Results 111 to 120 of about 595 (159)
Investigating Microperimetric Features in Bietti Crystalline Dystrophy Patients: A Cross-Sectional Longitudinal Study in a Large Cohort. [PDF]
Xu Y +12 more
europepmc +1 more source
High-Resolution Imaging of Patients with Bietti Crystalline Dystrophy with CYP4V2 Mutation
Kiyoko Gocho +9 more
doaj +1 more source
DISCREPANCY BETWEEN FUNDUS AUTOFLUORESCENCE ABNORMALITY AND VISUAL FIELD LOSS IN BIETTI CRYSTALLINE DYSTROPHY. [PDF]
Sakai D +9 more
europepmc +1 more source
Longitudinal Natural History Study of Visual Function in Bietti Crystalline Dystrophy: Implications for Early Intervention. [PDF]
Han X +5 more
europepmc +1 more source
Longitudinal characterisation of function and structure of Bietti crystalline dystrophy: report on a novel homozygous mutation in CYP4V2. [PDF]
Lockhart CM +7 more
europepmc +1 more source
Some of the next articles are maybe not open access.
Related searches:
Related searches:
Bietti crystalline dystrophy and choroidal neovascularisation
International Ophthalmology, 2010Bietti crystalline dystrophy is a rare autosomal recessive condition characterised by the presence of crystals in the retina and is followed by retinal and choroidal degeneration. We present a novel finding of juxtafoveal choroidal neovascularisation in Bietti crystalline dystrophy and demonstrate a spectral domain optical coherence tomography image of
Bhaskar Gupta
exaly +3 more sources
Inborn Errors of Metabolism: Bietti Crystalline Dystrophy
Advances in Experimental Medicine and Biology, 2018Bietti crystalline dystrophy (BCD) has been estimated to occur in 1 in 67,000 people; it is more common in people of East Asian descent.
Stephen H Tsang +2 more
exaly +3 more sources

