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Research 901–930 of 1000+
- Histologic Study of the Regeneration Process of Human Hair Follicles Grafted onto SCID Mice after Bulb Amputation
- Distribution of childhood skin diseases according to age and gender, a single institution experience
- Adverse cutaneous reactions to chemotherapeutic agents and cytokine therapy
- Management of High-energy Avulsive Ballistic Facial Injury: A Review of the Literature and Algorithmic Approach
- Histopathological insights into hair loss in Cronkhite-Canada syndrome: Diffuse anagen-telogen conversion precedes clinical hair loss progression
- Hair shaft abnormalities after chemotherapy and tamoxifen therapy in patients with breast cancer evaluated by optical coherence tomography
- Case 21-2012
- Skin diseases in consequence of endocrine alterations
- Cutaneous Blood Flow.
- Lucio Phenomenon: Sequelae of Neglected Leprosy
- Follicular red dots: a normal trichoscopy feature in patients with pigmentary disorders?
- Yellow dots in trichoscopy: relevance, clinical significance and peculiarities
- Thrombocytosis Associated with Low-Molecular-Weight Heparin
- Adult Group B Streptococcal Disease
- Assessment of Vitamin D Level in Patients of Alopecia Areata
- Microneedling as a successful treatment for alopecia X in two Pomeranian siblings
- Clinical picture of infectious syphilis
- Spironolactone May be a Cause of Hormonally Associated Vestibulodynia and Female Sexual Arousal Disorder
- Beau's Lines
- Chemotherapy-Induced Hair Loss: The Use of Biomarkers for Predicting Alopecic Severity and Treatment Efficacy
- Dermatological problems following spinal cord injury in Korean patients
- Autoimmune gastritis and parietal cell reactivity in two children with abnormal intestinal permeability
- Analysis of histological and microRNA profiles changes in rabbit skin development
- Skin health and integrity
- Commentary
- Hyperadrenocorticism in Ferrets
- Changes in murine hair with dietary selenium excess or deficiency
- Alterações dermatológicas em pacientes oncológicos – adultos e crianças
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- THE FREQUENCY OF VISCERAL AND PHENOTYPIC MARKERS IN PATIENTS WITH THE COMBINATION OF UNDIFFERENTIATED CONNECTIVE TISSUE DISEASE AND GASTROESOPHAGEAL REFLUX DISEASE