Table of Contents Table of Contents
Previous Page  28 / 60 Next Page
Information
Show Menu
Previous Page 28 / 60 Next Page
Page Background

74

JCPSLP

Volume 18, Number 2 2016

Journal of Clinical Practice in Speech-Language Pathology

Kate Anderson

is a researcher and lecturer in disability and

inclusion at Deakin University, Melbourne, Australia.

Paul Andres

is

an occupational therapist and AAC consultant at Prentke-Romich

Deutschland, in Germany.

Correspondence to:

Dr Kate Anderson

Deakin University

email:

Kate.anderson2@deakin.edu.au

References

Anderson, K. L., Balandin, S., & Stancliffe, R. J. (2014).

Australian parents’ experiences of speech generating

device (SGD) service delivery.

Developmental

Neurorehabilitation

,

17

(2), 75–83.

Anderson, K. L., Balandin, S., & Stancliffe, R. J. (2016).

“It’s got to be more than that”: Parents and speech-

language pathologists discuss training content for families

with a new speech generating device.

Disability and

Rehabilitation: Assistive Technology

,

11

(5), 375–384.

Blackburn, C., & Read, J. (2005). Using the Internet? The

experiences of parents of disabled children.

Child: Care,

Health and Development

,

31

(5), 507–515.

Disability Reform Council. (2015).

National Disability

Insurance Scheme: A framework for information, linkages,

and capacity building

. [On-line policy document]. Retrieved

from

http://www.ndis.gov.au/sites/default/files/ILC-Policy-

Framework.pdf

Eastin, M. S. (2001). Credibility assessments of online

health information: The effects of source expertise

and knowledge of content. [Electronic resource].

Journal of Computer-Mediated Communication

,

6

(4).

doi:10.1111/j.1083-6101.2001.tb00126.x

Eysenbach, G., Yihune, G., Lampe, K., Cross, P., &

Brickley, D. (2000).

MedCERTAIN: quality management,

certification and rating of health information on the

Net

. Paper presented at the Proceedings of the AMIA

Symposium, 230–234. [Electronic resource]. Retrieved from

http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2244104/

Fox, S. (2006).

Online health search 2006

. Pew Internet

& American Life Project. Retrieved from http://www.

pewinternet.org/2006/10/29/online-health-search-2006/

Fox, S., & Duggan, M. (2013).

Health online 2013

. Pew

Internet & American Life Project. Retrieved from http://

www.pewinternet.org/2013/01/15/health-online-2013/

Greenberg, L., D’Andrea, G., & Lorence, D. (2004).

Setting the public agenda for online health search: A white

paper and action agenda. [Electronic resource].

Journal

of Medical Internet Research

,

6

(2), e18. doi:10.2196/

jmir.6.2.e18

Hallgren, K. A. (2012). Computing inter-rater reliability for

observational data: An overview and tutorial.

Tutorials in

Quantitative Methods for Psychology

,

8

(1), 23.

Hemsley, B., Dann, S., Palmer, S., Allan, M., & Balandin,

S. (2015). “We definitely need an audience”: Experiences

of Twitter, Twitter networks and tweet content in adults with

severe communication disabilities who use augmentative

and alternative communication (AAC).

Disability and

Rehabilitation

,

37

(17), 1531–1542.

Kunst, H., & Khan, K. S. (2002). Quality of web-based

medical information on stable COPD: Comparison of non-

commercial and commercial websites.

Health Information &

Libraries Journal

,

19

(1), 42–48.

Porter, A., & Edirippulige, S. (2007). Parents of deaf

children seeking hearing loss-related information on the

internet: The Australian experience.

Journal of Deaf Studies

and Deaf Education

,

12

(4): 518–529.

Rice, R. E. (2006). Influences, usage, and outcomes of

Internet health information searching: Multivariate results

from the Pew surveys.

International Journal of Medical

Informatics

,

75

(1), 8–28.

Roche, M. I., & Skinner, D. (2009). How parents search,

interpret, and evaluate genetic information obtained from

the internet.

Journal of Genetic Counseling

,

18

(2), 119–129.

Spink, A., & Jansen, B. J. (2004). A study of web search

trends.

Webology

,

1

(2), 4.

Zaidman-Zait, A., & Jamieson, J. R. (2007). Providing

web-based support for families of infants and young

children with established disabilities.

Infants & Young

Children

,

20

(1), 11–25.