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Research 391–420 of 1000+
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- A New Office Based Protocol to Reverse AGA Miniaturization at Early and Advanced Stages
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- A rare cutis verticis gyrata secondary to cerebriform intradermal nevus: case report and literature review
- TRP Channels in Skin Biology and Pathophysiology
- Skin Development and Disease: A Molecular Perspective
- A girl with loose anagen hair syndrome and concurrent uncombable hair syndrome
- Polycystic Ovary Syndrome in the Context of Pituitary Adenomas: Prevalence, Pathophysiology and Clinical Management
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- Annual Convention in the Time of COVID
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Computational Drug Repositioning in Cardiorenal Disease: Opportunities, Challenges, and Approaches
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Oral minoxidil in trichology: A review
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Endocrinology
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Unleashing the Furry Beast: Exploring the Fascinating World of Hypertrichosis Lanuginosa
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Update on Melasma—Part I: Pathogenesis