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The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 3, 2006
Delta subunit susceptibility variants E177A and R220H associated with complex epilepsy alter channel gating and surface expression of alpha4beta2delta GABAA receptors
Hua-Jun Feng, Jing-Qiong Kang, Luyan Song, et al.
The Australian and New Zealand Journal of Psychiatry
|
October 31, 2022
Management of cardiovascular disease risk in people with comorbid mental illness: A cross sectional study in Australian general practice
Genevieve Coorey, Anna Campain, John Mulley, et al.
BMC Primary Care
|
June 21, 2022
Utilisation of government-subsidised chronic disease management plans and cardiovascular care in Australian general practices
Genevieve Coorey, Anna Campain, John Mulley, et al.
Plos One
|
April 28, 2017
Examination of an eHealth literacy scale and a health literacy scale in a population with moderate to high cardiovascular risk: Rasch analyses
Sarah S Richtering, Rebecca Morris, Sze-Ee Soh, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
June 22, 2010
Mosaicism of a missense SCN1A mutation and Dravet syndrome in a Roma/Gypsy family
Dimitar N Azmanov, Sashka Zhelyazkova, Petya S Dimova, et al.
Human Molecular Genetics
|
August 22, 2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
Tim Cundy, Madhuri Hegde, Dorit Naot, et al.
NPJ Digital Medicine
|
September 23, 2020
A digital health intervention for cardiovascular disease management in primary care (CONNECT) randomized controlled trial
Julie Redfern, Genevieve Coorey, John Mulley, et al.
Epilepsia
|
April 18, 2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy
Gianpiero L Cavalleri, Nicole M Walley, Nicole Soranzo, et al.
The Lancet Regional Health. Western Pacific
|
February 22, 2024
Overcoming silos in health care systems through meso-level organisations - a case study of health reforms in New South Wales, Australia
David Peiris, Anne-Marie Feyer, Justine Barnard, et al.
American Journal of Human Genetics
|
June 9, 2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation
Patrick Tarpey, Josep Parnau, Matthew Blow, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 22) with videos related to
Sort By:
Page
of 3
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
February 3, 2006
Delta subunit susceptibility variants E177A and R220H associated with complex epilepsy alter channel gating and surface expression of alpha4beta2delta GABAA receptors
Hua-Jun Feng, Jing-Qiong Kang, Luyan Song, et al.
The Australian and New Zealand Journal of Psychiatry
|
October 31, 2022
Management of cardiovascular disease risk in people with comorbid mental illness: A cross sectional study in Australian general practice
Genevieve Coorey, Anna Campain, John Mulley, et al.
BMC Primary Care
|
June 21, 2022
Utilisation of government-subsidised chronic disease management plans and cardiovascular care in Australian general practices
Genevieve Coorey, Anna Campain, John Mulley, et al.
Plos One
|
April 28, 2017
Examination of an eHealth literacy scale and a health literacy scale in a population with moderate to high cardiovascular risk: Rasch analyses
Sarah S Richtering, Rebecca Morris, Sze-Ee Soh, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
June 22, 2010
Mosaicism of a missense SCN1A mutation and Dravet syndrome in a Roma/Gypsy family
Dimitar N Azmanov, Sashka Zhelyazkova, Petya S Dimova, et al.
Human Molecular Genetics
|
August 22, 2002
A mutation in the gene TNFRSF11B encoding osteoprotegerin causes an idiopathic hyperphosphatasia phenotype
Tim Cundy, Madhuri Hegde, Dorit Naot, et al.
NPJ Digital Medicine
|
September 23, 2020
A digital health intervention for cardiovascular disease management in primary care (CONNECT) randomized controlled trial
Julie Redfern, Genevieve Coorey, John Mulley, et al.
Epilepsia
|
April 18, 2007
A multicenter study of BRD2 as a risk factor for juvenile myoclonic epilepsy
Gianpiero L Cavalleri, Nicole M Walley, Nicole Soranzo, et al.
The Lancet Regional Health. Western Pacific
|
February 22, 2024
Overcoming silos in health care systems through meso-level organisations - a case study of health reforms in New South Wales, Australia
David Peiris, Anne-Marie Feyer, Justine Barnard, et al.
American Journal of Human Genetics
|
June 9, 2004
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation
Patrick Tarpey, Josep Parnau, Matthew Blow, et al.
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of 3