Results 31 to 40 of about 8,062 (235)

Adult onset coats disease in a 56-year-old male: An atypical presentation

Medical Journal of Dr. D.Y. Patil University, 2015
Coats disease is a congenital retinal vascular disease, which is seen commonly in childhood and remits and exacerbates throughout life. However, it is not rare for coats disease to present in adulthood for the first time.
Bodhraj Dhawan, Ankur Goel, Rajbir Singh, Vipan Vig   +3 more
doaj   +1 more source

Assessing Photoreceptor Structure Associated with Ellipsoid Zone Disruptions Visualized with Optical Coherence Tomography [PDF]

, 2016
Purpose: To compare images of photoreceptor layer disruptions obtained with optical coherence tomography (OCT) and adaptive optics scanning light ophthalmoscopy (AOSLO) in a variety of pathologic states.Methods: Five subjects with photoreceptor ellipsoid
Carroll, Joseph, Cooper, Robert F., Dubra, Alfredo, Flatter, John A., Han, Dennis P., Langlo, Christopher S., Neitz, Maureen, Pennesi, Mark E., Robison, Scott, Scoles, Drew, Weinberg, David V.   +10 more
core   +2 more sources

Triple Therapy Management of Macular Telangiectasia

Delhi Journal of Ophthalmology, 2015
We report the case of a 65 year old lady presenting with sudden diminution of vision in her right eye (RE) with the best corrected visual acuity (BCVA) being counting fingers at 1 metre.
Hammad Rashid Nasti, Vipan Vig, Bodhraj Dhawan, Taranpreet Kaur   +3 more
doaj   +1 more source

Unilateral Nevoid Telangiectasis: Report of Five Cases [PDF]

, 2010
Unilateral nevoid telangiectasia (UNT) is a rare cutaneous disorder characterized by superficial telangiectasias distributed unilaterally. UNT can be congenital or acquired.
Canan Aslan, Cuyan Demirkesen, Pembegül Güneş, Zehra Aşiran Serdar, Şirin Yaşar   +4 more
core   +1 more source

Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data [PDF]

, 2017
Infantile or early onset is estimated to occur in around 10% of all facioscapulohumeral dystrophy (FSHD) patients. Although small series of early onset FSHD patients have been reported, comprehensive data on the clinical phenotype is missing.
Brouwer, Oebele F., Dorobek, Malgorzata, Erasmus, Corrie E., Goselink, Rianne J. M., Mah, Jean K., Nikolic, Ana, Okkersen, Kees, Padberg, George W., Schreuder, Tim H. A., Tupler, Rossella, Van Engelen, Baziel G. M., Voermans, Nicol C.   +11 more
core   +5 more sources

Glicose como causa e tratamento de necrose cutânea

Jornal Vascular Brasileiro
Resumo A escleroterapia continua sendo um dos procedimentos mais executados pelos cirurgiões vasculares brasileiros. O conhecimento das suas complicações é imprescindível para que possamos evitá-las.
Marcelo Luiz Brandão, Amina Muhamad Mota Mustafá, Jordana Lopes Costa   +2 more
doaj   +1 more source

Telangiectasia retiniana parafoveal unilateral Unilateral parafoveal retinal telangiectasis

Revista Brasileira de Oftalmologia, 2007
Telangiectasia retiniana é um termo inicialmente proposto por Reese, em 1956. Caracteriza-se por uma anormalidade vascular retiniana, com dilatação irregular e incompetência dos vasos.
Mário Martins dos Santos Motta, Jacqueline Coblentz   +1 more
doaj   +1 more source

Non-homologous end-joining pathway associated with occurrence of myocardial infarction: gene set analysis of genome-wide association study data [PDF]

, 2013
<p>Purpose: DNA repair deficiencies have been postulated to play a role in the development and progression of cardiovascular disease (CVD). The hypothesis is that DNA damage accumulating with age may induce cell death, which promotes formation of ...
A Choudhury, A Torkamani, AL Dixon, AP Bazo, B Arcidiacono, Bastiaan T. Heijmans, BJ Lamarche, Brendan M. Buckley, C Matthews, CD Ragnauth, Consortium Wellcome Trust Case Control, D Thorne, David J. Stott, E Durand, E Poch, F Gizard, G Bauriedel, G Macintyre, G Perez-Rivero, G Voghel, GJ Williams, GS Stewart, H Gui, H Schunkert, Henk-Jan Guchelaar, HY Shyu, Ian Ford, IS Ockene, J Shepherd, J Shepherd, J. Wouter Jukema, Jeanine J. Houwing-Duistermaat, Jeffrey J. W. Verschuren, Joris Deelen, JR Mercer, K Allen-Brady, K Wang, LS Waters, M Corral-Debrinski, M Durik, M Kanehisa, M Mahmoudi, M Satoh, MA Loizidou, MF Moffatt, MG Andreassi, MK Shimada, ML Rossi, ML Sampietro, Naveed Sattar, NJ Samani, OK Mirzoeva, P. Eline Slagboom, S Furukawa, S Knudsen, S Mahabir, S Ozturk, S Purcell, S Purcell, S Trompet, SC Liu, Sergey Korolev, Stella Trompet, T Minamino, T Zeller, V Borde, V Borde, WR Agema, X Xie, Y Li, YB Park   +70 more
core   +3 more sources

Case for diagnosis [PDF]

Anais Brasileiros de Dermatologia, 2014
The Osler-Weber-Rendu syndrome or Hereditary Hemorrhagic Telangiectasia (HHT) is a systemic fibrovascular dysplasia characterized by defects in the elastic and vascular walls of blood vessels, making them varicose and prone to disruptions.
Juliana Catucci Boza, Timotio Volnei Dorn, Fabiana Bazanella de Oliveira, Renato Marchiori Bakos   +3 more
doaj   +1 more source

SUBFOVEAL NODULE IN COATS' DISEASE: Toward an Updated Classification Predicting Visual Prognosis. [PDF]

, 2017
To determine the prevalence, clinical characteristics and nature of subfoveal nodules in Coats' disease and the associated impact on the long-term visual outcome.
Daruich, A.L., Matet, A., Moulin, A.P., Munier, F.L., Tran, H.V.   +4 more
core   +1 more source