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Research 211–240 of 362
- Rapidly progressive diffuse fibrosing alopecia
- Diagnosis and Management of Hair Loss in Pediatric
- An analytical study of serum ferritin, vitamin D, and thyroid function in females with diffuse hair loss
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Towards Defining the Pathogenesis of the Hairless Phenotype
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Telogen Effluvium: A Review
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Genetic hair and nail disorders
- A review of modern surgical hair restoration techniques
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- A novel missense mutation in the mouse hairless gene causes irreversible hair loss: Genetic and molecular analyses of Hrm1Enu
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Mutations in the Serum/Glucocorticoid Regulated Kinase 3 (Sgk3) Are Responsible for the Mouse Fuzzy (fz) Hair Phenotype
- Molecular Basis for Hair Loss in Mice Carrying a Novel Nonsense Mutation (<i>Hr<sup>rh-R</sup></i>) in the Hairless Gene (<i>Hr</i>)
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Fibrosing Alopecia in a Pattern Distribution: A Case Report and Literature Review
- The role of trichoscopy beyond hair and scalp diseases: A review
- Colored dots on trichoscopy—beware of artifacts
- Assessment, reliability, and validity of trichoscopy in the evaluation of alopecia in women
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
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- Trichoscopic Features, Clinical Correlates, and Risk Prediction in Female Pattern Hair Loss: A Retrospective Case-Control Study
- Laboratory Workup and Histopathology
- Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report
- A Cross-sectional Observational Study to Correlate the Trichoscopic Findings of Female Pattern Hair Loss with the Disease Severity and Underlying Histopathological Changes