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Research 31–60 of 1000+
- ELECTROLYSIS VERSUS HIGH FREQUENCY CURRENTS IN THE TREATMENT OF HYPERTRICHOSIS
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Congenital hypotrichosis due to short anagen
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Congenital atrichia and hypotrichosis
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Generalized hypertrichosis associated with the use of interleukin 17 blockers in 2 patients with psoriasis
- Combined Alopecia Areata and Acquired Hypertrichosis Lanuginosa in Celiac Disease- A Rarest Phenomenon
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Acquired hypertrichosis lanuginosa: Case report and review of the literature
- Facial hypertrichosis after isotretinoin therapy: Is it a side effect or coincidence?
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Irreversible alopecia universalis during treatment with pegylated interferon-ribavirin for chronic hepatitis C virus infection: Case report and published work review
- A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Becker's Melanosis and Hypertrichosis*
- Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Autosomal recessive woolly hair/hypotrichosis with homozygous mutation in the <i>LIPH</i> gene: a case report
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Disorders of hair in children
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- ORAL MINOXIDIL EFFICACY AND SAFETY IN MALE ANDROGENETIC ALOPECIA - A LITERATURE REVIEW
- PRIDE syndrome with lumbosacral hypertrichosis
- Biology and Genetics of Hair