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Research 61–90 of 880
- A 6-Month, Prospective, Multi-arm Study for the Efficacy of Standardized Nutraceuticals to Improve Hair Fiber Thickness and Strength
- Regenerative Potential of Adipose Tissue–Derived Exosomes in Treating Hair Shaft Abnormalities: A Case Report
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- CLINICAL AND LABORATORY EVALUATION OF AIDS TRICHOPATHY
- Congenital atrichia and hypotrichosis
- Hair diseases: a big problem on a small surface
- Biotin
- Genetic Hair Disorders: A Review
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Pregnancy and Skin
- Micronutrients in hair loss
- The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene
- Hair and Nails
- <i>Hoxc13</i> mutant mice lack external hair
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- A Clinical Review of Trichorrhexis Nodosa
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Pili trianguli et canaliculi as a phenotypic subtype in patients with central centrifugal cicatricial alopecia: A scanning electron microscopy study
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Trichothiodystrophy in a child with occult learning disorder
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Netherton Syndrome
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Zinc-responsive Acral Hyperkeratosis as a Sequele of Acrodermatitis Enteropathica
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Netherton Syndrome – Responding to Oral Retinoids