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Publications by Lisa Latchney

Phenotypic Diversity in Autosomal-Dominant Cone-Rod Dystrophy Elucidated by Adaptive Optics Retinal Imaging

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2017English

Related publications

Autosomal Dominant Cone-Rod Dystrophy With Negative Electroretinogram.

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
1995English

Phenotype of Autosomal Dominant Cone–rod Dystrophy Due to the R838C Mutation of the GUCY2D Gene Encoding Retinal Guanylate Cyclase-1

Eye
MedicineArtsSensory SystemsOphthalmologyHumanities
2006English

Spondylometaphyseal Dysplasia-Cone-Rod Dystrophy Syndrome

2020English

Influence of Wave-Front Sampling in Adaptive Optics Retinal Imaging

Biomedical Optics Express
BiotechnologyOpticsAtomicMolecular Physics,
2017English

Novel CDHR1 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Novel C8ORF37 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Rod-Cone Dystrophy in Spinocerebellar Ataxia Type 1

Archives of Ophthalmology
2011English

Autosomal Dominant Limb-Girdle Muscular Dystrophy Type 1A

2020English

Combined Adaptive Optics: Optical Coherence Tomography and Adaptive Optics: Scanning Laser Ophthalmoscopy System for Retinal Imaging

2009English

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