Purpose: To analyze ocular biometric parameters alterations of the posterior pole and choroidal abnormalities in patients with neurofibromatosis type 1 (NF1) by adopting multimodal imaging, especially focusing on the role of novel diagnostic devices like swept-source optical coherence tomography angiography (SS-OCTA). Methods: In this prospective, case-controlled study, patients with NF1 and age-matched control subjects were quantitatively analyzed by using multimodal imaging. All the subjects underwent confocal scanning laser ophthalmoscopy (SLO), SS-OCT and SS-OCTA examinations. Results: SS-OCT analysis revealed a lower macular retinal nerve fiber layer (RNFL) thickness in patients with NF1 compared with those with suspected NF1 (95.0±15....
Purpose: To investigate choroidal changes in patients with Vogt-Koyanagi-Harada disease (VKH) using ...
Purpose: Lafora disease is a genetic neurodegenerative metabolic disorder caused by insoluble polygl...
Aim: To describe a distinctive spectrum of retinal microvascular abnormalities in 12 patients with n...
PurposeTo analyze ocular biometric parameters alterations of the posterior pole and choroidal abnorm...
PURPOSE: To analyze and classify neurofibromatosis type 1 (NF1) related retinal vascular abnormaliti...
PURPOSE: To evaluate the prevalence, the vascular features, and the clinical diagnostic implication ...
Purpose: To analyze biometric changes and prevalence of refractive in patients with neurofibromatosi...
Purpose: Only a few reports in the literature have investigated the presence of ocular abnormalities...
BACKGROUND/AIMS: A normal structural and functional choroid is essential in supplying blood flow to...
PURPOSE: The aim of this study was to provide a classification of the different retinal vascular ar...
PURPOSE: To evaluate peripapillary retinal nerve fiber layer, macular retinal nerve fiber layer, an...
Purpose: The aim of this study is to evaluate ocular surface morphological and functional changes in...
PURPOSE The aim of this study was to evaluate the anterior segment angle parameters using anterior s...
Optical coherence tomography (OCT) is an imaging method for non-invasive, in vivo visualisation of t...
BACKGROUND: Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder involving aberrant ...
Purpose: To investigate choroidal changes in patients with Vogt-Koyanagi-Harada disease (VKH) using ...
Purpose: Lafora disease is a genetic neurodegenerative metabolic disorder caused by insoluble polygl...
Aim: To describe a distinctive spectrum of retinal microvascular abnormalities in 12 patients with n...
PurposeTo analyze ocular biometric parameters alterations of the posterior pole and choroidal abnorm...
PURPOSE: To analyze and classify neurofibromatosis type 1 (NF1) related retinal vascular abnormaliti...
PURPOSE: To evaluate the prevalence, the vascular features, and the clinical diagnostic implication ...
Purpose: To analyze biometric changes and prevalence of refractive in patients with neurofibromatosi...
Purpose: Only a few reports in the literature have investigated the presence of ocular abnormalities...
BACKGROUND/AIMS: A normal structural and functional choroid is essential in supplying blood flow to...
PURPOSE: The aim of this study was to provide a classification of the different retinal vascular ar...
PURPOSE: To evaluate peripapillary retinal nerve fiber layer, macular retinal nerve fiber layer, an...
Purpose: The aim of this study is to evaluate ocular surface morphological and functional changes in...
PURPOSE The aim of this study was to evaluate the anterior segment angle parameters using anterior s...
Optical coherence tomography (OCT) is an imaging method for non-invasive, in vivo visualisation of t...
BACKGROUND: Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder involving aberrant ...
Purpose: To investigate choroidal changes in patients with Vogt-Koyanagi-Harada disease (VKH) using ...
Purpose: Lafora disease is a genetic neurodegenerative metabolic disorder caused by insoluble polygl...
Aim: To describe a distinctive spectrum of retinal microvascular abnormalities in 12 patients with n...