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Research 271–300 of 1000+
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- An ancestral recipe of “Champigny Saumure” to be used tepid by topical way could be useful to combat Patton-Lynch’s Erosive pustular dermatosis of the scalp
- Birt–Hogg–Dubé syndrome
- Natural Remedies for Hypercholesteremia
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Ichthyosis
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Trichoscopy in genetic hair shaft abnormalities
- Morphea: progress to date and the road ahead
- Bacterial Diseases of the Skin
- Recessive Epidermolysis Bullosa Simplex Phenotype Reproduced in Vitro
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- ESCITALOPRAM
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Trichohyalin is a Potential Major Autoantigen in Human Alopecia Areata
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Fullerene C<sub>60</sub> with cytoprotective and cytotoxic potential: prospects as a novel treatment agent in Dermatology?
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Immunologic adverse reactions of β-blockers and the skin (Review)
- Efficacy of Platelet-Rich Plasma Therapy in Oral Lichen Planus: A Systematic Review
- [Cutaneous manifestations of zinc deficiency in ethylic cirrhosis].
- The Link Between Obesity and the Skin
- Reversible alopecia in Vogt-Koyanagi-Harada disease and sympathetic ophthalmia
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Off-label uses of retinoids in dermatology
- Cutaneous Adverse Events of Tyrosine Kinase Inhibitors in Endocrine Tumors: Clinical Features, Mechanisms, and Management Strategies