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Research 481–510 of 1000+
- Society for Endocrinology Clinical Practice Guideline for the Evaluation of Androgen Excess in Women
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- TRANSMEDCON 2022: E-Poster Abstracts
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Lean Women with Polycystic Ovary Syndrome
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Botulinum Toxin Off-Label Use in Dermatology: A Review
- Scalp Itch: A Systematic Review
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- Pathological findings in a case of stiff person syndrome with anti‐GAD antibodies
- Premature graying of hair
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- Anagen effluvium
- Oral Supplementation with l-Cystine, <i>Serenoa repens</i>, <i>Cucurbita pepo</i>, and <i>Pygeum africanum</i> in Chronic Telogen Effluvium and Androgenetic Alopecia: A Double-Blind, Placebo-Controlled, Randomized Clinical Study
- Role of caffeine in the management of androgenetic alopecia
- A case of hidradenitis suppurativa with treatment effective by finasteride
- Diabetes, ovarian tumor, hyperparathyroidism, and papillary cancer: A chance association?
- Caring for women with polycystic ovary syndrome
- Adams–Oliver syndrome: new evidence in variable expressivity?
- Creatine phosphokinase levels and isotretinoin therapy
- Androgen excess: a hallmark of polycystic ovary syndrome
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Alopecia: Association with Resistance to Thyroid Hormones
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- CLINICAL UPDATES IN HAIR
- Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells