Search
for
Sort by
Research 61–90 of 113
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Mechanisms of proton inhibition and sensitization of the cation channel TRPV3
- Micronutrients in hair loss
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Vitiligo and Its Mimics in Childhood: A Diagnostic Framework for Hypopigmented Disorders
- Cutaneous manifestations associated with substance use disorders
- Natural phenylethanoid glycoside forsythoside A alleviates androgenetic alopecia by selectively inhibiting TRPV3 channels in mice
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Acne Vulgaris
- Alopecia and periorificial dermatitis in biotin-responsive multiple carboxylase deficiency
- Biotinidase Deficiency Accompanying Hair Changes and Periorificial Lesions: A Case Report
- Reflectance Confocal Microscopy of Adult Periorificial Dermatitis: A Case Report
- Skin signs of nutritional disorders.
- Biotin deficiency complicating parenteral alimentation: Diagnosis, metabolic repercussions, and treatment
- Acrodermatitis Enteropathica
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Olmsted syndrome
- Brandt Syndrome
- Dermatitis as a Presenting Sign of Cystic Fibrosis
- Acrodermatitis Enteropathica in an adult: a case report
- Cutaneous manifestations of methylmalonic and propionic acidaemia: a description based on 38 cases
- A case of acrodermatitis enteropathica misdiagnosed as staphylococcal scalded skin syndrome
- An overview of zinc and its importance in dermatology-Part II: The association of zinc with some dermatologic disorders
- BOOK REVIEWS
- Nutrition and Hair
- Oral Manifestations of Hematologic and Nutritional Diseases
- Experiences From a Combined Dermatology and Rheumatology Clinic
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- Acrodermatitis enteropathica in the pediatric population: a literature review of real-world studies
- Acquired Acrodermatitis Enteropathica in a 28-Year-Old Male with Type 1 Diabetes