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- Dermatología en la Práctica Médica General Vol. 13
- Dermatological care of gender‐diverse patients in Australia
- A Rare Case Report of Congenital Adrenal Hyperplasia: 46XX at Tertiary Care Centre, Visnagar, North Gujarat.
- Managing Acne in Individuals with Polycystic Ovarian Syndrome
- The Role of Hormonal Imbalances in Amenorrhea
- Care Considerations and Management of Transgender Individuals After Kidney Transplantation: A Single Institution Experience and Literature Review
- An affirming approach to caring for transgender and gender-diverse youth
- SAT646 Cutaneous Manifestations In Adults With Gender Dysphoria Under Treatment Hormonal In External Consultation Of The Hospital De San José , Bogotá Colombia
- Sebaceous gland diseases: clinical picture risk factors and treatment
- Die Menopause und ihre Auswirkungen auf Haut und Haare
- (053) Multidisciplinary Treatment of Transgender Woman with Severe Gender Dysphoria and Comorbid Psychiatric Disorders - Case Report
- PSSD,PFS,PRSD: A perspective for aetiology and treatment
- VIJAYA-The one who fights to win
- ODP292 A Xanthomatous Hypophysitis: Always Think Twice Before Pituitary Resection.
- A Case of Sheehan Syndrome Presenting with Pancytopenia and Dilated Cardiomyopathy: A Rare Combination
- Nothing about us, without us: Are we asking the right questions in transgender research?
- SUN-287 A Case of Ectopic Neurohypophysis
- Frontal fibrosing alopecia: follow-up of a brazilian group
- Contents
- Transgender Health Simplified: A Concise Guide to the Gynecologist
- Hair and Scalp Variation Related to Gender
- CHAPTER 1 Facial Feminization Surgery: A Global Approach
- Dermatologic care of the transgender patient - eScholarship
- Frontal Fibrosing Alopecia
- Female sexual dysfunction
- Incidence of alopecia from endocrine therapies in cancer
- Onychomatricoma with classic features: Case report and review of the literature
- Details always tell a big story: Importance of physical symptoms in evaluation of secondary causes of depression
- A case report of a novel homozygote mutation causing severe Leydig cell hypoplasia: insights in the coexistence of nonsense mutation and polymorphism in the same LHCGR gene locus
- Transsexualism