Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jessica Mackay"'
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 9, Iss 1, Pp 1-13 (2017)
Abstract Background Rett syndrome is a severe neurodevelopmental disorder associated with mutations in the MECP2 gene. Irregular breathing patterns and abdominal bloating are prominent but poorly understood features. Our aims were to characterize the
Externí odkaz:
https://doaj.org/article/54d1c83d00b14a2f978a4c9578885e38
Publikováno v:
Lecture Notes in Networks and Systems ISBN: 9783031280726
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::61de8a5aa47807be8501543030e7c42e
https://doi.org/10.1007/978-3-031-28073-3_30
https://doi.org/10.1007/978-3-031-28073-3_30
Publikováno v:
ELT Journal. 75:418-431
This study examines the results of an intervention conducted with adult EFL learners in Barcelona, Spain, to foster engagement with the target language outside class time. As part of the programme, the messaging service WhatsApp was used to carry out
Autor:
Nitin Kapur, Andrew Tai, Jenny Downs, Elaine Tham, Chris Seton, Yassmin Musthaffa, Peter Jacoby, Patricia Crock, Greg Blecher, Gillian M. Nixon, Charles F. Verge, Komal Vora, Antony R Lafferty, Cara Schofield, Andrew Wilson, Helen Leonard, Geoff Ambler, Philip Bergman, Daan Caudri, Catherine S. Choong, Jessica Mackay
Publikováno v:
Journal of Autism and Developmental Disorders, 52(9), 3877-3889. Springer New York
Prader-Willi syndrome (PWS) is a rare genetic disorder characterised by neurodevelopmental delays, hyperphagia, difficulties with social communication and challenging behaviours. Individuals require intensive supervision from caregivers which may neg
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33b98a188b75e12ced8c13a7cd3754bf
https://pure.eur.nl/en/publications/219e78a3-1f63-4637-9cd1-e0c1562e0124
https://pure.eur.nl/en/publications/219e78a3-1f63-4637-9cd1-e0c1562e0124
Publikováno v:
Computer Assisted Language Learning. 35:1946-1974
WhatsApp is a powerful tool for L2 learning because of its capacity to promote interaction between teacher and student, as well as among students. Its use has also been shown to support ubiquitous ...
Autor:
Catherine S. Choong, Jessica Mackay, Jenny Downs, Greg Blecher, Andrew C. Wilson, Chris Seton, Nora Shields, Charles F. Verge, Helen Leonard, Cara Schofield, Jaqueline Curran, Yassmin Musthaffa, Philip Bergman, Kate Milner, Aleisha Nielsen, Jessica Harper, Geoffrey R Ambler, Komal Vora, Daan Caudri, Gillian M. Nixon, Patricia Crock, Antony R Lafferty, Zoe McCallum, Nitin Kapur, Andrew Tai, Elaine Tham
Publikováno v:
Journal of Paediatrics and Child Health, 55(9), 1029-1037. Wiley-Blackwell Publishing Ltd
Journal of Paediatrics and Child Health
Journal of Paediatrics and Child Health
Prader‐Willi syndrome (PWS) is a rare genetic condition with multi‐system involvement. The literature was reviewed to describe neurodevelopment and the behavioural phenotype, endocrine and metabolic disorders and respiratory and sleep functioning
Autor:
Jessica Mackay
Publikováno v:
System. 81:50-62
This study analyses the effects of a specifically-designed Ideal L2 self intervention based on the principles outlined in Dornyei’s (2005 , 2009) proposal of the L2 Motivational Self System (L2MSS). Activities designed to enhance and develop the Id
Pesticide seed treatments (PST) which contain fungicides and insecticides are commonly used in agriculture; however, little is known about their effect on soil microbial communities and soil health...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30cfe2bc3b198eb5cc3dd87714047cd7
https://doi.org/10.1002/essoar.10501281.1
https://doi.org/10.1002/essoar.10501281.1
Publikováno v:
Developmental Medicine & Child Neurology. 60:951-957
Aim Respiratory illness is a major cause of morbidity and mortality in Rett syndrome. This study investigated respiratory morbidity and relationships with age, mutation type, feeding, and walking status. Method Families registered with the InterRett
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 9, Iss 1, Pp 1-13 (2017)
Journal of Neurodevelopmental Disorders
Journal of Neurodevelopmental Disorders
Background Rett syndrome is a severe neurodevelopmental disorder associated with mutations in the MECP2 gene. Irregular breathing patterns and abdominal bloating are prominent but poorly understood features. Our aims were to characterize the abnormal