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Research 31–60 of 1000+
- Hair follicle dystrophy in a litter of domestic cats resembling lanceolate hair mutant mice
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- What does acne genetics teach us about disease pathogenesis?
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- The Use of Human Dermal Papillae Conditioned Medium (HDPCM) on Aplasia Cutis Congenita in Lower Extremity due to Intrauterine Varicella Infection
- Dermatologic manifestations of endocrine disorders
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Superficial temporal artery flap for reconstruction of complex facial defects: A new algorithm
- Familial congenital generalized hypertrichosis
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Polarized microscopy in genetic hair disorders: case series
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- Pathologic Quiz Case: An Anterior Neck Mass in a 5-Month-Old Female Infant
- Successful treatment of ulcerated infantile hemangioma associated with PELVIS syndrome using oral propanolol
- Hair and Nail Relationship
- Ichthyoses
- Top applications of dermatologic ultrasonography that can modify management
- Contents
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Breast Embryology, Anatomy, and Physiology
- Omenn syndrome in a 10-month-old male with athymia and VACTERL association
- 864 Catalytic-dependent and -independent activities of Polycomb repressive complex 1 differentially regulate skin stem cell specification
- Congenital hypotrichosis due to short anagen
- Male fertility and skin diseases