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Research 691–720 of 1000+
- Cutaneous signs in COVID ‐19 patients: A review
- Decreased Serum Ferritin is Associated With Alopecia in Women
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- EVALUATION OF ASSOCIATION OF ANTHROPOMETRIC INDICES WITH STRESS RESPONSE IN PCOS POPULATION
- Incidence of adverse cutaneous drug reactions in a Mexican sample: an exploratory study on their association to tumour necrosis factor alpha TNF2 allele
- Basal cell carcinoma of the scalp shows distinct features from the face in Asians
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Wnt1/βcatenin injury response activates the epicardium and cardiac fibroblasts to promote cardiac repair
- An Update of Congenital Adrenal Hyperplasia
- Keratin disorders: from gene to therapy
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase
- Endocrine Influences on Hair Growth
- Androgen receptors and their biology
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- JunB defines functional and structural integrity of the epidermo-pilosebaceous unit in the skin
- Premature graying of hair
- Fluoroquinolone-induced serious, persistent, multisymptom adverse effects
- Hydrogen peroxide and monoethanolamine are the key causative ingredients for hair dye-induced dermatitis and hair loss
- Lichen planus and other cutaneous manifestations in chronic hepatitis C: pre- and post-interferon-based treatment prevalence vary in a cohort of patients from low hepatitis C virus endemic area
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Diagnostic approach to low‐renin hypertension
- The Basic Science of Hair Biology
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Hypersensitivity Reactions to Anticoagulant Drugs
- Congenital adrenal hyperplasia
- Thyroid hormone action on skin.