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Research 271–300 of 1000+
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Sex Hormone-Binding Globulin (SHBG) as an Early Biomarker and Therapeutic Target in Polycystic Ovary Syndrome
- Are sex discordant outcomes in COVID-19 related to sex hormones?
- Skin diseases in consequence of endocrine alterations
- Upregulation of interfollicular epidermal and hair infundibulum β-catenin expression in Gsdma3 mutant mice
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Association of Cyp11a Gene with Polycystic Ovarian Syndrome Patients in Lahore, Pakistan
- Polycystic Ovarian Syndrome - What is New
- STUDY OF CUTANEOUS MANIFESTATIONS IN THYROID DISORDERS
- Polycystic Ovary Syndrome in Adolescents
- Abstracts Pt.30
- Cutaneous Lupus Erythematosus
- Use of chemotherapy during human pregnancy
- Alopecia areata
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Morpho-Regulation of Ectodermal Organs
- Interferon in the treatment of cutaneous T-cell lymphoma
- The role of lymphocytes in the development and treatment of alopecia areata
- Prolactin: an emerging force along the cutaneous–endocrine axis
- Oral Manifestations of Hematologic and Nutritional Diseases
- Alopecia areata update
- Human TSC2-null fibroblast-like cells induce hair follicle neogenesis and hamartoma morphogenesis
- Graham Little-Piccardi-Lassueur syndrome associated with androgen insensitivity syndrome (testicular feminization)
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Genetic basis of polycystic ovary syndrome
- Long COVID syndrome: An unfolding enigma
- Association of AR rs6152G/A gene polymorphism with susceptibility to polycystic ovary syndrome in Chinese women
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Secretory phospholipase A2-IIA overexpressing mice exhibit cyclic alopecia mediated through aberrant hair shaft differentiation and impaired wound healing response