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Arundhati Dev Borman

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Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|February 8, 2018
Nonaccidental injury presenting as unilateral retinal detachment in two infantsKrishanthy Sornalingam, Arundhati Dev Borman, Jane Ashworth
JIMD Reports|March 6, 2023
Autonomic instability, arrhythmia and visual impairment in a new presentation of <i>MTFMT</i>-related mitochondrial diseaseCaoimhe Howard, Arundhati Dev-Borman, John Stokes, et al.
Archives of Disease in Childhood|July 6, 2023
Nutritional blindness from avoidant-restrictive food intake disorder - recommendations for the early diagnosis and multidisciplinary management of children at risk from restrictive eatingSarah Schimansky, Haneen Jasim, Lucy Pope, et al.
Investigative Ophthalmology & Visual Science|September 3, 2010
A survey of DNA variation of C2ORF71 in probands with progressive autosomal recessive retinal degeneration and controlsPanagiotis I Sergouniotis, Zheng Li, Donna S Mackay, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
Ophthalmology|April 4, 2017
Benign Yellow Dot Maculopathy: A New Macular PhenotypeArundhati Dev Borman, Aleksandra Rachitskaya, Martina Suzani, et al.
Molecular Vision|November 9, 2011
RDH12 retinopathy: novel mutations and phenotypic descriptionDonna S Mackay, Arundhati Dev Borman, Phillip Moradi, et al.
Human Mutation|December 31, 2013
A homozygous mutation in the TUB gene associated with retinal dystrophy and obesityArundhati Dev Borman, Laura R Pearce, Donna S Mackay, et al.
Investigative Ophthalmology & Visual Science|May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic studyArundhati Dev Borman, Louise A Ocaka, Donna S Mackay, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|February 8, 2018
Nonaccidental injury presenting as unilateral retinal detachment in two infantsKrishanthy Sornalingam, Arundhati Dev Borman, Jane Ashworth
JIMD Reports|March 6, 2023
Autonomic instability, arrhythmia and visual impairment in a new presentation of <i>MTFMT</i>-related mitochondrial diseaseCaoimhe Howard, Arundhati Dev-Borman, John Stokes, et al.
Archives of Disease in Childhood|July 6, 2023
Nutritional blindness from avoidant-restrictive food intake disorder - recommendations for the early diagnosis and multidisciplinary management of children at risk from restrictive eatingSarah Schimansky, Haneen Jasim, Lucy Pope, et al.
Investigative Ophthalmology & Visual Science|September 3, 2010
A survey of DNA variation of C2ORF71 in probands with progressive autosomal recessive retinal degeneration and controlsPanagiotis I Sergouniotis, Zheng Li, Donna S Mackay, et al.
JAMA Ophthalmology|August 1, 2014
Clinical and molecular characterization of enhanced S-cone syndrome in childrenSarah Hull, Gavin Arno, Panagiotis I Sergouniotis, et al.
Investigative Ophthalmology & Visual Science|February 12, 2011
Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutationsDonna S Mackay, Louise A Ocaka, Arundhati Dev Borman, et al.
Ophthalmology|April 4, 2017
Benign Yellow Dot Maculopathy: A New Macular PhenotypeArundhati Dev Borman, Aleksandra Rachitskaya, Martina Suzani, et al.
Molecular Vision|November 9, 2011
RDH12 retinopathy: novel mutations and phenotypic descriptionDonna S Mackay, Arundhati Dev Borman, Phillip Moradi, et al.
Human Mutation|December 31, 2013
A homozygous mutation in the TUB gene associated with retinal dystrophy and obesityArundhati Dev Borman, Laura R Pearce, Donna S Mackay, et al.
Investigative Ophthalmology & Visual Science|May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic studyArundhati Dev Borman, Louise A Ocaka, Donna S Mackay, et al.
Pageof 2