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Research 151–180 of 1000+
- Nonclassic Congenital Adrenal Hyperplasia: An Overview
- Trichorrhexis Nodosa Secondary to Argininosuccinicaciduria
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Early Onset Werner Syndrome
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Follicular ichthyosis
- Biotin: overview of the treatment of diseases of cutaneous appendages and of hyperseborrhea
- Cutaneous Manifestations of Endocrine Disease
- Hair Shaft Dysplasias
- Congenital generalized hypertrichosis: the skin as a clue to complex malformation syndromes
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- Unruly hair
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Hair loss
- Itchy Black Hair Bristles on Back
- Hair and Nail Manifestations of Systemic Disease
- Acquired progressive kinking of the hair in a Korean female adolescent
- Acquired Uncombable Hair
- Analysis of Chemical Components in Cosmetics and Their Effects on Human Health and Controversies
- A clinical case of familial alopecia areata in combination with immune pathology
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review