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Research 271–300 of 1000+
- Long COVID syndrome: An unfolding enigma
- Skin diseases in consequence of endocrine alterations
- 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
- Diseases of Periocular Hair
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Janus kinase inhibitors for alopecia areata: a review of clinical data
- Dissecting hair breakage in alopecia areata: the central role of dysregulated cysteine homeostasis
- Longer TA repeat but not V89L polymorphisms in the SRD5A2 gene may confer acne risk in the Chinese population
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- A brief report on PCOS: and its inducing model
- Solitary Basaloid Follicular Hamartoma: A Report of Two Cases.
- The necessity of investigations to clarify sex and racial disparities in pathophysiology of Long COVID
- Polycystic Ovarian Syndrome - What is New
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- A study of cutaneous manifestations of systemic lupus erythematosus in Malwa region of India
- STUDY OF CUTANEOUS MANIFESTATIONS IN THYROID DISORDERS
- Polycystic Ovary Syndrome in Adolescents
- Abstracts Pt.30
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency