Search Results - Peter van Hasselt
- Showing 1 - 6 results of 6
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Imaging flow cytometry-based cellular screening elucidates pathophysiology in individuals with Variants of Uncertain Significance by Irena Muffels, Hans R. Waterham, Giuseppina D’Alessandro, Guido Zagnoli-Vieira, Michael Sacher, Dirk J. Lefeber, Celine Van der Vinne, Chaim M. Roifman, Koen L.I. van Gassen, Holger Rehmann, Désirée Y. van Haaften–Visser, Edward E. S. Nieuwenhuis, Stephen P. Jackson, Sabine A. Fuchs, Femke van Wijk, Peter van Hasselt
Published 2025Artigo -
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Evolutionary conservation of the fidelity of transcription by Claire Chung, Bert M. Verheijen, Zoe Navapanich, Eric McGann, Sarah J. Shemtov, Guan-Ju Lai, Payal Arora, Atif Towheed, Suraiya Haroon, Ágnes Holczbauer, Sharon Chang, Zarko Manojlovic, Stephen Simpson, W. Kelley Thomas, Craig D. Kaplan, Peter van Hasselt, H. T. Marc Timmers, Dorothy A. Erie, Lin Chen, Jean-François Goût, Marc Vermulst
Published 2023Artigo -
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Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management by Lucia Laugwitz, Daphne H. Schoenmakers, Laura Adang, Stefanie Beck‐Woedl, Caroline Bergner, Geneviève Bernard, Annette Bley, Audrey Boyer, Valeria Calbi, Hanka Dekker, Florian Eichler, Erik A. Eklund, Francesca Fumagalli, Francesco Gavazzi, Sabine Grønborg, Peter van Hasselt, Mirjam Langeveld, Caroline A. Lindemans, Fanny Mochel, Andreas Øberg, Dipak Ram, Elise F. Saunier-Vivar, Lüdger Schöls, Michael S. Scholz, Caroline Sevin, Ayelet Zerem, Nicole I. Wolf, Samuel Groeschel
Published 2024Artigo -
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ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies by Éva Morava, Vera Tiemes, Christian Thiel, Nathalie Seta, Pascale de Lonlay, Hans de Klerk, Margot F. Mulder, M. Estela Rubio‐Gozalbo, Gepke Visser, Peter van Hasselt, Dafne D. G. Horovitz, Carolina Fischinger Moura de Souza, Ida Vanessa Döederlein Schwartz, Andrew Green, Mohammed Al‐Owain, Graciella Uziel, Sabine Sigaudy, B. Chabrol, Franc‐Jan van Spronsen, Martin Steinert, Eleni Komini, Donald Wurm, Andrea Bevot, Addelkarim Ayadi, Karin Huijben, Marli Dercksen, Peter Witters, Jaak Jaeken, Gert Matthijs, Dirk J. Lefeber, Ron A. Wevers
Published 2016Artigo -
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Erratum to: ALG6‐CDG: a recognizable phenotype with epilepsy, proximal muscle weakness, ataxia and behavioral and limb anomalies by Éva Morava, Vera Tiemes, Christian Thiel, Nathalie Seta, Pascale de Lonlay, Hans de Klerk, Margot F. Mulder, M. Estela Rubio‐Gozalbo, Gepke Visser, Peter van Hasselt, Dafne D. G. Horovitz, Carolina Fischinger Moura de Souza, Ida Vanessa Döederlein Schwartz, Andrew Green, Mohammed Al‐Owain, Graciella Uziel, Sabine Sigaudy, B. Chabrol, Franc‐Jan van Spronsen, Martin Steinert, Eleni Komini, Donald Wurm, Andrea Bevot, Addelkarim Ayadi, Karin Huijben, Marli Dercksen, Peter Witters, Jaak Jaeken, Gert Matthijs, Dirk J. Lefeber, Ron A. Wevers
Published 2016Errata/Corrigenda
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