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Research 121–150 of 1000+
- Piggyback‐Acquired Hypertrichosis
- Minoxidil-induced hypertrichosis in a child with alopecia areata
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- The impact of obesity on the folliculosebaceous unit
- Contextualización histórica y social de la remoción del vello púbico femenino
- A guide to diagnosis and management of hypertrichosis
- Momentary fluke of cyclosporine in incidental repigmentation and hypertrichosis of hair
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Influence of Extended Photoperiod Using Blue Light Masks on Hypertrichosis, Coat Condition and General Health Parameters in Horses with Pituitary Pars Intermedia Dysfunction
- Hypertrichosis Induced by Minoxidil: A Case of Systemic Absorption from Scalp Occlusion
- Hair Changes due to Drugs
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- Association between epidermal growth factor and epidermal growth factor receptor gene polymorphisms and susceptibility to alopecia areata in Korean population
- Localized Acquired Hypertrichosis Associated with the Application of a Splint
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hypotrichosis with juvenile macular dystrophy
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- A Look Back at Hair Restoration through History
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report