Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Christina Trout"'
Autor:
Aparna Ajjarapu, Shawna ME. Feely, Michael E. Shy, Christina Trout, Stephan Zuchner, Steven A. Moore, Katherine D. Mathews
Publikováno v:
Case Reports in Neurology, Pp 1-1 (2023)
Dominant mutations in serine palmitoyltransferase long chain base subunit 1 (SPTLC1), a known cause of hereditary sensory autonomic neuropathy type 1 (HSAN1), are a recently identified cause of juvenile amyotrophic lateral sclerosis (JALS) with slow
Externí odkaz:
https://doaj.org/article/3d0bf05c17e4433e9a51434f5dbe929e
Autor:
Jennifer G Andrews, Shree Pandya, Christina Trout, Treeva Jaff, Dennis Matthews, Christopher Cunniff, F John Meaney
Publikováno v:
SAGE Open Medicine, Vol 7 (2019)
Introduction: Information on use of palliative care services among individuals with Duchenne and Becker muscular dystrophy is scant despite the clearly documented need. Methods: We examined associations between uptake of palliative care services by 2
Externí odkaz:
https://doaj.org/article/cf26540a05d14ae1a11b5618c30533de
Autor:
Kristin M Conway, Katy Eichinger, Christina Trout, Paul A Romitti, Katherine D Mathews, Shree K Pandya
Publikováno v:
SAGE Open Medicine, Vol 7 (2019)
Purpose: To collect information about the needs of families affected by childhood-onset dystrophinopathies residing in the United States. Methods: Individuals with an eligible dystrophinopathy were identified by the Muscular Dystrophy Surveillance, T
Externí odkaz:
https://doaj.org/article/b0a981e0ed034b70b7ff3f82e9adfcb3
Autor:
James Poysky, Melissa Gibbons, Janet Hoskin, Norbert J. Weidner, Kathi Kinnett, Mary K. Colvin, Christina Trout, Mario Damiani, Scott Moreland
Publikováno v:
Pediatrics. 142:S99-S109
In this article, we outline a comprehensive plan for the psychosocial management of patients with Duchenne muscular dystrophy (DMD) across the life span. In 2010, the Centers for Disease Control and Prevention sponsored the development of multidiscip
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33c19f467d830f524b3fe446dc494a87
https://doi.org/10.1542/peds.2018-0333l
https://doi.org/10.1542/peds.2018-0333l
Autor:
Garey Noritz, David J. Birnkrant, Angela Blackwell, James Naprawa, Leanne M Ward, Christina Trout, Katharine Bushby, Annie Kennedy, Susan D. Apkon, David R. Weber, Linda H. Cripe, James Poysky, Mary K. Colvin, Kathi Kinnett, Carla M. Bann, Natalie Street, Adrienne R. Herron
Publikováno v:
The Lancet Neurology. 17:445-455
Summary Improvements in the function, quality of life, and longevity of patients with Duchenne muscular dystrophy (DMD) have been achieved through a multidisciplinary approach to management across a range of health-care specialties. In part 3 of this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b8871b503a2be76e687e0c5589b1ae2
https://doi.org/10.1016/s1474-4422(18)30026-7
https://doi.org/10.1016/s1474-4422(18)30026-7
Autor:
Marie Ritzo, Alexandra McArthur, Kathryn R. Wagner, Annie Kennedy, Laura E. Case, Garey Noritz, Christina Trout, Elizabeth Vroom, Paula R. Clemens
Publikováno v:
Pediatrics. 142(Suppl 2)
The care of individuals with Duchenne muscular dystrophy (DMD) now extends into adulthood. Childhood to adulthood transition planning is an important aspect of care, affecting health outcomes as well as other important aspects of adult life. In this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bfa1e64847ad6f84f9bca9c207d7f1b
https://pubmed.ncbi.nlm.nih.gov/30275255
https://pubmed.ncbi.nlm.nih.gov/30275255
Autor:
Christina Westfield, Jennifer Andrews, Deborah J. Fox, Katherine D. Mathews, Emma Ciafaloni, Christopher Cunniff, Dennis J. Matthews, Shree Pandya, Kristin M Conway, Christina Trout, F. John Meaney
Publikováno v:
Pediatrics. 142(1)
BACKGROUND: Duchenne muscular dystrophy (DMD) is an X-linked disorder characterized by progressive muscle weakness and multisystem involvement. Recent advances in management of individuals with DMD have prolonged survival. Lack of standardized care s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28eb6668c992873d0976d9f044b00704
https://pubmed.ncbi.nlm.nih.gov/29925575
https://pubmed.ncbi.nlm.nih.gov/29925575
Publikováno v:
PLoS Currents.
Introduction Care Considerations supported by the Centers for Disease Control and Prevention for the management of Duchenne muscular dystrophy were published in 2010, but there has been limited study of implementation in the United States. Methods A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4e1df6ebaff6fb374ed2beffecc97a47
https://doi.org/10.1371/currents.md.5f533e6e60ee172d6bf6b2b8375dfadf
https://doi.org/10.1371/currents.md.5f533e6e60ee172d6bf6b2b8375dfadf
Autor:
Ying Zhang, Pangaja Paramsothy, Paul A. Romitti, Kristin Caspers Conway, Joyce Oleszek, Christina Trout, Katherine D. Mathews
Publikováno v:
Journal of Developmental & Behavioral Pediatrics. 36:455-463
Objective To describe the occurrence of selected neurobehavioral concerns among males with a dystrophinopathy and to explore the associations with corticosteroid or supportive device use. Methods Medical record abstraction of neurobehavioral concerns
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0545680e8a99564d5bf54556e9fe978
https://doi.org/10.1097/dbp.0000000000000177
https://doi.org/10.1097/dbp.0000000000000177
Autor:
Treeva A. Jaff, Jennifer Andrews, Dennis J. Matthews, F. John Meaney, Christina Trout, Christopher Cunniff, Shree Pandya
Publikováno v:
SAGE Open Medicine
SAGE Open Medicine, Vol 7 (2019)
SAGE Open Medicine, Vol 7 (2019)
Introduction: Information on use of palliative care services among individuals with Duchenne and Becker muscular dystrophy is scant despite the clearly documented need. Methods: We examined associations between uptake of palliative care services by 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3671d3cebb74f0af0c8315b031ca3aa9
https://doi.org/10.1177/2050312119840518
https://doi.org/10.1177/2050312119840518