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Research 91–120 of 1000+
- Disorders of hair growth : diagnosis and treatment
- Becker's Nevus Syndrome
- Disorders of the Hair and Nails
- Pathology in Practice
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Generalized hypertrichosis due to secukinumab in a patient with moderate psoriasis: A case of serendipity or zemblanity?
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- Congenital adrenal hyperplasia
- Ciclosporin-Induced Generalised Hypertrichosis in a Transgender Woman Receiving Testosterone Blockers
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study
- Management of congenital ichthyoses: European guidelines of care, part two
- Congenital Triangular Alopecia (Brauer Nevus)
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Omeprazole-induced hypertrichosis in two children
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report