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

D Irvine

Showing results (471-480 of 487) with videos related to

Pageof 49
Sort By:
Journal of the American Academy of Dermatology|March 14, 2020
The Alopecia Areata Consensus of Experts (ACE) study: Results of an international expert opinion on treatments for alopecia areataNekma Meah, Dmitri Wall, Katherine York, et al.
Journal of the American Academy of Dermatology|September 14, 2020
The Alopecia Areata Consensus of Experts (ACE) study part II: Results of an international expert opinion on diagnosis and laboratory evaluation for alopecia areataNekma Meah, Dmitri Wall, Katherine York, et al.
Nature Genetics|January 6, 2009
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosisYaran Wen, Yang Liu, Yiming Xu, et al.
Nature Genetics|June 4, 2013
High-density genotyping study identifies four new susceptibility loci for atopic dermatitisDavid Ellinghaus, Hansjörg Baurecht, Jorge Esparza-Gordillo, et al.
Nature|August 11, 2015
Mutations in DCHS1 cause mitral valve prolapseRonen Durst, Kimberly Sauls, David S Peal, et al.
Orphanet Journal of Rare Diseases|October 17, 2015
Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutationsSandra Mercier, Sébastien Küry, Emmanuelle Salort-Campana, et al.
Human Mutation|September 17, 2013
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformationNicole Revencu, Laurence M Boon, Antonella Mendola, et al.
The British Journal of Dermatology|October 17, 2015
Propranolol in the treatment of infantile haemangiomas: lessons from the European Propranolol In the Treatment of Complicated Haemangiomas (PITCH) Taskforce surveyE Wedgeworth, M Glover, A D Irvine, et al.
JAMA Dermatology|March 3, 2021
A Global eDelphi Exercise to Identify Core Domains and Domain Items for the Development of a Global Registry of Alopecia Areata Disease Severity and Treatment Safety (GRASS)Dmitri Wall, Nekma Meah, Katherine York, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 23, 2025
Statement from the frontal fibrosing alopecia international expert alliance: SOFFIA 2024Nekma Meah, Jane Li, Dmitri Wall, et al.
Pageof 49

Showing results (471-480 of 487) with videos related to

Sort By:
Pageof 49
Journal of the American Academy of Dermatology|March 14, 2020
The Alopecia Areata Consensus of Experts (ACE) study: Results of an international expert opinion on treatments for alopecia areataNekma Meah, Dmitri Wall, Katherine York, et al.
Journal of the American Academy of Dermatology|September 14, 2020
The Alopecia Areata Consensus of Experts (ACE) study part II: Results of an international expert opinion on diagnosis and laboratory evaluation for alopecia areataNekma Meah, Dmitri Wall, Katherine York, et al.
Nature Genetics|January 6, 2009
Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosisYaran Wen, Yang Liu, Yiming Xu, et al.
Nature Genetics|June 4, 2013
High-density genotyping study identifies four new susceptibility loci for atopic dermatitisDavid Ellinghaus, Hansjörg Baurecht, Jorge Esparza-Gordillo, et al.
Nature|August 11, 2015
Mutations in DCHS1 cause mitral valve prolapseRonen Durst, Kimberly Sauls, David S Peal, et al.
Orphanet Journal of Rare Diseases|October 17, 2015
Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutationsSandra Mercier, Sébastien Küry, Emmanuelle Salort-Campana, et al.
Human Mutation|September 17, 2013
RASA1 mutations and associated phenotypes in 68 families with capillary malformation-arteriovenous malformationNicole Revencu, Laurence M Boon, Antonella Mendola, et al.
The British Journal of Dermatology|October 17, 2015
Propranolol in the treatment of infantile haemangiomas: lessons from the European Propranolol In the Treatment of Complicated Haemangiomas (PITCH) Taskforce surveyE Wedgeworth, M Glover, A D Irvine, et al.
JAMA Dermatology|March 3, 2021
A Global eDelphi Exercise to Identify Core Domains and Domain Items for the Development of a Global Registry of Alopecia Areata Disease Severity and Treatment Safety (GRASS)Dmitri Wall, Nekma Meah, Katherine York, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 23, 2025
Statement from the frontal fibrosing alopecia international expert alliance: SOFFIA 2024Nekma Meah, Jane Li, Dmitri Wall, et al.
Pageof 49