Kết quả tìm kiếm - D. Rating

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  1. 1
    Sulthiame as Monotherapy in Children with Benign Childhood Epilepsy with Centrotemporal Spikes: A 6‐Month Randomized, Double‐Blind, Placebo‐Controlled Study

    Sulthiame as Monotherapy in Children with Benign Childhood Epilepsy with Centrotemporal Spikes: A 6‐Month Randomized, Double‐Blind, Placebo‐Controlled Study Bằng D. Rating, Christian Wolf, Thomas Bast

    Được phát hành 2000
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    Artigo
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  2. 2
    Incidence of Epilepsies and Epileptic Syndromes in Children and Adolescents: A Population‐Based Prospective Study in Germany

    Incidence of Epilepsies and Epileptic Syndromes in Children and Adolescents: A Population‐Based Prospective Study in Germany Bằng Christine M. Freitag, Theodor W. May, Margarete Pfäfflin, Stephan König, D. Rating

    Được phát hành 2001
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    Artigo
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  3. 3
    Large neutral amino acids block phenylalanine transport into brain tissue in patients with phenylketonuria

    Large neutral amino acids block phenylalanine transport into brain tissue in patients with phenylketonuria Bằng Joachim Pietz, Roland Kreis, André Rupp, Ertan Mayatepek, D. Rating, Chris Boesch, H. J. Bremer

    Được phát hành 1999
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    Artigo
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  4. 4
    Succinic semialdehyde dehydrogenase deficiency: an inborn error of gamma-aminobutyric acid metabolism

    Succinic semialdehyde dehydrogenase deficiency: an inborn error of gamma-aminobutyric acid metabolism Bằng K. Michael Gibson, Lawrence Sweetman, William L. Nyhan, C. Jakobs, D. Rating, H. Siemes, F. Hanefeld

    Được phát hành 1983
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    Artigo
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  5. 5
    Change of seizure frequency in pregnant epileptic women.

    Change of seizure frequency in pregnant epileptic women. Bằng D. Schmidt, R. Canger, G. Avanzini, Dina Battino, C. Cusi, G. Beck‐Mannagetta, S. Koch, D. Rating, Diéter Janz

    Được phát hành 1983
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    Artigo
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  6. 6
    Levetiracetam in the treatment of neonatal seizures: A pilot study

    Levetiracetam in the treatment of neonatal seizures: A pilot study Bằng Alexandra Fürwentsches, Cornelia Bußmann, Georgia Ramantani, Friedrich Ebinger, Heike Philippi, Johannes Pöschl, Susanne Schubert‐Bast, D. Rating, Thomas Bast

    Được phát hành 2010
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  7. 7
    EEG and MEG Source Analysis of Single and Averaged Interictal Spikes Reveals Intrinsic Epileptogenicity in Focal Cortical Dysplasia

    EEG and MEG Source Analysis of Single and Averaged Interictal Spikes Reveals Intrinsic Epileptogenicity in Focal Cortical Dysplasia Bằng Thomas Bast, Oezdin Oezkan, Sabine Rona, Christoph Stippich, Angelika Seitz, André Rupp, Susanne Fauser, Josef Zentner, D. Rating, Michael Scherg

    Được phát hành 2004
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    Artigo
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  8. 8
    Status epilepticus in children with Alpers’ disease caused by <i>POLG1</i> mutations: EEG and MRI features

    Status epilepticus in children with Alpers’ disease caused by <i>POLG1</i> mutations: EEG and MRI features Bằng Nicole I. Wolf, Shamima Rahman, Bernhard Schmitt, Jan‐Willem Taanman, Andrew Duncan, Inga Harting, Gabriele Wohlrab, Friedrich Ebinger, D. Rating, Thomas Bast

    Được phát hành 2008
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  9. 9
    Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: Diagnostic tools for a new inborn error of metabolism

    Creatine deficiency syndrome caused by guanidinoacetate methyltransferase deficiency: Diagnostic tools for a new inborn error of metabolism Bằng Andreas Schulze, Thomas Heß, Ron A. Wevers, Ertan Mayatepek, Peter Bachert, Bart Marescau, Michael V. Knopp, Peter Paul De Deyn, H. J. Bremer, D. Rating

    Được phát hành 1997
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    Artigo
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  10. 10
    Levetiracetam in children with refractory epilepsy: A multicenter open label study in Germany

    Levetiracetam in children with refractory epilepsy: A multicenter open label study in Germany Bằng Joachim Opp, Ingrid Tuxhorn, Theodor W. May, Gerhard Kluger, Adelheid Wiemer‐Kruel, G Kurlemann, G Gross-Selbeck, D. Rating, Ulrich Brandl, U Bettendorf, Christoph Härtel, Elisabeth Korn‐Merker

    Được phát hành 2005
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    Artigo
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  11. 11
    Clinical characteristics in focal cortical dysplasia: a retrospective evaluation in a series of 120 patients

    Clinical characteristics in focal cortical dysplasia: a retrospective evaluation in a series of 120 patients Bằng Susanne Fauser, Hans‐Jürgen Huppertz, Thomas Bast, Karl Strobl, Georgios Pantazis, Dirk-Matthias Altenmueller, Bertram Feil, Sabine Rona, Christoph Kurth, D. Rating, Rudolf Korinthenberg, Bernhard J. Steinhoff, Benedikt Volk, Andreas Schulze‐Bonhage

    Được phát hành 2006
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    Artigo
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  12. 12
    Identification of biallelic<i>LRRK1</i>mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneity

    Identification of biallelic<i>LRRK1</i>mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneity Bằng Aritoshi Iida, Weirong Xing, M. Docx, Tomoki Nakashima, Zheng Wang, Mamori Kimizuka, Wim Van Hul, D. Rating, Jürgen W. Spranger, H Ohashi, Noriko Miyake, Naomichi Matsumoto, Subburaman Mohan, Gen Nishimura, Geert Mortier, Shiro Ikegawa

    Được phát hành 2016
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    Artigo
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  13. 13
    <i>NUBPL</i> mutations in patients with complex I deficiency and a distinct MRI pattern

    <i>NUBPL</i> mutations in patients with complex I deficiency and a distinct MRI pattern Bằng Sietske H. Kevelam, Richard J. Rodenburg, Nicole I. Wolf, Patrick Ferreira, Roelineke J. Lunsing, Leo Nijtmans, Anne Mitchell, H Arroyo, D. Rating, Adeline Vanderver, Carola G.M. van Berkel, Truus E. M. Abbink, Peter Heutink, Marjo S. van der Knaap

    Được phát hành 2013
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    Artigo
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  14. 14
    Safety and effectiveness of hormonal treatment versus hormonal treatment with vigabatrin for infantile spasms (ICISS): a randomised, multicentre, open-label trial

    Safety and effectiveness of hormonal treatment versus hormonal treatment with vigabatrin for infantile spasms (ICISS): a randomised, multicentre, open-label trial Bằng Finbar O’Callaghan, Stuart W. Edwards, Fabienne Dietrich Alber, Eleanor Hancock, Anthony L. Johnson, Colin Kennedy, Marcus Likeman, Andrew Lux, Mark T. Mackay, Andrew A. Mallick, Richard Newton, Melinda Nolan, Ronit Pressler, D. Rating, Bernhard Schmitt, Christopher Verity, John Osborne

    Được phát hành 2016
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    Artigo
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  15. 15
    The underlying etiology of infantile spasms (West syndrome): Information from the International Collaborative Infantile Spasms Study (<scp>ICISS</scp>)

    The underlying etiology of infantile spasms (West syndrome): Information from the International Collaborative Infantile Spasms Study (<scp>ICISS</scp>) Bằng John Osborne, Stuart W. Edwards, Fabienne Dietrich Alber, Eleanor Hancock, Anthony L. Johnson, Colin Kennedy, Marcus Likeman, Andrew Lux, Mark T. Mackay, Andrew A. Mallick, Richard Newton, Melinda Nolan, Ronit Pressler, D. Rating, Bernhard Schmitt, Christopher Verity, Finbar O’Callaghan

    Được phát hành 2019
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  16. 16
    Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy

    Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathy Bằng Dorien Lugtenberg, Tjitske Kleefstra, Astrid Oudakker, Willy M. Nillesen, Helger G. Yntema, Andreas Tzschach, Martine Raynaud, D. Rating, Hubert Journel, Jamel Chelly, Cyril Goizet, Didier Lacombe, Jean‐Michel Pédespan, Bernard Échenne, Gholamali Tariverdian, Declan O’Rourke, Mary D. King, Andrew Green, Margriet van Kogelenberg, Hilde Van Esch, Jozef Gécz, Ben C.J. Hamel, Hans van Bokhoven, Arjan P.M. de Brouwer

    Được phát hành 2008
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    Artigo
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  17. 17
    Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti–Boltshauser syndrome)

    Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti–Boltshauser syndrome) Bằng Alessia Micalizzi, Andrea Poretti, Marta Romani, Monia Ginevrino, Tommaso Mazza, Chiara Aiello, Ginevra Zanni, Bastian Baumgartner, Renato Borgatti, Knut Brockmann, Ana Camacho, Gaetano Cantalupo, Martin Haeusler, Christiane Hikel, Andrea Klein, Giorgia Mandrile, Eugenio Mercuri, D. Rating, Romina Romaniello, Filippo M. Santorelli, Mareike Schimmel, Luigina Spaccini, Serap Teber, Arpad von Moers, Sarah Wente, Andreas Ziegler, Andrea Zonta, Enrico Bertini, Eugen Boltshauser, Enza Maria Valente

    Được phát hành 2016
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  18. 18
    Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum

    Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum Bằng Anne Thorwarth, Sarah Schnittert-Hübener, Pamela Schrumpf, Ines Müller, Sabine Jyrch, Christof Dame, Heike Biebermann, Gunnar Kleinau, Juri Katchanov, Markus Schuelke, Grit Ebert, Anne Steininger, Carsten G. Bönnemann, Knut Brockmann, H.‐J. Christen, Patricia Crock, Francis deZegher, Matthias Griese, Jacqueline Hewitt, Sten A. Ivarsson, Christoph Hübner, Klaus Kapelari, Barbara Plecko, D. Rating, Iva Stoeva, Hans‐Hilger Ropers, Annette Grüters, Reinhard Ullmann, Heiko Krude

    Được phát hành 2014
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  19. 19
    Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial

    Vigabatrin with hormonal treatment versus hormonal treatment alone (ICISS) for infantile spasms: 18-month outcomes of an open-label, randomised controlled trial Bằng Finbar O’Callaghan, Stuart W. Edwards, Fabienne Dietrich Alber, Mario Cortina‐Borja, Eleanor Hancock, Anthony L. Johnson, Colin Kennedy, Marcus Likeman, Andrew Lux, Mark T. Mackay, Andrew A. Mallick, Richard Newton, Melinda Nolan, Ronit Pressler, D. Rating, Bernhard Schmitt, Christopher Verity, John Osborne, Maysara Abdel Aziz, Triloknath Acharya, Carolyn Adcock, Robert Jones, Rachel Howells, Ben Marsh, Kemi Adejare, Rashmi Adiga, Mary Wheater, Mansoor Ahmed, Mohammad Sawal, Chhavi Goel, Mas Ahmed, Michael Alber, Markus Wolff, Susanne Ruf, Asya M Al-Kharusi, Hassan Al-Moasseb, Ruchi Arora, R.C. Beach, Patricia Atkinson, Kunle Ayonrinde, Pronab Bala, Nicola Bamford, Nagi Barakat, Nigel Basheer, Peter Baxter, Santosh Mordekar, Chris Rittey, Ingo Borggraefe, Peter Borusiak, Sabine Cagnoli, Richard Brown, Sophie Calvert, Sophie Calvert, Duncan Cameron, Ramesh Chaniyil, Ravi Chinthapalli, Gabriel Chow, William Whitehouse, V. Clarke, Chris Cooper, Alexane Datta, Selwyn D'Costa, Christian de Goede, Helen Basu, David Deekollu, Adela Della Marina, Penelope Dison, Colin Dunkley, Megan M. Eaton, Julie Ellison, R. C. B. Pugh, Penny Fallon, Hani Faza, Imti Choonara, Richard E. Morton, Mal Ratnayaka, Colin D. Ferrie, Amanda Freeman, Stephen Warriner, María del Carmen García, Malihe Ghazavi, Frances Gibbon, J. M. Gibbs, Des Ginbey, Iolanda Guarino, Rajesh Gupta, Mary Hanlon, Siân Harris, Paul Munyard, Cheryl Hemingway, Christin Eltze, Marios Kaliakatsos, V. Murugan, Robert Robinson, Jeen Tan, Daniel Hindley, Adrian Hughes, Akmal Hussain, Greg Boden, Munir A. Hussain

    Được phát hành 2018
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  20. 20
    Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in <i>POLR3A</i>, <i>POLR3B</i>, and <i>POLR1C</i>

    Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in <i>POLR3A</i>, <i>POLR3B</i>, and <i>POLR1C</i> Bằng Félixe Pelletier, Stefanie Perrier, Ferdy Kurniawan Cayami, Amytice Mirchi, Stéphan Saïkali, Luan T. Tran, Nicole Ulrick, Kether Guerrero, Emmanouil Rampakakis, Rosalina M.L. van Spaendonk, Sakkubai Naidu, Daniela Pohl, William T. Gibson, Michelle Demos, Cyril Goizet, Ingrid Tejera-Martin, Ana Potic, Brent L. Fogel, Bernard Brais, Michel Sylvain, Guillaume Sébire, Charles Marques Lourenço, Joshua L. Bonkowsky, Coriene E. Catsman‐Berrevoets, Pedro Soares Pinto, Sandya Tirupathi, Petter Strømme, Ton de Grauw, Dorota Gieruszczak‐Białek, Ingeborg Krägeloh‐Mann, Hanna Mierzewska, Heike Philippi, Julia Rankin, Tahir Atık, Brenda Banwell, William Benko, Astrid Blaschek, Annette Bley, Eugen Boltshauser, Drago Bratkovic, Klára Brožová, Icíar Cimas, Christopher Clough, Bernard Corenblum, Argirios Dinopoulos, Gail Dolan, Flavio Faletra, Raymond Fernandez, Janice M. Fletcher, María Eugenia García, Paolo Gasparini, Janina Gburek‐Augustat, Dolores González Morón, Aline I. Hamati, Inga Harting, Christoph Hertzberg, Alan Hill, Grace M. Hobson, A. Micheil Innes, Marcelo Kauffman, Susan M. Kirwin, Gerhard Kluger, Petra Kolditz, Urania Kotzaeridou, Roberta La Piana, Eriskay Liston, W. McClintock, Meriel McEntagart, Fiona McKenzie, Serge B. Melançon, Anjum Misbahuddin, Mohnish Suri, Fernando Montón, Sébastien Moutton, Raymond P. Murphy, Miriam Nickel, Hüseyin Önay, Simona Orcesi, Ferda Özkınay, Steffi Patzer, Hélio Pedro, Sandra Pekić, M. Pineda, Amy Pizzino, Barbara Plecko, Bwee Tien Poll‐The, Vera Popović, D. Rating, Marie‐France Rioux, N. Rodríguez-Espinosa, Anne Ronan, John R. Østergaard, Elsa Rossignol, Rocío Sánchez‐Carpintero, Anna Schossig, Nesrin Şenbil, Laura Roos, Cathy A. Stevens, Matthis Synofzik, László Sztriha

    Được phát hành 2020
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