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Research 241–270 of 1000+
- Woolly hair nevus
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Role of the Wnt signaling pathway in keratoacanthoma
- Intraretinal variation in disease severity in the Oat mouse model of gyrate atrophy
- Alopecia Universalis Associated with a Mutation in the Human <i>hairless</i> Gene
- Subcellular localization of the five members of the human steroid 5α-reductase family
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- Targeting integrin pathways: mechanisms and advances in therapy
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Severe Hypernatremia as Presentation of Netherton Syndrome
- SEBACEOUS ADENITIS IN AKITA DOG – CASE REPORT
- Hair loss in children.
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Approach to the adult female patient with diffuse nonscarring alopecia
- Premature graying of hair
- REVIEW OF SO-CALLED ASEPTIC NEUTROPHILIC DERMATOSES
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- Hemoglobinopathy and Systemic Lupus: A Rare Association
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- 9. Immunology and Genetics
- Hair shaft disorders
- Insulin resistance is increased in alopecia areata patients
- Skin
- A Review on Ayurvedic Niadanatmak Concept of Khalityavyadhi
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Unruly hair
- The clinical spectrum of parathyroid disease
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child