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Publications by Shalesh Kaushal
Results at 2 Years After Gene Therapy for RPE65-Deficient Leber Congenital Amaurosis and Severe Early-Childhood–Onset Retinal Dystrophy
Ophthalmology
Ophthalmology
Treatment of Leber Congenital Amaurosis Due toRPE65Mutations by Ocular Subretinal Injection of Adeno-Associated Virus Gene Vector: Short-Term Results of a Phase I Trial
Human Gene Therapy
Molecular Medicine
Genetics
Molecular Biology
Related publications
Correction: Leber Congenital Amaurosis/Early-Onset Severe Retinal Dystrophy: Clinical Features, Molecular Genetics and Therapeutic Interventions
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Leber Congenital Amaurosis RPE65: 7 Years Follow Up
Gaceta Medica de Mexico
Medicine
Leber Congenital Amaurosis
Differential Proteomics and Functional Research Following Gene Therapy in a Mouse Model of Leber Congenital Amaurosis
PLoS ONE
Multidisciplinary
Hypomorphic Mutations Identified in the Candidate Leber Congenital Amaurosis Gene CLUAP1
Genetics in Medicine
Medicine
Genetics
Pharmacological and rAAV Gene Therapy Rescue of Visual Functions in a Blind Mouse Model of Leber Congenital Amaurosis
PLoS Medicine
Biochemistry
Biotechnology
Molecular Biology
Cell Biology
Medicine
Mutation Screen of the TUB Gene in Patients With Retinitis Pigmentosa and Leber Congenital Amaurosis
Experimental Eye Research
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular
Compound Heterozygous Novel Frameshift Variants in the PROM1 Gene Result in Leber Congenital Amaurosis
Cold Spring Harbor molecular case studies
Biochemistry
Molecular Medicine
Genetics
Molecular and Clinical Analysis of 27 German Patients With Leber Congenital Amaurosis
PLoS ONE
Multidisciplinary
