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Research 841–870 of 1000+
- Circle hairs involving the extremities in a young girl
- Dermatoscopy: Alternative uses in daily clinical practice
- The Effect of Copper Supplementation on the Brindled Mouse
- Remarkable Improvement of Nail Changes in Alopecia Areata Universalis with 10 Months of Treatment with Tofacitinib: A Case Report
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Urinary steroids in women with androgenic alopecia
- The involvement of Elf5 in regulating keratinocyte proliferation and differentiation processes in skin
- A Review on-Types and Treatment of Alopecia
- Isolated eyebrow and eyelash trichotillomania mimicking alopecia areata
- Dermal Changes in Osteoporosis Following Prolonged Treatment with Human Growth Hormone
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Myeloproliferative disorder associated with alopecia universalis
- Accidental Poisoning with Autumn Crocus
- P146 A multicentre retrospective study evaluating the real-world efficacy and safety of ritlecitinib in the treatment of alopecia areata
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Az alopecia areata kezelésében alkalmazott baricitinib hatásosságának és biztonságosságának retrospektív vizsgálata = Efficacy and safety of baricitinib treatment in alopecia areata:a retrospective analysis
- Clouston’s Syndrome-A Case Report
- Schimmelpenning syndrome with dydimosis aplasticosebacea in a one-month-old girl
- Molecular studies of Hutchinson-Gilford progeria syndrome
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- Integrated Safety Analysis of Ritlecitinib for the Treatment of Alopecia Areata (AA) From the Phase 2 and Phase 3 ALLEGRO Clinical Trial Program
- Carbon finance opportunities: There are excellent funding opportunities available to hydro developers in the new Carbon market
- Trichorhinophalangeal Syndrome
- Netherton Syndrome Associated with Growth Hormone Deficiency
- Kératose pilaire
- Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions
- Unusual Dermatologic Findings in an Extremely Low Birthweight Infant: The Genetic Diagnosis
- Rapunzel Syndrome as a Rare Presentation of Trichobezoar
- PRIDE syndrome with lumbosacral hypertrichosis
- Hypotrichosis with juvenile macular dystrophy