A Search Service for Abbreviation / Long Form

■ Abbreviation / Long Form : STGD / Stargardt disease

[Related PubMed/MEDLINE]
Total Number of Papers: 133
[Display Entries]
100 entries :
     (Publication year, Descending)
100 entries :
     (Publication year, Ascending)
>> all entries
[Entries Per Page]
 per page
Page Control
Page: of
Abbreviation:   STGD  (>> Co-occurring Abbreviation)
Long Form:   Stargardt disease
 Abbreviation Variation
 Long Form Variation
 Pair(Abbreviation/Long Form) Variation
No. Year Title Co-occurring Abbreviation
2022 ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease. CRD
2022 Choroidal vascularity index in eyes with central macular atrophy secondary to age-related macular degeneration and Stargardt disease. AMD, CVI, MA, TCA
2021 Clinical and Genetic Spectrum of Stargardt Disease in Argentinean Patients. ---
2021 High-resolution images in macular disorders. AO, CSC, FAF, OCT, RP
2021 Microvascular and metabolic alterations in retinitis pigmentosa and Stargardt disease. no-ME-RP, OCTA, RO, RP
2021 Motion-Based Acuity Task: Full Visual Field Measurement of Shape and Motion Perception. RDKs, RP
2021 Non-syndromic inherited retinal diseases in Poland: Genes, mutations, and phenotypes. IRDs, NGS, RP
2021 Outer nuclear layer relevance in visual function correlated to quantitative enface OCT parameters in Stargardt disease. BCVA, C-ONL-T, CR-T, OCT, RPE
2021 Retinal Vascular Abnormalities in Different Types of Inherited Retinal Dystrophies Assessed by Optical Coherence Tomography Angiography. CRD, IRDs, RP, SCP and DCP, VDs
10  2021 Targeted next-generation sequencing identifies ABCA4 mutations in Chinese families with childhood-onset and adult-onset Stargardt disease. NGS
11  2020 Automated classification of normal and Stargardt disease optical coherence tomography images using deep learning. CNN, JSS, OCT
12  2020 Deep Learning-Based Classification of Inherited Retinal Diseases Using Fundus Autofluorescence. BD, CNN, FAF, IRD, PRC-AUC, RP
13  2020 Exome sequencing analysis identifies novel homozygous mutation in ABCA4 in a Chinese family with Stargardt disease. WES
14  2020 Formulation and efficacy of ECO/pRHO-ABCA4-SV40 nanoparticles for nonviral gene therapy of Stargardt disease in a mouse model. ---
15  2020 Living with Stargardt disease: insights from patients and their parents. ---
16  2020 Novel variants associated with Stargardt disease in Chinese patients. NGS, UTRs
17  2020 Progressive Choriocapillaris Impairment in ABCA4 Maculopathy Is Secondary to Retinal Pigment Epithelium Atrophy. CC, OCTA, RPE, SW-AF
18  2020 Retinal Glial and Choroidal Vascular Pathology in Donors Clinically Diagnosed With Stargardt Disease. FFB
19  2020 Saccadic movements assessment in eccentric fixation: A study in patients with Stargardt disease. ---
20  2020 Simultaneous expression of two pathogenic genes in four Chinese patients affected with inherited retinal dystrophy. adRP, arRP, HEDEP, IRDs, RP
21  2020 Systemic administration of the di-apocarotenoid norbixin (BIO201) is neuroprotective, preserves photoreceptor function and inhibits A2E and lipofuscin accumulation in animal models of age-related macular degeneration and Stargardt disease. AMD, BLD, RPE
22  2020 Thinner temporal peripapillary retinal nerve fibre layer in Stargardt disease detected by optical coherence tomography. OCT, RNFL
23  2020 [Morphological and functional indicators of retinal pigment epithelium and photoreceptor apparatus in inherited retinal diseases]. AF, CP, CRD, EOG, G-ERG, IRD, OCT, PR, RP, RPE
24  2019 An ABCA4 loss-of-function mutation causes a canine form of Stargardt disease. ABCA4, RPE
25  2019 Application of targeted exome and whole-exome sequencing for Chinese families with Stargardt disease. ---
26  2019 Characterisation of vascular changes in different stages of Stargardt disease using double swept-source optical coherence tomography angiography. CC, FAZ, ORCC, SCP/DCP
27  2019 Choroidal Patterns in Stargardt Disease: Correlations with Visual Acuity and Disease Progression. BCVA, OCT, OCTA
28  2019 Correlation between Choriocapillaris Density and Retinal Sensitivity in Stargardt Disease. CA, CC, DA, MP, NA, PPCA, SS WF OCTA
29  2019 Correlation of Outer Retinal Degeneration and Choriocapillaris Loss in Stargardt Disease Using En Face Optical Coherence Tomography and Optical Coherence Tomography Angiography. CC, CCVD, IS/OS, OCTA, RPE
30  2019 Fluorescence Lifetime Patterns of Retinal Pigment Epithelium Atrophy in Patients with Stargardt Disease and Age-Related Macular Degeneration. AMD, RPE
31  2019 Genetic Spectrum of ABCA4-Associated Retinal Degeneration in Poland. ABCA4, CRD, IRDs, MIPs, RFLP, RP
32  2019 Genotypic profile and phenotype correlations of ABCA4-associated retinopathy in Koreans. ABCA4-RD, CRD, IRDs, RP
33  2019 Impact of segmentation density on spectral domain optical coherence tomography assessment in Stargardt disease. ONL, OS, ProgStar, RPE, SD-OCT
34  2019 Macular hyperpigmentary changes in ABCA4-Stargardt disease. AMD, FAF, ffERG, VA
35  2019 Multimodal evaluation of central and peripheral alterations in Stargardt disease: a pilot study. OCT, OCTA, UWF
36  2019 Non-viral Gene Therapy for Stargardt Disease with ECO/pRHO-ABCA4 Self-Assembled Nanoparticles. WT
37  2019 OCTA-Based Identification of Different Vascular Patterns in Stargardt Disease. CMT, HF, OCT, OCTA, VD, VR, VT
38  2019 Perceptual learning in patients with Stargardt disease. ---
39  2018 CFH Y402H polymorphism in Italian patients with age-related macular degeneration, retinitis pigmentosa, and Stargardt disease. AMD, RP
40  2018 Clinical and Genetic Characteristics Analysis of Korean Patients with Stargardt Disease Using Targeted Exome Sequencing. ABCA4, ELOVL4, PROM1
41  2018 Contrast sensitivity deficits in patients with mutation-proven inherited retinal degenerations. CS, IRD, QCSF, RCD, SD-OCT
42  2018 EDI OCT evaluation of choroidal thickness in Stargardt disease. CT
43  2018 Hyperreflective foci in Stargardt disease: 1-year follow-up. HF
44  2018 Stargardt Disease. FAF, hyperAF
45  2018 Stargardt Phenotype Associated With Two ELOVL4 Promoter Variants and ELOVL4 Downregulation: New Possible Perspective to Etiopathogenesis? ELOVL4, VLC-PUFA
46  2018 Treatments for dry age-related macular degeneration and Stargardt disease: a systematic review. AMD, EME, HTA, VA
47  2017 A Novel ABCA4 Mutation Associated with a Late-Onset Stargardt Disease Phenotype: A Hypomorphic Allele? ---
49  2017 Comparative analysis of autofluorescence and OCT angiography in Stargardt disease. CC, FAF, OCTA, RPE
50  2017 Functional changes at the preferred retinal locus in subjects with bilateral central vision loss. AMD, BCEA, CVL, MSs, PRL
51  2017 Morpho-functional analysis of Stargardt Disease for reading. BCVA, FAF, OCT
52  2017 Novel compound heterozygous mutations in ABCA4 in a Chinese pedigree with Stargardt disease. ---
53  2017 Optical Coherence Tomography Angiography Findings in Stargardt Disease. CC, DCP, ILM, IPL, mfERG, MT, OCTA, PERG, SCP, VD
54  2017 Peripheral Visual Fields in ABCA4 Stargardt Disease and Correlation With Disease Extent on Ultra-widefield Fundus Autofluorescence. ffERG, UWF-FAF, VA
55  2017 Quantifying the Rate of Ellipsoid Zone Loss in Stargardt Disease. EZ, FAF, ICC, OCT, RPE, SD-OCT
56  2017 Reading Ability and Quality of Life in Stargardt Disease. ETDRS, VRQoL
57  2017 Reading Performance Improvements in Patients with Central Vision Loss without Age-Related Macular Degeneration after Undergoing Personalized Rehabilitation Training. AFVD, CVL, MMD, QoL, RRP, VAs
58  2017 Reliability and Repeatability of Cone Density Measurements in Patients With Stargardt Disease and RPGR-Associated Retinopathy. AOSLO, RPGR
59  2017 STARGARDT DISEASE: Beyond Flecks and Atrophy. BrM, EZ
60  2017 The Epidemiology of Stargardt Disease in the United Kingdom. BOSU
61  2017 Unravelling the Complexity of Inherited Retinal Dystrophies Molecular Testing: Added Value of Targeted Next-Generation Sequencing. BMD, IRDs, LCA, NGS, RP, USH
62  2017 [Contribution of multimodal imaging in the various stages of Stargardt disease]. FA, FAF, ICGA, RPE, SD-OCT
63  2016 Analysis of ELOVL4 and PRPH2 genes in Turkish Stargardt disease patients. ---
64  2016 Dark Atrophy: An Optical Coherence Tomography Angiography Study. AMD, EDI-OCT, FA, FAF, GA, ICGA, OCTA, RPE
65  2016 Dietary profile of patients with Stargardt's disease and Retinitis Pigmentosa: is there a role for a nutritional approach? RP
66  2016 Fluorescence Lifetime Imaging in Stargardt Disease: Potential Marker for Disease Progression. FLIO
67  2016 Focal Choroidal Excavation in Retinal Dystrophies. FCE, RP
68  2016 Test-Retest Variability of Functional and Structural Parameters in Patients with Stargardt Disease Participating in the SAR422459 Gene Therapy Trial. BCVA, CI, ETDRS, HOV, RC, SD-OCT, SKP, SVF
69  2015 Cerebral Involvement in Stargardt's Disease: A VBM and TBSS Study. BCVA, DTI, ERG, GM, OCT, T1W, TBSS, VBM, WM
70  2015 Choroidal Thickness in Eyes With Central Geographic Atrophy Secondary to Stargardt Disease and Age-Related Macular Degeneration. AMD, CT, FAF, GA, RPD, SD
71  2015 Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel Analysis. ---
72  2015 Identification of Novel Mutations in ABCA4 Gene: Clinical and Genetic Analysis of Indian Patients with Stargardt Disease. ---
73  2015 [The molecular genetic and clinical findings in two probands with Stargardt disease]. SD-OCT
74  2014 Association between genotype and phenotype in families with mutations in the ABCA4 gene. ABCA4, arRP, CRD, ff-ERG, mERG, OCT
75  2014 Causes and consequences of inherited cone disorders. ACHM, CDs, COD, CRD
76  2014 Clinical and molecular characteristics of childhood-onset Stargardt disease. SD-OCT
77  2014 Efficient gene delivery to the cone-enriched pig retina by dual AAV vectors. AAV, IRDs
78  2014 Molecular diagnosis of putative Stargardt disease by capture next generation sequencing. CNGS
79  2014 Multifunctional PEG retinylamine conjugate provides prolonged protection against retinal degeneration in mice. AMD, GFL, PEG
80  2013 Biofeedback rehabilitation of eccentric fixation in patients with Stargardt disease. BCEA, BCVA, BF
81  2013 Characterization of stargardt disease using polarization-sensitive optical coherence tomography and fundus autofluorescence imaging. FAF, PS-OCT
82  2013 Effective delivery of large genes to the retina by dual AAV vectors. AAV
83  2013 Phenotype/genotype correlation in a case series of Stargardt's patients identifies novel mutations in the ABCA4 gene. BCVA
84  2013 Subretinal Fibrosis in Stargardt's Disease with Fundus Flavimaculatus and ABCA4 Gene Mutation. FFM
85  2012 Correlation between photoreceptor layer integrity and visual function in patients with Stargardt disease: implications for gene therapy. IS/OS
86  2012 Functional Analysis of Retinal Flecks in Stargardt Disease. FAF, RPE, SD-OCT
87  2012 Molecular diagnosis of putative Stargardt Disease probands by exome sequencing. WES
88  2012 The dark atrophy with indocyanine green angiography in Stargardt disease. FA, ICGA, SD-OCT
89  2011 Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease. AF, AOSLO
90  2011 Transition zones between healthy and diseased retina in choroideremia (CHM) and Stargardt disease (STGD) as compared to retinitis pigmentosa (RP). CHM, Fd, OR, OS, RP, TZ
91  2010 DHA supplementation for late onset Stargardt disease: NAT-3 study. BCVA, DHA, LE, mfERG, RE
92  2010 In vivo visualization of photoreceptor layer and lipofuscin accumulation in stargardt's disease and fundus flavimaculatus by high resolution spectral-domain optical coherence tomography. BCVA, FFM, HD-OCT, IS, OS, PR, RPE, VM
93  2010 Inhibition of the visual cycle by A2E through direct interaction with RPE65 and implications in Stargardt disease. LRAT, RPE
94  2009 Comparison of high-resolution melting analysis with denaturing high-performance liquid chromatography for mutation scanning in the ABCA4 gene. arCRD, arRP, DHPLC, HRM
95  2009 Lipofuscin and autofluorescence metrics in progressive STGD. AF, FDAF, FIAF, GA
96  2009 Novel mutations in of the ABCR gene in Italian patients with Stargardt disease. ---
97  2008 Correlation of visual function impairment and OCT findings in patients with Stargardt disease and fundus flavimaculatus. BCVA, FFM, OCT
98  2008 Evaluation of macular abnormalities in Stargardt's disease using optical coherence tomography and scanning laser ophthalmoscope microperimetry. BCVA, SLO
99  2008 Evaluation of the common variants of the ABCA4 gene in families with Stargardt disease and autosomal recessive retinitis pigmentosa. RP
100  2008 Evidence of widespread retinal dysfunction in patients with stargardt disease and morphologically unaffected carrier relatives. CS, LSF, mfERG