Search
for
Sort by
Research 931–960 of 1000+
- Trichoscopic patterns of nonscarring alopecia's
- Alopecia in Harlequin mutant mice is associated with reduced AIF protein levels and expression of retroviral elements
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- AB023. An atypical clinical presentation of alopecia in two patients with systemic lupus erythematosus
- Age-related diffuse chronic telogen effluvium- type alopecia in female squirrel monkeys (Saimiri boliviensis boliviensis).
- Dermatologic Signs in Patients with Eating Disorders
- Alopecias in lupus erythematosus
- Short Anagen Syndrome
- Telogen Effluvium
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A Novel Model System to Identify Cellular and Molecular Defects Underlying Rare Genetic Disorders
- Low-dose oral minoxidil in a case of short anagen syndrome
- Tinea Capitis: Bedside Diagnosis by Dermoscopy
- Moniletherix
- Recent Progress in Prostaglandin F<sub>2</sub><i><sub>α</sub></i>Ethanolamide (Prostamide F<sub>2</sub><i><sub>α</sub></i>) Research and Therapeutics
- Clinico-mycological profile and trichoscopic findings among pediatric tinea capitis patients: A cross-sectional study from northern India (Haryana)
- Common data base programs for accelerator physics
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- The Pathobiology of Skin Aging
- Skin signs in anorexia nervosa
- Central centrifugal cicatricial alopecia – an approach to diagnosis and management
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions