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Research 541–570 of 1000+
- Hypersensitivity Reactions to Anticoagulant Drugs
- Dermatologic manifestations of COVID‐19: a comprehensive systematic review
- Skin disorders in elderly subjects
- Biochemistry of epidermal stem cells
- Pregnancy and Skin
- METHOTREXATE FOR GENERALIZED PUSTULAR PSORIASIS IN A 2-YEAR-OLD CHILD
- Skin disease in pregnancy
- The Genetics of Human Skin Disease
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Alopecia as a rare but distinct manifestation of pemphigus vulgaris
- Exfoliative cutaneous lupus erythematosus in German shorthaired pointer dogs: disease development, progression and evaluation of three immunomodulatory drugs (ciclosporin, hydroxychloroquine, and adalimumab) in a controlled environment
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- ADVANCES IN PSORIASIS THERAPY
- Erosive pustular dermatosis of the scalp: a multicentre study
- Cutaneous adverse reactions linked to targeted anticancer therapies bortezomib and lenalidomide for multiple myeloma: new drugs, old side effects
- REVIEW OF SO-CALLED ASEPTIC NEUTROPHILIC DERMATOSES
- FOX FORDYCE DISEASE IN A PREPUBERTAL GIRL
- Dermatologic Reactions to Targeted Therapy
- Lupus erythematosus: considerations about clinical, cutaneous and therapeutic aspects
- Topical minoxidil sensitization in androgenic alopecia
- Spontaneous cutaneous adverse drug reaction reports—An analysis of a 10‐year dataset in Singapore
- A study on dermatoses of pregnancy
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Nanocarrier Systems for Transdermal Drug Delivery
- Skin health of community-living older people: a scoping review
- Spectrum of mucocutaneous manifestations in human immunodeficiency virus-infected patients and its correlation with CD4 lymphocyte count
- GEOGRAPHIC TONGUE IN TWO CHILDREN WITH NONPUSTULAR PSORIASIS
- Incidence of skin diseases diagnosed in a public institution: comparison between 2003 and 2014
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Beau's Lines