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Research 391–420 of 1000+
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Design and development of cosmeceutical cream for hyperpigmentation and anti-aging
- Bio-Catalytic Action of Pseudomonas DL17 on Environmental Contaminant Sunset Yellow FCF
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Combined activity of selenite-resistant bacteria and Pisum sativum sprout extract against Malassezia furfur: A preliminary qualitative evaluation
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Ayurvedic Approach in Management of Vata-Kaphaja Artavdushti (PCOS)
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- 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
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Assessment of scalp hair survivin in patients with premature greying of hair
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- Pictorial Essay on Hair Loss; the Result of Head Bones Displacement
- Polycystic Ovarian Syndrome - What is New
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Inherited Epidermolysis Bullosa: A Clinical Case
- Alopecia Areata in 12 years old female treated with Oral Azathioprine: A case report and review
- WNT10B (wingless-type MMTV integration site family)
- Phylloid terminal hair nevus: A unique clinical entity
- Study of Skin Expression of MicroRNA-146a in Patients with Alopacia Areata
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- A study of cutaneous manifestations of systemic lupus erythematosus in Malwa region of India
- Natural Killer Group 2 Type D (NKG2D) Gene Polymorphism in Systemic Lupus Erythematosus-Suez Canal Region - Egypt
- Genetic Defects of Female Sexual Differentiation
- Androgen effects on the skin