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Research 61–90 of 1000+
- Analysis of pediatric dermatology inpatient consultations in a pediatric teaching hospital
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- The Coexistence of Trachyonychia and Mucocutaneous Lichen Planus: A Case Report
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Protein-Losing Enteropathy, Anasarca and Dermatological Manifestations on People of Advanced Age: Don't Overlook the Diagnostic Hypothesis of a Cronkhite Canada Syndrome
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Clouston’s Syndrome-A Case Report
- Clouston’s syndrome: a rare case report
- Geriatric Dermatology: Overview
- Trichothiodystrophy
- Cutaneous toxicities of cancer therapy
- Cutaneous Reactions to Chemotherapeutic Agents
- Acquired Zinc Deficiency Dermatosis in Man
- Alopecia areata: diagnosis and management
- Clinical Characteristics and Prognostic Factors in Early-Onset Alopecia Totalis and Alopecia Universalis
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- 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?
- Cutaneous Drug Eruptions Associated with the Use of New Oncological Drugs
- 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
- Prognostic factors that affect the response to topical treatment in patchy alopecia areata
- 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