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Research 211–240 of 1000+
- Evaluation of the relationship between androgenetic alopecia and demodex infestation
- Common causes of paediatric alopecia
- Understanding Polycystic Ovary Syndrome: A Comprehensive Guide
- Androgenetic alopecia in adolescents.
- Mutation des menschlichen hairless -Gens bei Atrichia universalis
- Monilethrix
- Alopezien und Hypotrichosen im Kindesalter
- Efficacy, Safety, and Real-World Aspects of Janus Kinase Inhibitors to Treat Patients With Alopecia Areata
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Approach to Alopecia in Dogs in Clinical Practice
- An unusual presentation of vitamin D dependent rickets type 2 with low 25 (OH) D3 levels and alopecia: a case report of two siblings
- 1,25-dihydroxyvitamin D resistance, rickets, and alopecia
- Pili torti in association with citrullinemia
- Rickets with alopecia: An inborn error of vitaminD metabolism
- 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
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Clouston’s syndrome: a rare case report
- Disease Prevention and Alleviation by Human Myoblast Transplantation
- Off-label uses of retinoids in dermatology
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Pvalb8, a Type of Oncomodulin, Regulates Neuromast Development and Auditory Function in Zebrafish
- Trichotillomania
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- Viva questions from the IJDVL
- Embolic Stroke as the Initial Manifestation of Systemic Lupus Erythematosus
- Androgenetic alopecia, hirsutism and hypertrichosis
- Skin Development and Disease: A Molecular Perspective
- Connexin mutations in human disease
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>