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Research 211–240 of 1000+
- Microneedles: Selected Applications for Pediatrics
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Presence and future of dermoscopy
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- The urine as a diagnostic key for a homozygous EGFR mutation
- Dermatological manifestations associated with COVID‐19: A comprehensive review of the current knowledge
- Multilineage-differentiating stress-enduring cells alleviate atopic dermatitis-associated behaviors in mice
- MOF-mediated histone H4 Lysine 16 acetylation governs mitochondrial and ciliary functions by controlling gene promoters
- Dermatoses of Pregnancy - Clues to Diagnosis, Fetal Risk and Therapy
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Transforming Growth Factor-??, Smad, and Collagen Expression Patterns in Fetal and Adult Keratinocytes
- Acne in children
- Vitamin B6 promotes the activation of primordial follicles through the PI3K/Akt signaling pathway
- Management of autoimmune associated alopecia areata
- 10.51847/ubmwCM2
- Hair and scalp disorders in ethnic populations
- Westwood Carolina Conference on Clinical Dermatology
- Hair loss and its management in children
- Delicious Dermatology: Baked-Up Eponyms
- Ichthyoses
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- Cutaneous and Oral Mucosal Lesions in Cri-du-chat Syndrome
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Dermatologic manifestations of endocrine disorders
- Stem cell secretome as a mechanism for restoring hair loss due to stress, particularly alopecia areata: narrative review
- Drug Induced Alopecia
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Multiple congenital smooth muscle hamartoma: A case report
- Subject Index
- Dermatologic manifestations of endocrine disorders