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Research 931–960 of 1000+
- Tentative reference ranges for calcium and strontium in Spanish children’ scalp-hair.
- Las alteraciones metabólicas y funcionales asociadas a la COVID-19
- Alopecia areata after severe allergic contact dermatitis to a permanent hair dye
- 1390 Lineage-committed fibroblast populations are more efficient at regenerating hair follicles in chamber grafting assays when compared to undifferentiated embryonic fibroblasts
- A cornerstone of hematological science
- The perception of donor gametes from male and female members of infertile couples
- Acute, diffuse and total alopecia
- A randomized, blinded, three-arm, multicenter trial comparing the efficacy and safety of fluconazole given once daily for 3 or 6 weeks with griseofulvin given once daily for 6 weeks in pediatric patients with tinea capitis
- Alopecia areata in the United States: Outpatient utilization and common prescribing patterns
- ダブルストロボレンジファインダの開発(特別講演)(画像センシングおよび一般)
- Single-cell analysis reveals fibroblast heterogeneity and myeloid-derived adipocyte progenitors in murine skin wounds
- Epithelial Wnt Ligand Secretion Is Required for Adult Hair Follicle Growth and Regeneration
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- Effects of 5-alpha reductase inhibitors on erectile function, sexual desire and ejaculation
- Reorganization of hair follicles in human skin organ culture induced by cultured human follicle-derived cells
- Role of Endolysosomes in Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Coronavirus Disease 2019 Pathogenesis: Implications for Potential Treatments
- An improved and rapid method to construct skin equivalents from human hair follicles and fibroblasts
- Skin steroidogenesis in health and disease
- The Role of Nutrition on Thyroid Function
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Sorafenib-induced eruption resembling pityriasis rubra pilaris
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Generalized hair loss induced by indinavir plus ritonavir therapy
- Re-identification of anonymised MRI head images with publicly available software: investigation of the current risk to patient privacy
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Biotin and Acetazolamide for Treatment of an Unusual Child With Autism Plus Lack of Nail and Hair Growth
- Winding the clock back on female androgenetic alopecia