Zobrazeno 1 - 10
of 111
pro vyhledávání: '"Erika, Tavares"'
Autor:
Sarah Rae, Jonathon Maguire, Mary Aglipay, Melanie Barwick, Karoon Danavan, Jess Haines, Jennifer Jenkins, Marie Klaassen, Myla E. Moretti, Frank Ong, Nav Persaud, Michelle Porepa, Sharon Straus, Erika Tavares, Andrew Willan, Catherine Birken
Publikováno v:
Trials, Vol 24, Iss 1, Pp 1-12 (2023)
Abstract Background The prevalence of overweight (15%) and obesity (6%) in children under 5 years of age in Canada are high, and young children with overweight and obesity are at increased risk of the development of chronic disease(s) in adulthood. P
Externí odkaz:
https://doaj.org/article/9c03b850743644fa98f89cff8f14300d
Autor:
Xuedi Li, Charles D. G. Keown-Stoneman, Cornelia M. Borkhoff, Peter D. Wong, Dana Arafeh, Erika Tavares, Sharon Thadani, Jonathon L. Maguire, Catherine S. Birken
Publikováno v:
PLoS ONE, Vol 18, Iss 4 (2023)
Background All longitudinal cohort studies strive for high participant retention, although attrition is common. Understanding determinants of attrition is important to inform and develop targeted strategies to improve study participation. We aimed to
Externí odkaz:
https://doaj.org/article/8fbc28d740634779924dda995ad46f85
Autor:
Leigh M. Vanderloo, Shelley M. Vanderhout, Erika Tavares, Jonathon Maguire, Sharon Straus, Catherine S. Birken
Publikováno v:
Trials, Vol 22, Iss 1, Pp 1-15 (2021)
Abstract Evidence generated from partnering with parents to design and conduct research together may be used to refine, adjust, and modify future research approaches. This study aimed to describe the initial approaches to parent engagement in the des
Externí odkaz:
https://doaj.org/article/9d0dd2c17c22429cb3dbb751cb905fcd
Autor:
Jacqueline Tizard, Selina Patel, John Waugh, Erika Tavares, Tjard Bergmann, Brian Gill, Janette Norman, Les Christidis, Paul Scofield, Oliver Haddrath, Allan Baker, David Lambert, Craig Millar
Publikováno v:
BMC Evolutionary Biology, Vol 19, Iss 1, Pp 1-13 (2019)
Abstract Background DNA barcoding utilises a standardised region of the cytochrome c oxidase I (COI) gene to identify specimens to the species level. It has proven to be an effective tool for identification of avian samples. The unique island avifaun
Externí odkaz:
https://doaj.org/article/2e7ee963c2654366ab5dc3b13a00431b
Autor:
Eman Saleh, Monika Grudzinska Pechhacker, Anjali Vig, Maanik Mehta, Jason Maynes, Anupreet Tumber, Erika Tavares, Ajoy Vincent, Kamiar Mireskandari, Elise Heon
Publikováno v:
Journal of American Association for Pediatric Ophthalmology and Strabismus. 26:202-205
Unilateral cataract can cause pediatric vision impairment. Although the majority of unilateral cataracts are idiopathic in nature, genetic causes have been reported. We present the case of a 4-week-old child of nonconsanguineous parents who was affec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cbec2d92ab2ba9b0df5b18b165308ac
https://doi.org/10.1016/j.jaapos.2022.03.013
https://doi.org/10.1016/j.jaapos.2022.03.013
Publikováno v:
Revista de Direito Ambiental e Socioambientalismo, Vol 2, Iss 2, Pp 107-129 (2016)
The National Solid Waste Policy is a milestone on the issue of management and management of solid waste in Brazil. But few Brazilian states monitor the traceability of hazardous waste. The overall objective of this paper is to analyze to what extent
Externí odkaz:
https://doaj.org/article/7f5540ec97fe470f99763473300f6aa5
Autor:
Erika Tavares Amaral Rabelo de Matos1 etarm13@gmail.com, Fernando Rangel Alvarez dos Santos2,3 frangel2005@gmail.com
Publikováno v:
Revista de Direito Ambiental e Socioambientalismo. jul-dez2016, Vol. 2 Issue 2, p107-129. 23p.
Autor:
Anna Dvaladze, Erika Tavares, Matteo Di Scipio, Graeme Nimmo, Monika K. Grudzinska‐Pechhacker, Tara Paton, Anupreet Tumber, Shuning Li, Christabel Eileen, Birgit Ertl‐Wagner, Eva Mamak, Georg Hoffmann, Christian R. Marshall, Dorothea Haas, Ertan Mayatepek, Andreas Schulze, Elise Heon, Ajoy Vincent
Publikováno v:
Clinical geneticsREFERENCES. 102(6)
Non-syndromic retinitis pigmentosa (NSRP) is a clinically and genetically heterogeneous group of disorders characterized by progressive degeneration of the rod and cone photoreceptors, often leading to blindness. The evolving association of syndromic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a37034bdaa16050594f895c70ba0166
https://pubmed.ncbi.nlm.nih.gov/35916082
https://pubmed.ncbi.nlm.nih.gov/35916082
Autor:
Anjali Vig, James A. Poulter, Daniele Ottaviani, Erika Tavares, Katerina Toropova, Anna Maria Tracewska, Antonio Mollica, Jasmine Kang, Oshini Kehelwathugoda, Tara Paton, Jason T. Maynes, Gabrielle Wheway, Gavin Arno, J.C. Ambrose, P. Arumugam, E.L. Baple, M. Bleda, F. Boardman-Pretty, J.M. Boissiere, C.R. Boustred, H. Brittain, M.J. Caulfield, G.C. Chan, C.E.H. Craig, L.C. Daugherty, A. de Burca, A. Devereau, G. Elgar, R.E. Foulger, T. Fowler, P. Furió-Tarí, J.M. Hackett, D. Halai, A. Hamblin, S. Henderson, J.E. Holman, T.J.P. Hubbard, K. Ibáñez, R. Jackson, L.J. Jones, D. Kasperaviciute, M. Kayikci, L. Lahnstein, K. Lawson, S.E.A. Leigh, I.U.S. Leong, F.J. Lopez, F. Maleady-Crowe, J. Mason, E.M. McDonagh, L. Moutsianas, M. Mueller, N. Murugaesu, A.C. Need, C.A. Odhams, C. Patch, D. Perez-Gil, D. Polychronopoulos, J. Pullinger, T. Rahim, A. Rendon, P. Riesgo-Ferreiro, T. Rogers, M. Ryten, K. Savage, K. Sawant, R.H. Scott, A. Siddiq, A. Sieghart, D. Smedley, K.R. Smith, A. Sosinsky, W. Spooner, H.E. Stevens, A. Stuckey, R. Sultana, E.R.A. Thomas, S.R. Thompson, C. Tregidgo, A. Tucci, E. Walsh, S.A. Watters, M.J. Welland, E. Williams, K. Witkowska, S.M. Wood, M. Zarowiecki, Kamron N. Khan, Martin McKibbin, Carmel Toomes, Manir Ali, Matteo Di Scipio, Shuning Li, Jamie Ellingford, Graeme Black, Andrew Webster, Małgorzata Rydzanicz, Piotr Stawiński, Rafał Płoski, Ajoy Vincent, Michael E. Cheetham, Chris F. Inglehearn, Anthony Roberts, Elise Heon
Publikováno v:
Genetics in Medicine
Purpose Determining the role of DYNC2H1 variants in nonsyndromic inherited retinal disease (IRD). Methods Genome and exome sequencing were performed for five unrelated cases of IRD with no identified variant. In vitro assays were developed to validat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c0d1392a5b005c16762f6fc0adb770b
http://europepmc.org/articles/PMC7708302
http://europepmc.org/articles/PMC7708302
Autor:
Erika Tavares, Monika K Grudzinska Pechhacker, Nicole M. Roslin, Anjali Vig, Ajoy Vincent, Elise Héon, Matteo Di Scipio, Anupreet Tumber
Publikováno v:
Ophthalmic Genetics. 41:457-464
S-adenosylhomocysteine hydrolase deficiency due to pathologic variants in AHCY gene is a rare neurometabolic disease for which no eye phenotype has been documented. Pathologic variants in CRB1 gene...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21531d9cc53234eacfcca433831b9d2d
https://doi.org/10.1080/13816810.2020.1790013
https://doi.org/10.1080/13816810.2020.1790013