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Research 31–60 of 1000+
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Biologics and Small Molecules for Inflammatory Nail Disorders: A Narrative Review
- Disorders of the Hair and Nails
- Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Nail Matrix Pathology in Cronkhite–Canada Syndrome: The First Case Report
- Skin features in myotonic dystrophy type 1: An observational study
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Selenium poisoning from consumption of contaminated wheat: a case series from rural Maharashtra, India
- Efficacy of modern methods for assessing the severity of alopecia areata
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- Epidermolysis bullosa in animals: a review
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Clinical and histological challenge in the differential diagnosis of diffuse alopecia: female androgenetic alopecia, telogen effluvium and alopecia areata – part I
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- Vitamin A toxicity: When one a day doesn't keep the doctor away
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- [Two cases of the rare Cronkhite-Canada syndrome].
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- A patient with diffuse hair loss
- A rare case of woolly hair with unusual associations
- Keratin disorders: from gene to therapy
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.