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Research 241–270 of 1000+
- Cutaneous lupus erythematosus
- Diet in dermatology: Revisited
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Acrodermatitis enteropathica – diagnostic challenges
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- New Pharmaceutical Concepts for Sebaceous Gland Diseases: Implementing Today’s Pre-Clinical Data into Tomorrow’s Daily Clinical Practice
- The Parathyroid Hormone Second Receptor PTH2R and its Ligand Tuberoinfundibular Peptide of 39 Residues TIP39 Regulate Intracellular Calcium and Influence Keratinocyte Differentiation
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Conditional Knockout in Mice Reveals the Critical Roles of Ppp2ca in Epidermis Development
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Collagen Involvement in Health, Disease, and Medicine
- Lean Women with Polycystic Ovary Syndrome
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- News in brief
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Alopecia Areata: A Review of the Genetic Variants and Immunodeficiency Disorders Associated with Alopecia Areata
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Contents Vol. 2, 2016
- An updated review on acne
- Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- A missense mutation in Lama3 causes androgen alopecia
- 454 Modeling epidermolysis bullosa simplex with cardiomyopathy using KLHL24-mutant pluripotent stem cells.