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Research 61–90 of 108
- Beyond the usual: a case of acrodermatitis enteropathica clinically resembling erythrokeratoderma variabilis
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Acquired Acrodermatitis Enteropathica in an Infant
- P78 Acrodermatitis enteropathica in children: clinical cases
- Activation of TRPV3 Regulates Inflammatory Actions of Human Epidermal Keratinocytes
- Biotin Deficiency in an Infant Fed with Amino Acid Formula
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- Biotin Is Required for the Zinc Homeostasis in the Skin
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- A study on efficacy of oral zinc therapy for treatment of acrodermatitis enteropathica
- TRPV3 Ion Channel: From Gene to Pharmacology
- Biotin Deficiency in Telogen Effluvium: Fact or Fiction?
- 76976 Association of Depression with Finasteride Stratified by Dosage and Diagnosis: A Retrospective Cohort Study Using the TriNetX Database
- Heterozygous Variants of the SLC39A4 Gene and Possible Increased Risk for Developing Acrodermatitis Enteropathica with Kaposi’s Varicelliform Eruption
- Inherited Acrodermatitis Enteropathica
- Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Recurrent pruritic polymorphic lesions associated with weight loss
- An Infant with Worsening Rash
- Zinc-responsive Acral Hyperkeratosis as a Sequele of Acrodermatitis Enteropathica
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Poster Presentations
- Molecular determinants for the chemical activation of the warmth-sensitive TRPV3 channel by the natural monoterpenoid carvacrol
- A Comprehensive Review of Acne Vulgaris
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Lack of classic histology should not prevent diagnosis of necrolytic acral erythema
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3