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Research 331–360 of 1000+
- Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene
- Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans
- Research Snippets
- Multiple basal cell carcinomas in a patient with myotonic dystrophy type 1
- Ectodermal Dysplasia: Variable Expressions
- 1322 A non-cell autonomous dermal hedgehog signaling mechanism for follicular neoplasia and induction
- Hair and nail disorders of childhood
- A Very Unusual Cause of Diarrhea in a 60-Year-Old Man
- Delayed Puberty
- Clinical Impact of Molecular Diagnostics in Endocrinology
- Kératose pilaire
- Disorders of the Hair and Nails
- Ulerythema ophryogenes (keratosis pilaris atrophicans faciei).
- Hirsutism
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Hair Loss in Children
- Pearly Pinna Papules in a Young Female
- Increasing of PCOs among Young Females
- Noninflammatory, Nonpruritic Alopecia of Horses
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Zebrafish Model of Hereditary Pigmentary Disorders
- IMMUNOLOGICAL AND GENETIC ASPECTS OF HEREDITARY ANTIBODY DEFICIENCIES
- AN UPDATE OF HAIR SHAFT DISORDERS
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Solitary Nodular Lesion Over Face
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Metabolic Syndrome in Androgenetic Alopecia in a Tertiary Care Centre in Goa: A Case Control Study During COVID-19 Pandemic
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Diagnosis, Management, and Associated Comorbidities of Polycystic Ovary Syndrome: A Narrative Review
- Polycystic ovary syndrome