{"id":142,"date":"2025-06-13T09:53:19","date_gmt":"2025-06-13T09:53:19","guid":{"rendered":"https:\/\/gracic.org\/?page_id=142"},"modified":"2026-05-13T13:38:03","modified_gmt":"2026-05-13T13:38:03","slug":"literatur-und-berichte-uber-hnrnph2","status":"publish","type":"page","link":"https:\/\/gracic.org\/?page_id=142","title":{"rendered":""},"content":{"rendered":"\t\t<div data-elementor-type=\"wp-page\" data-elementor-id=\"142\" class=\"elementor elementor-142\">\n\t\t\t\t<div class=\"elementor-element elementor-element-db03112 e-flex e-con-boxed e-con e-parent\" data-id=\"db03112\" data-element_type=\"container\">\n\t\t\t\t\t<div class=\"e-con-inner\">\n\t\t\t\t<div class=\"elementor-element elementor-element-8fae4ad animated-slow elementor-invisible elementor-widget elementor-widget-text-editor\" data-id=\"8fae4ad\" data-element_type=\"widget\" data-settings=\"{&quot;_animation&quot;:&quot;fadeIn&quot;}\" data-widget_type=\"text-editor.default\">\n\t\t\t\t<div class=\"elementor-widget-container\">\n\t\t\t\t\t\t\t\t\t<p>\u00a0<\/p><p><strong><u>Literatur:<\/u><\/strong><\/p><ul><li><strong>Varianten in\u00a0<em>HNRNPH2<\/em>auf dem X-Chromosom werden mit einer neurologischen Entwicklungsst\u00f6rung bei Frauen in Verbindung gebracht<\/strong>\u00a0Originalforschungsartikel von J.M. Bain\u00a0<em>et al<\/em>. (2016) Lesen Sie die Zusammenfassung\u00a0<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/27545675\">hier<\/a>\u00a0und die Zusammenfassung von\u00a0Simons Searchlight\u00a0<a href=\"https:\/\/www.simonssearchlight.org\/de\/forschungsprozess\/genetische-stoerungen-die-wir-untersuchen\/hnrnph2\/46545-2\/\">hier<\/a>.<\/li><\/ul><ol><li>Bain, J. M., Thornburg, O., Pan, C., Rome-Martin, D., Boyle, L., Fan, X., \u2026 &amp; Chung, W. K. (2021). Detailed Clinical and Psychological Phenotype of the X-linked HNRNPH2-Related Neurodevelopmental Disorder. Neurology Genetics, 7(1). \u25cb Salazar, R., Beenders, S., Thornburg, O., LaMarca, N., &amp; Bain, J. (2020). The Pediatric Evaluation of Disability Inventory Computer Adaptive Test in Individuals with HNRNPH2-Related Disorders (4177).<\/li><li>Salazar, R., Beenders, S., Thornburg, O., LaMarca, N., &amp; Bain, J. (2020). The Pediatric Evaluation of Disability Inventory Computer Adaptive Test in Individuals with HNRNPH2-Related Disorders (4177).<\/li><li>Rome-Martin, D., Thornburg, O., &amp; Bain, J. (2020). Evaluating the Use of OT Assessments in Individuals With the Ultra Rare Disease HNRNPH2 Gene Variant. American Journal of Occupational Therapy, 74(4_Supplement_1), 7411500032p1-7411500032p1.<\/li><li>Duong, T. T., Goldman, S., Zhang, H., Salazar, R., Beenders, S., Cornett, K. M., \u2026 &amp; Zanotto, D. Validation of Insole based Gait Analysis System in Young Children with a Neurodevelopmental Disorder and Autism Traits. In 2020 8th IEEE RAS\/EMBS International Conference for Biomedical Robotics and Biomechatronics (BioRob) (pp. 715-720). IEEE.<\/li><li>Salazar R, Beenders S, LaMarca N, Thornburg O, Bain J. Motor Function of Individuals with HNRNPH2-related Disorders. Poster session presented at: American Academy of Neurology Annual Meeting; 2019 May 4-10; Philadelphia, PA<\/li><\/ol>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t","protected":false},"excerpt":{"rendered":"<p>\u00a0 Literatur: Varianten in\u00a0HNRNPH2auf dem X-Chromosom werden mit einer neurologischen Entwicklungsst\u00f6rung bei Frauen in Verbindung gebracht\u00a0Originalforschungsartikel von J.M. Bain\u00a0et al. (2016) Lesen Sie die Zusammenfassung\u00a0hier\u00a0und die Zusammenfassung von\u00a0Simons Searchlight\u00a0hier. Bain, J. M., Thornburg, O., Pan, C., Rome-Martin, D., Boyle, L., Fan, X., \u2026 &amp; Chung, W. K. (2021). Detailed Clinical and Psychological Phenotype of the [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-142","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/gracic.org\/index.php?rest_route=\/wp\/v2\/pages\/142","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/gracic.org\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/gracic.org\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/gracic.org\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/gracic.org\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=142"}],"version-history":[{"count":14,"href":"https:\/\/gracic.org\/index.php?rest_route=\/wp\/v2\/pages\/142\/revisions"}],"predecessor-version":[{"id":511,"href":"https:\/\/gracic.org\/index.php?rest_route=\/wp\/v2\/pages\/142\/revisions\/511"}],"wp:attachment":[{"href":"https:\/\/gracic.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=142"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}