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Research 901–930 of 1000+
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- A Retrospective Study of Frontal Fibrosing Alopecia from North-East India
- Serum Vitamin D levels and Alopecia areata- A hospital based case-control study from North-India
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Considerations in the choice of a skin donor site for harvesting keratinocytes containing a high proportion of stem cells for culture in vitro
- Repigmentation by combined narrow‑band ultraviolet B/adipose‑derived stem cell transplantation in the mouse model: Role of Nrf2/HO‑1‑mediated Ca<sup>2+</sup> homeostasis
- Refractory pruritic Fox-Fordyce disease successfully treated with botulinum toxin type A
- Thrombophilia and Polycythemia in a Woman With Budd-Chiari Syndrome
- Peculiarities of long-COVID-19 and treatment strategy: a clinical case
- Molecular basis of androgen insensitivity
- Lichen planopilaris epidemiology: a retrospective study of 80 cases
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Abstract 14
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Disorders of sex development (DSD) 46.XY due to type 2 5-α reductase deficiency in three siblings: Case report from a low-resource setting
- SUN-287 A Case of Ectopic Neurohypophysis
- Unrevealing the Potential of Sansevieria trifasciata Prain Fraction for the Treatment of Androgenetic Alopecia by Inhibiting Androgen Receptors Based on LC-MS/MS Analysis, and In-Silico Studies
- Parathyroid adenoma with coeliac disease: primary or quaternary hyperparathyroidism?
- Visualising Androgen Receptor Activity in Male and Female Mice
- Pathology of Mouse Models of Accelerated Aging
- Hidradenitis Suppurativa as a Potential Subtype of Autoinflammatory Keratinization Disease
- Update on hidradenitis suppurativa: connecting the tracts
- Frontal Fibrosing Alopecia Coexisting with Lupus Erythematosus: Poor Response to Hydroxychloroquine
- Establishment of type II 5α-reductase over-expressing cell line as an inhibitor screening model
- Severe onycholysis in a card illusionist with alopecia areata universalis
- Evidence on Hidradenitis Suppurativa as an Autoinflammatory Skin Disease
- Atrichia with papular lesions
- Role of Aire and Notch4 Allelic Mutations in Alopecia Areata in C3H/HeJ Mice
- Frontal Fibrosing Alopecia: An Observational Single-Center Study of 306 Cases