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Research 631–660 of 1000+
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- Bioengineered skin organoids: from development to applications
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Evaluation of Premature Pubarche Cases: A Single CenterExperience
- Nonclassic Congenital Adrenal Hyperplasia: An Overview
- Premature isolated adrenarche in a six-year-old girl
- Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects
- Prematüre Pubarş Olgularının Değerlendirilmesi: Tek Merkez Deneyimi
- EFFECTS of SOME CHEMICALS in COSMETIC PRODUCTS on PREGNANT, FETUS and NEWBORN HEALTH
- Immunological control of skin development: from homeostasis to developmental pathologies
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Predominant expression of 5 alpha-reductase type 1 in pubic skin from normal subjects and hirsute patients.
- Familial congenital generalized hypertrichosis
- 46, XY Disorder of Sexual Development with Ambiguous Female External Genitalia: A Case Report
- Editorial: Retinoids — dermatologists’ drug of the decade
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Mister XX
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Delayed Diagnosis of Congenital Adrenal Hyperplasia Due to 3β-Hydroxysteroid Dehydrogenase Type 2 Deficiency
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Precocious puberty: the unlikely herald of Familial adenomatous polyposis in a young girl
- The diversity of sex development: What do conditions affecting sex development teach us about sexual diversity?
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- Alternative androgen pathways
- Eyelashes: Anatomical and Physiological Features, Eyelash Loss and Trichomegaly: Review
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- From the Elephant Man to Barbie Girl: Dissecting the Freak from the Margins to the Mainstream