with severe forms of androgen insensitivity syndrome
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Iatrogenic Cushing's Syndrome in a Patient With Salt-Wasting Congenital Adrenal Hyperplasia (SWCAH)
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- American Association of Clinical Endocrinologists Medical Guidelines for Clinical Practice for the Diagnosis and Treatment of Hyperandrogenic Disorders
- Diagnostic imaging in congenital adrenal hyperplasia – how does it help?
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- A recently characterized, underdiagnosed cause of female androgenetic alopecia and polycystic ovarian syndrome: non-classical 21 hydroxylase deficiency
- Wokeness in Our Practice