Results 91 to 100 of about 25,332 (224)

Double or nothing: red flag symptoms of critical carotid stenosis, a case report [PDF]

open access: yes, 2017
Background Detailed knowledge of every possible manifestation of Internal Carotid Artery (ICA) disease is important. For improving detection and a timely adoption of secondary prevention procedures or treatments.
Irene Gómez-Estévez   +4 more
core   +1 more source

Linfoma Burkitt del seno esfenoidal en pediatría: Reporte de caso Burkitt Lymphoma of the Sphenoid Sinus in Children: Case Report

open access: yesRevista 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
doaj  

A Gene Scan Study of RPE65 in Chinese Patients with Leber Congenital Amaurosis

open access: yesChinese 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
doaj   +1 more source

Amaurosis secondary to sphenoid mucocele

open access: yesInternational Archives of Otorhinolaryngology, 2011
Introduction: The mucocele of the sphenoide sinus its a benign rare lesion. Those lesions are probably diagnosed late because they are asymptomatic or cause non-specific symptoms. The clinical characteristics depend on its location and can include fronto-
Melo, Antonio Antunes   +3 more
doaj  

Terapía génica en enfermedades oculares [PDF]

open access: yes, 2018
Universidad de Sevilla.
Marín Robayo, Mónica
core  

A CEP290 C-Terminal Domain Complements the Mutant CEP290 of Rd16 Mice In Trans and Rescues Retinal Degeneration

open access: yesCell Reports, 2018
Summary: Mutations in CEP290 cause ciliogenesis defects, leading to diverse clinical phenotypes, including Leber congenital amaurosis (LCA). Gene therapy for CEP290-associated diseases is hindered by the 7.4 kb CEP290 coding sequence, which is difficult ...
Suddhasil Mookherjee   +10 more
doaj   +1 more source

Culture of the Aspirated Coronary Thromboembulus Specimen: A Peculiar Diagnostic Method for Infective Endocarditis

open access: yesCase Reports in Medicine, 2013
A 69-year-old man was admitted to our hospital for persistent fever, myalgias, articular pain, headache, and hypoaesthesia of the scalp. The clinical scenario was typical for giant-cell arteritis.
Massimo Slavich   +5 more
doaj   +1 more source

\u3cem\u3eIn vivo\u3c/em\u3e Dark-field Imaging of the Retinal Pigment Epithelium Cell Mosaic [PDF]

open access: yes, 2013
Non-invasive reflectance imaging of the human RPE cell mosaic is demonstrated using a modified confocal adaptive optics scanning light ophthalmoscope (AOSLO). The confocal circular aperture in front of the imaging detector was replaced with a combination
Dubra, Alfredo   +2 more
core   +1 more source

Home - About - Disclaimer - Privacy