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

David Orchard

Showing results (31-40 of 39) with videos related to

Pageof 4
Sort By:
You have reached the last page of results.This site can display upto 39 results.
The Australasian Journal of Dermatology|September 4, 2022
Discoid (nummular) eczema in the paediatric setting - An Australian/New Zealand narrativeSeamus McWhirter, Rachael Foster, Anne Halbert, et al.
The Australasian Journal of Dermatology|November 11, 2011
Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagenJohn Frew, Shueh W Lim, Alfred Klausseger, et al.
The Australasian Journal of Dermatology|May 14, 2024
Australian consensus: Treatment goals for moderate to severe psoriasis in the era of targeted therapies - Considerations for paediatric patientsPeter Foley, Patrick D Mahar, Saxon D Smith, et al.
The Australasian Journal of Dermatology|March 11, 2015
Adverse effects of topical corticosteroids in paediatric eczema: Australasian consensus statementEmma Mooney, Marius Rademaker, Rebecca Dailey, et al.
The Australasian Journal of Dermatology|August 6, 2025
Criteria for Commencing and Continuing Subsidised Janus Kinase Inhibitor Therapy in Australian Alopecia Areata Patients-Results From an Australian Expert Consensus ExerciseMeryl Thomas, Madeline Hankins, Emadodin Darchini-Maragheh, et al.
American Journal of Human Genetics|June 5, 2013
A recurrent PDGFRB mutation causes familial infantile myofibromatosisYee Him Cheung, Tenzin Gayden, Philippe M Campeau, et al.
European Journal of Human Genetics : EJHG|July 19, 2025
A new multisystem ERCC1-hepatorenal syndrome: insights from a clinical cohort, molecular pathogenesis, and management guidelinesSusan M White, Annelotte P Wondergem, Isa Breet, et al.
The Australasian Journal of Dermatology|March 3, 2017
Consensus statement for the treatment of infantile haemangiomas with propranololSarah L Smithson, Marius Rademaker, Susan Adams, et al.
Journal of Paediatrics and Child Health|June 1, 2026
Development of Multidisciplinary Consensus-Informed Guidance for the Management of Paediatric Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Among Clinicians From Australasian Tertiary Referral HospitalsPatrick David Mahar, Thomas Lee, David Orchard, et al.
Pageof 4

Showing results (31-40 of 39) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 39 results.
The Australasian Journal of Dermatology|September 4, 2022
Discoid (nummular) eczema in the paediatric setting - An Australian/New Zealand narrativeSeamus McWhirter, Rachael Foster, Anne Halbert, et al.
The Australasian Journal of Dermatology|November 11, 2011
Autosomal dominant bullous dermolysis of the newborn associated with a heterozygous missense mutation p.G1673R in type VII collagenJohn Frew, Shueh W Lim, Alfred Klausseger, et al.
The Australasian Journal of Dermatology|May 14, 2024
Australian consensus: Treatment goals for moderate to severe psoriasis in the era of targeted therapies - Considerations for paediatric patientsPeter Foley, Patrick D Mahar, Saxon D Smith, et al.
The Australasian Journal of Dermatology|March 11, 2015
Adverse effects of topical corticosteroids in paediatric eczema: Australasian consensus statementEmma Mooney, Marius Rademaker, Rebecca Dailey, et al.
The Australasian Journal of Dermatology|August 6, 2025
Criteria for Commencing and Continuing Subsidised Janus Kinase Inhibitor Therapy in Australian Alopecia Areata Patients-Results From an Australian Expert Consensus ExerciseMeryl Thomas, Madeline Hankins, Emadodin Darchini-Maragheh, et al.
American Journal of Human Genetics|June 5, 2013
A recurrent PDGFRB mutation causes familial infantile myofibromatosisYee Him Cheung, Tenzin Gayden, Philippe M Campeau, et al.
European Journal of Human Genetics : EJHG|July 19, 2025
A new multisystem ERCC1-hepatorenal syndrome: insights from a clinical cohort, molecular pathogenesis, and management guidelinesSusan M White, Annelotte P Wondergem, Isa Breet, et al.
The Australasian Journal of Dermatology|March 3, 2017
Consensus statement for the treatment of infantile haemangiomas with propranololSarah L Smithson, Marius Rademaker, Susan Adams, et al.
Journal of Paediatrics and Child Health|June 1, 2026
Development of Multidisciplinary Consensus-Informed Guidance for the Management of Paediatric Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Among Clinicians From Australasian Tertiary Referral HospitalsPatrick David Mahar, Thomas Lee, David Orchard, et al.
Pageof 4