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Seema Anand

Showing results (11-20 of 20) with videos related to

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The British Journal of Ophthalmology|June 21, 2023
Repeat corneal collagen cross-linking after failure of primary cross-linking in keratoconusDavid Maskill, Arthur Okonkwo, Charlotte Onsiong, et al.
Eye (London, England)|December 14, 2022
The cost of laser refractive surgery and supplementary sulcus lens implantation for pseudophakic ametropia and astigmatism, the leeds experienceArthur Okonkwo, Robert Blizzard, Seema Anand, et al.
Molecular Diagnosis & Therapy|July 28, 2025
Long-Range PCR and Nanopore Sequencing Enables High-Throughput Detection of TCF4 Trinucleotide Repeat Expansions in Fuchs Endothelial Corneal DystrophyBushra Alayed, Salina Siddiqui, Seema Anand, et al.
Eye (London, England)|October 19, 2022
Specialist nurse-led cross-linking service for Keratoconus, the Leeds experienceRita Prajapati, Alan Salada, Arthur Okonkwo, et al.
The British Journal of Ophthalmology|August 23, 2013
Cataract surgery outcome in eyes with keratoconusMartin P Watson, Seema Anand, Maninder Bhogal, et al.
Ophthalmology|April 4, 2006
Poststreptococcal syndrome uveitis: a descriptive case series and literature reviewShafiq Ur Rehman, Seema Anand, Aravind Reddy, et al.
Retina (Philadelphia, Pa.)|March 6, 2009
Macular dystrophy associated with the Arg172Trp substitution in peripherin/RDS: genotype-phenotype correlationSeema Anand, Eamonn Sheridan, Frances Cassidy, et al.
Molecular Vision|May 25, 2026
Targeted sequencing with single-molecule molecular inversion probes highlights a gap in understanding the cause of Fuchs endothelial corneal dystrophyBushra Alayed, Danah Albuainain, Salina Siddiqui, et al.
Nature Genetics|June 13, 2006
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)Eranga N Vithana, Patricio Morgan, Periasamy Sundaresan, et al.
Investigative Ophthalmology & Visual Science|October 18, 2011
Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconusKathryn P Burdon, Stuart Macgregor, Yelena Bykhovskaya, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
The British Journal of Ophthalmology|June 21, 2023
Repeat corneal collagen cross-linking after failure of primary cross-linking in keratoconusDavid Maskill, Arthur Okonkwo, Charlotte Onsiong, et al.
Eye (London, England)|December 14, 2022
The cost of laser refractive surgery and supplementary sulcus lens implantation for pseudophakic ametropia and astigmatism, the leeds experienceArthur Okonkwo, Robert Blizzard, Seema Anand, et al.
Molecular Diagnosis & Therapy|July 28, 2025
Long-Range PCR and Nanopore Sequencing Enables High-Throughput Detection of TCF4 Trinucleotide Repeat Expansions in Fuchs Endothelial Corneal DystrophyBushra Alayed, Salina Siddiqui, Seema Anand, et al.
Eye (London, England)|October 19, 2022
Specialist nurse-led cross-linking service for Keratoconus, the Leeds experienceRita Prajapati, Alan Salada, Arthur Okonkwo, et al.
The British Journal of Ophthalmology|August 23, 2013
Cataract surgery outcome in eyes with keratoconusMartin P Watson, Seema Anand, Maninder Bhogal, et al.
Ophthalmology|April 4, 2006
Poststreptococcal syndrome uveitis: a descriptive case series and literature reviewShafiq Ur Rehman, Seema Anand, Aravind Reddy, et al.
Retina (Philadelphia, Pa.)|March 6, 2009
Macular dystrophy associated with the Arg172Trp substitution in peripherin/RDS: genotype-phenotype correlationSeema Anand, Eamonn Sheridan, Frances Cassidy, et al.
Molecular Vision|May 25, 2026
Targeted sequencing with single-molecule molecular inversion probes highlights a gap in understanding the cause of Fuchs endothelial corneal dystrophyBushra Alayed, Danah Albuainain, Salina Siddiqui, et al.
Nature Genetics|June 13, 2006
Mutations in sodium-borate cotransporter SLC4A11 cause recessive congenital hereditary endothelial dystrophy (CHED2)Eranga N Vithana, Patricio Morgan, Periasamy Sundaresan, et al.
Investigative Ophthalmology & Visual Science|October 18, 2011
Association of polymorphisms in the hepatocyte growth factor gene promoter with keratoconusKathryn P Burdon, Stuart Macgregor, Yelena Bykhovskaya, et al.
Pageof 2