Zobrazeno 1 - 10
of 104
pro vyhledávání: '"Michael D. Sussman"'
Autor:
Cathleen E, Buckon, Susan E, Sienko, Eileen G, Fowler, Anita M, Bagley, Loretta A, Staudt, Mitell, Sison-Williamson, Kent R, Heberer, Craig M, McDonald, Michael D, Sussman
Publikováno v:
Journal of Neuromuscular Diseases. 9:321-334
Background: Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder, that is characterized by progressive muscle degeneration and loss of ambulation between 7–13 years of age. Novel pharmacological agents targeting the genetic d
Publikováno v:
Journal of children's orthopaedics. 16(6)
Background: Orthopedic treatment of flexed-knee gait consists of hamstring lengthening along with surgery at other levels. Transfer of the semitendinosus (hamstring transfer) was introduced to avoid increase of anterior pelvic tilt as well as reduce
Autor:
Susan Sienko, Michael D. Sussman, Charles d’Amato, Cathleen E. Buckon, Coleman Hilton, Camila Bedeschi De Mattos
Publikováno v:
Journal of Children's Orthopaedics
Purpose Pharmacologic doses of corticosteroid (CS) have been shown to ameliorate the progression of Duchenne muscular dystrophy (DMD) preserving strength, pulmonary function and ambulation as well as reducing the incidence of scoliosis. However, ther
Autor:
Michael D. Sussman
Publikováno v:
The Journal of bone and joint surgery. American volume. 103(20)
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:
Loretta A. Staudt, Michael D. Sussman, Craig M. McDonald, Anita Bagley, Mitell Sison-Williamson, Eileen Fowler, Kent Heberer, Cathleen E. Buckon, Susan Sienko
Publikováno v:
Gaitposture. 90
Background In boys with DMD, muscle weakness progresses in a proximal to distal pattern, leading to compensatory gait strategies, including hyperlordosis and equinus, that increase energy cost and accelerate the loss of walking capacity. Research que
Autor:
Kent Heberer, Anita Bagley, Cathleen E. Buckon, Eileen Fowler, Michael D. Sussman, Loretta A. Staudt, Craig M. McDonald, Susan Sienko
Publikováno v:
Muscle & Nerve. 57:401-406
Introduction: Natural history studies for Duchenne muscular dystrophy (DMD) have not included measures of community ambulation. Methods: Step activity (SA) monitors quantified community ambulation in 42 boys with DMD (4-16 years) with serial enrollme
Autor:
Eileen G, Fowler, Loretta A, Staudt, Kent R, Heberer, Susan E, Sienko, Cathleen E, Buckon, Anita M, Bagley, Michael D, Sussman, Craig M, McDonald
Publikováno v:
Musclenerve. 57(3)
Natural history studies for Duchenne muscular dystrophy (DMD) have not included measures of community ambulation.Step activity (SA) monitors quantified community ambulation in 42 boys (ages 4-16 years) with DMD with serial enrollment up to 5 years by
Autor:
Eileen Fowler, Kent Heberer, Cathleen E. Buckon, Susan Sienko, Mitell Sison-Williamson, Michael D. Sussman, Anita Bagley, Craig M. McDonald, Loretta A. Staudt
Publikováno v:
Gaitposture. 48
Duchenne muscular dystrophy (DMD) is an X-linked genetic neuromuscular disorder characterized by progressive proximal to distal muscle weakness. The success of randomized clinical trials for novel therapeutics depends on outcome measurements that are