Search research articles
Contact Us
Filters
Showing results (151-160 of 343) with videos related to
Page
of 35
Sort By:
The International Journal on Drug Policy
|
December 28, 2020
Non-medical cannabis use among Indigenous Canadians: A systematic review of prevalence and associated factors
Erica Wennberg, Ariane Lasry, Sarah B Windle, et al.
Postgraduate Medicine
|
October 26, 2012
Evaluation of the 9-item Patient Health Questionnaire (PHQ-9) as an assessment instrument for symptoms of depression in patients with multiple sclerosis
Kirsten Sjonnesen, Sandy Berzins, Kirsten M Fiest, et al.
The Patient
|
December 23, 2016
Perceived Benefits and Factors that Influence the Ability to Establish and Maintain Patient Support Groups in Rare Diseases: A Scoping Review
Vanessa C Delisle, Stephanie T Gumuchian, Danielle B Rice, et al.
BMJ Open
|
March 10, 2021
Effects of cosmetic and other camouflage interventions on appearance-related and psychological outcomes among adults with visible differences in appearance: a systematic review
Shadi Gholizadeh, Danielle B Rice, Andrea Carboni-Jiménez, et al.
The Patient
|
August 14, 2020
Perceived Benefits and Facilitators and Barriers to Providing Psychosocial Interventions for Informal Caregivers of People with Rare Diseases: A Scoping Review
Danielle B Rice, Andrea Carboni-Jiménez, Mara Cañedo-Ayala, et al.
Disability and Rehabilitation
|
August 30, 2021
Intensity of care and perceived burden among informal caregivers to persons with chronic medical conditions: a systematic review and meta-analysis
Andrea Carboni-Jiménez, Danielle B Rice, Brooke Levis, et al.
Journal of Clinical Epidemiology
|
April 17, 2020
Individual participant data meta-analyses (IPDMA): data contribution was associated with trial corresponding author country, publication year, and journal impact factor
Marleine Azar, Andrea Benedetti, Kira E Riehm, et al.
BMJ Open
|
March 4, 2018
Use of the nominal group technique to identify stakeholder priorities and inform survey development: an example with informal caregivers of people with scleroderma
Danielle B Rice, Mara Cañedo-Ayala, Kimberly A Turner, et al.
Plos One
|
March 19, 2014
The comparability of English, French and Dutch scores on the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F): an assessment of differential item functioning in patients with systemic sclerosis
Linda Kwakkenbos, Linda M Willems, Murray Baron, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
June 21, 2023
Clinical index to quantify the 1-year risk for common postpartum mental disorders at the time of delivery (PMH CAREPLAN): development and internal validation
Simone N Vigod, Natalie Urbach, Andrew Calzavara, et al.
Page
of 35
Search research articles
Search
Showing results (151-160 of 343) with videos related to
Sort By:
Page
of 35
The International Journal on Drug Policy
|
December 28, 2020
Non-medical cannabis use among Indigenous Canadians: A systematic review of prevalence and associated factors
Erica Wennberg, Ariane Lasry, Sarah B Windle, et al.
Postgraduate Medicine
|
October 26, 2012
Evaluation of the 9-item Patient Health Questionnaire (PHQ-9) as an assessment instrument for symptoms of depression in patients with multiple sclerosis
Kirsten Sjonnesen, Sandy Berzins, Kirsten M Fiest, et al.
The Patient
|
December 23, 2016
Perceived Benefits and Factors that Influence the Ability to Establish and Maintain Patient Support Groups in Rare Diseases: A Scoping Review
Vanessa C Delisle, Stephanie T Gumuchian, Danielle B Rice, et al.
BMJ Open
|
March 10, 2021
Effects of cosmetic and other camouflage interventions on appearance-related and psychological outcomes among adults with visible differences in appearance: a systematic review
Shadi Gholizadeh, Danielle B Rice, Andrea Carboni-Jiménez, et al.
The Patient
|
August 14, 2020
Perceived Benefits and Facilitators and Barriers to Providing Psychosocial Interventions for Informal Caregivers of People with Rare Diseases: A Scoping Review
Danielle B Rice, Andrea Carboni-Jiménez, Mara Cañedo-Ayala, et al.
Disability and Rehabilitation
|
August 30, 2021
Intensity of care and perceived burden among informal caregivers to persons with chronic medical conditions: a systematic review and meta-analysis
Andrea Carboni-Jiménez, Danielle B Rice, Brooke Levis, et al.
Journal of Clinical Epidemiology
|
April 17, 2020
Individual participant data meta-analyses (IPDMA): data contribution was associated with trial corresponding author country, publication year, and journal impact factor
Marleine Azar, Andrea Benedetti, Kira E Riehm, et al.
BMJ Open
|
March 4, 2018
Use of the nominal group technique to identify stakeholder priorities and inform survey development: an example with informal caregivers of people with scleroderma
Danielle B Rice, Mara Cañedo-Ayala, Kimberly A Turner, et al.
Plos One
|
March 19, 2014
The comparability of English, French and Dutch scores on the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-F): an assessment of differential item functioning in patients with systemic sclerosis
Linda Kwakkenbos, Linda M Willems, Murray Baron, et al.
The British Journal of Psychiatry : the Journal of Mental Science
|
June 21, 2023
Clinical index to quantify the 1-year risk for common postpartum mental disorders at the time of delivery (PMH CAREPLAN): development and internal validation
Simone N Vigod, Natalie Urbach, Andrew Calzavara, et al.
Page
of 35