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Research 271–300 of 1000+
- Diffuse hypotrichosis from early childhood
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Long-term safety and efficacy of Latisse (bimatoprost 0.03% solution) for treatment of eyelash hypotrichosis in subjects with chemotherapy induced and idiopathic hypotrichosis
- Bimatoprost in the treatment of eyelash hypotrichosis
- Congenital Hypotrichosis in a White-Tailed Deer Fawn from
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Congenital hypotrichosis - treatment with topical minoxidil and hair dye
- Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2%
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- BIOACTIVE AND PERIPHERAL ANDROGENS IN PREPUBERTAL SIMPLE HYPERTRICHOSIS
- Coexistence of acquired localized hypertrichosis and lipoatrophy after lupus panniculitis
- Acquired Localized Hypertrichosis Following Pressure Garment and/or Silicone Therapy in Burn Patients
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Localized Acquired Hypertrichosis After Long-Term Repeated Cupping Therapy: A Case Report
- Localized acquired hypertrichosis on a miner’s shoulder: case report
- From rare hypertrichosis to common alopecia: new pathways for hair regeneration
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Acquired Localized Hypertrichosis Following Cast Application for Fracture
- 494 Congenital generalized hypertrichosis with a copy number variation on chromosome 17q24
- 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
- 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
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript