Search
for
Sort by
Research 31–60 of 1000+
- Focal and Generalized Alopecia
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Biology and Genetics of Hair
- Trichodystrophies: A hair-raising differential diagnosis
- Cutaneous changes in patients with chronic renal failure on hemodialysis
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations
- HAIR AND SYSTEMATIC DISEASE
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Female Adolescent Hair Disorders
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Hair Disorders
- Drug Reactions Affecting Hair: Diagnosis
- The Genetics of Human Skin Disease
- TRICHOPATHOPHOBIA.
- Cutaneous drug reactions
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Hair Changes due to Drugs
- Drug-Induced Hair Loss and Hair Growth
- Polarized microscopy in genetic hair disorders: case series
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Thyroid hormone action on skin.
- Hair and Nail Relationship
- Hair Loss in Children
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Targeted Self-Assembled anti-NFκB AuNCs-Aptamer Nanoplatform for Precise Theranostics via Tailored Follicle Regeneration