Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jennifer M Chan"'
Autor:
Amy Weisman, Jennifer M. Chan, Chantal LaPointe, Kaye Sjoholm, Kristy Steinau, Kaycie Artus, Suci Widhiati, Rebecca Bodan, Michelle Wood, Julio C. Salas-Alanis, Anna Carolina Rocha, Beata Faitli, Phuong Khuu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Abstract Epidermolysis bullosa (EB) is characterized by skin fragility with blister formation occurring spontaneously or following minor trauma such as gentle pressure or friction. Current physiotherapy practice is based on anecdotal care, clinical e
Externí odkaz:
https://doaj.org/article/fa85efbd09ba491e9eefff01bce21607
Autor:
Jennifer M. Chan, Amy Weisman, Alex King, Susan Maksomski, Carrissa Shotwell, Claire Bailie, Helen Weaver, Rebecca Bodan, Estrella Guerrero, Matija Zmazek, Phuong Khuu
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-12 (2019)
Abstract The purpose of this article is to summarize the Dystrophic Epidermolysis Bullosa Research Association (DEBRA) International evidence-based Clinical Practice Guidelines (CPGs) for the provision of occupational therapy (OT) for children and ad
Externí odkaz:
https://doaj.org/article/e6a857f5ccbc4784b70a8accaa1f0ed3
Autor:
Beata Faitli, Julio C. Salas-Alanis, Michelle Wood, Jennifer M Chan, Amy Weisman, Chantal LaPointe, Kristy Steinau, Rebecca Cross Bodán, Anna Carolina Rocha, Phuong Khuu, Kaycie Artus, Kaye Sjoholm, Suci Widhiati
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-11 (2021)
Epidermolysis bullosa (EB) is characterized by skin fragility with blister formation occurring spontaneously or following minor trauma such as gentle pressure or friction. Current physiotherapy practice is based on anecdotal care, clinical expertise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f887fdbc465373fc60f60e0b9cfa496f
https://doi.org/10.1186/s13023-021-01997-w
https://doi.org/10.1186/s13023-021-01997-w
Background: Epidermolysis bullosa is a rare genetic skin disorder with four main types. One of the most debilitating subtypes is recessive dystrophic epidermolysis bullosa (RDEB). Patients experience frequent blister formation that occurs spontaneous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fbfa66b31ae3db4df6977080236527d2
https://doi.org/10.21203/rs.3.rs-41738/v1
https://doi.org/10.21203/rs.3.rs-41738/v1
Autor:
Joshua M. Abzug, Allison Allgier, Sarah Ashworth, Jamie Berggren, Matthew B. Burn, Alexandria L. Case, Jennifer M. Chan, Roger Cornwall, Jenny M. Dorich, Reeti R. Douglas, Kelly Anne Ferry, Theodore J. Ganley, Richard Gardner, Ritu Goel, Donald Goldsmith, Namrata Grampurohit, Elliot Greenberg, Christine A. Ho, Danielle A. Hogarth, Deborah Humpl, Gina Kim, Scott H. Kozin, Ryan Krochak, Amy L. Ladd, Amy Lake, Carolyn M. Levis, Kevin J. Little, Erin Meisel, Michelle Hsia, M.J. Mulcahey, Rebecca Neiduski, Scott Oishi, Heta Parikh, Meagan Pehnke, Nicholas Pulos, Lydia D. Rawlins, Roberta Ciocco, Daniel W. Safford, Sandra Schmieg, Apurva S. Shah, Francisco Soldado, Milan Stevanovic, Tami Konieczny, Kathleen Tate, Daniel Waltho, Heather Weesner, Aviva Wolff, Cheryl Zalieckas, Dan A. Zlotolow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9cdb480f5bcd6b437f5d349ff716720
https://doi.org/10.1016/b978-0-323-53091-0.01002-2
https://doi.org/10.1016/b978-0-323-53091-0.01002-2
Polydactyly, defined by the presence of greater than five digits on one limb, is one of the most common congenital anomalies treated by pediatric specialists. It can be defined by the location of the duplicated digits into preaxial (i.e., radial), po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ada7428a7c645981800c6c725dc8606c
https://doi.org/10.1016/b978-0-323-53091-0.00008-7
https://doi.org/10.1016/b978-0-323-53091-0.00008-7
Autor:
Jennifer M. Chan
Publikováno v:
The Journal of Hand Surgery. 37:1953-1954
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac58ff8e4e6679e937a956cbbb60e561
https://doi.org/10.1016/j.jhsa.2012.04.004
https://doi.org/10.1016/j.jhsa.2012.04.004