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Research 841–870 of 1000+
- Combined drug triads for synergic neuroprotection in retinal degeneration
- Myasthenia Gravis Coexisting With Primary Sjögren's Syndrome: Report of Three Cases and Literature Review
- Werner′s syndrome
- A bibliometric analysis of strabismus (from 2004 to 2023)
- Episodic Bilateral Corneal Edema Caused by Hair Groom Gel
- Recent Advances in the Role of Fibroblast Growth Factors in Hair Follicle Growth
- Pre-Clinical Cell-Based Therapy for Limbal Stem Cell Deficiency
- Treating Alopecia Areata: Current Practices Versus New Directions
- Case Series: Gene Expression Analysis in Canine Vogt-Koyanagi-Harada/Uveodermatologic Syndrome and Vitiligo Reveals Conserved Immunopathogenesis Pathways Between Dog and Human Autoimmune Pigmentary Disorders
- Polyglandular autoimmune syndrome type 4 with GAD antibody and dystonia
- Role of Growth Factors-Rich Plasma, Gel and Membrane in Dermal Wound Healing and Injured Tissue Restoration and Regeneration
- Retinoids in Hair Loss
- Efficacy and Safety of Rb‐bFGF in Hair Transplantation: A Prospective and Comparative Study
- Jarilla–Coffea extract: a natural cosmetic product that improves eyelash and eyebrow growth in women
- Does prostaglandin D<sub>2</sub> hold the cure to male pattern baldness?
- Effects of Skin Lightening Cream Agents – Hydroquinone and Kojic Acid, on the Skin of Adult Female Experimental Rats
- Male infertility and genitourinary birth defects: there is more than meets the eye
- Comparative Analysis of the Cutaneous Microbiome in Psoriasis Patients and Healthy Individuals—Insights into Microbial Dysbiosis: Final Results
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- Adverse Events in Isotretinoin Therapy: A Single-Arm Meta-Analysis
- The Silent Syndrome of Long COVID and Gaps in Scientific Knowledge: A Narrative Review
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Impact of Formulation Variables on Meloxicam spanlastics Preparation
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Impact of constant light exposure during pregnancy on skin of neonatal New Zealand rabbits: structural and ultrastructural study
- Moth-Eaten Symptomatic Syphilitic Alopecia Associated with Human Immunodeficiency Virus—A Case Report
- RAGE and Its Ligands in Melanoma
- The Possible Role of Antibodies in Alopecia: A Narrative Review