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G Robson

Showing results (371-380 of 456) with videos related to

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Ophthalmology|October 15, 2014
Clinical and molecular characteristics of childhood-onset Stargardt diseaseKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Investigative Ophthalmology & Visual Science|July 17, 2024
CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural HistoryThales A C de Guimaraes, Anthony G Robson, Isabela M C de Guimaraes, et al.
Retina (Philadelphia, Pa.)|April 14, 2011
Mutations in the USH1C gene associated with sector retinitis pigmentosa and hearing lossZubin Saihan, Polona Le Quesne Stabej, Anthony G Robson, et al.
JAMA Ophthalmology|July 9, 2016
Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular DystrophySarah Hull, Gavin Arno, Anthony G Robson, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 26, 2013
Effects of maternal exposure to phthalates and bisphenol A during pregnancy on gestational ageBarry Weinberger, Anna M Vetrano, Faith E Archer, et al.
The Canadian Journal of Infectious Diseases = Journal Canadien Des Maladies Infectieuses|March 15, 2012
Reduction in clinical response to empiric antimicrobial therapy of febrile granulocytopenic patients receiving TMP/SMX infection prophylaxisE J Bow, J L Pater, T J Louie, et al.
Stem Cell Reports|July 25, 2017
Enhanced Energetic State and Protection from Oxidative Stress in Human Myoblasts Overexpressing BMI1Silvia Dibenedetto, Maria Niklison-Chirou, Claudia P Cabrera, et al.
Progress in Retinal and Eye Research|January 26, 2024
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromesMichalis Georgiou, Anthony G Robson, Kaoru Fujinami, et al.
Progress in Retinal and Eye Research|August 30, 2020
The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapiesSamantha R De Silva, Gavin Arno, Anthony G Robson, et al.
Frontiers in Neuroscience|October 25, 2021
Structural and Functional Characteristics of Color Vision Changes in ChoroideremiaJasleen K Jolly, Matthew P Simunovic, Adam M Dubis, et al.
Pageof 46

Showing results (371-380 of 456) with videos related to

Sort By:
Pageof 46
Ophthalmology|October 15, 2014
Clinical and molecular characteristics of childhood-onset Stargardt diseaseKaoru Fujinami, Jana Zernant, Ravinder K Chana, et al.
Investigative Ophthalmology & Visual Science|July 17, 2024
CDH23-Associated Usher Syndrome: Clinical Features, Retinal Imaging, and Natural HistoryThales A C de Guimaraes, Anthony G Robson, Isabela M C de Guimaraes, et al.
Retina (Philadelphia, Pa.)|April 14, 2011
Mutations in the USH1C gene associated with sector retinitis pigmentosa and hearing lossZubin Saihan, Polona Le Quesne Stabej, Anthony G Robson, et al.
JAMA Ophthalmology|July 9, 2016
Characterization of CDH3-Related Congenital Hypotrichosis With Juvenile Macular DystrophySarah Hull, Gavin Arno, Anthony G Robson, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|June 26, 2013
Effects of maternal exposure to phthalates and bisphenol A during pregnancy on gestational ageBarry Weinberger, Anna M Vetrano, Faith E Archer, et al.
The Canadian Journal of Infectious Diseases = Journal Canadien Des Maladies Infectieuses|March 15, 2012
Reduction in clinical response to empiric antimicrobial therapy of febrile granulocytopenic patients receiving TMP/SMX infection prophylaxisE J Bow, J L Pater, T J Louie, et al.
Stem Cell Reports|July 25, 2017
Enhanced Energetic State and Protection from Oxidative Stress in Human Myoblasts Overexpressing BMI1Silvia Dibenedetto, Maria Niklison-Chirou, Claudia P Cabrera, et al.
Progress in Retinal and Eye Research|January 26, 2024
Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromesMichalis Georgiou, Anthony G Robson, Kaoru Fujinami, et al.
Progress in Retinal and Eye Research|August 30, 2020
The X-linked retinopathies: Physiological insights, pathogenic mechanisms, phenotypic features and novel therapiesSamantha R De Silva, Gavin Arno, Anthony G Robson, et al.
Frontiers in Neuroscience|October 25, 2021
Structural and Functional Characteristics of Color Vision Changes in ChoroideremiaJasleen K Jolly, Matthew P Simunovic, Adam M Dubis, et al.
Pageof 46