Search
for
Sort by
Research 30 of 130
- Hypotrichosis in a child with olmsted syndrome
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Late Management of Burns
- Dermatological Issues in a Child with Diabetes Mellitus
- Complex Regional Pain Syndrome Type I : measurements and treatment
- Transforming growth factor-β in stem cells and tissue homeostasis
- Skin manifestations of chronic kidney disease
- Male fertility and skin diseases
- Approach to Patients with Suspected Rheumatic Disease
- Specific Attention Areas in Scar Management: Specific Scar Management Depending on Anatomical Features (Face, Hair, Breast, Hand, Joints, Foot)
- Inherited Disorders of the Hair
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Interventions for morphea
- Ottawa, Ontario, Canada, February 13–16, 2013
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Applications of Marine Organism-Derived Polydeoxyribonucleotide: Its Potential in Biomedical Engineering
- Guía de Procedimientos en Cirugía Plástica Reconstructiva Vol. 4
- Harnessing the Biomimetic Effect of Macromolecular Crowding in the Cell-Derived Model of Clubfoot Fibrosis
- Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency
- Case Report: Hypopituitarism Masquerading As Failure to Thrive in a 75‐Year‐Old Woman
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Animals in Dermatology
- The Case Report on the Effectiveness of Infrared Light on Acid Burn Victim
- Mesenchymal stem cells paracrine proteins from three‐dimensional dynamic culture system promoted wound healing in third‐degree burn models
- Morphea: progress to date and the road ahead
- Biomechanical Factors in Psoriatic Disease: Defective Repair Exertion as a Potential Cause. Hypothesis Presentation and Literature Review
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Cloning of wrinkle-free, a previously uncharacterized mouse mutation, reveals crucial roles for fatty acid transport protein 4 in skin and hair development
- Ayurvedic management of systemic sclerosis - A case report
- SKIN MANIFESTATIONS OF RHEUMATOLOGICAL DISEASES