Search
for
Sort by
Research 61–90 of 1000+
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Cutaneous manifestations of systemic infection in children
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Treatment of acne vulgaris: a literature review / Lečenje običnih akni (acne vulgaris) – pregled literature
- Use of chemotherapy during human pregnancy
- Transforming growth factor-β in stem cells and tissue homeostasis
- Wnt signaling in skin organogenesis
- Regeneration of skin appendages and nerves: current status and further challenges
- Morphological Approach to Hair Disorders
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- The clinical spectrum of parathyroid disease
- Darier Sign: A Historical Note
- Platelet-rich fibrin in the management of oral mucosal lesions: a scoping review
- The Potential Application of Exosomes as Therapeutic Agents, Carriers, and Biomarkers in Skin Diseases
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications
- Aesthetics in Geriatrics Using Plasma and Its Fractions in India
- Inherited Epidermolysis Bullosa: A Clinical Case
- All Roads Go to the Nucleus: Integration of Signaling/Transcription Factor-Mediated and Epigenetic Regulatory Mechanisms in the Control of Skin Development and Regeneration
- The role of integrin alphavbeta6 in impaired wound healing and hair follicle regeneration
- Differences in cell subsets between sun-exposed and unexposed skin: preliminary single-cell sequencing and biological analysis from a single case
- Serenoa Repens (Saw Palmetto) for Lower Urinary Tract Symptoms (LUTS): The Evidence for Efficacy and Safety of Lipidosterolic Extracts. Part III
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- 14. Wound Healing; Cutaneous Therapy; Hair
- A rare case of multiple keratoacanthomas treated with oral acitretin and intralesional methotrexate
- Ectodermal Dysplasia: Variable Expressions
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Vitamin D-Dependent Rickets Type II with Alopecia: A Rare Case Report.