Search Results - Elise Davis
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Elastic lamina growth in the developing mouse aorta. by Elise Davis
Published 1995Artigo -
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A randomized controlled trial of the impact of therapeutic horse riding on the quality of life, health, and function of children with cerebral palsy by Elise Davis, Belinda Davies, Rory Wolfe, R RAADSVELD, Barbara Heine, Pam Thomason, Fiona Dobson, H. Kerr Graham
Published 2009Artigo -
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Exploring quality of life of children with cerebral palsy and intellectual disability: What are the important domains of life? by Elise Davis, Dinah Reddihough, Nada Murphy, Amy Epstein, Susan Reid, Andrew J. O. Whitehouse, Katrina Williams, Helen Leonard, Jenny Downs
Published 2017Artigo -
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Qualitative Analysis of Parental Observations on Quality of Life in Australian Children with Down Syndrome by Nada Murphy, Amy Epstein, Helen Leonard, Elise Davis, Dinah Reddihough, Andrew J. O. Whitehouse, Peter Jacoby, Jenny Bourke, Katrina Williams, Jenny Downs
Published 2017Artigo -
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Psychometric properties of the quality of life questionnaire for children with CP by Elizabeth Waters, Elise Davis, Andrew Mackinnon, Roslyn N. Boyd, H. Kerr Graham, Sing Kai Lo, Rory Wolfe, Richard J. Stevenson, Kristie Bjornson, Eve Blair, Peter Hoare, Ulrike Ravens‐Sieberer, Dinah Reddihough
Published 2006Artigo -
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Mutations in Fibrillin-1 Cause Congenital Scleroderma: Stiff Skin Syndrome by Bart Loeys, Elizabeth E. Gerber, Douglas L. Riegert‐Johnson, Sarah Iqbal, Pat Whiteman, Vivienne McConnell, Chandramouli Chillakuri, Daniela Macaya, Paul Coucke, Anne De Paepe, Daniel P. Judge, Fredrick M. Wigley, Elise Davis, Helen J. Mardon, Penny A. Handford, Douglas R. Keene, Lynn Y. Sakai, Harry C. Dietz
Published 2010Artigo -
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Loss-of-function mutations in ATP6V0A2 impair vesicular trafficking, tropoelastin secretion and cell survival by Vishwanathan Hucthagowder, Éva Morava, Uwe Kornak, Dirk J. Lefeber, Björn Fischer‐Zirnsak, Aikaterini Dimopoulou, Annika Aldinger, Ji-Won Choi, Elise Davis, Dianne Abuelo, Michael S. Adamowicz, Jumana Y. Al‐Aama, Lina Basel‐Vanagaite, Brianna Fernandez, Marie T. Greally, Gabriele Gillessen‐Kaesbach, Hülya Kayserili, Emmanuelle Lemyre, Mustafa Tekin, Seval Türkmen, Beyhan Tüysüz, Berrin Yüksel‐Konuk, Stefan Mundlos, Lionel Van Maldergem, Ron A. Wevers, Zsolt Urbán
Published 2009Artigo -
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Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen by U. Schwarze, Tim Cundy, Shawna M. Pyott, H. E. Christiansen, Madhuri Hegde, Ruud A. Bank, Gerard Pals, Arunkanth Ankala, Karen N. Conneely, Laurie Seaver, Suzanne M. Yandow, Ellen M. Raney, Dusica Babovic‐Vuksanovic, Joan M. Stoler, Ziva Ben‐Neriah, Reeval Segel, Sari Lieberman, Liesbeth Siderius, Aida I. Al‐Aqeel, Mark C. Hannibal, Lucas Hudgins, Elizabeth McPherson, Michele Clemens, Michael D. Sussman, Robert D. Steiner, John D. Mahan, Rosemarie Smith, Kwame Anyane‐Yeboa, Julia Wynn, Karen Chong, Tami Uster, Salim Aftimos, V. Reid Sutton, Elise Davis, In S. Kim, Mary Ann Weis, David R. Eyre, Peter H. Byers
Published 2012Artigo
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