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There are 19396 results for: content related to: The impact of having a sibling with an intellectual disability: parental perspectives in two disorders

  1. Investigating intellectual disability: A genetic perspective

    Journal of Paediatrics and Child Health

    Volume 39, Issue 7, September 2003, Pages: 492–506, NK Poplawski

    Article first published online : 16 SEP 2003, DOI: 10.1046/j.1440-1754.2003.00201.x

  2. ASD, ADHD, mental health conditions and psychopharmacology in neurogenetic syndromes: parent survey

    Journal of Intellectual Disability Research

    Volume 59, Issue 4, April 2015, Pages: 307–318, C. Reilly, J. Senior and L. Murtagh

    Article first published online : 25 JUN 2014, DOI: 10.1111/jir.12147

  3. You have full text access to this OnlineOpen article
    Is persistence of metabolic syndrome associated with poor health-related quality of life in non-diabetic Iranian adults? Tehran Lipid and Glucose Study

    Journal of Diabetes Investigation

    Volume 5, Issue 6, November 2014, Pages: 687–693, Parisa Amiri, Farhad Hosseinpanah, Sara Jalali-Farahani, Yadollah Mehrabi, Ali Montazeri and Fereidoun Azizi

    Article first published online : 25 MAR 2014, DOI: 10.1111/jdi.12222

  4. Behavioural phenotypes in the classroom: a qualitative study of parental and teacher knowledge of classroom guidelines and teacher views on best practices

    Journal of Research in Special Educational Needs

    Colin Reilly, Lelia Murtagh and Joyce Senior

    Article first published online : 13 JAN 2015, DOI: 10.1111/1471-3802.12097

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    Macrophage activation syndrome in juvenile systemic lupus erythematosus: A multinational multicenter study of thirty-eight patients

    Arthritis & Rheumatism

    Volume 60, Issue 11, November 2009, Pages: 3388–3399, Alessandro Parodi, Sergio Davì, Alejandra Beatriz Pringe, Angela Pistorio, Nicolino Ruperto, Silvia Magni-Manzoni, Paivi Miettunen, Brigitte Bader-Meunier, Graciela Espada, Gary Sterba, Seza Ozen, Dowain Wright, Claudia Saad Magalhães, Raju Khubchandani, Hartmut Michels, Patricia Woo, Antonio Iglesias, Dinara Guseinova, Claudia Bracaglia, Kristen Hayward, Carine Wouters, Alexei Grom, Marina Vivarelli, Alberto Fischer, Luciana Breda, Alberto Martini and Angelo Ravelli

    Article first published online : 29 OCT 2009, DOI: 10.1002/art.24883

  6. Aging in people with specific genetic syndromes: Rett syndrome

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 15, 1 August 2008, Pages: 1925–1932, Nicky S.J. Halbach, Eric E.J. Smeets, Connie T.R.M. Schrander-Stumpel, Henny H.J. van Schrojenstein Lantman de Valk, Marian A. Maaskant and Leopold M.G. Curfs

    Article first published online : 14 JUL 2008, DOI: 10.1002/ajmg.a.32361

  7. 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

  8. British Dietetic Association evidence-based guidelines for the dietary management of irritable bowel syndrome in adults

    Journal of Human Nutrition and Dietetics

    Volume 25, Issue 3, June 2012, Pages: 260–274, Y. A. McKenzie, A. Alder, W. Anderson, A. Wills, L. Goddard, P. Gulia, E. Jankovich, P. Mutch, L. B. Reeves, A. Singer, M. C. E. Lomer and on behalf of Gastroenterology Specialist Group of the British Dietetic Association

    Article first published online : 10 APR 2012, DOI: 10.1111/j.1365-277X.2012.01242.x

  9. Sweet's syndrome revisited: a review of disease concepts

    International Journal of Dermatology

    Volume 42, Issue 10, October 2003, Pages: 761–778, Philip R. Cohen and Razelle Kurzrock

    Article first published online : 2 OCT 2003, DOI: 10.1046/j.1365-4362.2003.01891.x

  10. Transcription Factor 4 and Myocyte Enhancer Factor 2C mutations are not common causes of Rett syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 4, April 2012, Pages: 713–719, Roksana Armani, Hayley Archer, Angus Clarke, Pradeep Vasudevan, Christiane Zweier, Gladys Ho, Sarah Williamson, Desiree Cloosterman, Nan Yang and John Christodoulou

    Article first published online : 1 MAR 2012, DOI: 10.1002/ajmg.a.34206

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    Rett syndrome: an eye-tracking study of attention and recognition memory

    Developmental Medicine & Child Neurology

    Volume 55, Issue 4, April 2013, Pages: 364–371, Susan A Rose, Aleksandra Djukic, Jeffery J Jankowski, Judith F Feldman, Iris Fishman and Maria Valicenti-Mcdermott

    Article first published online : 12 MAR 2013, DOI: 10.1111/dmcn.12085

  12. 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

  13. Salivary inflammatory exocrinopathy: diagnosis and treatment

    Australian Dental Journal

    Volume 28, Issue 2, April 1983, Pages: 87–94, David Wiesenfeld and Martin M. Ferguson

    Article first published online : 22 MAY 2009, DOI: 10.1111/j.1834-7819.1983.tb01085.x

  14. Central nervous system manifestations of mitochondrial disorders

    Acta Neurologica Scandinavica

    Volume 114, Issue 4, October 2006, Pages: 217–238, J. Finsterer

    Article first published online : 4 JUL 2006, DOI: 10.1111/j.1600-0404.2006.00671.x

  15. MECP2 mutations in Serbian Rett syndrome patients

    Acta Neurologica Scandinavica

    Volume 116, Issue 6, December 2007, Pages: 413–419, A. Djarmati, V. Dobričić, M. Kecmanović, P. Marsh, J. Jančić-Stefanović, C. Klein, M. Djurić and S. Romac

    Article first published online : 31 AUG 2007, DOI: 10.1111/j.1600-0404.2007.00893.x

  16. Barriers to diagnosis of a rare neurological disorder in China—Lived experiences of Rett syndrome families

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Pages: 1–9, Faye Lim, Jenny Downs, Jianghong Li, Xin-Hua Bao and Helen Leonard

    Article first published online : 21 NOV 2011, DOI: 10.1002/ajmg.a.34351

  17. Salivary flow and its relationship to oral signs and symptoms in patients with dry eyes

    Oral Diseases

    Volume 10, Issue 2, March 2004, Pages: 75–80, M Koseki, Y Maki, T Matsukubo, Y Ohashi and K Tsubota

    Article first published online : 25 FEB 2004, DOI: 10.1111/j.1354-523X.2003.00987.x

  18. You have free access to this content
    Ciliary biology: Understanding the cellular and genetic basis of human ciliopathies

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 151C, Issue 4, 15 November 2009, Pages: 263–280, Magdalena Cardenas-Rodriguez and Jose L. Badano

    Article first published online : 28 OCT 2009, DOI: 10.1002/ajmg.c.30227


    Family Court Review

    Volume 44, Issue 1, January 2006, Pages: 135–148, G. Kim Blank and Tara Ney

    Article first published online : 10 FEB 2006, DOI: 10.1111/j.1744-1617.2006.00072.x


    Family Court Review

    Volume 39, Issue 3, July 2001, Pages: 267–281, Justice R. James Williams

    Article first published online : 15 MAR 2005, DOI: 10.1111/j.174-1617.2001.tb00610.x