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Research 241–270 of 1000+
- The Nutrient–Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs
- Skin Manifestations in Primary Immunodeficient Children
- Endocrine-skin interactions
- <i>WNT10A</i> , dermatology and dentistry
- Types and Treatment of Hair Loss in Men and Women
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Diseases of Periocular Hair
- Hair and Scalp Dermatoscopy (Trichoscopy)
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Therapeutic approach and management of Marz-e-Shayb (Premature greying of hair) in the perspective of Unani medicine: A case study
- Mixing the Old with the New: Drug Repurposing for Immune Deficiency in the Era of Precision Medicine and Pediatric Genomics
- Polycystic Ovary Syndrome and Its Differential Diagnosis
- Do you know this syndrome? * Você conhece esta síndrome? *
- Oral Presentations
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Physiology and Medical Treatments for Alopecia
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Heterogeneity of Polymorphous Light Eruption: A Study of 105 Patients
- Hairless-knockout piglets generated using the clustered regularly interspaced short palindromic repeat/CRISPR-associated-9 exhibit abnormalities in the skin and thymus
- The involvement of androgens in human hair growth
- The first 20 years of skin of color dermatology: An era of advancements in skin, hair, and nail disorders
- Normal Hair Growth in Children
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Diagnosis and management of vascular Ehlers-Danlos syndrome: Experience of the UK national diagnostic service, Sheffield