Rezultati - Anneke I. den Hollander

Refine Results
  1. 1
    The complement system in age-related macular degeneration: A review of rare genetic variants and implications for personalized treatment

    The complement system in age-related macular degeneration: A review of rare genetic variants and implications for personalized treatment od Maartje J. Geerlings, Eiko K. de Jong, Anneke I. den Hollander

    Izdano 2016
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  2. 2
    Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies

    Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies od Anneke I. den Hollander, Aaron Black, Jean Bennett, Frans P.M. Cremers

    Izdano 2010
    Polni tekst Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  3. 3
    Composition and function of the Crumbs protein complex in the mammalian retina

    Composition and function of the Crumbs protein complex in the mammalian retina od Ilse Gosens, Anneke I. den Hollander, Frans P.M. Cremers, Ronald Roepman

    Izdano 2008
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  4. 4
    Omics Biomarkers in Ophthalmology

    Omics Biomarkers in Ophthalmology od Susette Lauwen, Eiko K. de Jong, Dirk J. Lefeber, Anneke I. den Hollander

    Izdano 2017
    Polni tekst Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  5. 5
    Non-syndromic retinal ciliopathies: translating gene discovery into therapy

    Non-syndromic retinal ciliopathies: translating gene discovery into therapy od Alejandro Estrada‐Cuzcano, Ronald Roepman, Frans P.M. Cremers, Anneke I. den Hollander, Dorus A. Mans

    Izdano 2012
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  6. 6
    Risk factors for progression of age‐related macular degeneration

    Risk factors for progression of age‐related macular degeneration od Thomas J. Heesterbeek, Laura Lorés‐Motta, Carel B. Hoyng, Yara T. E. Lechanteur, Anneke I. den Hollander

    Izdano 2020
    Polni tekst Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  7. 7
    The use of eplerenone in therapy‐resistant chronic central serous chorioretinopathy

    The use of eplerenone in therapy‐resistant chronic central serous chorioretinopathy od Myrte B. Breukink, Anneke I. den Hollander, Jan E.E. Keunen, Camiel J.F. Boon, Carel B. Hoyng

    Izdano 2014
    Polni tekst Polni tekst
    Carta
    Dodaj v priljubljene
    Shranjeno v:
  8. 8
    Nutritional Risk Factors for Age-Related Macular Degeneration

    Nutritional Risk Factors for Age-Related Macular Degeneration od Lebriz Ersoy, Tina Ristau, Yara Lechanteur, Moritz Hahn, Carel B. Hoyng, Bernd Kirchhof, Anneke I. den Hollander, Sascha Fauser

    Izdano 2014
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  9. 9
    Y chromosome mosaicism is associated with age-related macular degeneration

    Y chromosome mosaicism is associated with age-related macular degeneration od Felix Graßmann, Christina Kiel, Anneke I. den Hollander, Daniel E. Weeks, Andrew Lotery, Valentina Cipriani, Bernhard H. F. Weber

    Izdano 2018
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  10. 10
    Non-canonical roles of CFH in retinal pigment epithelial cells revealed by dysfunctional rare CFH variants

    Non-canonical roles of CFH in retinal pigment epithelial cells revealed by dysfunctional rare CFH variants od Sofie C.A. ten Brink, Louet Koolen, Caroline C. W. Klaver, Remko A. Bakker, Anneke I. den Hollander, Seba Almedawar

    Izdano 2025
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  11. 11
    Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290

    Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290 od Rob W.J. Collin, Anneke I. den Hollander, Saskia D. van der Velde-Visser, Jeannette Bennicelli, Jean Bennett, Frans P.M. Cremers

    Izdano 2012
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  12. 12
    A Multi-Omics Approach Identifies Key Regulatory Pathways Induced by Long-Term Zinc Supplementation in Human Primary Retinal Pigment Epithelium

    A Multi-Omics Approach Identifies Key Regulatory Pathways Induced by Long-Term Zinc Supplementation in Human Primary Retinal Pigment Epithelium od Eszter Emri, Elöd Körtvely, Sascha Dammeier, Franziska Klose, David Simpson, EYE-RISK Consortium Consortium, Anneke I. den Hollander, Marius Ueffing, Imre Lengyel

    Izdano 2020
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  13. 13
    The genetics and disease mechanisms of rhegmatogenous retinal detachment

    The genetics and disease mechanisms of rhegmatogenous retinal detachment od Birgit Marlies Govers, Ramon A. C. van Huet, Susanne Roosing, Sander Keijser, Leonoor I. Los, Anneke I. den Hollander, B. Jeroen Klevering

    Izdano 2023
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  14. 14
    Genomic Copy Number Variations of the Complement Component<i>C4B</i>Gene Are Associated With Chronic Central Serous Chorioretinopathy

    Genomic Copy Number Variations of the Complement Component<i>C4B</i>Gene Are Associated With Chronic Central Serous Chorioretinopathy od Myrte B. Breukink, Rosa L. Schellevis, Camiel J. F. Boon, Sascha Fauser, Carel B. Hoyng, Anneke I. den Hollander, Eiko K. de Jong

    Izdano 2015
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  15. 15
    A Homozygous Missense Mutation in the<i>IRBP</i>Gene (<i>RBP3</i>) Associated with Autosomal Recessive Retinitis Pigmentosa

    A Homozygous Missense Mutation in the<i>IRBP</i>Gene (<i>RBP3</i>) Associated with Autosomal Recessive Retinitis Pigmentosa od Anneke I. den Hollander, Terri L. McGee, Carmela Ziviello, Sandro Banfi, Thaddeus P. Dryja, Federico Gonzalez‐Fernandez, Debashis Ghosh, Eliot L. Berson

    Izdano 2009
    Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  16. 16
    Towards understanding CRUMBS function in retinal dystrophies

    Towards understanding CRUMBS function in retinal dystrophies od Mélisande Richard, Ronald Roepman, Wendy M. Aartsen, Agnes G.S.H. van Rossum, Anneke I. den Hollander, Elisabeth Knust, Jan Wijnholds, Frans P.M. Cremers

    Izdano 2006
    Polni tekst Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  17. 17
    Cell culture models to study retinal pigment epithelium-related pathogenesis in age-related macular degeneration

    Cell culture models to study retinal pigment epithelium-related pathogenesis in age-related macular degeneration od Kapil Bharti, Anneke I. den Hollander, Aparna Lakkaraju, Debasish Sinha, David Williams, Silvia C. Finnemann, Catherine Bowes Rickman, Goldis Malek, Patricia A. D’Amore

    Izdano 2022
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  18. 18
    Genetic Variants and Systemic Complement Activation Levels Are Associated With Serum Lipoprotein Levels in Age-Related Macular Degeneration

    Genetic Variants and Systemic Complement Activation Levels Are Associated With Serum Lipoprotein Levels in Age-Related Macular Degeneration od Constantin C. Paun, Lebriz Ersoy, Tina Schick, J.M.M. Groenewoud, Yara Lechanteur, Sascha Fauser, Carel B. Hoyng, Eiko K. de Jong, Anneke I. den Hollander

    Izdano 2015
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:
  19. 19
    Implications of genetic variation in the complement system in age-related macular degeneration

    Implications of genetic variation in the complement system in age-related macular degeneration od Sarah de Jong, Giuliana Gagliardi, Alejandro Garanto, Anita de Breuk, Yara Lechanteur, Suresh Katti, Lambert P. van den Heuvel, Elena B. Volokhina, Anneke I. den Hollander

    Izdano 2021
    Polni tekst
    Revisão
    Dodaj v priljubljene
    Shranjeno v:
  20. 20
    Basal Laminar Drusen Caused by Compound Heterozygous Variants in the CFH Gene

    Basal Laminar Drusen Caused by Compound Heterozygous Variants in the CFH Gene od Camiel J.F. Boon, B. Jeroen Klevering, Carel B. Hoyng, Marijke N. Zonneveld-Vrieling, Sander B. Nabuurs, Ellen A.W. Blokland, Frans P.M. Cremers, Anneke I. den Hollander

    Izdano 2008
    Polni tekst Polni tekst
    Artigo
    Dodaj v priljubljene
    Shranjeno v:

Iskalna orodja: