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Research 571–600 of 1000+
- Caring for women with polycystic ovary syndrome
- A Study on the Pattern of Genetic Inheritance of Polycystic Ovarian Syndrome
- Comparative Study Between 2% Minoxidil Topical Spray vs. Intradermal Injection (Mesotherapy) for Treatment of Androgenetic Alopecia in Female Patients: A Controlled, 4-month Randomized Trial
- Finding bald spots on chromosome 20p11
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Evidence based homoeopathy: A case report on androgenic alopecia in 23 year old male
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- Health Utility of Facial Angiofibroma associated with Tuberous Sclerosis Complex
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- A rare pediatric case of loose anagen hair syndrome
- Bhangra: Therapeutic and Pharmacological Actions in Shayb (Premature Greying of Hair)
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Hair shaft disorders
- From Hairline to Lipid Line: Prevalence and Spectrum of Dyslipidemia in Patients with Androgenetic Alopecia – A Hospital-Based Study
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- Persistent Papular Eruption in a Young Adult: Importance of Histopathology in Diagnosing Eruptive Vellus Hair Cysts
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Ultraviolet-Enhanced Trichoscopy—A New Tool to Assess Pili Annulati
- Exploring the Causal Relationship and Molecular Mechanisms Between Fasting Insulin and Androgenetic Alopecia: A Mendelian Randomization Study with Bioinformatics Analysis
- Therapeutic approach and management of Marz-e-Shayb (Premature greying of hair) in the perspective of Unani medicine: A case study
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Androgenic Alopecia and Homoeopathic Management
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS