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Journal of Substance Use and Addiction Treatment
|
September 18, 2025
Feasibility of direct induction onto long-acting injectable buprenorphine
Thileepan Naren, Dean Membrey, Paul MacCartney, et al.
Australian Journal of General Practice
|
May 5, 2025
Provision of a remote telehealth opioid substitution therapy clinic in a regional Victorian community
Sarah Garry, Paul MacCartney, Dean Membrey, et al.
European Journal of Immunology
|
September 19, 2014
Transient Treg-cell depletion in adult mice results in persistent self-reactive CD4(+) T-cell responses
Sofia N Nyström, Dorothée Bourges, Sarah Garry, et al.
Australian Journal of General Practice
|
February 8, 2026
Naltrexone: A safe and effective standard of care in treating alcohol use disorder
Thileepan Naren, Sarah Garry, Dean Membrey, et al.
European Journal of Medical Genetics
|
October 27, 2019
EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalities
Marie Shaw, Anna Winczewska-Wiktor, Magdalena Badura-Stronka, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 5) with videos related to
Sort By:
Page
of 1
Journal of Substance Use and Addiction Treatment
|
September 18, 2025
Feasibility of direct induction onto long-acting injectable buprenorphine
Thileepan Naren, Dean Membrey, Paul MacCartney, et al.
Australian Journal of General Practice
|
May 5, 2025
Provision of a remote telehealth opioid substitution therapy clinic in a regional Victorian community
Sarah Garry, Paul MacCartney, Dean Membrey, et al.
European Journal of Immunology
|
September 19, 2014
Transient Treg-cell depletion in adult mice results in persistent self-reactive CD4(+) T-cell responses
Sofia N Nyström, Dorothée Bourges, Sarah Garry, et al.
Australian Journal of General Practice
|
February 8, 2026
Naltrexone: A safe and effective standard of care in treating alcohol use disorder
Thileepan Naren, Sarah Garry, Dean Membrey, et al.
European Journal of Medical Genetics
|
October 27, 2019
EXOME REPORT: Novel mutation in ATP6V1B2 segregating with autosomal dominant epilepsy, intellectual disability and mild gingival and nail abnormalities
Marie Shaw, Anna Winczewska-Wiktor, Magdalena Badura-Stronka, et al.
Page
of 1