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Research 391–420 of 1000+
- Case 1: Severe acne – not just skin deep
- Hemoglobinopathy and Systemic Lupus: A Rare Association
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Evaluation of Premature Pubarche Cases: A Single CenterExperience
- 133 TIME LAGS BETWEEN VARIOUS MATURITY MEASURES AND SPERMACRCHE
- Clinical characteristics and risk factors of female precocious puberty
- Precocious puberty: the unlikely herald of Familial adenomatous polyposis in a young girl
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Stigmata of Liver Disease in a Cirrhotic Patient
- Lasers and Energy-Based Devices in Men
- Differences in anatomical area-specific wound healing in hidradenitis suppurativa/acne inversa after surgery
- An innovative technique of hydrosurgery in the treatment of osmidrosis
- Immune-mediated Coombs negative intravascular haemolysis in systemic lupus erythematosus (SLE)
- The secretory clear cell of the eccrine sweat gland as the probable source of excess sweat production in hyperhidrosis
- Fox-Fordyce Disease
- Premature isolated adrenarche in a six-year-old girl
- Diseases of the Hair
- An Adult With Hair Loss! a Rare Case of Non-Classical 3β Hydroxysteroid Dehydrogenase (3β HSD) Deficiency
- Hair Whorls in the Dog (<i>Canis familiaris</i>). I. Distribution
- Electrophoretic variability in human hair: Comparative sodium dodecyl sulfate‐polyacrylamide gel electrophoresis of body and head hair proteins
- Mechanism of action of androgen in hair follicles
- A case report of Graham-Little–Piccardi–Lassueur syndrome
- Frontal fibrosing alopecia: a survey in 16 patients
- Interaction between dermal papilla cells and follicular epithelial cells in vitro: effect of androgen.
- DIAGNOSIS AND MANAGEMENT OF HIRSUTISM
- THE USE OF TOFACITINIB IN THE TREATMENT OF IMMUNE-MEDIATED UNIVERSAL ALOPECIA IN A PATIENT WITH SYSTEMIC LUPUS ERYTHEMATOSUS: A CASE REPORT
- SAT-134 Postmenopausal Virilization: Rare Case of an Ovarian Tumor Not Easily Identified on Imaging
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Bilateral periorbital swelling as the presenting manifestation of recurrent breast carcinoma
- Graham–Little–Piccardi–Lassueur syndrome: case report and systematic review of a rare LPP variant