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Research 91–120 of 1000+
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Botulinum toxin A in the treatment of facial reflex sympathetic dystrophy: A case report
- Pretreatment with epidermal growth factor promotes primary hair recovery in the chemotherapy-induced alopecia
- Relation of Selenium, Vitamin E and Other Factors to Muscular Dystrophy in the Rabbit
- Efficacy and safety of glucocorticoids in the treatment of progressive muscular dystrophy in children: a systematic review and meta-analysis
- The Autoimmune Regulator (AIRE), Which Is Defective in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients, Is Expressed in Human Epidermal and Follicular Keratinocytes and Associates With the Intermediate Filament Protein Cytokeratin 17
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- A generalized reticulate eruption with scarring alopecia, vulvovaginitis, keratoderma, and 20-nail dystrophy in a 70-year-old woman
- A randomized, double-blind, placebo- and active-controlled, half-head study to evaluate the effects of platelet-rich plasma on alopecia areata
- The incidence and management of cutaneous adverse events of the epidermal growth factor receptor inhibitors
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Cutaneous Reactions to Chemotherapeutic Agents
- Acquired Zinc Deficiency Dermatosis in Man
- Alopecia areata: diagnosis and management
- Involvement of scalp and nails in lupus erythematosus
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Vitamin A toxicity: When one a day doesn't keep the doctor away
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- JAK inhibition in the treatment of alopecia areata – a promising new dawn?
- Retrospective review of diphencyprone in the treatment of alopecia areata
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Prognostic factors that affect the response to topical treatment in patchy alopecia areata
- Twenty nail onychomadesis: An unusual finding in Cronkhite–Canada syndrome