Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Andrew Y Finlay

Showing results (11-20 of 70) with videos related to

Pageof 7
Sort By:
American Journal of Clinical Dermatology|August 23, 2008
Can we define acne as a chronic disease? If so, how and when?Harald P M Gollnick, Andrew Y Finlay, Neil Shear, et al.
American Journal of Clinical Dermatology|June 4, 2009
Impact of topical calcineurin inhibitors on quality of life in patients with atopic dermatitisJohn R Ingram, Julie A Martin, Andrew Y Finlay
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|February 23, 2015
Equivalence of electronic and paper-based patient-reported outcome measuresNiloufar Campbell, Faraz Ali, Andrew Y Finlay, et al.
Clinics in Dermatology|November 18, 2018
Correlating the Dermatology Life Quality Index with psychiatric measures: A systematic reviewFaraz M Ali, Nutjaree Johns, Sam Salek, et al.
Dermatology (Basel, Switzerland)|October 10, 2017
How to Train to Discharge a Dermatology Outpatient: A ReviewA Harun, Andrew Y Finlay, M Sam Salek, et al.
BMC Dermatology|August 6, 2004
DLQI scores in vitiligo: reliability and validity of the Persian versionShahin Aghaei, Manouchehr Sodaifi, Peyman Jafari, et al.
Journal of Cosmetic Dermatology|September 16, 2008
An assessment of the efficacy of blue light phototherapy in the treatment of acne vulgarisSadia Ammad, Maria Gonzales, Chris Edwards, et al.
BMJ Open|May 2, 2022
Impact of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) on the quality of life of people with ME/CFS and their partners and family members: an online cross-sectional surveyJui Vyas, Nina Muirhead, Ravinder Singh, et al.
Journal of Patient-Reported Outcomes|May 9, 2025
Psychometric validation of the Spanish for Ecuador Family Reported Outcome Measure (FROM-16) and its application to measure impact on family members of patients with skin diseasesAndrea Cueva, Faraz M Ali, Jeffrey Johns, et al.
Medicina (Kaunas, Lithuania)|August 29, 2024
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Impact on Quality of Life (QoL) of Persons with ME/CFSNina L Muirhead, Jui Vyas, Rachel Ephgrave, et al.
Pageof 7

Showing results (11-20 of 70) with videos related to

Sort By:
Pageof 7
American Journal of Clinical Dermatology|August 23, 2008
Can we define acne as a chronic disease? If so, how and when?Harald P M Gollnick, Andrew Y Finlay, Neil Shear, et al.
American Journal of Clinical Dermatology|June 4, 2009
Impact of topical calcineurin inhibitors on quality of life in patients with atopic dermatitisJohn R Ingram, Julie A Martin, Andrew Y Finlay
Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|February 23, 2015
Equivalence of electronic and paper-based patient-reported outcome measuresNiloufar Campbell, Faraz Ali, Andrew Y Finlay, et al.
Clinics in Dermatology|November 18, 2018
Correlating the Dermatology Life Quality Index with psychiatric measures: A systematic reviewFaraz M Ali, Nutjaree Johns, Sam Salek, et al.
Dermatology (Basel, Switzerland)|October 10, 2017
How to Train to Discharge a Dermatology Outpatient: A ReviewA Harun, Andrew Y Finlay, M Sam Salek, et al.
BMC Dermatology|August 6, 2004
DLQI scores in vitiligo: reliability and validity of the Persian versionShahin Aghaei, Manouchehr Sodaifi, Peyman Jafari, et al.
Journal of Cosmetic Dermatology|September 16, 2008
An assessment of the efficacy of blue light phototherapy in the treatment of acne vulgarisSadia Ammad, Maria Gonzales, Chris Edwards, et al.
BMJ Open|May 2, 2022
Impact of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) on the quality of life of people with ME/CFS and their partners and family members: an online cross-sectional surveyJui Vyas, Nina Muirhead, Ravinder Singh, et al.
Journal of Patient-Reported Outcomes|May 9, 2025
Psychometric validation of the Spanish for Ecuador Family Reported Outcome Measure (FROM-16) and its application to measure impact on family members of patients with skin diseasesAndrea Cueva, Faraz M Ali, Jeffrey Johns, et al.
Medicina (Kaunas, Lithuania)|August 29, 2024
Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: Impact on Quality of Life (QoL) of Persons with ME/CFSNina L Muirhead, Jui Vyas, Rachel Ephgrave, et al.
Pageof 7