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Research 31–60 of 97
- Inherited Disorders of the Hair
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Update on Hidradenitis Suppurativa (Part I): Epidemiology, Pathogenesis, Severity assessment and Comorbidities
- Autoamputation in a 45-Year-Old Female with Systemic Lupus Erythematosus Overlap with Systemic Sclerosis: A Case Report
- Polarized microscopy in genetic hair disorders: case series
- M-CSF-Stimulated CD11b+ Myeloid Cells Induce Alopecia Areata in C3H/HeJ Mice
- Syndromes of Severe Insulin Resistance (SSIRs)
- Evaluating the Effects of Low-level Laser Therapy and Platelet-rich Plasma on Bone Calcium Content and Mechanical Properties at Tooth Extraction Sites: An Animal Study
- The PDGF/PDGFR pathway as a drug target
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Design of a RADA16-based self-assembling peptide nanofiber scaffold for biomedical applications
- Acne
- Acne and acneiform eruptions
- Syphilis: today
- Is Three-Dimensional Virtual Planning in Cranial Reconstruction for Advanced Cutaneous Squamous Cell Carcinoma of the Skull a Feasible Option?
- A brief lightening on medicinal activity and Pharmacological profile of plant Eclipta prostrata: A Review
- Cerebellar Medulloblastoma: Treatment by Irradiation of the Whole Central Nervous System
- Platelet-Rich Plasma Contains High Concentrations of DKK1, A Potent Inhibitor of Wnt Signaling that Limits Bone Regeneration and Hair Growth
- Changes in Color of Hair and Feathers
- Wedelolactone inhibits breast cancer-induced osteoclastogenesis by decreasing Akt/mTOR signaling
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Use of Leukocyte Platelet (L-PRF) Rich Fibrin in Diabetic Foot Ulcer with Osteomyelitis (Three Clinical Cases Report)
- Ultrastructural skin changes in Egyptian mandibuloacral dysplasia patients with p.Arg527Leu <i>LMNA</i> mutation and in their asymptomatic heterozygotic mothers
- TGFβ and cancer metastasis: an inflammation link
- Long-Term Intravital Imaging of the Cornea, Skin, and Hair Follicle by Multiphoton Microscope
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin
- Myotonic Dystrophy—A Progeroid Disease?