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J B Kerrison

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Retina (Philadelphia, Pa.)|August 18, 2001
Choroidal infarction, anterior ischemic optic neuropathy, and central retinal artery occlusion from polyarteritis nodosaC T Hsu, J B Kerrison, N R Miller, et al.
Ophthalmology|October 1, 1995
Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a caseJ B Kerrison, N Howell, N R Miller, et al.
American Journal of Ophthalmology|March 3, 2001
Sickle cell disease presenting with extensive peri-macular arteriolar occlusions in a nine-year-old boyN A Al-Abdulla, T A Haddock, J B Kerrison, et al.
Ophthalmic Genetics|January 23, 2002
Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1)J B Kerrison, R Giorda, T D Lenart, et al.
American Journal of Ophthalmology|January 23, 1998
Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12J B Kerrison, R K Koenekoop, V J Arnould, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 5, 1999
Atypical mass lesion associated with cat-scratch diseaseJ B Kerrison, M D Bennett, N J Newman, et al.
American Journal of Ophthalmology|December 22, 2000
Stages of improvement in visual fields after pituitary tumor resectionJ B Kerrison, M J Lynn, C A Baer, et al.
Genomics|May 1, 1996
A gene for autosomal dominant congenital nystagmus localizes to 6p12J B Kerrison, V J Arnould, M M Barmada, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 1999
Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3J B Kerrison, V J Arnould, J M Ferraz Sallum, et al.
American Journal of Ophthalmology|December 22, 2000
A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathyJ B Kerrison, N R Miller, F Hsu, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Retina (Philadelphia, Pa.)|August 18, 2001
Choroidal infarction, anterior ischemic optic neuropathy, and central retinal artery occlusion from polyarteritis nodosaC T Hsu, J B Kerrison, N R Miller, et al.
Ophthalmology|October 1, 1995
Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a caseJ B Kerrison, N Howell, N R Miller, et al.
American Journal of Ophthalmology|March 3, 2001
Sickle cell disease presenting with extensive peri-macular arteriolar occlusions in a nine-year-old boyN A Al-Abdulla, T A Haddock, J B Kerrison, et al.
Ophthalmic Genetics|January 23, 2002
Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1)J B Kerrison, R Giorda, T D Lenart, et al.
American Journal of Ophthalmology|January 23, 1998
Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12J B Kerrison, R K Koenekoop, V J Arnould, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|August 5, 1999
Atypical mass lesion associated with cat-scratch diseaseJ B Kerrison, M D Bennett, N J Newman, et al.
American Journal of Ophthalmology|December 22, 2000
Stages of improvement in visual fields after pituitary tumor resectionJ B Kerrison, M J Lynn, C A Baer, et al.
Genomics|May 1, 1996
A gene for autosomal dominant congenital nystagmus localizes to 6p12J B Kerrison, V J Arnould, M M Barmada, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|June 16, 1999
Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3J B Kerrison, V J Arnould, J M Ferraz Sallum, et al.
American Journal of Ophthalmology|December 22, 2000
A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathyJ B Kerrison, N R Miller, F Hsu, et al.
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