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C W Storimans

Showing results (1-10 of 6) with videos related to

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Nederlands Tijdschrift Voor Geneeskunde|December 24, 1994
[With an eye on... the champagne cork]J E Keunen, C W Storimans
Ophthalmic Paediatrics and Genetics|December 1, 1989
Rieger's eye anomaly and persistent hyperplastic primary vitreousC W Storimans, M J Van Schooneveld
European Journal of Ophthalmology|April 1, 1991
A new autosomal dominant vascular retinopathy syndromeC W Storimans, M J Van Schooneveld, J A Oosterhuis, et al.
The British Journal of Ophthalmology|November 26, 1998
Serotoninergic status in patients with hereditary vascular retinopathy syndromeC W Storimans, D Fekkes, A van Dalen, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 1, 1990
Familial vascular retinopathy. A preliminary reportC W Storimans, J A Oosterhuis, M J van Schooneveld, et al.
Brain : a Journal of Neurology|April 29, 1998
Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenonG M Terwindt, J Haan, R A Ophoff, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Nederlands Tijdschrift Voor Geneeskunde|December 24, 1994
[With an eye on... the champagne cork]J E Keunen, C W Storimans
Ophthalmic Paediatrics and Genetics|December 1, 1989
Rieger's eye anomaly and persistent hyperplastic primary vitreousC W Storimans, M J Van Schooneveld
European Journal of Ophthalmology|April 1, 1991
A new autosomal dominant vascular retinopathy syndromeC W Storimans, M J Van Schooneveld, J A Oosterhuis, et al.
The British Journal of Ophthalmology|November 26, 1998
Serotoninergic status in patients with hereditary vascular retinopathy syndromeC W Storimans, D Fekkes, A van Dalen, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|October 1, 1990
Familial vascular retinopathy. A preliminary reportC W Storimans, J A Oosterhuis, M J van Schooneveld, et al.
Brain : a Journal of Neurology|April 29, 1998
Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenonG M Terwindt, J Haan, R A Ophoff, et al.
Pageof 1