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Research 31–60 of 1000+
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- Hypertrichosis lanuginosa acquisita following cytotoxic chemotherapy
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- Hair Restoration Surgery in Patients with Pubic Atrichosis or Hypotrichosis
- Sequence and structure based assessment of non-synonymous SNPs in hypertrichosis universalis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Marie-unna hereditary hypotrichosis
- Cutaneous Granular Cell Tumor with Overlying Hypertrichosis in an Adult: A Rare Case Report
- Alopezien und Hypotrichosen im Kindesalter
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Dermatopathology and molecular genetics
- Hair Changes due to Drugs
- Capryloyl glycine and soy isoflavonoids in hypertrichosis: An experimental and placebo‐controlled clinical study
- Influence of Extended Photoperiod Using Blue Light Masks on Hypertrichosis, Coat Condition and General Health Parameters in Horses with Pituitary Pars Intermedia Dysfunction
- Biology and Genetics of Hair
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Diseases of Periocular Hair
- Enhancing the Growth of Natural Eyelashes: The Mechanism of Bimatoprost-Induced Eyelash Growth
- Polarized microscopy in genetic hair disorders: case series
- Adverse Dermatologic Effects of Cardiovascular Drug Therapy: Part III
- Laser Hair Reduction and Removal