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Research 61–90 of 1000+
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous 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
- Protein-Losing Enteropathy, Anasarca and Dermatological Manifestations on People of Advanced Age: Don't Overlook the Diagnostic Hypothesis of a Cronkhite Canada Syndrome
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Nail Involvement in Alopecia Areata: A Questionnaire-based Survey on Clinical Signs, Impact on Quality of Life and Review of the Literature
- Nail involvement in patients with moderate-to-severe alopecia areata treated with oral tofacitinib
- PA33 When bones speak through nails: insights from a paediatric case series
- Epidermolysis bullosa in animals: a review
- Pincer Nails – A Rare Manifestation of Systemic Lupus Erythematosus
- Vitamin A toxicity: When one a day doesn't keep the doctor away
- Toxicity of repeated oral intake of organic selenium, inorganic selenium, and selenium nanoparticles: A review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- A rare case of woolly hair with unusual associations
- Alopecia Areata: Prognostic Factors
- Prognostic Factors in Mexican Patients with Patchy and Other Types of Alopecia Areata
- Unraveling a Rare Case: Diarrhea, Alopecia, and Polyposis
- Pachyonychia congenita: Sporadic onset with mutation analysis
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Clinical Characteristics and Prognostic Factors in Early-Onset Alopecia Totalis and Alopecia Universalis
- A clinical study of Geriatric dermatoses at Tertiary care center in South India
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia