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Research 121–150 of 1000+
- Acne-Associated Syndromes
- Complementary and Alternative Treatments for Alopecia: A Comprehensive Review
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Diseases of Periocular Hair
- Acne and acneiform eruptions
- Psychodermatology
- Ichthyosis hystrix
- Ulerythema ophryogenes with multiple congenital anomalies
- Cystathionine β‐synthase‐deficient mice thrive on a low‐methionine diet
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Zinc Therapy in Dermatology: A Review
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- The association between serum zinc levels and subjective symptoms in zinc deficiency patients with chronic liver disease
- Synthesis and Actions of 5α-Reduced Metabolites of Testosterone in the Nervous System
- Application of Acyzol in the Context of Zinc Deficiency and Perspectives
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Adverse effects of 5α-reductase inhibitors: What do we know, don’t know, and need to know?
- Effects of hormonal treatment on dermatological outcome in transgender people: a multicentric prospective study (ENIGI)
- The Genus Astragalus Species as an Emerging Source of Bioactive Phytochemicals: A Review of Dermatological and Cosmetic Applications
- Low-Molecular-Weight Synthetic Antioxidants: Classification, Pharmacological Profile, Effectiveness and Trends
- Keratosis follicularis spinulosa decalvans in a female
- The effect of dietary modulation of sulfur amino acids on cystathionine β synthase–deficient mice
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- TONGUE, RED
- This Month in the Journal
- Congenital atrichia associated with situs inversus and mesocardia
- Advances in Bioprinting to Model Immune‐Mediated Skin Diseases
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes