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Research 61–90 of 1000+
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Hair physiology and its disorders
- Pathology in Practice
- 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
- 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
- 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)
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- 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
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Marie-unna hereditary hypotrichosis
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- 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
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- The eyelash comes to the fore
- Secondary cicatricial and other permanent alopecias
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless