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Research 151–180 of 1000+
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Novel agents for the treatment of alopecia
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Alopecia - the search for novel agents continues
- Acquired progressive kinking of hair affecting the scalp and eyelashes in an adult woman
- Hair loss in children.
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Androgenic Alopecia and Homoeopathic Management
- A Review on Ayurvedic Niadanatmak Concept of Khalityavyadhi
- Review Article - Changing trends in hair restoration surgery
- Family History and Risk of Hair Loss
- Evaluation of Hair Loss
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Central centrifugal cicatricial alopecia: challenges and solutions
- Dermatopathology and molecular genetics
- Hair Loss: A Harbinger of the Morbidities to Come!
- Bhangra: Therapeutic and Pharmacological Actions in Shayb (Premature Greying of Hair)
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Congenital atrichia and hypotrichosis
- The clinical spectrum of parathyroid disease
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- A Study on the Pattern of Genetic Inheritance of Polycystic Ovarian Syndrome
- Non-Neoplastic Disorders of Hair
- Androgens and hair loss
- <i>WNT10A</i> , dermatology and dentistry
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria