Search
for
Sort by
Research 61–90 of 1000+
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Mucocutaneous manifestations in children with human immunodeficiency virus infection
- Beard Alopecia: An Updated and Comprehensive Review of Etiologies, Presentation and Treatment
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Focal and Generalized Alopecia
- Trichoscopy in Hair Shaft Disorders
- Molecular Genetics of Alopecias
- Nonclassic Congenital Adrenal Hyperplasia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Hair loss and its management in children
- Hair Loss in Children
- Male Pattern Baldness
- Alopecia and its medical management
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Non-Edg family LPA receptors: the cutting edge of LPA research
- Morphological Approach to Hair Disorders
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Secondary cicatricial and other permanent alopecias
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Oral Manifestations of Hematologic and Nutritional Diseases
- Frontal Fibrosing Alopecia: An Update on Pathogenesis, Diagnosis, and Treatment
- Short anagen syndrome
- The Genetics of Human Skin Disease
- Advances in Hair Diseases
- Hair loss in infancy and childhood