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Research 31–60 of 71
- What Ages Hair?
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Break Dancing: A New Risk Factor for Scarring Hair Loss
- Diseases of Periocular Hair
- Disorders of hair
- Advances in Hair Diseases
- Diagnosis and management of hair loss in children
- Trichodystrophies: A hair-raising differential diagnosis
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Two females with hair loss
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Trichoscopy and Trichogram
- Westwood Carolina Conference on Clinical Dermatology
- [Trichothiodystrophy: a morphological and biochemical study].
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- New clinico‐genetic classification of trichothiodystrophy
- Central trichoptilosis with onycholysis
- Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Human hair production by scalp samples grafted onto nude mice. Biochemical data on normal human hair and the genetic defect trichothiodystrophy
- Hair Evaluation in Orthodontic Patients with Oligodontia
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- 675 Hair loss in hephaestin knockout mice is associated with iron deficiency
- Trichothiodystrophy in a child with occult learning disorder
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Metabolites from Macroalgae and Its Applications in the Cosmetic Industry: A Circular Economy Approach
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Trichoscopy in genetic hair shaft abnormalities
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1