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Research 151–180 of 1000+
- Pegylated-interferon-α<sub>2a</sub>in clinical practice: how to manage patients suffering from side effects
- Congenital atrichia and hypotrichosis
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Minoxidil and bilateral central serous chorioretinopathy in an adolescent girl: relationship or causality?
- Antihelminthic Drugs
- Clinical Profile and Outcomes of Patients With Systemic Lupus Erythematosus
- Congenital Atrichia: A Case Report
- Immunopathogenesis of Primary Cicatricial Alopecia
- CUTANEOUS SIDE-EFFECTS OF BETA-ADRENERGIC BLOCKERS
- Granulomatous pigmented purpuric dermatosis containing Propionibacterium acnes
- Alopecia Areata
- Woolly hair nevus
- Syphilis: A great imitator
- Molecular pathology of skin adnexal tumours
- The genetically programmed hair growth cycle and alopecia: what is there to know?
- Alopecia Areata and Alopecia Areata Incognita
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Gouty Alopecia: An Intriguing Manifestation of Disseminated Tophaceous Gout
- 879 Molecular network of Smads and Id2 genes in hair follicle stem cells regulation
- 878 Influence of bovine milk oligosaccharides on sebocyte lipid content and inflammatory mediators
- 883 Hair follicle bulb developed as 3D scaffold free microtissue
- Disorders of hair in children
- Secondary cicatricial and other permanent alopecias
- The Rotterdam Study: 2016 objectives and design update
- Leucine-Rich Repeat-Containing G-Protein-Coupled Receptors as Markers of Adult Stem Cells
- Severe cutaneous adverse reactions to drugs
- Interrelation of immunity and tissue repair or regeneration
- Roles for Msx and Dlx homeoproteins in vertebrate development
- The British Society for Rheumatology guideline for the management of systemic lupus erythematosus in adults
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes