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Research 31–60 of 1000+
- Skin features in myotonic dystrophy type 1: An observational study
- Biologics and Small Molecules for Inflammatory Nail Disorders: A Narrative Review
- Trichothiodystrophy
- 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
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- Clinical Characteristics and Prognostic Factors in Early-Onset Alopecia Totalis and Alopecia Universalis
- 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
- The disrupted balance between hair follicles and sebaceous glands in<i>Hoxc13</i>‐ablated rabbits
- 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
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A rare case of woolly hair with unusual associations
- Analysis of pediatric dermatology inpatient consultations in a pediatric teaching hospital
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Elkonyxis associated with habit-tic deformity: Two case reports
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- A Case of Cronkhite-Canada Syndrome Involving the Entire Gastrointestinal Tract
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families