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Research 721–750 of 1000+
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Congenital atrichia associated with situs inversus and mesocardia
- Substance P in keratosis follicularis spinulosa decalvans
- P latelet rich plasma application by dermapen microneedling and intradermal point‐by‐point injection methods, and their comparison with clinical findings and trichoscan in patients with androgenetic alopecia
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Value of dermoscopy for the diagnosis of monilethrix
- Osseous Metaplasia and Mature Bone Formation With Extramedullary Hematopoiesis in Trichilemmal Cyst
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Folliculin: A surprising molecular brake in the human hair follicle
- Effectiveness of Rosmarinus officinalis for Androgenetic Alopecia: A Literature Review
- Ectodermal Dysplasia: Variable Expressions
- Exploring the Dermoscopic Patterns in Tuberous Sclerosis
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Effect of Oral Minoxidil on Monilethrix
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- P-18 THREE BODY PROBLEM PATIENT: EHLER DANLOS SYNDROME COMBINED WITH HYPOPHOSPHATASIA AND FATTY ACID OXIDATION DEFECT
- Effectiveness of Exosome Treatment in Androgenetic Alopecia: Outcomes of a Prospective Study
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- PCSK9: From Nature’s Loss to Patient’s Gain
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Efficacy of Dupilumab in Treating Atopic Dermatitis With Recurrent Eczema Herpeticum in a Patient With DOCK8-Deficiency Hyper-IgE Syndrome: A Case Report
- Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa
- 464 Phenotypic heterogeneity of epidermolysis bullosa associated with the recurrent pathogenic variant p.(Arg2000Trp) in plectin
- Long-term Prophylaxis with Androgens in the management of Hereditary Angioedema (HAE) in emerging countries
- Editorial: Mechanisms and novel treatments of pigmentary disorders and skin regeneration
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Tricholemmoma and tricholemmal carcinoma and Cowden syndrome