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Research 61–90 of 1000+
- Trace element zinc and skin disorders
- Premature graying of hairs: Ayurveda perspective
- Acrodermatitis Enteropathica in an adult: a case report
- Diffuse Alopecia and Thyroid Atrophy in Sheep
- Vitamin D: More Than a “Bone-a-Fide” Hormone
- The Role of Nutrition in Immune-Mediated, Inflammatory Skin Disease: A Narrative Review
- Physiological Insights from the Vitamin D Receptor Knockout Mouse
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Vitamin D and the Parenteral Nutrition Patient
- Micronutrients in hair loss
- Zinc and Zinc Transporters in Dermatology
- Genomic prediction and genome-wide association studies of morphological traits and distraction index in Korean Sapsaree dogs
- Atypical presentation of Acrodermatitis enteropathica in a child: later onset with life-threatening severe extensive dermatitis and septic shock
- Gray Hair: From Preventive to Treatment
- Male androgenetic alopecia
- E-Poster
- Enteropathica Acrodermatitis Complicated by Necrotising Fasciitis in an Infant Admitted to the Paediatric Emergency Department of the Gabriel Touré University Hospital
- Oral Presentations
- TONGUE, RED
- European Society of Endocrinology Clinical Practice Guideline: Endocrine work-up in obesity
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Hereditary 1,25-Dihydroxyvitamin D Resistant Rickets due to a Mutation Causing Multiple Defects in Vitamin D Receptor Function
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Topical minoxidil therapy in hereditary androgenetic alopecia
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor
- Hereditary vitamin D-resistant rickets (HVDRR) owing to a heterozygous mutation in the vitamin D receptor
- Two New Unrelated Cases of Hereditary 1,25-Dihydroxyvitamin D-resistant Rickets with Alopecia resulting from the same Novel Nonsense Mutation in the Vitamin D Receptor Gene
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family