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Research 31–60 of 1000+
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- In this Issue
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly
- Dietary Vitamin A Impacts Refractory Telogen
- An essential role for <i>Rxrα</i> in the development of Th2 responses
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis
- Expert recommendations on supportive skin care for non‐surgical and surgical procedures
- Pathophysiology of the Behçet's Disease
- Novel skin phenotypes revealed by a genome-wide mouse reverse genetic screen
- Menkes Syndrome Presenting as Myoclonic Seizures: Neuroimaging and EEG Observations
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- TONGUE, RED
- In Vitro Stability and Preclinical Safety Evaluation of High-Dose Intravitreal Topotecan in Rabbits: Impact of Dose and Concentration
- Nailfold capillaroscopy alterations in androgenetic alopecia: A cross-sectional study
- Confocal microscopy and optical coherence tomography of inflammatory skin diseases in hairs and pilosebaceous units: A systematic review
- Roles of <i>jumonji</i> and <i>jumonji</i> family genes in chromatin regulation and development
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Making the head: Caspases in life and death
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Interventional studies for polycystic ovarian syndrome in children and adolescents
- Comorbidities in alopecia areata: A systematic review and meta-analysis
- TGF-β Family Signaling in Epithelial Differentiation and Epithelial–Mesenchymal Transition
- Cutaneous lupus erythematosus
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Male fertility and skin diseases
- Retinoids for Chemoprophylaxis of Nonmelanoma Skin Cancer
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome