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Research 241–270 of 1000+
- Linking diet to acne metabolomics, inflammation, and comedogenesis: an update
- The pathophysiology of polycystic ovary syndrome: trying to understand PCOS and its endocrinology
- Cutaneous reactions to recombinant cytokine therapy
- Primary cicatricial alopecia
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- The roles of Wnt/β‐catenin pathway in tissue development and regenerative medicine
- Are the cutaneous manifestations during or due to SARS-CoV-2 infection/COVID-19 frequent or not? Revision of possible pathophysiologic mechanisms
- Androgen receptors and their biology
- Interventions for nail psoriasis
- Skin Manifestations in Primary Immunodeficient Children
- Autoimmunity and autoimmune co-morbidities in psoriasis
- TOXIC EPIDERMAL NECROLYSIS
- Nanoparticles in wound healing from hope to promise from promise to routine
- Exploring the Drug Repurposing Versatility of Valproic Acid as a Multifunctional Regulator of Innate and Adaptive Immune Cells
- Acquired scalp alopecia. Part I: A review
- Congenital hair loss disorders: Rare, but not too rare
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Polycystic ovary syndrome (PCOS)
- SLE and Serum Complement: Causative, Concomitant or Coincidental?
- Therapeutic Applications of Nanoemulsion Based Drug Delivery Systems: A Review of Patents in Last Two Decades
- TCL1 transgenic mouse model as a tool for the study of therapeutic targets and microenvironment in human B-cell chronic lymphocytic leukemia
- Toxic shock syndrome: Recent developments in pathogenesis
- Azelaic Acid: Mechanisms of Action and Clinical Applications
- Stress and Psychoneuroimmunologic Factors in Dermatology
- Guidelines of care for superficial mycotic infectionsof the skin: Tinea capitis and tinea barbae
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Hair Transplantation Controversies
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Serum lipocalin-2 as an insulin resistance marker in patients with polycystic ovary syndrome
- Role of stem/progenitor cells in reparative disorders