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Research 121–150 of 1000+
- Clinical features, therapeutic outcomes and recovery period of long COVID
- Prostate cancer and androgenic alopecia
- Global Landscapes of Human Phenotypic Variation in Inherited Traits
- Therapeutics for COVID-19 and post COVID-19 complications: An update
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Lichen planus pigmentosus: a clinico‐pathological study in a Caucasian population from North Africa
- Concept of tinea capitis
- BJD Editor's Choice
- Identification of the Ovine Keratin-Associated Protein 22-1 (KAP22-1) Gene and Its Effect on Wool Traits
- Prevalence of functional disorders of androgen excess in unselected premenopausal women: a study in blood donors
- Primary Scarring Alopecias
- Hair disorders associated with autoimmune connective tissue diseases.
- Clinical and Dermoscopic Approaches to Diagnosis of Frontal Fibrosing Alopecia: Results From a Multicenter Study of the International Dermoscopy Society
- Ottawa, Ontario, Canada, February 13–16, 2013
- Scarring Alopecia
- Folliculocentric tinea versicolor: a case report
- Genetic basis of polycystic ovary syndrome
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- 5α-Reductase type 2 gene variant associations with prostate cancer risk, circulating hormone levels and androgenetic alopecia
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- Genetic Variants at 20p11 Confer Risk to Androgenetic Alopecia in the Chinese Han Population
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Integrative analysis of rare copy number variants and gene expression data in alopecia areata implicates an aetiological role for autophagy
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Investigation of variants of the aromatase gene (CYP19A1) in female pattern hair loss
- Minoxidil Sulfotransferase Enzyme (SULT1A1) genetic variants predicts response to oral minoxidil treatment for female pattern hair loss
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope