Search
for
Sort by
Research 31–60 of 1000+
- Role of the Wnt signaling pathway in keratoacanthoma
- Acne
- Parry-Romberg Syndrome: A Rare Case with Diagnostic Challenges and Orthodontic Implications
- Cosmetic Considerations in Dark-Skinned Patients
- Evaluation of the palatal wound healing effect of wound dressing carrying GSK-3 antagonist tideglusib on rats
- Psychodermatology U.K.
- General Dermatology
- 14 Rhytidectomy
- Literature Reviews
- Syndromes of Severe Insulin Resistance (SSIRs)
- Progeroide Syndrome
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Pathologic Quiz Case: An Anterior Neck Mass in a 5-Month-Old Female Infant
- Ectodermal Dysplasia: Variable Expressions
- Drug-associated gingival disorders: a retrospective pharmacovigilance assessment using disproportionality analysis
- Tissue engineering strategies combining molecular targets against inflammation and fibrosis, and umbilical cord blood stem cells to improve hampered muscle and skin regeneration following cleft repair
- Efficacy of platelet-rich plasma and concentrated growth factor in treating androgenetic alopecia – A retrospective study
- Stimulation of ectodermal organ development by Ectodysplasin-A1
- The Lysosomal Protease Cathepsin L Is an Important Regulator of Keratinocyte and Melanocyte Differentiation During Hair Follicle Morphogenesis and Cycling
- E-Poster
- Myotonic Dystrophy—A Progeroid Disease?
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- The Spectrum of Scarring in Craniofacial Wound Repair
- A clinical study of cutaneous changes in pregnancy
- Odontogenic Keratocysts Arise from Quiescent Epithelial Rests and Are Associated with Deregulated Hedgehog Signaling in Mice and Humans
- The role of platelet-rich plasma in biomedicine: A comprehensive overview
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?