Search
for
Sort by
Research 61–90 of 1000+
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Alopecia Areata of the Nails: Diagnosis and Management
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Vitamin A toxicity: When one a day doesn't keep the doctor away
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Primary hypothyroidism with exuberant dermatological manifestations
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- [Two cases of the rare Cronkhite-Canada syndrome].
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Transglutaminase Activity Is Conserved in Stratified Epithelia and Skin Appendages of Mammals and Birds
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Prophylaxis and Management of Skin Toxicities
- Toxicity of repeated oral intake of organic selenium, inorganic selenium, and selenium nanoparticles: A review
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Collagen Involvement in Health, Disease, and Medicine
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Peculiarities of clinical course and diagnostic of alopecia areata with comorbidity. Clinical observations
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Monilethrix – Case report of a rare disease
- Progress in the Use of Platelet-rich Plasma in Aesthetic and Medical Dermatology.
- Evaluation of Clinical and Oral Findings in Patients with Epidermolysis bullosa
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Acute selenium poisoning by paradise nuts (Lecythis ollaria)