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Ian M MacDonald

Showing results (51-60 of 130) with videos related to

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Expert Review of Molecular Diagnostics|July 1, 2004
Choroideremia gene testingIan M MacDonald, Christina Sereda, Kerry McTaggart, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
Analysis of a large choroideremia dataset does not suggest a preference for inclusion of certain genotypes in future trials of gene therapyPaul R Freund, Yuri V Sergeev, Ian M MacDonald
Ophthalmic Genetics|June 6, 2003
A novel syndrome of congenital lid and punctal anomalies, corneal and chorioretinal dystrophyThomas K M Lee, Marc Hébert, Ian M MacDonald
Journal of Ophthalmic & Vision Research|September 1, 2020
Ocular Gene Therapy with Adeno-associated Virus Vectors: Current Outlook for Patients and ResearchersGeoffrey A Casey, Kimberly M Papp, Ian M MacDonald
Advances in Experimental Medicine and Biology|December 21, 2011
Serum biomarkers and trafficking defects in peripheral tissues reflect the severity of retinopathy in three brothers affected by choroideremiaNatalia Strunnikova, Wadih M Zein, Chris Silvin, et al.
JIMD Reports|September 9, 2020
Improved electroretinographic responses following dietary intervention in a patient with Refsum diseaseMatthew D Benson, Ian M MacDonald, Melissa Sheehan, et al.
American Journal of Ophthalmology|June 3, 2015
Communicating the promise for ocular gene therapies: challenges and recommendationsShelly Benjaminy, Stephanie P Kowal, Ian M MacDonald, et al.
Experimental Eye Research|December 18, 2024
Genetic variants in PIKFYVE: A review of ocular phenotypesEhsan Misaghi, Peter Kannu, Ian M MacDonald, et al.
Biomolecules|January 13, 2021
Zebrafish Models of Photoreceptor Dysfunction and DegenerationNicole C L Noel, Ian M MacDonald, W Ted Allison
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 19, 2016
Brothers with ocular motor apraxia, juvenile nephronophthisis, and mild cerebellar defectsStephanie C Chan, Jaspreet Rayat, Yves Sauvé, et al.
Pageof 13

Showing results (51-60 of 130) with videos related to

Sort By:
Pageof 13
Expert Review of Molecular Diagnostics|July 1, 2004
Choroideremia gene testingIan M MacDonald, Christina Sereda, Kerry McTaggart, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
Analysis of a large choroideremia dataset does not suggest a preference for inclusion of certain genotypes in future trials of gene therapyPaul R Freund, Yuri V Sergeev, Ian M MacDonald
Ophthalmic Genetics|June 6, 2003
A novel syndrome of congenital lid and punctal anomalies, corneal and chorioretinal dystrophyThomas K M Lee, Marc Hébert, Ian M MacDonald
Journal of Ophthalmic & Vision Research|September 1, 2020
Ocular Gene Therapy with Adeno-associated Virus Vectors: Current Outlook for Patients and ResearchersGeoffrey A Casey, Kimberly M Papp, Ian M MacDonald
Advances in Experimental Medicine and Biology|December 21, 2011
Serum biomarkers and trafficking defects in peripheral tissues reflect the severity of retinopathy in three brothers affected by choroideremiaNatalia Strunnikova, Wadih M Zein, Chris Silvin, et al.
JIMD Reports|September 9, 2020
Improved electroretinographic responses following dietary intervention in a patient with Refsum diseaseMatthew D Benson, Ian M MacDonald, Melissa Sheehan, et al.
American Journal of Ophthalmology|June 3, 2015
Communicating the promise for ocular gene therapies: challenges and recommendationsShelly Benjaminy, Stephanie P Kowal, Ian M MacDonald, et al.
Experimental Eye Research|December 18, 2024
Genetic variants in PIKFYVE: A review of ocular phenotypesEhsan Misaghi, Peter Kannu, Ian M MacDonald, et al.
Biomolecules|January 13, 2021
Zebrafish Models of Photoreceptor Dysfunction and DegenerationNicole C L Noel, Ian M MacDonald, W Ted Allison
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|June 19, 2016
Brothers with ocular motor apraxia, juvenile nephronophthisis, and mild cerebellar defectsStephanie C Chan, Jaspreet Rayat, Yves Sauvé, et al.
Pageof 13