Results 61 to 70 of about 30,124 (290)
Histology of non-melanoma skin cancers. An Update [PDF]
, 2017 Non-melanoma skin cancer (NMSC) is the most frequently diagnosed cancer in humans. Several different non-melanoma skin cancers have been reported in the literature, with several histologic variants that frequently cause important differential diagnoses ...
Cantisani, Carmen +4 more
core +2 more sources
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.Summary Background and Objectives People with skin disease often experience stigmatization in health and body care settings, significantly impacting their quality of life. This parallel‐group randomized controlled trial evaluated a face‐to‐face group seminar aimed at reducing stigma towards people with skin disease among health and body care ...
Juliane Traxler +5 more
wiley +1 more source
A neglected case of Klippel Trenaunay Weber syndrome
Journal of Orthopedics, Traumatology and Rehabilitation, 2015 This congenital vascular disorder is described by a “triad” of symptoms affecting one or more limbs. The “triad” constitutes varicose veins, cutaneous hemangioma, with bone and soft tissue hypertrophy.
Vikram Khanna +3 more
doaj +1 more source
, 2015 thesisPort wine stains are capillary malformations that are typically located in the dermis of the head and neck. They affect 0.3% of the population. Current theories suggest that port wine stains are caused by somatic mutations that disrupt vascular ...
Wright, Karol Lynne
core
Rudimentary meningocele: remnant of a neural tube defect? [PDF]
, 2001 Background: Rudimentary meningocele, a malformation in which meningothelial elements are present in the skin and subcutaneous tissue, has been described in the past, under a variety of different terms and has also been referred to as cutaneous meningioma.
El Shabrawi-Caelen, Laila +5 more
core +1 more source
Efficacy of 577‐nm Pro‐Yellow laser in port wine stain treatment
Dermatologic Therapy, 2019 A port‐wine stain (PWS) is a congenital capillary malformation that is seen in 0.3–0.5% of newborns. Although many types of lasers have been used to treat PWSs, few studies have investigated the efficacy of 577‐nm Pro‐Yellow lasers. The aim of this study
G. Sarac, Y. Kapıcıoğlu
semanticscholar +1 more source
Journal of Prosthodontics, EarlyView.Abstract Purpose To evaluate the shade variability and stability of interim and definitive tooth‐colored restorative materials by comparing manufacturer‐claimed shades to a universal shade guide before and after thermocycling. Materials and Methods Eight commercially available tooth‐colored restorative materials were tested, including conventional ...
Amal Alfaraj +2 more
wiley +1 more source
TNOA Journal of Ophthalmic Science and ResearchWe report a case of 6-year-old boy presented with dimness of vision having a past history of recurrent seizure for last four years and was found to have glaucoma in both eyes.
Pallabi R Chaudhuri +3 more
doaj +1 more source
Klippel–trenaunay syndrome: A case report with radiological review
Medical Journal of Dr. D.Y. Patil University, 2016 Klippel–Trenaunay Syndrome is a congenital disorder with a rare incidence of 3-5/1,00,000. It is characterized by a triad of capillary malformation (hemangioma or port-wine stain), venous varicosities, and bony or, soft-tissue hypertrophy.
Amit T Kharat +3 more
doaj +1 more source
Maintenance and degradation of proteins in intact and severed axons: Implications for the mechanism of long-term survival of anucleate crayfish axons [PDF]
, 1995 Protein maintenance and degradation are examined in the severed distal (anucleate) portions of crayfish medial giant axons (MGAs), which remain viable for over 7 months following axotomy.
Bittner, George D. +2 more
core +1 more source