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Research 391–420 of 1000+
- 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
- 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
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study
- Management of congenital ichthyoses: European guidelines of care, part two
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- 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
- 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
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Multiple congenital smooth muscle hamartoma: A case report
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Congenital Trichomegaly of the Eyelashes
- Localized Acquired Hypertrichosis Associated with the Application of a Splint