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Research 661–690 of 1000+
- Diffuse hypotrichosis from early childhood
- 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
- Acquired hypertrichosis lanuginosa: Case report and review of the literature
- Acquired Hypertrichosis Lanuginosa: A Rare Cutaneous Paraneoplastic Syndrome
- Generalized hypertrichosis after treatment with topical minoxidil
- What are the Factors That Induce Paradoxical Hypertrichosis After Laser Hair Removal?
- Traumatic panniculitis with localized hypertrichosis: Two new cases and considerations
- Localized Hypertrichosis in Subsiding Psoriatic Plaques
- <i>FOXN1</i> Duplication and Congenital Hypertrichosis
- Acquired Localized Hypertrichosis Induced by Rivastigmine
- Indirect Exposure to Topical Minoxidil Causing Generalized Hypertrichosis in Children: A Report of Two Cases
- Combined Alopecia Areata and Acquired Hypertrichosis Lanuginosa in Celiac Disease- A Rarest Phenomenon
- Facial hypertrichosis after isotretinoin therapy: Is it a side effect or coincidence?
- PRIDE syndrome with lumbosacral hypertrichosis
- A child with generalized hypertrichosis due to secondary topical minoxidil exposure
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- 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
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family