Výsledky vyhledávání - Cacha Peeters‐Scholte

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  1. 1
    Neuroprotective strategies following perinatal hypoxia-ischemia: Taking aim at NOS

    Neuroprotective strategies following perinatal hypoxia-ischemia: Taking aim at NOS Autor M. Albrecht, Karina Zitta, Floris Groenendaal, Frank van Bel, Cacha Peeters‐Scholte

    Vydáno 2019
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  2. 2
    Effects of Allopurinol and Deferoxamine on Reperfusion Injury of the Brain in Newborn Piglets after Neonatal Hypoxia-Ischemia

    Effects of Allopurinol and Deferoxamine on Reperfusion Injury of the Brain in Newborn Piglets after Neonatal Hypoxia-Ischemia Autor Cacha Peeters‐Scholte, Kees P. J. Braun, Johanna G. Koster, Nicole Kops, Klas Blomgren, Giuseppe Buonocore, Sylvia van Buul‐Offers, Henrik Hagberg, Klaas Nicolay, Frank van Bel, Floris Groenendaal

    Vydáno 2003
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  3. 3
    Nitric Oxide Synthase Inhibition as a Neuroprotective Strategy Following Hypoxic–Ischemic Encephalopathy: Evidence From Animal Studies

    Nitric Oxide Synthase Inhibition as a Neuroprotective Strategy Following Hypoxic–Ischemic Encephalopathy: Evidence From Animal Studies Autor Laurent M. A. Favié, Arlette R. Cox, Agnes van den Hoogen, Cora H. Nijboer, Cacha Peeters‐Scholte, Frank van Bel, Toine C. G. Egberts, Carin M. A. Rademaker, Floris Groenendaal

    Vydáno 2018
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  4. 4
    Neuroprotection by Selective Nitric Oxide Synthase Inhibition at 24 Hours After Perinatal Hypoxia-Ischemia

    Neuroprotection by Selective Nitric Oxide Synthase Inhibition at 24 Hours After Perinatal Hypoxia-Ischemia Autor Cacha Peeters‐Scholte, Johanna G. Koster, Wouter B. Veldhuis, Evelyn van den Tweel, Changlian Zhu, Nicole Kops, Klas Blomgren, Dop Bär, Sylvia van Buul‐Offers, Henrik Hagberg, Klaas Nicolay, Frank van Bel, Floris Groenendaal

    Vydáno 2002
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  5. 5
    From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care

    From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care Autor Maayke A. de Koning, Monique C. Haak, P. N. Adama van Scheltema, Cacha Peeters‐Scholte, Tamara T. Koopmann, Esther Nibbeling, Emmelien Aten, Nicolette S. den Hollander, Claudia Ruivenkamp, Mariëtte J.V. Hoffer, Gijs W.E. Santen

    Vydáno 2019
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  6. 6
    Male patients affected by mosaic PCDH19 mutations: five new cases

    Male patients affected by mosaic PCDH19 mutations: five new cases Autor Iris Lange, Patrick Rump, Rinze F. Neuteboom, Paul B. Augustijn, K. Hodges, A. I. Kistemaker, Oebele F. Brouwer, Grazia M.S. Mancini, Hadas Newman, Yvonne J. Vos, Katherine L. Helbig, Cacha Peeters‐Scholte, Marjolein Kriek, N. Knoers, Dick Lindhout, Bobby P.C. Koeleman, Marjan J. A. van Kempen, Eva H. Brilstra

    Vydáno 2017
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  7. 7
    Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study

    Incidence of acquired demyelinating syndromes of the CNS in Dutch children: a nationwide study Autor I. A. Ketelslegers, Coriene E. Catsman‐Berrevoets, Rinze F. Neuteboom, M. E. Boon, K. G. J. van Dijk, Merijn Eikelenboom, R. H. J. M. Gooskens, Erik H. Niks, W. C. G. Overweg‐Plandsoen, E Peeters, Cacha Peeters‐Scholte, Bwee Tien Poll‐The, J. F. Rijk-van Andel, Johnny P.A. Samijn, I. Snoeck, Hans Stroink, R. Jeroen Vermeulen, Aad Verrips, Johan S.H. Vles, Michèl A.A.P. Willemsen, Rob Rodrigues Pereira, Rogier Q. Hintzen

    Vydáno 2012
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  8. 8
    De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila

    De novo loss-of-function mutations in WAC cause a recognizable intellectual disability syndrome and learning deficits in Drosophila Autor Dorien Lugtenberg, Margot R.F. Reijnders, Michaela Fencková, Emilia K. Bijlsma, Raphael Bernier, Bregje W.M. van Bon, Eric Smeets, Anneke T. Vulto‐van Silfhout, Daniëlle G.M. Bosch, Evan E. Eichler, Heather C. Mefford, Gemma L. Carvill, Ernie M.H.F. Bongers, Janneke Schuurs-Hoeijmakers, Claudia Ruivenkamp, Gijs W.E. Santen, Anouk den Braber, Cacha Peeters‐Scholte, Sabine Kuenen, Patrik Verstreken, Rolph Pfundt, Helger G. Yntema, Petra F. de Vries, Joris A. Veltman, Alexander Hoischen, Christian Gilissen, Bert B.A. de Vries, Annette Schenck, Tjitske Kleefstra, Lisenka E.L.M. Vissers

    Vydáno 2016
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  9. 9
    Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective study

    Incidence and outcome of acquired demyelinating syndromes in Dutch children: update of a nationwide and prospective study Autor Casper L. de Mol, Yu Yi M. Wong, E Daniëlle van Pelt, I. A. Ketelslegers, Dewi P. Bakker, M. E. Boon, Kees P. J. Braun, K. G. J. van Dijk, Merijn Eikelenboom, Marc Engelen, Karin Geleijns, Charlotte A. Haaxma, J.M.F. Niermeijer, Erik H. Niks, E Peeters, Cacha Peeters‐Scholte, Bwee Tien Poll‐The, R Portier, J.F. de Rijk-van Andel, Johnny P.A. Samijn, H.M. Schippers, I. Snoeck, Hans Stroink, R. Jeroen Vermeulen, Aad Verrips, Frank Visscher, Johan S.H. Vles, Michèl A.A.P. Willemsen, Coriene E. Catsman‐Berrevoets, Rogier Q. Hintzen, R. F. Neuteboom

    Vydáno 2018
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  10. 10
    De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders

    De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders Autor Sara Reynhout, Sandra Jansen, Dorien Haesen, Siska Van Belle, Sonja A. de Munnik, Ernie M.H.F. Bongers, Jolanda Schieving, Carlo Marcelis, Jeanne Amiel, Marlène Rio, Heather M. McLaughlin, Roger L. Ladda, Susan L. Sell, Marjolein Kriek, Cacha Peeters‐Scholte, Paulien A. Terhal, Koen L.I. van Gassen, Nienke E. Verbeek, Sonja Henry, Jessica Scott Schwoerer, Saleem Malik, Nicole Revençu, Carlos R. Ferreira, Ellen F. Macnamara, Hilde M. H. Braakman, Elise Brimble, Maura Ruzhnikov, Matias Wagner, Philip Harrer, Dagmar Wieczorek, Alma Kuechler, Barak Tziperman, Ortal Barel, Bert B.A. de Vries, Christopher T. Gordon, Veerle Janssens, Lisenka E.L.M. Vissers

    Vydáno 2018
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  11. 11
    Biallelic <i>ADAM22</i> pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsy

    Biallelic <i>ADAM22</i> pathogenic variants cause progressive encephalopathy and infantile-onset refractory epilepsy Autor Marieke M van der Knoop, Reza Maroofian, Yuko Fukata, Yvette van Ierland, Ehsan Ghayoor Karimiani, Anna‐Elina Lehesjoki, Mikko Muona, Anders Paetau, Yuri Miyazaki, Yoko Hirano, Laila Selim, Marina de França, Rodrigo Ambrósio Fock, Christian Beetz, Claudia Ruivenkamp, Alison Eaton, Francois D Morneau-Jacob, Lena Sagi‐Dain, Lilach Shemer-Meiri, Amir Peleg, Jumana Haddad‐Halloun, D.J. Kamphuis, Cacha Peeters‐Scholte, Semra Hız Kurul, Rita Horváth, Hanns Lochmüller, David Murphy, Stephan Waldmüller, Stephanie Spranger, David Overberg, Alison M. Muir, Abolfazl Rad, Barbara Vona, Firdous Abdulwahad, Sateesh Maddirevula, Inna Povolotskaya, V. Yu. Voinova, Vykuntaraju K. Gowda, Varunvenkat M. Srinivasan, Fowzan S. Alkuraya, Heather C. Mefford, Majid Alfadhel, Tobias B. Haack, Pasquale Striano, Mariasavina Severino, Masaki Fukata, Yvonne Hilhorst‐Hofstee, Henry Houlden

    Vydáno 2022
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  12. 12
    De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

    De novo mutations in ATP1A3 cause alternating hemiplegia of childhood Autor Erin L. Heinzen, Kathryn J. Swoboda, Yuki Hitomi, Fiorella Gurrieri, Sophie Nicole, Boukje de Vries, Francesco Danilo Tiziano, Bertrand Fontaine, Sophie Nicole, Sinéad B. Heavin, Eleni Panagiotakaki, Sophie Nicole, Fiorella Gurrieri, Giovanni Neri, Boukje de Vries, Stephany C Koelewijn, Jessica T. Kamphorst, Marije A. Geilenkirchen, Nadine Pelzer, Laura Laan, Joost Haan, Michel D. Ferrari, Arn van den Maagdenberg, Claudio Zucca, Maria Teresa Bassi, F Franchini, Rosaria Vavassori, Melania Giannotta, Giuseppe Gobbi, Tiziana Granata, Nardo Nardocci, Elisa De Grandis, E. Veneselli, Michela Stagnaro, Fiorella Gurrieri, Giovanni Neri, Federico Vigevano, Eleni Panagiotakaki, Claudia Oechsler, Alexis Arzimanoglou, Sophie Nicole, Melania Giannotta, Giuseppe Gobbi, Miriam Ninan, Brian Neville, Friedrich Ebinger, Carmen Fons, Jaume Campistol, David Kemlink, Soňa Nevšímalová, Laura Laan, Cacha Peeters‐Scholte, Arn van den Maagdenberg, Paul Casaer, Giorgio Casari, Guenter Sange, Georg Spiel, Filippo Martinelli Boneschi, Claudio Zucca, Maria Teresa Bassi, Tsveta Schyns, Francis P. Crawley, Dominique Poncelin, Rosaria Vavassori, Stefania Fiori, Emanuela Abiusi, Lorena Di Pietro, Matthew Sweney, Tara Newcomb, Louis Viollet, Chad D. Huff, Lynn B. Jorde, Sandra P. Reyna, Kelley J. Murphy, Kevin V. Shianna, Curtis Gumbs, Latasha Little, Kenneth Silver, Louis J. Ptáček, Joost Haan, Michel D. Ferrari, Ann Bye, Geoffrey Herkes, Charlotte M Whitelaw, David Webb, Bryan J. Lynch, Peter Uldall, Mary D. King, Ingrid E. Scheffer, Giovanni Neri, Alexis Arzimanoglou, Arn M. J. M. van den Maagdenberg, Sanjay M. Sisodiya, Mohamad A. Mikati, David B. Goldstein

    Vydáno 2012
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