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Research 241–270 of 1000+
- Personalized Medicine in the Field of Inflammatory Skin Disorders
- Hormonal and Genetic Controls of Hirsutism: Link Between hyperprolactinemia, Polycystic ovary syndrome and Hirsutism
- Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response
- Interplay between fibroblast growth factor 9 (FGF9) and CD44 underlies 46,XY disorders of sex development in Kruppel‐like factor 1 (KLF‐1)‐E325K‐associated congenital dyserythropoietic anaemia (CDA‐IV)
- The laboratory in the multidisciplinary diagnosis of differences or disorders of sex development (DSD)
- A case of cutis verticis gyrata developing in a patient with primary scarring alopecia: A unique presentation of a rare disorder
- Evaluation of the Environmental Risk Factors and Comorbidities in Patients with Lichen Planopilaris: A Case-Control Study
- Keratin disorders: from gene to therapy
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- 1363 Hair follicle growth and pigmentation during ageing
- Characterization of an autoimmune condition associated with AEC syndrome
- Biology of the hair follicle and mechanisms of nonscarring and scarring alopecia
- Cicatricial (Scarring) Alopecias
- Sex hormones and acne
- Genetic Variants Associated with Hyperandrogenemia in PCOS Pathophysiology
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Combination Antiretroviral Therapy and the Risk of Myocardial Infarction
- Alopecia areata: a comprehensive review of clinical, immunologic, and genetic perspectives
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- 236 Wnt/planar cell polarity impairment and the genetics of yellow nail syndrome
- Genetics and Epigenetics of Polycystic Ovary Syndrome
- Keratosis Follicularis Spinulosa Decalvans. What Syndrome Is This?
- The genetics of alopecia areata: New approaches, new findings, new treatments
- The gene for autosomal dominant hidrotic ectodermal dysplasia (Clouston syndrome) in a large Indian family maps to the 13q11-q12.1 pericentromeric region
- New Horizons in the Genetics of Polycystic Ovary Syndrome: From Predisposition to Precision Medicine.
- Genetics Poly Cystic Ovary Syndrome
- The Basic Science of Hair Biology
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- Disorders of Keratinization