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Retina (Philadelphia, Pa.)
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August 18, 2001
Choroidal infarction, anterior ischemic optic neuropathy, and central retinal artery occlusion from polyarteritis nodosa
C 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 case
J 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 boy
N 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 6p12
J 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 disease
J 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 resection
J B Kerrison, M J Lynn, C A Baer, et al.
Genomics
|
May 1, 1996
A gene for autosomal dominant congenital nystagmus localizes to 6p12
J 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 18q12.2-12.3
J 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 neuropathy
J B Kerrison, N R Miller, F Hsu, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
Retina (Philadelphia, Pa.)
|
August 18, 2001
Choroidal infarction, anterior ischemic optic neuropathy, and central retinal artery occlusion from polyarteritis nodosa
C 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 case
J 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 boy
N 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 6p12
J 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 disease
J 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 resection
J B Kerrison, M J Lynn, C A Baer, et al.
Genomics
|
May 1, 1996
A gene for autosomal dominant congenital nystagmus localizes to 6p12
J 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 18q12.2-12.3
J 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 neuropathy
J B Kerrison, N R Miller, F Hsu, et al.
Page
of 4