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Research 271–300 of 483
- Psoriasis of the Scalp
- Hair Shaft Dysplasias
- Keratin disorders: from gene to therapy
- Interferon in the treatment of cutaneous T-cell lymphoma
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Beyond Expectations
- Management of congenital ichthyoses: European guidelines of care, part two
- Oral Retinoids in Dermatology
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Trichoscopy in Hair Shaft Disorders
- Alternative uses of dermoscopy in daily clinical practice: An update
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- METHOTREXATE FOR GENERALIZED PUSTULAR PSORIASIS IN A 2-YEAR-OLD CHILD
- Group IID, IIE, IIF and III secreted phospholipase A2s
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Síndrome do nevo de Becker
- MINOXIDIL FOR MALE-PATTERN BALDNESS
- FOX FORDYCE DISEASE IN A PREPUBERTAL GIRL
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Ppp2r2a Knockout Mice Reveal That Protein Phosphatase 2A Regulatory Subunit, PP2A-B55α, Is an Essential Regulator of Neuronal and Epidermal Embryonic Development
- GEOGRAPHIC TONGUE IN TWO CHILDREN WITH NONPUSTULAR PSORIASIS
- Hair loss
- Molecular Genetics of Alopecias
- CUTANEOUS MASTOCYTOSIS IN CHILDREN: AN INDIAN EXPERIENCE