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Research 211–240 of 1000+
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- 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
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Bioactive Proteolytic Enzymes Chymotrypsin and Papain as Adjuvants to Laser Hair Removal: Reducing the Risk of Paradoxical Hypertrichosis in Women with Facial Hirsutism
- 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
- 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
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation