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Research 271–300 of 1000+
- Hair and nail involvement in lupus erythematosus
- Clinical characterization of men with long QT syndrome and torsades de pointes associated with hypogonadism: A review and pharmacovigilance study
- Elevated fasting insulin is associated with cardiovascular and metabolic risk in women with polycystic ovary syndrome
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Enhanced viability and neural differential potential in poor post-thaw hADSCs by agarose multi-well dishes and spheroid culture
- METABOLIC DISOEDEKS AND HAIE GEOWTH
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Successful induction of oral tolerance in Netherton syndrome
- The Function of Zinc in Animal, Plant, and Human Nutrition
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Molecular Genetics of Alopecias
- The clinical spectrum of parathyroid disease
- Androgen profile in Chinese women with polycystic ovary syndrome in their reproductive years
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Infertility: Evaluation and Initial Management
- Polycystic ovary syndrome: diagnosis and management of related infertility
- Lipedematous Alopecia: Clinical, Histopathological, and Trichoscopic Findings of a Single Case and Review of the Literature
- Debatable Topics in PCOS Patients
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Variations in anterior segment parameters among different phenotypes of polycystic ovary syndrome
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- The Skin and Subcutaneous Tissues
- Woolly Antics between the Sheaths
- Book Reviews
- Alopecia and Its homoeopathic treatment
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations