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10.1007/978-1-4419-1399-9_38 http://scihub22266oqcxt.onion/10.1007/978-1-4419-1399-9_38 C4862575!4862575!20238033     free     free     free       Adv+Exp+Med+Biol 2010 ; 664 (ä): 333-40 Nephropedia Template TP {{tp|p=20238033|t=2010. Advances in Imaging of Stargardt Disease |pdf=|usr=}}{{20238033}} gab.com Text Advances in Imaging of Stargardt Disease JO: Adv Exp Med Biol http://www.kidney.de/pget.php?&tw=1&pmid=20238033 #FOAvip Stargardt disease (STGD1) is an autosomal-recessively inherited condition often associated with mutations in ABCA4 and characterized by accumulation of autofluorescent lipofuscin deposits in the retinal pigment epithelium (RPE). Non-invasive imaging techniques including fundus autofluorescence (FAF), spectral domain optical coherence tomography (SD-OCT) and adaptive optics scanning laser ophthalmoscopy (AOSLO) have the potential to improve understanding of vision loss in patients with STGD. We describe a comprehensive approach to the study of patients with STGD. Measures of retinal structure and FAF were correlated with visual function including best-corrected visual acuity (BCVA), color vision, kinetic and static perimetry, fundus-guided microperimetry and full-field and multi-focal electroretinography. Mutation analysis of the ABCA4 gene was carried out by sequencing the complete coding region. Preliminary data suggest that a combination of imaging modalities may provide a sensitive measure of disease progression and response to experimental therapies in patients with STGD. Twit Text FOAVip Advances in Imaging of Stargardt Disease ????Adv Exp Med Biol http://www.kidney.de/pget.php?&tw=1&pmid=20238033 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=20238033 #FOAvip English Wikipedia <ref>{{Cite pmid|20238033}}</ref> Advances in Imaging of Stargardt Disease #MMPMID20238033 Chen Y; Roorda A; Duncan JL Adv Exp Med Biol 2010[]; 664 (ä): 333-40 PMID20238033show ga Stargardt disease (STGD1) is an autosomal-recessively inherited condition often associated with mutations in ABCA4 and characterized by accumulation of autofluorescent lipofuscin deposits in the retinal pigment epithelium (RPE). Non-invasive imaging techniques including fundus autofluorescence (FAF), spectral domain optical coherence tomography (SD-OCT) and adaptive optics scanning laser ophthalmoscopy (AOSLO) have the potential to improve understanding of vision loss in patients with STGD. We describe a comprehensive approach to the study of patients with STGD. Measures of retinal structure and FAF were correlated with visual function including best-corrected visual acuity (BCVA), color vision, kinetic and static perimetry, fundus-guided microperimetry and full-field and multi-focal electroretinography. Mutation analysis of the ABCA4 gene was carried out by sequencing the complete coding region. Preliminary data suggest that a combination of imaging modalities may provide a sensitive measure of disease progression and response to experimental therapies in patients with STGD. äAdvances in Imaging of Stargardt Disease (epmc).pdf DeepDyve Pubget Overpricing