Search
for
Sort by
Research 571–600 of 1000+
- Clinical Usefulness of Non-Invasive Metabolic-Associated Fatty Liver Disease Risk Assessment Methods in Patients with Full-Blown Polycystic Ovary Syndrome in Relation to the MRI Examination with the Ideal IQ Sequence
- Diffuse congenital hypotrichosis simplex with associated hair shaft fragility
- Congenital hair loss disorders: Rare, but not too rare
- Office Diagnosis of Hair Shaft Defects
- Genetic hair and nail disorders
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- Hair Shaft Disorders
- Hair and nail disorders of childhood
- Alopecia in children
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Hair loss in children.
- Hair Loss in Children
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Disorders of hair growth : diagnosis and treatment
- Hair and Scalp Dermatoscopy (Trichoscopy)
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Tricorrexis nodosa localizada
- Acquired Localized Trichorrhexis Nodosa Secondary to Cultural Practices
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- The evolving landscape of eyebrow reconstruction: from traditional flaps to minimally invasive techniques and regenerative medicine
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Human stratum corneum proteomics reveals cross‐linking of a broad spectrum of proteins in cornified envelopes
- Distinct genotype-phenotype patterns in non-syndromic hereditary hypotrichosis: a multicenter Chinese cohort
- [Monilethrix is a hereditary hair shaft disorder].
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Low prevalence of twisted hair in anorexia nervosa
- Congenital triangular alopecia: A close mimicker of alopecia areata
- Keratins: the hair shaft's backbone revealed