Results 81 to 90 of about 18,407 (215)
Síndrome de isquemia ocular: manifestaciones clínicas, diagnóstico y evolución tras el tratamiento
Revista de la Facultad de Ciencias Médicas de Córdoba, 2019 Ocular ischemia syndrome is caused by ocular chronic hypoperfusion due to stenosis or occlusion of the ipsilateral common or internal carotid artery. We present the case of a 58-year-old male with recurrent unilateral amaurosis fugax, ophthalmological ...
Abel Alejandro Sanabria Sanchinel +3 more
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Internal carotid artery thrombosis and its evolution documented by computed tomography angiography
Clinics and Practice, 2011 A case of a 79-year-old man, affected by persistent right eye blindness after multiple episodes of transient left hemiparesis and right eye amaurosis. Brain computed tomography (Angio CT) well documented right internal carotid artery (ICA) plaque with a ...
Silvia Olivato +3 more
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Amaurosis fugax: risk factors and prevalence of significant carotid stenosis
, 2016 Pia Kvickström,1 Bertil Lindblom,2,3 Göran Bergström,4,5 Madeleine Zetterberg2,3 1Department of Ophthalmology, Skaraborg Hospital, Skövde, 2Department of Clinical Neuroscience/Ophthalmology, Institute of Neuroscience and Physiology ...
Kvickström P +3 more
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Exudative vasculopathy in a child with Leber congenital amaurosis
, 2014 Leber congenital amaurosis is a severe retinal dystrophy that causes blindness or severe visual impairment, usually before the age of 1 year. We present the case of a 13-year-old girl with Leber congenital amaurosis who developed an exudative ...
Patel, Chirag +2 more
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Non-coding RNA Research, 2019 A recent study published to screen RPE65 in 187 families with Leber Congenital Amaurosis (LCA) by Zilin Zhong in 2019. There are seven novel variants were identified in RPE65, which was associated with LCA, but among only five were missense mutations [(c.
Zainularifeen Abduljaleel
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Spliceosome-Mediated Pre-mRNA trans-Splicing Can Repair CEP290 mRNA
Molecular Therapy: Nucleic Acids, 2018 Ocular gene therapy with recombinant adeno-associated virus (AAV) has shown vector-mediated gene augmentation to be safe and efficacious in the retina in one set of diseases (retinitis pigmentosa and Leber congenital amaurosis (LCA) caused by RPE65 ...
Scott J. Dooley +5 more
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Amaurosis fugax: the results of arteriography in 59 patients.
, 1983 Fifty-nine patients had arteriography because of episodes of amaurosis fugax. Only one third of them had atherosclerotic lesions potentially treatable by carotid endarterectomy.
S F Putman +4 more
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Revista Argentina de Radiología, 2011 Se reporta un caso de linfoma Burkitt del seno esfenoidal en un paciente de sexo masculino, de 3 años de edad, de raza caucásica. Presentaba un cuadro clínico de 10 días de evolución con deterioro del sensorio, vómitos y amaurosis bilateral y, por ...
Jorge Docampo +5 more
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A Gene Scan Study of RPE65 in Chinese Patients with Leber Congenital Amaurosis
Chinese Medical Journal, 2017 Background: Leber congenital amaurosis (LCA) is a visual disease which is caused by RPE65 mutations and results in retinal degeneration and severe vision loss in early infancy. According to previous researches, mutations of the RPE65 gene account for 16%
Jing Liu, Juan Bu
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