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Research 211–240 of 232
- Nutritional Disorders of the Hair and Their Management
- Nutritional Dermatoses in the Hospitalized Patient
- Gut microbes and skin disease, gut-brain-skin axis: A review
- Patologías dermatológicas de origen nutricional en los pequeños animales: una revisión
- Combination of secukinumab and acitretin for generalized pustular psoriasis: A case report and review of literature
- Study of The Experimentally Zinc Deficiency in Iraqi Local Breed Goats
- Addressing Androgenetic Alopecia-A Complex Disorder-with a Multilateral Treatment Strategy
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- Determinants of iron, zinc, and copper concentrations in the hair of dogs and cats
- Ernährungsstörungen des Haares und deren Management
- The Nutrient–Skin Connection: Diagnosing Eating Disorders Through Dermatologic Signs
- A comprehensive investigation of biochemical status in patients with telogen effluvium: Analysis of Hb, ferritin, vitamin B12, vitamin D, thyroid function tests, zinc, copper, biotin, and selenium levels
- Mapping Human Skin: One Sequenced Cell at a Time
- Serum Zinc Concentration in Patients with Alopecia Areata
- Micronutrient Deficiencies and Digital Computerized Phototrichogram Analysis in Telogen Effluvium: A Retrospective Correlation Study in a Tertiary Medical Center
- Oxidative DNA damage level in relationship to zinc status in patients complaining hair fall, in Duhok city, Krg-Iraq: A case-control study
- Seborrheic dermatitis and pityriasis sicca: A review
- Bariatric Surgery-Induced Telogen Effluvium (Bar SITE): Case Report and a Review of Hair Loss Following Weight Loss Surgery
- 078 The transmembrane protein LRIG1 regulates receptor tyrosine kinases in skin development and homeostasis
- Subject Index
- TONGUE, RED
- Author Index
- Acrodermatitis Enteropathica
- Polarization Microscopy of Hair in Acrodermatitis Enteropathica
- Acrodermatitis dysmetabolica in an infant with maple syrup urine disease
- Acrodermatitis Enteropathica‐like Eruption in an Infant with Nonketotic Hyperglycinemia
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of 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
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Acrodermatitis continua resistant to etanercept: Therapeutic challenge and Unfortunate outcome