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Research 421–450 of 1000+
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Birt–Hogg–Dubé syndrome
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Ectodermal Dysplasia: Variable Expressions
- Netherton Syndrome – Responding to Oral Retinoids
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Bachmann–Bupp syndrome and treatment
- Netherton Syndrome
- Stem cell-based therapies for alopecia areata: a narrative review
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Recent advances in the genetics of alopecia areata
- Polycystic ovary syndrome
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Hyperandrogenism in polycystic ovarian syndrome and role of CYP gene variants: a review
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- Keratosis follicularis spinulosa decalvans in a family
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- A review of hyperandrogenism state in polycystic ovarian syndrome
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Ichthyosis with confetti: clinics, molecular genetics and management
- Trichothiodystrophy: Current Concepts
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Defolliculated (Dfl): A Dominant Mouse Mutation Leading to Poor Sebaceous Gland Differentiation and Total Elimination of Pelage Follicles
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- The Diagnosis and Treatment of Hair and Scalp Diseases
- Cellular Senescence and Aging in Myotonic Dystrophy