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Janneke J C van Lith-Verhoeven

Showing results (1-10 of 14) with videos related to

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Molecular Vision|May 2, 2003
Genetic heterogeneity of butterfly-shaped pigment dystrophy of the foveaJanneke J C van Lith-Verhoeven, Frans P M Cremers, Bellinda van den Helm, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 11, 2007
Novel compound heterozygous TULP1 mutations in a family with severe early-onset retinitis pigmentosaAnneke I den Hollander, Janneke J C van Lith-Verhoeven, Maarten L Arends, et al.
Ophthalmology|October 1, 2014
Dominant cystoid macular dystrophyNicole T M Saksens, Ramon A C van Huet, Janneke J C van Lith-Verhoeven, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 15, 2003
A peculiar autosomal dominant macular dystrophy caused by an asparagine deletion at codon 169 in the peripherin/RDS geneJanneke J C van Lith-Verhoeven, Bellinda van den Helm, August F Deutman, et al.
Acta Ophthalmologica|December 10, 2014
A prospective, observational, open-label, multicentre study to investigate the daily treatment practice of ranibizumab in patients with neovascular age-related macular degenerationFreekje van Asten, Kim U Evers-Birkenkamp, Janneke J C van Lith-Verhoeven, et al.
The British Journal of Ophthalmology|May 17, 2007
Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatusCamiel J F Boon, Mary J van Schooneveld, Anneke I den Hollander, et al.
Investigative Ophthalmology & Visual Science|December 24, 2003
The benign concentric annular macular dystrophy locus maps to 6p12.3-q16Janneke J C van Lith-Verhoeven, Carel B Hoyng, Bellinda van den Helm, et al.
Ophthalmology|September 18, 2014
Mutations in MFSD8, encoding a lysosomal membrane protein, are associated with nonsyndromic autosomal recessive macular dystrophySusanne Roosing, L Ingeborgh van den Born, Riccardo Sangermano, et al.
Ophthalmology|July 14, 2009
Genetic etiology and clinical consequences of complete and incomplete achromatopsiaAlberta A H J Thiadens, Niki W R Slingerland, Susanne Roosing, et al.
Ophthalmology|January 19, 2010
Comprehensive analysis of the achromatopsia genes CNGA3 and CNGB3 in progressive cone dystrophyAlberta A H J Thiadens, Susanne Roosing, Rob W J Collin, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Molecular Vision|May 2, 2003
Genetic heterogeneity of butterfly-shaped pigment dystrophy of the foveaJanneke J C van Lith-Verhoeven, Frans P M Cremers, Bellinda van den Helm, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|July 11, 2007
Novel compound heterozygous TULP1 mutations in a family with severe early-onset retinitis pigmentosaAnneke I den Hollander, Janneke J C van Lith-Verhoeven, Maarten L Arends, et al.
Ophthalmology|October 1, 2014
Dominant cystoid macular dystrophyNicole T M Saksens, Ramon A C van Huet, Janneke J C van Lith-Verhoeven, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 15, 2003
A peculiar autosomal dominant macular dystrophy caused by an asparagine deletion at codon 169 in the peripherin/RDS geneJanneke J C van Lith-Verhoeven, Bellinda van den Helm, August F Deutman, et al.
Acta Ophthalmologica|December 10, 2014
A prospective, observational, open-label, multicentre study to investigate the daily treatment practice of ranibizumab in patients with neovascular age-related macular degenerationFreekje van Asten, Kim U Evers-Birkenkamp, Janneke J C van Lith-Verhoeven, et al.
The British Journal of Ophthalmology|May 17, 2007
Mutations in the peripherin/RDS gene are an important cause of multifocal pattern dystrophy simulating STGD1/fundus flavimaculatusCamiel J F Boon, Mary J van Schooneveld, Anneke I den Hollander, et al.
Investigative Ophthalmology & Visual Science|December 24, 2003
The benign concentric annular macular dystrophy locus maps to 6p12.3-q16Janneke J C van Lith-Verhoeven, Carel B Hoyng, Bellinda van den Helm, et al.
Ophthalmology|September 18, 2014
Mutations in MFSD8, encoding a lysosomal membrane protein, are associated with nonsyndromic autosomal recessive macular dystrophySusanne Roosing, L Ingeborgh van den Born, Riccardo Sangermano, et al.
Ophthalmology|July 14, 2009
Genetic etiology and clinical consequences of complete and incomplete achromatopsiaAlberta A H J Thiadens, Niki W R Slingerland, Susanne Roosing, et al.
Ophthalmology|January 19, 2010
Comprehensive analysis of the achromatopsia genes CNGA3 and CNGB3 in progressive cone dystrophyAlberta A H J Thiadens, Susanne Roosing, Rob W J Collin, et al.
Pageof 2