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Research 841–870 of 1000+
- Case number 19th of perforating necrobiosis lipoidica worldwide
- 199 Impairment of notch 1 signaling is a common defect in lesions from patients with hidradenitis suppurativa
- Study of effect of myoinositol on menstrual irregularities and skin problems in polycystic ovarian syndrome cases
- Acne
- Recognizing polycystic ovary syndrome in the primary care setting
- Clinicopathologic and Morphologic Analysis of the Adrenal Gland in Pomeranians with Non-Illness Alopecia
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- Human hair production by scalp samples grafted onto nude mice. Biochemical data on normal human hair and the genetic defect trichothiodystrophy
- Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion
- Single cell deciphering of pruritic keloids: the interaction between fibroblasts and Schwann cells through the Midkine signaling
- Effective Treatment of Folliculitis Decalvans With a Combination of Oral Isotretinoin and Rifampicin
- Erosive Pustular Dermatosis of the Scalp Arising on Long-Standing Burn Scars: A Report of Three Cases and Brief Review of Literature
- Behavioral Welfare Research for the Management of Sanctuary Chimpanzees (Pan troglodytes)
- Phospholipase's role in maintaining and restoring skin and hair health
- The Burden of Disease in Alopecia Areata: Canadian Online Survey of Patients and Caregivers
- Polyglandular Autoimmune Syndrome Type 3D : A Case Report
- Nutraceutical Intervention of Seeds in the Treatment of Poly Cystic Ovarian Syndrome; A Systematic Review
- Photosensitivity reaction induced by finasteride
- Prevalence and Predictors of Impaired Glucose Tolerance and Diabetes Mellitus Type 2 in Patients with Polycystic Ovary Syndrome
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- The Shaven (Sha) Mutation, Chromosome 15
- Assessment of efficacy and safety of dapsone gel 5% in the treatment of acne vulgaris
- [Construction and identification of mouse model with conditional knockout of p75 neurotrophin receptor gene in epidermal cells by Cre-loxP system].
- Zebrafish Model of Hereditary Pigmentary Disorders
- Characterization of novel TMEM173 mutation with additive IFIH1 risk allele
- A Teenage Girl with Unexpected Pubertal Changes
- Association of Androgenic Alopecia with Metabolic Syndrome
- Clinical Analysis of 1,360 Patients Presenting with Male Pattern Hair Loss
- Epidermis-specific ablation of claudin-1 in adult mice demonstrates the essential role of a tight junction barrier in skin homeostasis