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Research 30 of 828
- Fractography of human hair
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- A New Case of Isolated Trichothiodystrophy
- <i>Hoxc13</i> mutant mice lack external hair
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Clinical relevance of hair microscopy in alopecia
- Alopecia in a 19-Month-Old Boy
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Thyroid hormone action on skin.
- The clinical spectrum of parathyroid disease
- Disorders of hair in children
- Structural and Molecular Hair Abnormalities in Trichothiodystrophy
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Monilethrix
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Experimental Production of Cutaneous Calcinosis and Sclerosis with Dihydrotachysterol (AT-10) 1
- HAIR AND SYSTEMATIC DISEASE
- Trichoscopy in Hair Shaft Disorders
- Clinical Signs of Hair Damage
- Ethnic Hair Disorders
- Sparse hair in a female toddler
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Central trichoptilosis with onycholysis
- Ayurvedic Management of Osteoporosis W.S.R. to Asthikshaya- A Pilot Study
- Bubble Hair Deformity Induced by Bathroom Heating Lamp: A Report of Two Cases
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis