Zobrazeno 1 - 10
of 29
pro vyhledávání: '"RETINAL DEPOSITS"'
Publikováno v:
Clinical Ophthalmology, Vol Volume 13, Pp 1379-1399 (2019)
GP García-García,1 M Martínez-Rubio,1 MA Moya-Moya,1 JJ Pérez-Santonja,1 J Escribano2,31Department of Ophthalmology, General University Hospital of Alicante, Alicante 03010, Spain; 2Cooperative Research Network on Ophthalmology (OftaRed), Visual
Externí odkaz:
https://doaj.org/article/88999669c742478e94951beebaa04277
Autor:
Sina J. Sabet, Andrew R. Carey
Publikováno v:
Ophthalmic Genetics. 43:116-119
Wolfram Syndrome is a rare genetic disorder usually inherited in an autosomal recessive manner. The acronym DIDMOAD characterizes the classic constellation of findings: diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. However, othe
Publikováno v:
Clinical & Experimental Ophthalmology. 47:952-954
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Rosa Dolz Marco, Sumit Randhir Singh, Jay Chhablani, Unni Nair, Vishal Govindahari, Dhanya V Nair, Roberto Gallego-Pinazo, Bindu Rajesh
Publikováno v:
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Scientific Reports, Vol 9, Iss 1, Pp 1-8 (2019)
Central serous chorioretinopathy (CSCR) is characterised by choroidal hyperpermeability which results in neurosensory detachments (NSD) along with numerous retinal pigment epithelium (RPE) alterations such as RPE atrophy. Fundus autofluorescence (FAF
Publikováno v:
JAMA ophthalmology. 136(6)
Autor:
Miguel Hage Amaro, Luiz Augusto Siqueira Silva, Cristina Muccioli, Jorge Mitre, Mario Martins do Santos Motta, Joao Jorge Amaral Nassaralla, Teruo Aihara
Publikováno v:
Revista Brasileira de Oftalmologia, Vol 74, Iss 1, Pp 49-52 (2015)
The aim of this paper is to do a review of Drusen-like beneath retinal deposits in type II mesangiocapillary glomerulonephritis. Drusenlike beneath retinal deposits in type II mesangiocapillary glomerulonephritis appear to develop at an early age, of
Publikováno v:
Neuro-ophthalmology (Aeolus Press). 42(6)
Ocular features of Gaucher disease include gaze abnormalities, corneal clouding, ocular deposits and pigmentary changes in the macula. We report the presence of bilateral fovea sparing macular deposits in a 21-year-old woman with type 3 Gaucher disea
Autor:
David R. Hinton, Carol A. Miller, Shawn Kile, David S. Boyer, Dieu-Trang Fuchs, Joel A. Pearlman, Sally A. Frautschy, William Au, Maya Koronyo-Hamaoui, Ernesto Barron, Keith L. Black, Austin Blanco, Adeel Ashfaq, Yosef Koronyo, Gregory M. Cole, David Biggs, Steven Verdooner
Publikováno v:
JCI Insight. 2
Background Noninvasive detection of Alzheimer's disease (AD) with high specificity and sensitivity can greatly facilitate identification of at-risk populations for earlier, more effective intervention. AD patients exhibit a myriad of retinal patholog
Kniha
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.