Zobrazeno 1 - 10
of 79
pro vyhledávání: '"David J. Birnkrant"'
Publikováno v:
Pediatric Pulmonology. 58:1627-1630
Autor:
David J Birnkrant, John C Carter
Publikováno v:
Thorax. 77(8)
Autor:
David J. Birnkrant, John C Carter
Publikováno v:
Pediatric Pulmonology. 56:738-746
Neuromuscular respiratory medicine has traditionally focused on assisted lung ventilation and mucus clearance. These therapies have prolonged survival for patients with Duchenne muscular dystrophy (DMD). However, the field is rapidly evolving in a ne
Autor:
David J Birnkrant, Luca Bello, Russell J Butterfield, John C Carter, Linda H Cripe, Timothy P Cripe, Douglas A McKim, Deipanjan Nandi, Elena Pegoraro
The life-limiting complications of Duchenne muscular dystrophy (DMD) include loss of lung function and progressive cardiomyopathy; when patients are treated with assisted ventilation, cardiac function becomes the main determinant of survival. Therapy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08d27844351eab3027c85b1ae310dfc5
http://hdl.handle.net/11577/3443641
http://hdl.handle.net/11577/3443641
Autor:
David J. Birnkrant, Jane B. Black
Publikováno v:
Pediatric Pulmonology. 55:2542-2546
Neuromuscular cardiopulmonary medicine is entering a new and exciting phase, with studies that assess the respiratory effect of emerging genetic and molecular therapies. In this year's neuromuscular Year in Review, we focus on Duchenne muscular dystr
Autor:
Jonathan D. Finder, John T. Kissel, Hemant Sawnani, David J. Birnkrant, Michelle Eagle, Lisa F. Wolfe, Michael D. Sussman, Daniel W. Sheehan, Richard M. Kravitz, Joshua O. Benditt, Richard Shell
Publikováno v:
Pediatrics. 142:S62-S71
In 2010, Care Considerations for Duchenne Muscular Dystrophy, sponsored by the Centers for Disease Control and Prevention, was published in Lancet Neurology, and in 2018, these guidelines were updated. Since the publication of the first set of guidel
Autor:
Norbert J. Weidner, Susan D. Apkon, David J. Birnkrant, Michael D. Sussman, Ben Alman, William G. Mackenzie, Robert D. Fitch, Robert K. Lark
Publikováno v:
Pediatrics. 142:S82-S89
Orthopedic care is an important aspect of the overall management of patients with Duchenne muscular dystrophy (DMD). In addition to progressive muscle weakness and loss of function, patients may develop joint contractures, scoliosis, and osteoporosis
Autor:
David J. Birnkrant, Leanne M Ward
Publikováno v:
Pediatrics. 142:S1-S4
* Abbreviation: DMD — : Duchenne muscular dystrophy In 2010, Bushby et al1,2 published the first-ever international comprehensive guidance on the diagnosis and management of patients with Duchenne muscular dystrophy (DMD) for practitioners. These r
Publikováno v:
J Clin Sleep Med
STUDY OBJECTIVES: Due to a limited number of pediatric sleep centers, the aim was to test the feasibility of ambulatory polysomnography (PSG-home) in a group of French children suspected of OSA. METHODS: Children undergoing one-night PSG-home, with t
Publikováno v:
Clinics in Chest Medicine. 39:377-389
Muscular dystrophies represent a complex, varied, and important subset of neuromuscular disorders likely to require the care of a pulmonologist. The spectrum of conditions encapsulated by this subset ranges from severe and fatal congenital muscular d