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Research 181–210 of 1000+
- Learning from nudity: lessons from the nude phenotype
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Androgenetic alopecia in men
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- Transgenic mice display hair loss and regrowth overexpressing mutant <i>Hr</i> gene
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Expert consensus on the management of telogen effluvium in India
- Telogen Effluvium
- An analytical study of serum ferritin, vitamin D, and thyroid function in females with diffuse hair loss
- Trichoscopy as an essential diagnostic technique for hair and scalp disorders in skin of color: A case-control study
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- Molecular Genetics of Human Hair Diseases
- Hypotrichosis in a child with olmsted syndrome
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- A clinico-epidemiological study of scalp hair loss in children (0–18 years) in Kota Region, South-East Rajasthan
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Moth-eaten alopecia and beyond: Syphilitic alopecia - Revisited
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Receptor activator of NF-κB (RANK) stimulates the proliferation of epithelial cells of the epidermo-pilosebaceous unit
- Progressive Hair Loss and Myocardial Degeneration in Rough Coat Mice: Reduced Lysyl Oxidase-Like (LOXL) in the Skin and Heart