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Research 661–690 of 1000+
- Age-associated inflammation connects RAS-induced senescence to stem cell dysfunction and epidermal malignancy
- Growth hormone substitution in adult growth hormone‐deficient men augments androgen effects on the skin
- Extra-Intestinal Manifestation of Celiac Disease in Children
- Diagnosis and treatment of polonium poisoning
- Finasteride for female androgenetic alopecia
- TREATMENT OF REFRACTORY HYPERTENSION
- A Feature-Preserving Hair Removal Algorithm for Dermoscopy Images
- 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
- Experience with oral tofacitinib in 8 adolescent patients with alopecia universalis
- Skin-Derived Stem Cells for Wound Treatment Using Cultured Epidermal Autografts: Clinical Applications and Challenges
- Hereditary 1,25‐Dihydroxyvitamin D–Resistant Rickets Due to an Opal Mutation Causing Premature Termination of the Vitamin D Receptor
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Measures of Adult Systemic Lupus Erythematosus: Disease Activity and Damage
- In Search of New Therapeutics—Molecular Aspects of the PCOS Pathophysiology: Genetics, Hormones, Metabolism and Beyond
- Lichen Planopilaris: Retrospective Study and Stepwise Therapeutic Approach
- Long-Term Treatment of Refractory Hypertensive Patients With Minoxidil
- Therapy and Antifungal Susceptibility Profile of Microsporum canis
- Treatment of Alopecia Areata With Squaric Acid Dibutylester
- Direct-Acting Vasodilators
- Viral-Associated Trichodysplasia of Immunosuppression
- Studies on the biochemistry and morphology of freshly isolated and maintained rat hair follicles
- Acquired perforating dermatosis in renal and diabetic patients
- Polarity signaling ensures epidermal homeostasis by coupling cellular mechanics and genomic integrity
- Genetic studies on the functional relevance of the protein prenyltransferases in skin keratinocytes
- Alopecia Due to Psychotropic Medications
- 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
- Fatal Toxic Epidermal Necrolysis Associated With Cetuximab in a Patient With Colon Cancer
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Harlequin fetus with abnormal lamellar granules and giant mitochondria
- Fibroblasts in Diabetic Foot Ulcers