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Research 151–180 of 1000+
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Adverse Reactions to Oral Retinoids An Update
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Hairless is a nuclear receptor corepressor essential for skin function
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Dermatologic manifestations of endocrine disorders
- Genetic Defects of Female Sexual Differentiation
- 559 Visualization of sweat suppression following botulinum toxin A by soluble microneedle arrays
- Challenges in treatment of patients with non-classic congenital adrenal hyperplasia
- Polarized microscopy in genetic hair disorders: case series
- Alopecia in Belgian Blue crossbred calves: a case series
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Ptosis in childhood
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Trichoscopy in hair disorders in darker skin: An approach to diagnosis
- Pioneers in Dermatology and Venereology: An Interview with Professor Danilo V. Stevanovic
- Unveiling the Nuances of Adult Female Acne: A Comprehensive Exploration of Epidemiology, Treatment Modalities, Dermocosmetics, and the Menopausal Influence
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Genetic screening of non-classic CAH females with hyperandrogenemia identifies a novel CYP11B1 gene mutation
- Clinical and trichoscopic characteristics of temporal triangular alopecia: A multicenter study
- Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome
- A rare case of pigmented nodular alopecic lesion on the scalp
- Disruption of the temporally regulated cloaca endodermal β-catenin signaling causes anorectal malformations