Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Joyce M. C. Teng"'
Autor:
Kalyani Marathe, Joyce M. C. Teng, Scott Guenthner, Christopher G. Bunick, Steven Kempers, Kimmie Eads, Leslie Castelo-Soccio, Alan M. Mendelsohn, Jessica Raiz, Dédée F. Murrell
Publikováno v:
Dermatology and Therapy, Vol 13, Iss 6, Pp 1255-1264 (2023)
Abstract Introduction Treatment with oral retinoids can be effective in patients with congenital ichthyosis (CI) but may be associated with clinically significant laboratory changes. In this Phase 2b CONTROL study analysis, we characterize the effect
Externí odkaz:
https://doaj.org/article/0589bfedc89443abbc72105e37c33aed
Autor:
Dedee F Murrell, Joyce M C Teng, Scott Guenthner, Kalyani Marathe, Steven Kempers, Kimmie Eads, Leslie Castelo-Soccio, Alan M Mendelsohn, Jessica Raiz, Christopher G Bunick
Publikováno v:
Clinical and Experimental Dermatology.
BackgroundIn two severe congenital ichthyosis subtypes, autosomal recessive lamellar ichthyosis (ARCI-LI) and X-linked recessive ichthyosis (XLRI), cutaneous manifestations include widespread scaling. Approved topical treatment options are limited to
Autor:
Joyce M. C. Teng, Dawn H. Siegel
Publikováno v:
Nature Cardiovascular Research. 1:535-536
Autor:
Jessica G. Labadie, Sarah A. Ibrahim, Brandon Worley, Bianca Y. Kang, Uros Rakita, Sarah Rigali, Kenneth A. Arndt, Eric Bernstein, Jeremy A. Brauer, Sunandana Chandra, Aashish Didwania, Catherine DiGiorgio, Mattias Donelan, Jeffrey S. Dover, Hassan Galadari, Roy G. Geronemus, Mitchel P. Goldman, Merete Haedersdal, George Hruza, Omar A. Ibrahimi, Arielle Kauvar, Kristen M. Kelly, Andrew C. Krakowski, Rachel Miest, Jeffrey S. Orringer, David M. Ozog, E. Victor Ross, Peter R. Shumaker, Joseph F. Sobanko, Kathleen Suozzi, Mark B. Taylor, Joyce M. C. Teng, Nathan S. Uebelhoer, Jill Waibel, Molly Wanner, Ina Ratchev, Rachel E. Christensen, Emily Poon, Corinne H. Miller, Murad Alam
Publikováno v:
Labadie, J G, Ibrahim, S A, Worley, B, Kang, B Y, Rakita, U, Rigali, S, Arndt, K A, Bernstein, E, Brauer, J A, Chandra, S, Didwania, A, Digiorgio, C, Donelan, M, Dover, J S, Galadari, H, Geronemus, R G, Goldman, M P, Haedersdal, M, Hruza, G, Ibrahimi, O A, Kauvar, A, Kelly, K M, Krakowski, A C, Miest, R, Orringer, J S, Ozog, D M, Ross, E V, Shumaker, P R, Sobanko, J F, Suozzi, K, Taylor, M B, Teng, J M C, Uebelhoer, N S, Waibel, J, Wanner, M, Ratchev, I, Christensen, R E, Poon, E, Miller, C H & Alam, M 2022, ' Evidence-Based Clinical Practice Guidelines for Laser-Assisted Drug Delivery ', JAMA Dermatology, vol. 158, no. 10, pp. 1193-1201 . https://doi.org/10.1001/jamadermatol.2022.3234
JAMA dermatology, vol 158, iss 10
JAMA dermatology, vol 158, iss 10
ImportanceLaser-assisted drug delivery (LADD) is used for various medical and cosmetic applications. However, there is insufficient evidence-based guidance to assist clinicians performing LADD.ObjectiveTo develop recommendations for the safe and effe
Publikováno v:
Journal of Vascular Anomalies. 3:e047
Publikováno v:
Skinmed. 18(4)
Autor:
Joanna H, Tu, Joyce M C, Teng
Publikováno v:
Dermatologic therapy. 30(2)
The management of trichoepitheliomas is challenging, especially in children. This challenge is exemplified in patients with multiple trichoepitheliomas who present with progression of lesion count and size despite treatment with current strategies, i
Publikováno v:
Dermatologic therapy. 28(2)
Keratitis-ichthyosis-deafness (KID) syndrome is a rare hereditary cornification disorder resulting from mutations in connexin 26, a protein important for intercellular communication. In addition to the characteristic clinical triad of congenital bila
Autor:
Sherry M, Youssef, Joyce M C, Teng
Publikováno v:
Journal of drugs in dermatology : JDD. 11(7)
Lichen striatus (LS) is an uncommon linear dermatosis that is primarily seen in children from 4 months to 15 years of age. While some of these eruptions are asymptomatic, others can be quite pruritic. In darker-skinned individuals, post-inflammatory
Publikováno v:
Pediatric dermatology. 28(2)
Sclerodermatous graft-versus-host disease (sGVHD) is a rare, late complication of hematopoietic cell transplantation. Classified as a variant of chronic graft-versus-host disease, sGVHD is thought to be predominantly an immune-mediated response chara