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Research 61–90 of 1000+
- Bimatoprost in the treatment of eyelash hypotrichosis
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Cutaneous changes in patients with chronic renal failure on hemodialysis
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Trichodystrophies: A hair-raising differential diagnosis
- HAIR AND SYSTEMATIC DISEASE
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Hair Disorders
- Female Adolescent Hair Disorders
- Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations
- Drug-Induced Hair Loss and Hair Growth
- Biology and Genetics of Hair
- Drug Reactions Affecting Hair: Diagnosis
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- Genital Rejuvenation: The Next Frontier in Medical and Cosmetic Dermatology
- TRICHOPATHOPHOBIA.
- Cutaneous drug reactions
- Vorasidenib-Induced Trichomegaly and Hypertrichosis: a New Side Effect in a Patient with Diffuse Astrocytoma
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Hair Changes due to Drugs
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- Polarized microscopy in genetic hair disorders: case series
- Hypotrichosis congenita (KRT71 mutation) in Hereford cattle in Uruguay