Search
for
Sort by
Research 421–450 of 1000+
- Acne Vulgaris
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Tricholemmoma and tricholemmal carcinoma and Cowden syndrome
- New developments in the molecular treatment of ichthyosis: review of the literature
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Steroidogenic Factor-1 Lineage Origin of Skin Lesions in Carney Complex Syndrome
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Discreet monilethrix: De novo mutation on the example of polish families
- Keratosis Follicularis Squamosa in Unilateral Buttock: A Case Report and Review of Literature in China
- Clouston’s syndrome: a rare case report
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Analogs of human genetic skin disease in domesticated animals
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Collagen Involvement in Health, Disease, and Medicine
- Prevalence, Symptomatology and Herbal Management of Polycystic Ovarian Syndrome
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- Biomedical applications of organoids in genetic diseases