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Research 121–150 of 1000+
- MULTIPLE HEMANGIOMAS OF THE TONGUE AND ORAL CAVITY IN A MYOTONIC DYSTROPHY TYPE 1 PATIENT: A CASE REPORT
- Abstract ED05-04: Presurgical models to effectively screen preventive agents
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Value of dermoscopy for the diagnosis of monilethrix
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- Claves diagnósticas en displasias pilosas II
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Poster presentationsDP11 Bright, eosinophilic intracytoplasmic inclusion bodies: a rare presentation of acquired epidermodysplasia verruciformis with widespread human papillomavirus infection in a transplant recipient
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Forensic DNA Phenotyping
- Photobiomodulation: A Systematic Review of the Oncologic Safety of Low-Level Light Therapy for Aesthetic Skin Rejuvenation
- Optical Behavior of Human Skin Substitutes: Absorbance in the 200–400 nm UV Range
- Loss of ‘Epidermal Melanin Unit’ Integrity in Human Skin During Melanoma-Genesis
- Usefulness of Dermoscopy to Provide Accurate Assessment of Skin Cancers
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- The developmental basis of fingerprint pattern formation and variation
- Myotonic Dystrophy—A Progeroid Disease?
- Skin Development and Disease: A Molecular Perspective
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Proliferative and Non-Proliferative Lesions of the Rat and Mouse Integument
- Dermatologic Care of the Transplant Patient