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Research 541–570 of 1000+
- Alopecia areata
- Protein-Losing Enteropathy, Anasarca and Dermatological Manifestations on People of Advanced Age: Don't Overlook the Diagnostic Hypothesis of a Cronkhite Canada Syndrome
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Zinc: an undervalued microelement in research and treatment
- Valproic acid monotherapy induced longitudinal melanonychia
- Clinical cases of Darier-White follicular dyskeratosis
- Kudo Zero Sugar Collagen Anti-Aging Support Gummies Skincare & Beauty Reduces | Wrinkles & Fine Lines[WORK OR HOAX]
- SYMPTOMATOLOGY AND TREATMENT OF COVID-19 AFFECTING SKIN APPENDAGES: A NARRATIVE REVIEW BEYOND COVID-TOES.
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Biotin - facts and hopes
- Cutaneous manifestations of chronic kidney disease - A cross sectional study
- Peculiarities of clinical course and diagnostic of alopecia areata with comorbidity. Clinical observations
- Uncombable hair syndrome and beyond
- The Effects of the Oral Supplementation with a Natural Keratin Hydrolysate (Kera-Diet®) on Hair and Nails: Randomized, Placebo and Benchmark-Controlled Clinical Trial on Healthy Females
- Clinical and dermoscopic patterns of childhood alopecia areata in a tertiary care centre in North India
- Increased serum interleukin-17A levels correlate with disease severity and poor prognostic factors in patients with alopecia areata
- An Open-label Experience Trial to Evaluate the Effects of a Novel Supplement and Hair Serum Combination on Hair, Skin and Nails in Healthy Women
- Clouston’s Syndrome-A Case Report
- Impact of Coronavirus in a Dermatology Outpatient Clinic: A Single-Center Retrospective Study
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Clouston’s syndrome: a rare case report
- Assessment of anti-ageing effects of oral choline-stabilized orthosilicic acid on hair, skin and nails: an open label, non-randomized interventional study
- SPECIFIC ECTODERMAL ENHANCERS CONTROL THE EXPRESSION OF<i>Hoxc</i>GENES IN DEVELOPING MAMMALIAN INTEGUMENTS
- P095 The Very Interesting Small Bowel Lesions of Cronkhite-Canada Syndrome
- Review of Keratin Disorders
- 092 Novel biallelic RIPK4 mutations cause ectodermal dysplasia with cutaneous syndactyly
- 169 Clinical features, etiologic factors, treatment, and comorbidities of palmoplantar pustulosis: a retrospective single-center study
- Daclizumab