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Research 91–120 of 232
- Trichoscopy findings in loose anagen hair syndrome: rectangular granular structures and solitary yellow dots
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Congenital atrichia and hypotrichosis
- The hair shaft: normality, abnormality, and genetics
- Genetic Susceptibility to Alopecia
- Trichodystrophies: A hair-raising differential diagnosis
- Hair shaft disorders
- Hair Loss in Children
- Hair and Scalp Dermatoscopy (Trichoscopy)
- Inherited Disorders of the Hair
- Hair Loss in Children
- Diagnosis and management of hair loss in children
- Role of Trichoscopy in Children's Scalp and Hair Disorders
- Skin, Genetic Defects, and Aging
- Amino Acid Content of Damaged Human Hair
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Subject Index
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Genetic Hair Disorders: A Review
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Diseases of Periocular Hair
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Hair shaft disorders in children – An update
- Current Genetics in Hair Diseases
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias