Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Ann Schwentker"'
Autor:
Dorothy M. Supp, Jennifer M. Hahn, Kelly A. Combs, Kevin L. McFarland, Ann Schwentker, Raymond E. Boissy, Steven T. Boyce, Heather M. Powell, Anne W. Lucky
Publikováno v:
Cell Transplantation, Vol 28 (2019)
The blistering disease recessive dystrophic epidermolysis bullosa (RDEB) is caused by mutations in the gene encoding collagen VII (COL7), which forms anchoring fibrils that attach the epidermis to the dermis. Cutaneous gene therapy to restore COL7 ex
Externí odkaz:
https://doaj.org/article/abcfe7ae4538485ab5c75f5e748d3f6a
Autor:
Priya D. Bolikal, Katrina Peariso, Marissa Vawter-Lee, Benjamin T. Kerrey, Mary Frey, Joshua K. Schaffzin, Ronine Zamor, Ann Schwentker, William T. O’Brien
Publikováno v:
Journal of Child Neurology. 36:421-431
Acute flaccid myelitis is an emerging neurologic disease, first described in 2014 and predominantly affecting young children. Acute flaccid myelitis cases tend to spike every 2 years, in the late summer to fall, and the next peak is expected in 2020.
Autor:
Heather M. Powell, Raymond E. Boissy, Steven T. Boyce, Kelly A. Combs, Ann Schwentker, Anne W. Lucky, Kevin L. McFarland, Dorothy M. Supp, Jennifer M. Hahn
Publikováno v:
Cell Transplantation
Cell Transplantation, Vol 28 (2019)
Cell Transplantation, Vol 28 (2019)
The blistering disease recessive dystrophic epidermolysis bullosa (RDEB) is caused by mutations in the gene encoding collagen VII (COL7), which forms anchoring fibrils that attach the epidermis to the dermis. Cutaneous gene therapy to restore COL7 ex
Autor:
Ann Schwentker
Publikováno v:
The Journal of bone and joint surgery. American volume. 103(8)
Autor:
Amanda M. Rusk, Anne W. Lucky, Jens Goebel, Anita P. Sheth, Ann Schwentker, Marc G. Schecter, Anita Gupta, Meghan M. Crute
Publikováno v:
Pediatric dermatologyREFERENCES. 37(6)
Trichodysplasia spinulosa is a rare disorder caused by the ubiquitous trichodysplasia spinulosa-associated polyomavirus (TSPyV) and characterized clinically by predominately centrofacial, but often generalized, folliculocentric papules with protubera
Publikováno v:
Pediatric dermatologyREFERENCES. 37(1)
Porokeratosis ptychotropica is an unusual variant of porokeratosis characterized by papules and plaques located on the buttocks and gluteal cleft and showing multiple coronoid lamellae on histology. In this case report, we present the longitudinal cl
Publikováno v:
Journal of Pediatric Genetics. :189-197
Microtia is a genetic condition affecting the external ears and presents clinically along a wide spectrum: minimally affected ears are small with minor shape abnormalities; extremely affected ears lack all identifiable structures, with the most extre
Publikováno v:
Plastic and Reconstructive Surgery Global Open
Plastic and Reconstructive Surgery, Global Open, Vol 5, Iss 11, p e1547 (2017)
Plastic and Reconstructive Surgery, Global Open, Vol 5, Iss 11, p e1547 (2017)
Background:. Hypertrophic scar formation is unpredictable and poorly understood, afflicting both the pediatric and adult populations. Treatment methods with conservative and invasive approaches have low rates of compliance and high rates of morbidity
Autor:
Darlene M. Sparkman, Christopher J. van Belle, Anthony T. Vu, Ann Schwentker, Kevin P. Yakuboff
Publikováno v:
The Journal of hand surgery. 43(5)
Purpose Brachial plexus birth injuries with multiple nerve root avulsions present a particularly difficult reconstructive challenge because of the limited availability of donor nerves. The contralateral C7 has been described for brachial plexus recon
Publikováno v:
Plastic and Reconstructive Surgery. 123:939-948
Background: The authors previously showed that neurolysis in obstetrical brachial plexus palsy resulted in improved function in some patients at 1 year's follow-up. In this study, the hypothesis that the long-term outcome of neuroma-in-continuity res