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Research 511–540 of 1000+
- Alopecia in women submitted to childhood X-ray epilation for tinea capitis treatment
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Insulin resistance is increased in alopecia areata patients
- CLINICAL UPDATES IN HAIR
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Evidence based homoeopathy: A case report on androgenic alopecia in 23 year old male
- Health Utility of Facial Angiofibroma associated with Tuberous Sclerosis Complex
- A Review on Ayurvedic Niadanatmak Concept of Khalityavyadhi
- Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome
- Review Article - Changing trends in hair restoration surgery
- Alopecia and its medical management
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Frontal pseudoalopecia in history: Part 1—Fashionable forms
- Gestational diabetes mellitus and COVID-19, clinical characteristics and review of the literature
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- 46,XY DSD due to impaired androgen production
- Oral Manifestations of Hematologic and Nutritional Diseases
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Alopecia and Hirsuties
- Androgenetic, Diffuse and Senescent Alopecia in Men: Practical Evaluation and Management
- Congenital atrichia and hypotrichosis
- Alopecia: Association with Resistance to Thyroid Hormones
- The clinical spectrum of parathyroid disease
- Hyperandrogenism in polycystic ovary syndrome and adrenal hyperplasia: finding differences to make a specific diagnosis
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child