Search Results - Walraedt, Sophie

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  1. 1
    Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families

    Mutations in Splicing Factor Genes Are a Major Cause of Autosomal Dominant Retinitis Pigmentosa in Belgian Families by Van Cauwenbergh, Caroline, Coppieters, Frauke, Roels, Dimitri, De Jaegere, Sarah, Flipts, Helena, De Zaeytijd, Julie, Walraedt, Sophie, Claes, Charlotte, Fransen, Erik, Van Camp, Guy, Depasse, Fanny, Casteels, Ingele, de Ravel, Thomy, Leroy, Bart P, De Baere, Elfride

    Published in PloS one
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  2. 2
    Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy

    Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy by de Muijnck, Cansu, Haer-Wigman, Lonneke, van Everdingen, Judith A. M., Lushchyk, Tanya, Heutinck, Pam A. T., van Dooren, Marieke F., Kievit, Anneke J. A., Verhoeven, Virginie J. M., Simon, Marleen E. H., Wasmann, Rosemarie A., Notting, Irene C., De Baere, Elfride, Walraedt, Sophie, De Zaeytijd, Julie, Van den Broeck, Filip, Leroy, Bart P., Boon, Camiel J. F., van Genderen, Maria M.

    Published in Scientific reports
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  3. 3
    Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital Experience

    Paediatric cataract surgery with 27G vitrectomy instrumentation: the Ghent University Hospital Experience by Chan, Hwei Wuen, Van den Broeck, Filip, Cools, Axelle, Walraedt, Sophie, Joniau, Inge, Verdin, Hannah, Balikova, Irina, Van Nuffel, Stefaan, Delbeke, Patricia, De Baere, Elfride, Leroy, Bart P., Nerinckx, Fanny

    Published in Frontiers in medicine
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  4. 4
    Hypotonia and delayed motor development as an early presentation of Lowe syndrome: case report and literature review

    Hypotonia and delayed motor development as an early presentation of Lowe syndrome: case report and literature review by David, Sara, De Waele, Kathleen, De Wilde, Bram, Faes, Franny, Vanakker, Olivier, Walraedt, Sophie, Prytuła, Agnieszka

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  5. 5
    Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus

    Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus by AlMoallem, Basamat, Bauwens, Miriam, Walraedt, Sophie, Delbeke, Patricia, De Zaeytijd, Julie, Kestelyn, Philippe, Meire, Françoise, Janssens, Sandra, van Cauwenbergh, Caroline, Verdin, Hannah, Hooghe, Sally, Kumar Thakur, Prasoon, Coppieters, Frauke, De Leeneer, Kim, Devriendt, Koenraad, Leroy, Bart P, De Baere, Elfride

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  6. 6
    Diplopia as presenting sign of Turcot syndrome

    Diplopia as presenting sign of Turcot syndrome by Ninclaus, Virginie G. S., Walraedt, Sophie, Baert, Edward, Laureys, Geneviève, Leroy, Bart P., De Zaeytijd, Julie

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  7. 7
    Hypotonia and delayed motor development as an early presentation of Lowe syndrome: case report and literature review

    Hypotonia and delayed motor development as an early presentation of Lowe syndrome: case report and literature review by David, Sara, De Waele, Kathleen, De Wilde, Bram, Faes, Franny, Vanakker, Olivier, Walraedt, Sophie, Prytuła, Agnieszka

    Published in Acta Clinica Belgica
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