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- Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
- Disorders of Keratinization
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- HAIR LOSS IN WOMEN
- Multiorgan Dysfunction in a 7-Month-Old Boy With Developmental Delay and Poor Growth
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
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