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Ian M MacDonald

Showing results (71-80 of 130) with videos related to

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Archives of Ophthalmology (Chicago, Ill. : 1960)|August 19, 2007
Clinical and functional findings in choroideremia due to complete deletion of the CHM geneMarco Mura, Christina Sereda, Monica M Jablonski, et al.
Retina (Philadelphia, Pa.)|August 12, 2017
THE NATURAL HISTORY OF FULL-FIELD STIMULUS THRESHOLD DECLINE IN CHOROIDEREMIAIoannis S Dimopoulos, Paul R Freund, Jacob A Knowles, et al.
Investigative Ophthalmology & Visual Science|August 28, 2009
Mutations in ASCC3L1 on 2q11.2 are associated with autosomal dominant retinitis pigmentosa in a Chinese familyNingdong Li, Han Mei, Ian M MacDonald, et al.
Molecular Genetics and Metabolism|April 3, 2004
Cofactor treatment improves ATP synthetic capacity in patients with oxidative phosphorylation disordersBarbara J Marriage, M Thomas Clandinin, Ian M Macdonald, et al.
Molecular Vision|May 3, 2014
Molecular genetic diagnostic techniques in choroideremiaMira J B Furgoch, Jacqueline Mewes-Arès, Alina Radziwon, et al.
Analytical Biochemistry|February 11, 2003
The use of lymphocytes to screen for oxidative phosphorylation disordersBarbara J Marriage, M Thomas Clandinin, Ian M MacDonald, et al.
Investigative Ophthalmology & Visual Science|September 8, 2018
Crystals and Fatty Acid Abnormalities Are Not Present in Circulating Cells From Choroideremia PatientsAlina Radziwon, Woo Jung Cho, Artur Szkotak, et al.
Ophthalmic Genetics|January 13, 2025
Inferior sectoral chorioretinopathy in two patients with novel heterozygous <i>KIF11</i> mutationsAmit V Mishra, Rosanna Martens, Carolin Aizouki, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|October 15, 2011
Re: analysis of the publication volume of Canadian ophthalmology departments from 2005 to 2009: a systematic review of the literatureChristopher J Rudnisky, Karim F Damji, Matthew T S Tennant, et al.
Progress in Retinal and Eye Research|July 10, 2022
Zebrafish and inherited photoreceptor disease: Models and insightsNicole C L Noel, W Ted Allison, Ian M MacDonald, et al.
Pageof 13

Showing results (71-80 of 130) with videos related to

Sort By:
Pageof 13
Archives of Ophthalmology (Chicago, Ill. : 1960)|August 19, 2007
Clinical and functional findings in choroideremia due to complete deletion of the CHM geneMarco Mura, Christina Sereda, Monica M Jablonski, et al.
Retina (Philadelphia, Pa.)|August 12, 2017
THE NATURAL HISTORY OF FULL-FIELD STIMULUS THRESHOLD DECLINE IN CHOROIDEREMIAIoannis S Dimopoulos, Paul R Freund, Jacob A Knowles, et al.
Investigative Ophthalmology & Visual Science|August 28, 2009
Mutations in ASCC3L1 on 2q11.2 are associated with autosomal dominant retinitis pigmentosa in a Chinese familyNingdong Li, Han Mei, Ian M MacDonald, et al.
Molecular Genetics and Metabolism|April 3, 2004
Cofactor treatment improves ATP synthetic capacity in patients with oxidative phosphorylation disordersBarbara J Marriage, M Thomas Clandinin, Ian M Macdonald, et al.
Molecular Vision|May 3, 2014
Molecular genetic diagnostic techniques in choroideremiaMira J B Furgoch, Jacqueline Mewes-Arès, Alina Radziwon, et al.
Analytical Biochemistry|February 11, 2003
The use of lymphocytes to screen for oxidative phosphorylation disordersBarbara J Marriage, M Thomas Clandinin, Ian M MacDonald, et al.
Investigative Ophthalmology & Visual Science|September 8, 2018
Crystals and Fatty Acid Abnormalities Are Not Present in Circulating Cells From Choroideremia PatientsAlina Radziwon, Woo Jung Cho, Artur Szkotak, et al.
Ophthalmic Genetics|January 13, 2025
Inferior sectoral chorioretinopathy in two patients with novel heterozygous <i>KIF11</i> mutationsAmit V Mishra, Rosanna Martens, Carolin Aizouki, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|October 15, 2011
Re: analysis of the publication volume of Canadian ophthalmology departments from 2005 to 2009: a systematic review of the literatureChristopher J Rudnisky, Karim F Damji, Matthew T S Tennant, et al.
Progress in Retinal and Eye Research|July 10, 2022
Zebrafish and inherited photoreceptor disease: Models and insightsNicole C L Noel, W Ted Allison, Ian M MacDonald, et al.
Pageof 13