Search Results - Peter Uldall

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  1. 1
    Modified Atkins diet to children and adolescents with medical intractable epilepsy

    Modified Atkins diet to children and adolescents with medical intractable epilepsy by Susanne Weber, Christian Mølgaard, KarenTaudorf, Peter Uldall

    Published 2008
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  2. 2
    The misdiagnosis of epilepsy in children admitted to a tertiary epilepsy centre with paroxysmal events

    The misdiagnosis of epilepsy in children admitted to a tertiary epilepsy centre with paroxysmal events by Peter Uldall, Jørgen Alving, L.K. Hansen, M Kibaek, Jette Buchholt

    Published 2006
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  3. 3
    Predictors for early diagnosis of cerebral palsy from national registry data

    Predictors for early diagnosis of cerebral palsy from national registry data by Jakob Bie Granild‐Jensen, Gija Rackauskaite, Esben Meulengracht Flachs, Peter Uldall

    Published 2015
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  4. 4
    Epilepsy and cerebral palsy: Characteristics and trends in children born in 1976–1998

    Epilepsy and cerebral palsy: Characteristics and trends in children born in 1976–1998 by Élodie Sellier, Peter Uldall, Eulália Calado, Sólveig Sigurðardóttir, Maria Giulia Torrioli, Mary Jane Platt, Christine Cans

    Published 2011
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  5. 5
    Congenital anomalies in children with cerebral palsy: a population‐based record linkage study

    Congenital anomalies in children with cerebral palsy: a population‐based record linkage study by Judith Rankin, Christine Cans, Ester Garne, Allan Colver, Helen Dolk, Peter Uldall, Emmanuelle Amar, INGEBORGE KRAGELOH‐MANN

    Published 2009
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  6. 6
    Implications of the International Paediatric Multiple Sclerosis Study Group consensus criteria for paediatric acute disseminated encephalomyelitis: a nationwide validation study

    Implications of the International Paediatric Multiple Sclerosis Study Group consensus criteria for paediatric acute disseminated encephalomyelitis: a nationwide validation study by Magnus Spangsberg Boesen, Morten Blinkenberg, Nils Koch‐Henriksen, Lau Caspar Thygesen, Peter Uldall, Melinda Magyari, Alfred Peter Born

    Published 2018
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  7. 7
    Multiplicity and early gestational age contribute to an increased risk of cerebral palsy from assisted conception: a population-based cohort study

    Multiplicity and early gestational age contribute to an increased risk of cerebral palsy from assisted conception: a population-based cohort study by Dorte Hvidtjørn, Jakob Grove, Diana Schendel, Claus Sværke, Laura A. Schieve, Peter Uldall, E. Ernst, Bo Jacobsson, Poul Thorsen

    Published 2010
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  8. 8
    Epilepsy and risk of death and sudden unexpected death in the young: A nationwide study

    Epilepsy and risk of death and sudden unexpected death in the young: A nationwide study by Anders G. Holst, Bo Gregers Winkel, Bjarke Risgaard, Jonas B. Nielsen, Peter Rasmussen, Stig Haunsø, Anne Sabers, Peter Uldall, Jacob Tfelt‐Hansen

    Published 2013
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  9. 9
    Parental socioeconomic status and risk of cerebral palsy in the child: evidence from two Nordic population-based cohorts

    Parental socioeconomic status and risk of cerebral palsy in the child: evidence from two Nordic population-based cohorts by Ingeborg Forthun, Katrine Strandberg‐Larsen, Allen J. Wilcox, Dag Moster, Tanja Gram Petersen, Torstein Vik, Rolv T. Lie, Peter Uldall, Mette Christophersen Tollånes

    Published 2018
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  10. 10
    What constitutes cerebral palsy in the twenty‐first century?

    What constitutes cerebral palsy in the twenty‐first century? by Hayley Smithers‐Sheedy, Nadia Badawi, Eve Blair, Christine Cans, Kate Himmelmann, Ingeborg Krägeloh‐Mann, Sarah McIntyre, Jennie Slee, Peter Uldall, Linda Watson, Meredith Wilson

    Published 2013
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  11. 11
    Automated EEG source imaging: A retrospective, blinded clinical validation study

    Automated EEG source imaging: A retrospective, blinded clinical validation study by Amir G. Baroumand, Pieter van Mierlo, Gregor Strobbe, Lars H. Pinborg, Martin Fabricius, Guido Rubboli, Anne-Mette Leffers, Peter Uldall, Bo Jespersen, Jannick Brennum, Otto Mølby Henriksen, Sándor Beniczky

    Published 2018
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  12. 12
    European study of frequency of participation of adolescents with and without cerebral palsy

    European study of frequency of participation of adolescents with and without cerebral palsy by Susan Ishøy Michelsen, Esben Meulengracht Flachs, Mogens Trab Damsgaard, Jacqueline Parkes, Kathryn Parkinson, Marion Rapp, Catherine Arnaud, Malin Nystrand, Allan Colver, Jérôme Fauconnier, Heather O Dickinson, Marco Marcelli, Peter Uldall

    Published 2013
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  13. 13
    Use of paracetamol, ibuprofen or aspirin in pregnancy and risk of cerebral palsy in the child

    Use of paracetamol, ibuprofen or aspirin in pregnancy and risk of cerebral palsy in the child by Tanja Gram Petersen, Zeyan Liew, Anne‐Marie Nybo Andersen, Guro L. Andersen, Per Kragh Andersen, Torben Martinussen, Jørn Olsen, Cristina Rebordosa, Mette Christophersen Tollånes, Peter Uldall, Allen J. Wilcox, Katrine Strandberg‐Larsen

    Published 2017
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  14. 14
    Mutational Analysis of the Defective Protease in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis, a Neurodegenerative Lysosomal Storage Disorder

    Mutational Analysis of the Defective Protease in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis, a Neurodegenerative Lysosomal Storage Disorder by David E. Sleat, Rosalie M. Gin, István Sohár, Krystyna E. Wisniewski, Susan Sklower-Brooks, Raju K. Pullarkat, David N. Palmer, Terry J. Lerner, Rose-Mary Boustany, Peter Uldall, A. N. Siakotos, Robert Donnelly, Peter Lobel

    Published 1999
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  15. 15
    Electromagnetic source imaging in presurgical workup of patients with epilepsy

    Electromagnetic source imaging in presurgical workup of patients with epilepsy by Lene Duez, Hatice Tankişi, Peter Orm Hansen, Per Sidenius, Anne Sabers, Lars H. Pinborg, Martin Fabricius, György Rásonyi, Guido Rubboli, Birthe Pedersen, Anne-Mette Leffers, Peter Uldall, Bo Jespersen, Jannick Brennum, Otto Mølby Henriksen, Anders Fuglsang‐Frederiksen, Sándor Beniczky

    Published 2019
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  16. 16
    The role of <i> <scp>SLC</scp> 2A1 </i> mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of <scp>GLUT</scp> 1 deficiency syndrome

    The role of <i> <scp>SLC</scp> 2A1 </i> mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of <scp>GLUT</scp> 1 deficiency syndrome by Jan Larsen, Katrine M. Johannesen, Jakob Ek, Shan Tang, Carla Marini, Susanne Blichfeldt, Maria Kibæk, Sarah von Spiczak, Sarah Weckhuysen, Mimoza Frangu, Bernd A. Neubauer, Peter Uldall, Pasquale Striano, Federico Zara, Rebecca Kleiss, Michael A. Simpson, Hiltrud Muhle, Marina Nikanorova, Birgit Jepsen, Niels Tommerup, Ulrich Stephani, Renzo Guerrini, Morten Dunø, Helle Hjalgrim, Deb K. Pal, Ingo Helbig, Rikke S. Møller

    Published 2015
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  17. 17
    Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies

    Gene Panel Testing in Epileptic Encephalopathies and Familial Epilepsies by Rikke S. Møller, Line H.G. Larsen, Katrine M. Johannesen, Inga Talvik, Tiina Talvik, Ulvi Vaher, María J. Miranda, Muhammad Farooq, Jens Erik Nielsen, Lene Lavard Svendsen, Ditte B. Kjelgaard, Karen Markussen Linnet, Qin Hao, Peter Uldall, Mimoza Frangu, Niels Tommerup, Shahid Mahmood Baig, Uzma Abdullah, Alfred Peter Born, Pia Gellert, Marina Nikanorova, Kern Olofsson, Birgit Jepsen, Dragan Marjanović, Lana I.K. Al-Zehhawi, Sofia J. Peñalva, B Krag-Olsen, Klaus Brusgaard, Helle Hjalgrim, Guido Rubboli, Deb K. Pal, Hans A. Dahl

    Published 2016
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  18. 18
    Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

    Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry by Louis Viollet, Gustavo Glusman, Kelley J. Murphy, Tara Newcomb, Sandra P. Reyna, Matthew Sweney, B.E. Nelson, Frédérick Andermann, Eva Andermann, Gyula Acsádi, Richard L. Barbano, Candida Brown, Mary E. Brunkow, Harry T. Chugani, Sarah Cheyette, Abigail Collins, Suzanne D. DeBrosse, David J. Galas, Jennifer Friedman, Lee Hood, Chad Huff, Lynn B. Jorde, Mary D. King, Bernie LaSalle, Richard J. Leventer, Aga Lewelt, Mylynda Massart, Mario Merida, Louis J. Ptác̆ek, Jared C. Roach, Robert S. Rust, Francis Renault, Terry D. Sanger, Márcio A Sotero de Menezes, Rachel B. Tennyson, Peter Uldall, Yue Zhang, Mary L. Zupanc, Winnie Xin, Kenneth Silver, Kathryn J. Swoboda

    Published 2015
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  19. 19
    Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2

    Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2 by Derek Neilson, Mark D. Adams, Caitlin M.D. Orr, Deborah K. Schelling, Robert M. Eiben, Douglas S. Kerr, Jane Anderson, Alexander G. Bassuk, Ann Bye, Anne-Marie Childs, Antonia Clarke, Yanick J. Crow, Maja Di Rocco, Christian Dohna‐Schwake, Gregor Dueckers, Alfonso Fasano, Artemis Gika, Dimitris Gionnis, Mark Gorman, Padraic J. Grattan‐Smith, Annette Hackenberg, Alice Kuster, Markus Lentschig, Eduardo López‐Laso, Elysa J. Marco, Sotiria Mastroyianni, Julie Perrier, Thomas Schmitt‐Mechelke, Serenella Servidei, Angeliki Skardoutsou, Peter Uldall, Marjo S. van der Knaap, Karrie Goglin, David L. Tefft, Cristin Aubin, Philip L. De Jager, David A. Hafler, Matthew L. Warman

    Published 2009
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  20. 20
    <i>STXBP1</i> encephalopathy

    <i>STXBP1</i> encephalopathy by Hannah Stamberger, Marina Nikanorova, Marjolein H. Willemsen, Patrizia Accorsi, Marco Angriman, Hartmut Baier, Ira Benkel-Herrenbrueck, Valérie Benoît, M Budetta, Almuth Caliebe, Gaetano Cantalupo, Giuseppe Capovilla, Gianluca Casara, Carolina Courage, Marie Deprez, Anne Destrèe, Robertino Dilena, Corrie E. Erasmus, Madeleine Fannemel, Roar Fjær, Lucio Giordano, Katherine L. Helbig, Henrike Heyne, Joerg Klepper, Gerhard Kluger, Damien Lederer, Monica Lodi, Oliver Maier, Andreas Merkenschlager, Nina Michelberger, Carlo Minetti, Hiltrud Muhle, Judith Phalin, Keri Ramsey, Antonino Romeo, Jens Schallner, Ina Schanze, Marwan Shinawi, Kristel Sleegers, Katalin Štěrbová, Steffen Syrbe, Monica Traverso, Andreas Tzschach, Peter Uldall, Rudy Van Coster, Hélène Verhelst, Maurizio Viri, Susan Winter, Markus Wolff, Martin Zenker, Leonardo Zoccante, Peter De Jonghe, Ingo Helbig, Pasquale Striano, Johannes R. Lemke, Rikke S. Møller, Sarah Weckhuysen

    Published 2016
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