Suchergebnisse - E Peeters

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  1. 1
    Onset of intractability and its course over time: The Dutch study of epilepsy in childhood

    Onset of intractability and its course over time: The Dutch study of epilepsy in childhood von Ada T. Geerts, Oebele F. Brouwer, Hans Stroink, Cees van Donselaar, Boudewijn Peters, E Peeters, Willem F. Arts

    Veröffentlicht 2012
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  2. 2
    Course and outcome of childhood epilepsy: A 15‐year follow‐up of the Dutch Study of Epilepsy in Childhood

    Course and outcome of childhood epilepsy: A 15‐year follow‐up of the Dutch Study of Epilepsy in Childhood von Ada T. Geerts, Willem F. Arts, Hans Stroink, E Peeters, Oebele F. Brouwer, Boudewijn Peters, Laura Laan, Cees van Donselaar

    Veröffentlicht 2010
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  3. 3
    Safety and pharmacokinetics of intravenous levetiracetam infusion as add‐on in status epilepticus

    Safety and pharmacokinetics of intravenous levetiracetam infusion as add‐on in status epilepticus von J.W.F. Uges, Marc D. Van Huizen, Jeroen Engelsman, Erik B. Wilms, Daan J. Touw, E Peeters, Charles J. Vecht

    Veröffentlicht 2008
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  4. 4
    Effects of prehabilitation and rehabilitation including a home-based component on physical fitness, adherence, treatment tolerance, and recovery in patients with non-small cell lung cancer: A systematic review

    Effects of prehabilitation and rehabilitation including a home-based component on physical fitness, adherence, treatment tolerance, and recovery in patients with non-small cell lun... von Elisabeth J.M. Driessen, Marieke E. Peeters, Bart C. Bongers, Huub Maas, Gerbern P. Bootsma, Nico L. van Meeteren, Maryska L.G. Janssen‐Heijnen

    Veröffentlicht 2017
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  5. 5
    Long term outcome of benign childhood epilepsy with centrotemporal spikes: Dutch Study of Epilepsy in Childhood

    Long term outcome of benign childhood epilepsy with centrotemporal spikes: Dutch Study of Epilepsy in Childhood von Petra M.C. Callenbach, Paul A.D. Bouma, Ada T. Geerts, Willem F. Arts, Hans Stroink, E Peeters, Cees A. van Donselaar, A. C. B. Peters, Oebele F. Brouwer

    Veröffentlicht 2010
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  6. 6
    Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlations

    Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlations von Marcel Nelen, Hannie Kremer, Irene B. M. Konings, F. Schoute, Anton J van Essen, Rainer Koch, C. Geoffrey Woods, Jean‐Pierre Fryns, Ben C.J. Hamel, Lies H. Hoefsloot, E Peeters, George W. Padberg

    Veröffentlicht 1999
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  7. 7
    Concerted action of kinesins KIF5B and KIF13B promotes efficient secretory vesicle transport to microtubule plus ends

    Concerted action of kinesins KIF5B and KIF13B promotes efficient secretory vesicle transport to microtubule plus ends von Andrea Serra-Marques, Maud Martin, Eugene A. Katrukha, Ilya Grigoriev, Cathelijn A.E. Peeters, Qingyang Liu, Peter Jan Hooikaas, Yao Yao, Veronika Solianova, Ihor Smal, Lotte B. Pedersen, Erik Meijering, Lukas C. Kapitein, Anna Akhmanova

    Veröffentlicht 2020
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  8. 8
    Increased PI3K/Akt activity and deregulated humoral immune response in human PTEN deficiency

    Increased PI3K/Akt activity and deregulated humoral immune response in human PTEN deficiency von Gertjan J. Driessen, Hanna IJspeert, Marjolein Wentink, Helger G. Yntema, P. Martin van Hagen, Arthur van Strien, Giorgia Bucciol, Özgür Çoğulu, Margreet Trip, Willy M. Nillesen, E Peeters, Ingrid Pico‐Knijnenburg, Barbara H. Barendregt, Marta Rizzi, Jacques J. M. van Dongen, Necil Kütükçüler, Mirjam van der Burg

    Veröffentlicht 2016
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  9. 9
    MAP7 family proteins regulate kinesin-1 recruitment and activation

    MAP7 family proteins regulate kinesin-1 recruitment and activation von Peter Jan Hooikaas, Maud Martin, Tobias Mühlethaler, Gert-Jan Kuijntjes, Cathelijn A.E. Peeters, Eugene A. Katrukha, Luca Ferrari, Riccardo Stucchi, Daan G.F. Verhagen, Wilhelmina E. van Riel, Ilya Grigoriev, Maarten Altelaar, Casper C. Hoogenraad, Stefan Rüdiger, Michel O. Steinmetz, Lukas C. Kapitein, Anna Akhmanova

    Veröffentlicht 2019
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  10. 10
    Localization of the gene for Cowden disease to chromosome 10q22–23

    Localization of the gene for Cowden disease to chromosome 10q22–23 von Marcel Nelen, G.W. Padberg, E Peeters, Albert Y. Lin, Bellinda van den Helm, Rune R. Frants, V. Goulon, Alisa M. Goldstein, M.M.M van Reen, D.F. Eastern, Rosalind A. Eeles, Shirley Hodgson, John J. Mulvihill, Victoria A. Murday, M. A. Tucker, Edwin C.M. Mariman, Theo M. Starink, B. A. J. Ponder, Hans‐Hilger Ropers, Hannie Kremer, Michel Longy, Charis Eng

    Veröffentlicht 1996
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  11. 11
    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 von 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

    Veröffentlicht 2012
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  12. 12
    Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation

    Xq28 duplications including MECP2 in five females: Expanding the phenotype to severe mental retardation von Emilia K. Bijlsma, Andrew Collins, Filomena Tiziana Papa, María‐Isabel Tejada, Patricia G. Wheeler, E Peeters, A.C.J. Gijsbers, Jiddeke M. van de Kamp, Marjolein Kriek, Monique Losekoot, A.J. Broekma, John A. Crolla, Marzia Pollazzon, Mafalda Mucciolo, Eleni Katzaki, Vittoria Disciglio, Maria Immacolata Ferreri, Annabella Marozza, Maria Antonietta Mencarelli, Cinzia Castagnini, Laura Dosa, Francesca Ariani, Francesca Mari, Roberto Canitano, Joussef Hayek, M.P. Botella, Blanca Gener, Marina Mata Adolfo Mínguez, Alessandra Renieri, Claudia Ruivenkamp

    Veröffentlicht 2012
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  13. 13
    Long-term neuropsychological outcome following pediatric anti-NMDAR encephalitis

    Long-term neuropsychological outcome following pediatric anti-NMDAR encephalitis von Marienke A.A.M. de Bruijn, Femke K. Aarsen, Marielle P. van Oosterhout, Marieke M van der Knoop, Coriene E. Catsman‐Berrevoets, Marco W.J. Schreurs, Anna E.M. Bastiaansen, Peter A.E. Sillevis Smitt, Rinze F. Neuteboom, Maarten J. Titulaer, Paul B. Augustijn, Dewi P. Bakker, Maartje Boon, Elisabeth A. Cats, Merijn Eikelenboom, Marc Engelen, C.P.W. Geleijns, Charlotte A. Haaxma, Joost Nicolai, J.M.F. Niermeijer, Erik H. Niks, E Peeters, R Portier, André B. Rietman, H.M. Schippers, Aad Verrips, Marie‐Claire Y. de Wit

    Veröffentlicht 2018
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  14. 14
    Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan

    Mutations in ISPD cause Walker-Warburg syndrome and defective glycosylation of α-dystroglycan von Tony Roscioli, Erik‐Jan Kamsteeg, Karen Buysse, Isabelle Maystadt, Jeroen van Reeuwijk, Christa van den Elzen, Ellen van Beusekom, Moniek Riemersma, Rolph Pfundt, Lisenka E.L.M. Vissers, Margit Schraders, Umut Altunoğlu, Michael F. Buckley, Han G. Brunner, Bernard Grisart, Huiqing Zhou, Joris A. Veltman, Christian Gilissen, Grazia M.S. Mancini, P. Delrée, Michèl A.A.P. Willemsen, Danijela Petković Ramadža, David Chitayat, Christopher Bennett, Eamonn Sheridan, E Peeters, Gita Tan-Sindhunata, C E de Die-Smulders, Koenraad Devriendt, Hülya Kayserili, Osama Abd El-Fattah El-Hashash, Derek L. Stemple, Dirk J. Lefeber, Yung‐Yao Lin, Hans van Bokhoven

    Veröffentlicht 2012
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  15. 15
    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 von 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

    Veröffentlicht 2018
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  16. 16
    The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families

    The phenotypic spectrum of Schaaf-Yang syndrome: 18 new affected individuals from 14 families von Michael D. Fountain, Emmelien Aten, Megan T. Cho, Jane Juusola, Magdalena Walkiewicz, Joseph W. Ray, Fan Xia, Yaping Yang, Brett H. Graham, Carlos A. Bacino, Lorraine Potocki, Arie van Haeringen, Claudia Ruivenkamp, Pedro Mancías, Hope Northrup, Mary K. Kukolich, Marjan M. Weiss, Conny M.A. van Ravenswaaij‐Arts, Inge B. Mathijssen, Sébastien Levesque, Naomi Meeks, Jill A. Rosenfeld, Danielle Lemke, Ada Hamosh, M. E. Suzanne Lewis, Simone Race, Laura Stewart, Beverly N. Hay, Andrea M. Lewis, Rita Guerreiro, José Brás, Marcia P. Martins, G Derksen‐Lubsen, E Peeters, Connie T. R. M. Stumpel, Alexander P.A. Stegmann, Levinus A. Bok, Gijs W.E. Santen, Christian P. Schaaf

    Veröffentlicht 2016
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