Search
for
Sort by
Research 211–240 of 254
- Hearing impairment in patients with alopecia areata
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- The Suppression Effects of Fat Mass and Obesity Associated Gene on the Hair Follicle-Derived Neural Crest Stem Cells Differentiating into Melanocyte by N6-Methyladenosine Modifying Microphthalmia-Associated Transcription Factor
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- AN UPDATE OF HAIR SHAFT DISORDERS
- CD99 Is Strongly Expressed in Basal Cells of the Normal Adult Epidermis and Some Subpopulations of Appendages: Comparison with Developing Fetal Skin
- Trichothiodystrophy: Current Concepts
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Trichothiodystrophy in a child with occult learning disorder
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Mechanotransductive Differentiation of Hair Follicle Stem Cells Derived from Aged Eyelid Skin into Corneal Endothelial-Like Cells
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Two novel CreER<sup>T2</sup> transgenic mouse lines to study melanocytic cells in vivo
- Trichoscopy in genetic hair shaft abnormalities
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Dermatoscopy of hair shaft disorders
- Targeting Superficial or Nodular Basal Cell Carcinoma with Topically Formulated Small Molecule Inhibitor of Smoothened
- Chemotherapy for children with medulloblastoma
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Frontal fibrosing alopecia: a review of eleven patients
- Murine skin-derived multipotent papillary dermal fibroblast progenitors show germline potential in vitro
- Usefulness of Dermoscopy to Provide Accurate Assessment of Skin Cancers
- Diseases of Hair
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Diseases of Hair
- Induction of cardiomyocyte‑like cells from hair follicle cells in mice