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Research 931–960 of 1000+
- Therapeutic Applications of Hair Follicle Transplantation Beyond Hair Restoration
- Clinical characteristics and risk factors of female precocious puberty
- Precocious puberty: the unlikely herald of Familial adenomatous polyposis in a young girl
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- 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
- Hair Transplantation to the Axillae
- Evaluation of Premature Pubarche Cases: A Single CenterExperience
- Scalp Dermatology for the Hair Restoration Surgeon Trichotemnomania
- 133 TIME LAGS BETWEEN VARIOUS MATURITY MEASURES AND SPERMACRCHE
- In vitro assessment of some deodorant ingredients and determination of malodor inhibiting potentials of ascorbic acid, orlistat and mastic gum
- Interaction between dermal papilla cells and follicular epithelial cells in vitro: effect of androgen.
- The secretory clear cell of the eccrine sweat gland as the probable source of excess sweat production in hyperhidrosis
- Interaction between dermal papilla cells and follicular epithelial cells in vitro: effect of androgen
- Premature isolated adrenarche in a six-year-old girl
- Electrophoretic variability in human hair: Comparative sodium dodecyl sulfate‐polyacrylamide gel electrophoresis of body and head hair proteins
- Hair Whorls in the Dog (<i>Canis familiaris</i>). I. Distribution
- A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
- Graham–Little–Piccardi–Lassueur syndrome: case report and systematic review of a rare LPP variant
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Prematüre Pubarş Olgularının Değerlendirilmesi: Tek Merkez Deneyimi
- Expression of mRNA for androgen receptor, 5alpha-reductase and 17beta-hydroxysteroid dehydrogenase in human dermal papilla cells
- DIAGNOSIS AND MANAGEMENT OF HIRSUTISM
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- BCG'osis
- ALOPÉCIA CICATRICIAL E SÍNDROME RARA: DESAFIOS DIAGNÓSTICOS EM DERMATOLOGIA NA ATENÇÃO PRIMÁRIA À SAÚDE
- A Rare association of Mauriac syndrome and Van-Wyk Grumbach syndrome found in a young Saudi girl with poorly controlled type 1 Diabetes and Hypothyroidism: A Case Report and Brief literature review
- Diseases of the Hair
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- An Adult With Hair Loss! a Rare Case of Non-Classical 3β Hydroxysteroid Dehydrogenase (3β HSD) Deficiency