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Research 751–780 of 1000+
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- Male Pattern Baldness
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Clomiphene Citrate versus Letrozole for Ovulation Induction in PCOS: A Comparative Study
- Reversal of andro-genetic alopecia in a male. A spironolactone effect?
- Cardiometabolic risk factors in women with non-classic congenital adrenal hyperplasia
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child
- Saw palmetto (Serenoa repens) in androgenic alopecia An effective phytotherapy
- Efektivitas Terapi Minoksidil pada Alopesia Androgenetik: Studi in Vivo
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Challenges in the Diagnosis of Simple-Virilizing Congenital Adrenal Hyperplasia: A Case Report
- Hemoglobinopathy and Systemic Lupus: A Rare Association
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- 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
- 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