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Research 91–120 of 1000+
- Frontal Fibrosing Alopecia Mimicking Alopecia Syphilitica
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Acquired hypertrichosis lanuginosa: Case report and review of the literature
- Frontal fibrosing alopecia: a review of eleven patients
- Philosophy and technique in hair restoration surgery
- Medical therapy for frontal fibrosing alopecia: A review and clinical approach
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Generalized hypertrichosis after 5% minoxidil solution in trichorhinophalangeal syndrome: A case report and review of the literatures
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Monilethrix
- Dermatoscopy case of the month: Trichodysplasia spinulosa
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- Hypotrichosis with juvenile macular dystrophy
- Sarcoidosis Presenting as Frontal Fibrosing Alopecia: A Master Mimicker or a Coincidental Finding?
- Hypotrichosis in a child with olmsted syndrome
- Zinc transporter ZIP13 G289R variant from Spondylocheirodysplastic Ehlers-Danlos syndrome (SCD-EDS) is associated with abnormal hair quality
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- A rare case of woolly hair with unusual associations
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Monilethrix in three generations
- Rapidly progressive diffuse fibrosing alopecia
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Global behavior of solutions in a chemotaxis model for alopecia areata with signal-dependent sensitivity
- Netherton Syndrome
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- S3886 Concurrent Management of Crohn's Ileitis and Alopecia Universalis With Upadacitinib
- Moniletherix