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There are 10638 results for: content related to: The heritability of avoidant and dependent personality disorder assessed by personal interview and questionnaire

  1. Periodontal tissue engineering with stem cells from the periodontal ligament of human retained deciduous teeth

    Journal of Periodontal Research

    Volume 48, Issue 1, February 2013, Pages: 105–116, K. Ji, Y. Liu, W. Lu, F. Yang, J. Yu, X. Wang, Q. Ma, Z. Yang, L. Wen and K. Xuan

    Version of Record online : 8 AUG 2012, DOI: 10.1111/j.1600-0765.2012.01509.x

  2. Preliminary Functional Assessment and Classification of DEPDC5 Variants Associated with Focal Epilepsy

    Human Mutation

    Volume 36, Issue 2, February 2015, Pages: 200–209, Melissa van Kranenburg, Marianne Hoogeveen-Westerveld and Mark Nellist

    Version of Record online : 27 NOV 2014, DOI: 10.1002/humu.22723

  3. You have full text access to this OnlineOpen article
    DEPDC5 variants increase fibrosis progression in Europeans with chronic hepatitis C virus infection


    Volume 63, Issue 2, February 2016, Pages: 418–427, Maria Antonella Burza, Benedetta Maria Motta, Rosellina Margherita Mancina, Piero Pingitore, Carlo Pirazzi, Saverio Massimo Lepore, Rocco Spagnuolo, Patrizia Doldo, Cristina Russo, Veronica Lazzaro, Janett Fischer, Thomas Berg, Alessio Aghemo, Cristina Cheroni, Raffaele De Francesco, Silvia Fargion, Massimo Colombo, Christian Datz, Felix Stickel, Luca Valenti and Stefano Romeo

    Version of Record online : 18 DEC 2015, DOI: 10.1002/hep.28322

  4. DEPDC5 does it all: Shared genetics for diverse epilepsy syndromes

    Annals of Neurology

    Volume 75, Issue 5, May 2014, Pages: 631–633, Annapurna Poduri

    Version of Record online : 8 MAY 2014, DOI: 10.1002/ana.24160

  5. Familial focal epilepsy with focal cortical dysplasia due to DEPDC5 mutations

    Annals of Neurology

    Volume 77, Issue 4, April 2015, Pages: 675–683, Stéphanie Baulac, Saeko Ishida, Elise Marsan, Catherine Miquel, Arnaud Biraben, Dang Khoa Nguyen, Doug Nordli, Patrick Cossette, Sylvie Nguyen, Virginie Lambrecq, Mihaela Vlaicu, Maïlys Daniau, Franck Bielle, Eva Andermann, Frederick Andermann, Eric Leguern, Francine Chassoux and Fabienne Picard

    Version of Record online : 13 MAR 2015, DOI: 10.1002/ana.24368

  6. Mutations in mammalian target of rapamycin regulator DEPDC5 cause focal epilepsy with brain malformations

    Annals of Neurology

    Volume 75, Issue 5, May 2014, Pages: 782–787, Ingrid E. Scheffer, Sarah E. Heron, Brigid M. Regan, Simone Mandelstam, Douglas E. Crompton, Bree L. Hodgson, Laura Licchetta, Federica Provini, Francesca Bisulli, Lata Vadlamudi, Jozef Gecz, Alan Connelly, Paolo Tinuper, Michael G. Ricos, Samuel F. Berkovic and Leanne M. Dibbens

    Version of Record online : 14 APR 2014, DOI: 10.1002/ana.24126

  7. You have full text access to this OnlineOpen article
    DEPDC5 mutations are not a frequent cause of familial temporal lobe epilepsy


    Volume 56, Issue 10, October 2015, Pages: e168–e171, Pasquale Striano, Elena Serioli, Lia Santulli, Ida Manna, Angelo Labate, Emanuela Dazzo, Elena Pasini, Antonio Gambardella, Roberto Michelucci, Salvatore Striano and Carlo Nobile

    Version of Record online : 27 JUL 2015, DOI: 10.1111/epi.13094

  8. You have free access to this content
    Mutations in the mammalian target of rapamycin pathway regulators NPRL2 and NPRL3 cause focal epilepsy

    Annals of Neurology

    Volume 79, Issue 1, January 2016, Pages: 120–131, Michael G. Ricos, Bree L. Hodgson, Tommaso Pippucci, Akzam Saidin, Yeh Sze Ong, Sarah E. Heron, Laura Licchetta, Francesca Bisulli, Marta A. Bayly, James Hughes, Sara Baldassari, Flavia Palombo, Epilepsy Electroclinical Study Group, Margherita Santucci, Stefano Meletti, Samuel F. Berkovic, Guido Rubboli, Paul Q. Thomas, Ingrid E. Scheffer, Paolo Tinuper, Joel Geoghegan, Andreas W. Schreiber and Leanne M. Dibbens

    Version of Record online : 12 DEC 2015, DOI: 10.1002/ana.24547

  9. Blends of ultrasonically devulcanized and virgin carbon black filled ethylene–propylene–diene monomer rubbers

    Journal of Applied Polymer Science

    Volume 92, Issue 1, 5 April 2004, Pages: 132–138, Jushik Yun and A. I. Isayev

    Version of Record online : 27 JAN 2004, DOI: 10.1002/app.13668

  10. Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy

    Annals of Neurology

    Volume 79, Issue 4, April 2016, Pages: 522–534, Richard D. Bagnall, Douglas E. Crompton, Slavé Petrovski, Lien Lam, Carina Cutmore, Sarah I. Garry, Lynette G. Sadleir, Leanne M. Dibbens, Anita Cairns, Sara Kivity, Zaid Afawi, Brigid M. Regan, Johan Duflou, Samuel F. Berkovic, Ingrid E. Scheffer and Christopher Semsarian

    Version of Record online : 2 FEB 2016, DOI: 10.1002/ana.24596

  11. Role of IFN-λs,IFN-λs related genes and the DEPDC5 gene in Hepatitis B virus-related liver disease

    Journal of Viral Hepatitis

    Volume 21, Issue 7, July 2014, Pages: e29–e38, N. Ma, X. Zhang, F. Yu, P. Gao, Q. Fan, L. Liu and D. Liu

    Version of Record online : 20 FEB 2014, DOI: 10.1111/jvh.12235

  12. Novel DEPDC5 mutations causing familial focal epilepsy with variable foci identified

    Clinical Genetics

    Volume 84, Issue 4, October 2013, Pages: 341–342, A Kaur

    Version of Record online : 21 AUG 2013, DOI: 10.1111/cge.12239

  13. The Anxious Cluster of Personality Disorders: A Review

    Personality Disorders, Volume 8

    Mario Maj, Hagop S. Akiskal, Juan E. Mezzich, Ahmed Okasha, Pages: 349–403, 2005

    Published Online : 4 NOV 2005, DOI: 10.1002/0470090383.ch5

  14. sgk1, a member of an RNA cluster associated with cell death in a model of Parkinson's disease

    European Journal of Neuroscience

    Volume 21, Issue 2, January 2005, Pages: 301–316, Christine C. Stichel, Bodo Schoenebeck, Montserrat Foguet, Barbara Siebertz, Verian Bader, Xin Ran Zhu and Hermann Lübbert

    Version of Record online : 20 JAN 2005, DOI: 10.1111/j.1460-9568.2005.03859.x

  15. You have full text access to this OnlineOpen article
    Familial cortical dysplasia type IIA caused by a germline mutation in DEPDC5

    Annals of Clinical and Translational Neurology

    Volume 2, Issue 5, May 2015, Pages: 575–580, Thomas Scerri, Jessica R. Riseley, Greta Gillies, Kate Pope, Rosemary Burgess, Simone A. Mandelstam, Leanne Dibbens, Chung W. Chow, Wirginia Maixner, Anthony Simon Harvey, Graeme D. Jackson, David J. Amor, Martin B. Delatycki, Peter B. Crino, Samuel F. Berkovic, Ingrid E. Scheffer, Melanie Bahlo, Paul J. Lockhart and Richard J. Leventer

    Version of Record online : 12 MAR 2015, DOI: 10.1002/acn3.191

  16. DEPDC5 mutations in genetic focal epilepsies of childhood

    Annals of Neurology

    Volume 75, Issue 5, May 2014, Pages: 788–792, Dennis Lal, Eva M. Reinthaler, Julian Schubert, Hiltrud Muhle, Erik Riesch, Gerhard Kluger, Kamel Jabbari, Amit Kawalia, Christine Bäumel, Hans Holthausen, Andreas Hahn, Martha Feucht, Birgit Neophytou, Edda Haberlandt, Felicitas Becker, Janine Altmüller, Holger Thiele, Johannes R. Lemke, Holger Lerche, Peter Nürnberg, Thomas Sander, Yvonne Weber, Fritz Zimprich and Bernd A. Neubauer

    Version of Record online : 14 APR 2014, DOI: 10.1002/ana.24127

  17. A recurrent mutation in DEPDC5 predisposes to focal epilepsies in the French-Canadian population

    Clinical Genetics

    Volume 86, Issue 6, December 2014, Pages: 570–574, C. Martin, C. Meloche, M.-F. Rioux, D.K. Nguyen, L. Carmant, E. Andermann, M. Gravel and P. Cossette

    Version of Record online : 27 NOV 2013, DOI: 10.1111/cge.12311

  18. Mammalian target of rapamycin pathway mutations cause hemimegalencephaly and focal cortical dysplasia

    Annals of Neurology

    Volume 77, Issue 4, April 2015, Pages: 720–725, Alissa M. D'Gama, Ying Geng, Javier A. Couto, Beth Martin, Evan A. Boyle, Christopher M. LaCoursiere, Amer Hossain, Nicole E. Hatem, Brenda J. Barry, David J. Kwiatkowski, Harry V. Vinters, A. James Barkovich, Jay Shendure, Gary W. Mathern, Christopher A. Walsh and Annapurna Poduri

    Version of Record online : 26 FEB 2015, DOI: 10.1002/ana.24357

  19. Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia


    Volume 57, Issue 6, June 2016, Pages: 994–1003, Sarah Weckhuysen, Elise Marsan, Virginie Lambrecq, Cécile Marchal, Mélanie Morin-Brureau, Isabelle An-Gourfinkel, Michel Baulac, Martine Fohlen, Christine Kallay Zetchi, Margitta Seeck, Pierre de la Grange, Bart Dermaut, Alfred Meurs, Pierre Thomas, Francine Chassoux, Eric Leguern, Fabienne Picard and Stéphanie Baulac

    Version of Record online : 13 MAY 2016, DOI: 10.1111/epi.13391

  20. Association of germline or somatic TP53 missense mutation with oncogene amplification in tumors developed in patients with Li-Fraumeni or Li-Fraumeni-like syndrome

    Genes, Chromosomes and Cancer

    Volume 50, Issue 7, July 2011, Pages: 535–545, Waka Sugawara, Yasuhito Arai, Fumio Kasai, Yuiko Fujiwara, Masayuki Haruta, Rie Hosaka, Kazunori Nishida, Masashi Kurosumi, Yasuhito Kobayashi, Kiwamu Akagi and Yasuhiko Kaneko

    Version of Record online : 11 APR 2011, DOI: 10.1002/gcc.20878