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- Trichothiodystrophy
- TTNPB Promotes Human Pluripotent Stem Cell‐to‐Neural Stem Cell Transition via Modulation of Chromatin Accessibility and the S‐(5′‐adenosyl)‐L‐homocysteine/Choline Metabolic Network
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Tricotiodistrofia. Reporte de un caso
- Diagnosis of an indistinct Leydig cell tumor by positron emission tomography-computed tomography
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Trichothiodystrophy: Current Concepts
- Botulinum Toxin Off-Label Use in Dermatology: A Review
- Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Advances in hair growth
- Recent omics advances in hair aging biology and hair biomarkers analysis
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Topical minoxidil and dietary supplement for the treatment of chemotherapy-induced alopecia in childhood: a retrospective cohort study
- Design of In Vitro Hair Follicles for Different Applications in the Treatment of Alopecia—A Review
- Keratinocyte Stem Cells: Role in Aging
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Hydrogels: current biomedical applications and future directions
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Hair Shaft Dysplasias
- Congenital atrichia and hypotrichosis
- Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome
- Hair Loss in Children
- Hair and scalp disorders
- HAIR AND SYSTEMATIC DISEASE