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Research 211–240 of 1000+
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- Treatments of hereditary hair loss (alopecia)
- Recent Advances in the Pathogenesis of Autoimmune Hair Loss Disease Alopecia Areata
- Diagnosis and management of hair loss in children
- 17927 A pilot study of intrascalp platelet-rich plasma injections for hair loss in Nigerian patients
- Associaton of Insulin Resistance Linked Diseases and Hair Loss in Elderly Men. Finnish Population-based Study
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- Exome analysis for Cronkhite-Canada syndrome: A case report
- Hashimoto Thyroiditis - A Comprehensive Review
- Chapter-02 Androgenic Alopecia and Hirsutism
- Nonsegmental Vitiligo and Autoimmune Mechanism
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Generalized Vitiligo Associated Autoimmune Diseases in Japanese Patients Their Families
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Alopecias
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Using the zebrafish lateral line to uncover novel mechanisms of action and prevention in drug-induced hair cell death
- AN OVERVIEW ON POLYCYSTIC OVARIAN SYNDROME
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Mapping of a novel locus for keratosis follicularis squamosa on chromosome 7p14.3–7p12.1
- Acquired and inheritedhair disorders
- Oral Presentations
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- HAIR AND SYSTEMATIC DISEASE
- Selective Pituitary Resistance to Thyroid Hormone: Clinical Hyperthyroidism with High TSH on Levothyroxine Administration in I-131 Ablated “Graves Disease”