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Research 181–210 of 1000+
- Targeted Skin Overexpression of the Mineralocorticoid Receptor in Mice Causes Epidermal Atrophy, Premature Skin Barrier Formation, Eye Abnormalities, and Alopecia
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- A Comprehensive Review on Skin Pigmentation-Types, Causes, and Treatment
- An update of polycystic ovary syndrome: causes and therapeutics options
- Temporal triangular alopecia and a review of 52 past cases
- Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- Enhancing the diagnostic yield of monogenic diabetes in unresolved cases with early-onset hyperglycemia
- BH26 First reported case of lichen planopilaris in siblings: evidence for a genetic link?
- BG02: Muir‐Torre syndrome: a case of unusual coexisting genetic mutations
- Case report: a study of the clinical characteristics and genetic variants of post-finasteride syndrome patients
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature
- Association of JAK 1 and JAK 2 gene polymorphism with alopecia areata risk: a case–control genetic study
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- THE PATHOGENESIS OF ALOPECIA AREATA
- Eyebrow Loss
- The reasons and solutions for lipsotrichia and pelada phenomenon
- The possibilities of correction of premature greying of hair and involutive hair changes
- Women’s hair loss: pathophysiological, diagnostic and therapeutic aspects
- A review of the etiologies, clinical characteristics, and treatment of canities
- Late presentation of myotonic dystrophy
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Age-related hair changes in men: Mechanisms and management of alopecia and graying
- The aetiopathogenesis of acne vulgaris - what's new?
- The cat with alopecia
- Androgenetic alopecia: Update on etiology
- PA31 Congenital alopecia areata: a systematic review
- Inherited Disorders of the Hair
- Pathogenesis and management of TRPV3-related Olmsted syndrome