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

Erin F Mathes

Showing results (21-30 of 38) with videos related to

Pageof 4
Sort By:
Pediatric Dermatology|May 26, 2017
An Atopic Dermatitis Management Algorithm for Primary Care Providers and Assessment of Its Usefulness as a Clinical ToolMaria E Miyar, Megan Brown, Karina L Vivar, et al.
Pediatric Dermatology|March 21, 2017
Eosinophilic Pustular Folliculitis in Children after Stem Cell Transplantation: An Eruption Distinct from Graft-Versus-Host DiseaseMartin Theiler, Vikash S Oza, Erin F Mathes, et al.
Pediatric Radiology|July 6, 2015
MRI phenotypes of localized intravascular coagulopathy in venous malformationsKevin S H Koo, Christopher F Dowd, Erin F Mathes, et al.
JAMA Dermatology|September 22, 2021
Mapping of Segmental and Partial Segmental Infantile Hemangiomas of the Face and ScalpAlyson A Endicott, Sarah L Chamlin, Beth A Drolet, et al.
Clinics in Dermatology|August 21, 2022
Milestones 2.0: An advancement in competency-based assessment for dermatologyKiran Motaparthi, Laura Edgar, William D Aughenbaugh, et al.
Journal of the American Academy of Dermatology|October 24, 2024
Outcomes of the American Board of Dermatology focused Practice Improvement program 2016-2023Erik Stratman, Stanley Miller, Murad Alam, et al.
Blood Vessels, Thrombosis & Hemostasis|February 2, 2026
Alpelisib, a PI3Kα inhibitor, effectively treats vascular anomalies with diverse genotypes and phenotypesDeeti J Pithadia, Marina J Heskel, Arman Shotayev, et al.
The Journal of Experimental Medicine|January 20, 2016
A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70Alice Y Chan, Divya Punwani, Theresa A Kadlecek, et al.
Pediatric Dermatology|September 21, 2022
Multicenter retrospective review of pulsed dye laser in nonulcerated infantile hemangiomaSonal D Shah, Erin F Mathes, Eulalia Baselga, et al.
Human Molecular Genetics|November 26, 2015
Dominant de novo DSP mutations cause erythrokeratodermia-cardiomyopathy syndromeLynn M Boyden, Chen Y Kam, Angela Hernández-Martín, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
Pediatric Dermatology|May 26, 2017
An Atopic Dermatitis Management Algorithm for Primary Care Providers and Assessment of Its Usefulness as a Clinical ToolMaria E Miyar, Megan Brown, Karina L Vivar, et al.
Pediatric Dermatology|March 21, 2017
Eosinophilic Pustular Folliculitis in Children after Stem Cell Transplantation: An Eruption Distinct from Graft-Versus-Host DiseaseMartin Theiler, Vikash S Oza, Erin F Mathes, et al.
Pediatric Radiology|July 6, 2015
MRI phenotypes of localized intravascular coagulopathy in venous malformationsKevin S H Koo, Christopher F Dowd, Erin F Mathes, et al.
JAMA Dermatology|September 22, 2021
Mapping of Segmental and Partial Segmental Infantile Hemangiomas of the Face and ScalpAlyson A Endicott, Sarah L Chamlin, Beth A Drolet, et al.
Clinics in Dermatology|August 21, 2022
Milestones 2.0: An advancement in competency-based assessment for dermatologyKiran Motaparthi, Laura Edgar, William D Aughenbaugh, et al.
Journal of the American Academy of Dermatology|October 24, 2024
Outcomes of the American Board of Dermatology focused Practice Improvement program 2016-2023Erik Stratman, Stanley Miller, Murad Alam, et al.
Blood Vessels, Thrombosis & Hemostasis|February 2, 2026
Alpelisib, a PI3Kα inhibitor, effectively treats vascular anomalies with diverse genotypes and phenotypesDeeti J Pithadia, Marina J Heskel, Arman Shotayev, et al.
The Journal of Experimental Medicine|January 20, 2016
A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70Alice Y Chan, Divya Punwani, Theresa A Kadlecek, et al.
Pediatric Dermatology|September 21, 2022
Multicenter retrospective review of pulsed dye laser in nonulcerated infantile hemangiomaSonal D Shah, Erin F Mathes, Eulalia Baselga, et al.
Human Molecular Genetics|November 26, 2015
Dominant de novo DSP mutations cause erythrokeratodermia-cardiomyopathy syndromeLynn M Boyden, Chen Y Kam, Angela Hernández-Martín, et al.
Pageof 4