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Research 451–480 of 1000+
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Epidemiology and burden of alopecia areata: a systematic review
- Identification of Ovine KRTAP28-1 and Its Association with Wool Fibre Diameter
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Identification of the Ovine Keratin-Associated Protein 21-1 Gene and Its Association with Variation in Wool Traits
- Clinical recognition and management of alopecia in women of color,
- An audit of dermatoses at Baqai Institute of Skin Diseases, Karachi
- Clinical, Dermoscopic and In-Vivo Reflectance Confocal Microscopy Evaluation of a Case of Graham Little-Piccardi-Lassueur Syndrome Successfully Treated with Narrowband-UVB Phototherapy
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- Pigmentary Puzzle: A Rare Case of Hyperpigmented Cutaneous Sarcoidosis
- Retiform Sertoli-Leydig Cell Ovarian Tumour Presenting with Psammoma Bodies: A Rare Case Report
- Hair loss in women
- An overview of scalp dermatoses in a tertiary care institute
- THE PATHOGENESIS OF ALOPECIA AREATA
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Bilaterally Symmetrical Alopecia With Reticulated Hyperpigmentation
- Central Centrifugal Cicatricial Alopecia
- Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Variation in the ovine trichohyalin gene and its association with wool curvature
- Female Androgenetic (?) Alopecia
- Tofacitinib Citrate for the Treatment of Nail Dystrophy Associated With Alopecia Universalis
- Molecular Analysis of the ABCA4 Gene Mutations in Patients with Stargardt Disease Using Human Hair Follicles
- Male-pattern baldness susceptibility locus at 20p11
- Lichen planopilaris epidemiology: a retrospective study of 80 cases
- Prevalence, comorbidities, and treatment patterns of Japanese patients with alopecia areata: A descriptive study using Japan medical data center claims database
- Identification of the Ovine Keratin-Associated Protein 26-1 Gene and Its Association with Variation in Wool Traits
- Association Between Interleukin 18 Polymorphisms and Alopecia Areata in Koreans
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia