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Research 961–990 of 1000+
- Health Messages
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Hair Loss in Systemic Disease
- The Hair Shedding Visual Scale: A Quick Tool to Assess Hair Loss in Women
- Diseases on Hair Follicles Leading to Hair Loss Part I: Nonscarring Alopecias
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Genotype–Phenotype Correlation in Children With Congenital Adrenal Hyperplasia due to 21‐Hydroxylase Deficiency Using Next Generation Sequencing
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- 481 Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Cutaneous manifestations of endocrine diseases in children
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Stem-cell therapy in dermatology – Challenges and opportunities
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- The naked truth: Sphynx and Devon Rex cat breed mutations in KRT71
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Tracing selection signatures in the pig genome gives evidence for selective pressures on a unique curly hair phenotype in Mangalitza
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Prevalence and Predictors of Premature Graying of Hair Before the Age of 30: A Cross‐Sectional Study in Saudi Arabia
- Alopecia areata
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Effects of SLC45A2 and GPNMB on Melanin Deposition Based on Transcriptome Sequencing in Chicken Feather Follicles
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Coloration in Equine: Overview of Candidate Genes Associated with Coat Color Phenotypes
- Dermatologic care of patients with differences of sex development