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Research 91–120 of 1000+
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Association of Acne Tarda with Endocrinological Disorders
- Allopregnanolone in the bed nucleus of the stria terminalis modulates contextual fear in rats
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- <i>WNT10A</i> , dermatology and dentistry
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS
- HAIR AND SYSTEMATIC DISEASE
- Menopause, skin and common dermatoses. Part 4: oral disorders
- Zinc Spray for Treatment of Acrodermatitis Enteropathica: A Case Report
- Oral Presentations
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Ehlers-Danlos syndrome: From bedside to bench
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Vitamins and Alopecia
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair
- Marie-unna hereditary hypotrichosis
- TRP Channels in Skin Biology and Pathophysiology
- Skin Development and Disease: A Molecular Perspective
- Ptosis in childhood
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- The interplay of oxidative stress and immune dysfunction in Hashimoto’s thyroiditis and polycystic ovary syndrome: a comprehensive review
- The Hormonal Background of Hair Loss in Non-Scarring Alopecias
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome