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There are 40038 results for: content related to: Abnormal movements in Rett syndrome are present before the regression period: A case study

  1. Hand stereotypies distinguish Rett syndrome from autism disorder

    Movement Disorders

    Volume 27, Issue 8, July 2012, Pages: 1060–1062, Sylvie Goldman and Teresa Temudo

    Article first published online : 18 JUN 2012, DOI: 10.1002/mds.25057

  2. You have free access to this content
    Poster Presentations

    Movement Disorders

    Volume 27, Issue S1, June 2012, Pages: S1–S523,

    Article first published online : 19 JUN 2012, DOI: 10.1002/mds.25051

  3. Evolution of stereotypies in adolescents and women with Rett syndrome

    Movement Disorders

    Volume 24, Issue 9, 15 July 2009, Pages: 1379–1383, Aglaia Vignoli, Francesca La Briola and Maria Paola Canevini

    Article first published online : 7 MAY 2009, DOI: 10.1002/mds.22595

  4. Rett syndrome: An overlooked diagnosis in women with stereotypic hand movements, psychomotor retardation, Parkinsonism, and dystonia?

    Movement Disorders

    Volume 22, Issue 3, 15 February 2007, Pages: 387–389, Emmanuel Roze, Valérie Cochen, Sophie Sangla, Thierry Bienvenu, Anne Roubergue, Smaranda Leu-Semenescu and Marie Vidaihet

    Article first published online : 10 JAN 2007, DOI: 10.1002/mds.21276

  5. Atypical stereotypies and vocal tics in Rett syndrome: An illustrative case

    Movement Disorders

    Volume 23, Issue 4, 15 March 2008, Pages: 622–624, Teresa Temudo, Paula Freitas, Jorge Sequeiros, Patricia Maciel and Guiomar Oliveira

    Article first published online : 16 JAN 2008, DOI: 10.1002/mds.21939

  6. Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype

    American Journal of Medical Genetics Part A

    Volume 118A, Issue 2, 15 April 2003, Pages: 103–114, Linda S. Weaving, Sarah L. Williamson, Bruce Bennetts, Mark Davis, Carolyn J. Ellaway, Helen Leonard, Meow-Keong Thong, Martin Delatycki, Elizabeth M. Thompson, Nigel Laing and John Christodoulou

    Article first published online : 25 NOV 2002, DOI: 10.1002/ajmg.a.10053

  7. Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type

    Movement Disorders

    Volume 23, Issue 10, 30 July 2008, Pages: 1384–1390, Teresa Temudo, Elisabete Ramos, Karin Dias, Clara Barbot, Jose P. Vieira, Ana Moreira, Eulalia Calado, Ines Carrilho, Guiomar Oliveira, Antonio Levy, Maria Fonseca, Alexandra Cabral, Pedro Cabral, Joao P Monteiro, Luis Borges, Roseli Gomes, Manuela Santos, Jorge Sequeiros and Patricia Maciel

    Article first published online : 30 MAY 2008, DOI: 10.1002/mds.22115

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    Early postnatal behavioral changes in the Mecp2-308 truncation mouse model of Rett syndrome

    Genes, Brain and Behavior

    Volume 9, Issue 2, March 2010, Pages: 213–223, B. De Filippis, L. Ricceri and G. Laviola

    Article first published online : 2 NOV 2009, DOI: 10.1111/j.1601-183X.2009.00551.x

  9. Social impairments in Rett syndrome: characteristics and relationship with clinical severity

    Journal of Intellectual Disability Research

    Volume 56, Issue 3, March 2012, Pages: 233–247, W. E. Kaufmann, E. Tierney, C. A. Rohde, M. C. Suarez-Pedraza, M. A. Clarke, C. F. Salorio, G. Bibat, I. Bukelis, D. Naram, D. C. Lanham and S. Naidu

    Article first published online : 8 MAR 2011, DOI: 10.1111/j.1365-2788.2011.01404.x

  10. MECP2 gene mutations in non-syndromic X-linked mental retardation: Phenotype–genotype correlation

    American Journal of Medical Genetics Part A

    Volume 123A, Issue 2, 1 December 2003, Pages: 129–139, Marie Gomot, Chantal Gendrot, Alain Verloes, Martine Raynaud, Albert David, Helger G. Yntema, Sabine Dessay, Vera Kalscheuer, Suzanne Frints, Philippe Couvert, Sylvain Briault, Sophie Blesson, Annick Toutain, Jamel Chelly, Vincent Desportes and Claude Moraine

    Article first published online : 29 MAY 2003, DOI: 10.1002/ajmg.a.20247

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    Early speech–language development in females with Rett syndrome: focusing on the preserved speech variant

    Developmental Medicine & Child Neurology

    Volume 54, Issue 5, May 2012, Pages: 451–456, PETER B MARSCHIK, GIORGIO PINI, KATRIN D BARTL-POKORNY, MARTIN DUCKWORTH, MARKUS GUGATSCHKA, RALF VOLLMANN, MICHELE ZAPPELLA and CHRISTA EINSPIELER

    Article first published online : 21 FEB 2012, DOI: 10.1111/j.1469-8749.2012.04123.x

  12. Enhanced low-frequency oscillatory activity of the subthalamic nucleus in a patient with dystonia

    Movement Disorders

    Volume 27, Issue 8, July 2012, Pages: 1063–1066, Wolf-Julian Neumann, Julius Huebl, Christof Brücke, Maria Herrojo Ruiz, Andreas Kupsch, Gerd-Helge Schneider and Andrea A. Kühn

    Article first published online : 14 JUN 2012, DOI: 10.1002/mds.25078

  13. Atypical presentations and specific genotypes are associated with a delay in diagnosis in females with Rett syndrome

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 10, October 2010, Pages: 2535–2542, Stephanie Fehr, Jenny Downs, Ami Bebbington and Helen Leonard

    Article first published online : 2 SEP 2010, DOI: 10.1002/ajmg.a.33640

  14. High frequency of Parkin exon rearrangements in Mexican-mestizo patients with early-onset Parkinson's disease

    Movement Disorders

    Volume 27, Issue 8, July 2012, Pages: 1047–1051, Jorge Luis Guerrero Camacho, Nancy Monroy Jaramillo, Petra Yescas Gómez, Mayela Rodríguez Violante, Catherine Boll Woehrlen, Ma. Elisa Alonso Vilatela and Marisol López López

    Article first published online : 6 JUL 2012, DOI: 10.1002/mds.25030

  15. Intraoperative x-ray to measure distance between DBS leads: A reliability study

    Movement Disorders

    Volume 27, Issue 8, July 2012, Pages: 1056–1059, Leo Verhagen Metman, Julie G. Pilitsis, Glenn T. Stebbins, Maarten Bot and Roy A.E. Bakay

    Article first published online : 12 JUN 2012, DOI: 10.1002/mds.25056

  16. Short latency afferent inhibition in Parkinson's disease patients with dementia

    Movement Disorders

    Volume 27, Issue 8, July 2012, Pages: 1052–1055, Ozlem Celebi, Çağrı Mesut Temuçin, Bulent Elibol and Esen Saka

    Article first published online : 17 MAY 2012, DOI: 10.1002/mds.25040

  17. FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome

    Clinical Genetics

    Volume 82, Issue 6, December 2012, Pages: 569–573, S Takahashi, N Matsumoto, A Okayama, N Suzuki, A Araki, K Okajima, H Tanaka and A Miyamoto

    Article first published online : 16 DEC 2011, DOI: 10.1111/j.1399-0004.2011.01819.x

  18. Medical care of adolescents and women with Rett syndrome: An Italian study

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Pages: 13–18, Aglaia Vignoli, Francesca La Briola, Angela Peron, Katherine Turner, Miriam Savini, Francesca Cogliati, Silvia Russo and Maria Paola Canevini

    Article first published online : 2 DEC 2011, DOI: 10.1002/ajmg.a.34367

  19. Phenotypic manifestations of MECP2 mutations in classical and atypical rett syndrome

    American Journal of Medical Genetics Part A

    Volume 126A, Issue 2, 15 April 2004, Pages: 129–140, Carolyn Schanen, Elisa J.F. Houwink, Naghmeh Dorrani, Jane Lane, Ruth Everett, Alice Feng, Rita M. Cantor and Alan Percy

    Article first published online : 24 OCT 2003, DOI: 10.1002/ajmg.a.20571

  20. Rett syndrome: Of girls and mice—Lessons for regression in autism

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 10, Issue 2, May 2004, Pages: 154–158, Daniel G. Glaze

    Article first published online : 7 SEP 2004, DOI: 10.1002/mrdd.20030