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Showing results (771-780 of 854) with videos related to

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Ophthalmology|July 30, 2018
Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single CenterBrian P Brooks, Wadih M Zein, Amy H Thompson, et al.
Frontiers in Endocrinology|November 6, 2023
Case Report: Insulin hypersensitivity in youth with type 1 diabetesEinas H Alkhatib, Jody B Grundman, Anna M Adamusiak, et al.
Investigative Ophthalmology & Visual Science|November 7, 2018
The Henle Fiber Layer in Albinism: Comparison to Normal and Relationship to Outer Nuclear Layer Thickness and Foveal Cone DensityDaniel J Lee, Erica N Woertz, Alexis Visotcky, et al.
American Journal of Human Genetics|November 28, 2016
Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and DeafnessAman George, Dina J Zand, Robert B Hufnagel, et al.
JCI Insight|January 25, 2022
Photoreceptor degeneration in ABCA4-associated retinopathy and its genetic correlatesMaximilian Pfau, Catherine A Cukras, Laryssa A Huryn, et al.
Investigative Ophthalmology & Visual Science|October 23, 2018
Minimal Efficacy of Nitisinone Treatment in a Novel Mouse Model of Oculocutaneous Albinism, Type 3Ighovie F Onojafe, Lucyanne H Megan, Madeline G Melch, et al.
Plos One|March 16, 2017
Cellular and molecular defects in a patient with Hermansky-Pudlak syndrome type 5Joshi Stephen, Tadafumi Yokoyama, Nathanial J Tolman, et al.
Science Translational Medicine|November 2, 2018
Antisense oligonucleotides targeting mutant Ataxin-7 restore visual function in a mouse model of spinocerebellar ataxia type 7Chenchen Niu, Thazah P Prakash, Aneeza Kim, et al.
Frontiers in Aging Neuroscience|March 26, 2021
Persistent Dark Cones in Oligocone Trichromacy Revealed by Multimodal Adaptive Optics OphthalmoscopyJoanne Li, Tao Liu, Oliver J Flynn, et al.
Pharmacology & Therapeutics|June 29, 2023
Retina and RPE lipid profile changes linked with ABCA4 associated Stargardt's maculopathyMitra Farnoodian, Devika Bose, Francesca Barone, et al.
Pageof 86

Showing results (771-780 of 854) with videos related to

Sort By:
Pageof 86
Ophthalmology|July 30, 2018
Joubert Syndrome: Ophthalmological Findings in Correlation with Genotype and Hepatorenal Disease in 99 Patients Prospectively Evaluated at a Single CenterBrian P Brooks, Wadih M Zein, Amy H Thompson, et al.
Frontiers in Endocrinology|November 6, 2023
Case Report: Insulin hypersensitivity in youth with type 1 diabetesEinas H Alkhatib, Jody B Grundman, Anna M Adamusiak, et al.
Investigative Ophthalmology & Visual Science|November 7, 2018
The Henle Fiber Layer in Albinism: Comparison to Normal and Relationship to Outer Nuclear Layer Thickness and Foveal Cone DensityDaniel J Lee, Erica N Woertz, Alexis Visotcky, et al.
American Journal of Human Genetics|November 28, 2016
Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and DeafnessAman George, Dina J Zand, Robert B Hufnagel, et al.
JCI Insight|January 25, 2022
Photoreceptor degeneration in ABCA4-associated retinopathy and its genetic correlatesMaximilian Pfau, Catherine A Cukras, Laryssa A Huryn, et al.
Investigative Ophthalmology & Visual Science|October 23, 2018
Minimal Efficacy of Nitisinone Treatment in a Novel Mouse Model of Oculocutaneous Albinism, Type 3Ighovie F Onojafe, Lucyanne H Megan, Madeline G Melch, et al.
Plos One|March 16, 2017
Cellular and molecular defects in a patient with Hermansky-Pudlak syndrome type 5Joshi Stephen, Tadafumi Yokoyama, Nathanial J Tolman, et al.
Science Translational Medicine|November 2, 2018
Antisense oligonucleotides targeting mutant Ataxin-7 restore visual function in a mouse model of spinocerebellar ataxia type 7Chenchen Niu, Thazah P Prakash, Aneeza Kim, et al.
Frontiers in Aging Neuroscience|March 26, 2021
Persistent Dark Cones in Oligocone Trichromacy Revealed by Multimodal Adaptive Optics OphthalmoscopyJoanne Li, Tao Liu, Oliver J Flynn, et al.
Pharmacology & Therapeutics|June 29, 2023
Retina and RPE lipid profile changes linked with ABCA4 associated Stargardt's maculopathyMitra Farnoodian, Devika Bose, Francesca Barone, et al.
Pageof 86