Search Results - "Staudt, Loretta"

Selective voluntary motor control influences knee joint torque, work and power in children with spastic cerebral palsy by Fowler, Eileen G., Vuong, Andy, Staudt, Loretta A., Greenberg, Marcia B., Mesler, Sophia A., Chen, Keren, Stearns-Reider, Kristen M.

“…Children with spastic cerebral palsy (CP) have damage to the corticospinal tracts that are responsible for selective motor control (SMC). Force, velocity and…”
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Selective Control Assessment of the Lower Extremity (SCALE): development, validation, and interrater reliability of a clinical tool for patients with cerebral palsy by FOWLER, EILEEN G, STAUDT, LORETTA A, GREENBERG, MARCIA B, OPPENHEIM, WILLIAM L

“…Normal selective voluntary motor control (SVMC) can be defined as the ability to perform isolated joint movement without using mass flexor/extensor patterns or…”
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Lower‐extremity selective voluntary motor control in patients with spastic cerebral palsy: increased distal motor impairment by FOWLER, EILEEN G, STAUDT, LORETTA A, GREENBERG, MARCIA B

“…Aim  Multiple impairments contribute to motor deficits in spastic cerebral palsy (CP). Selective voluntary motor control (SVMC), namely isolation of joint…”
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Longitudinal community walking activity in Duchenne muscular dystrophy by Fowler, Eileen G., Staudt, Loretta A., Heberer, Kent R., Sienko, Susan E., Buckon, Cathleen E., Bagley, Anita M., Sussman, Michael D., McDonald, Craig M.

“…ABSTRACT Introduction Natural history studies for Duchenne muscular dystrophy (DMD) have not included measures of community ambulation. Methods Step activity…”
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Expression of SRP-9001 dystrophin and stabilization of motor function up to 2 years post-treatment with delandistrogene moxeparvovec gene therapy in individuals with Duchenne muscular dystrophy by Mendell, Jerry R, Shieh, Perry B, McDonald, Craig M, Sahenk, Zarife, Lehman, Kelly J, Lowes, Linda P, Reash, Natalie F, Iammarino, Megan A, Alfano, Lindsay N, Sabo, Brenna, Woods, Jeremy D, Skura, Christy L, Mao, Howard C, Staudt, Loretta A, Griffin, Danielle A, Lewis, Sarah, Wang, Shufang, Potter, Rachael A, Singh, Teji, Rodino-Klapac, Louise R

“…Delandistrogene moxeparvovec (SRP-9001) is an investigational gene transfer therapy designed for targeted expression of SRP-9001 dystrophin protein, a…”
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Brain Metabolism During A Lower Extremity Voluntary Movement Task in Children With Spastic Cerebral Palsy by Fowler, Eileen G, Oppenheim, William L, Greenberg, Marcia B, Staudt, Loretta A, Joshi, Shantanu H, Silverman, Daniel H S

“…Reduced selective voluntary motor control (SVMC) is a primary impairment due to corticospinal tract (CST) injury in spastic cerebral palsy (CP). There are few…”
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Functional outcome measures in young, steroid-naïve boys with Duchenne muscular dystrophy by Mayhew, Anna G, Moat, Dionne, McDermott, Michael P., Eagle, Michelle, Griggs, Robert C., King, Wendy M., James, Meredith K., Muni-Lofra, Robert, Shillington, Alison, Gregson, Sarah, Pallant, Lindsey, Skura, Christy, Staudt, Loretta A., Eichinger, Katy, McMurchie, Heather, Rabb, Rosanna, Di Marco, Marina, Brown, Sarah, Zanin, Riccardo, Arnoldi, Maria Teresa, McIntyre, Melissa, Wilson, Amelia, Alfano, Lindsay N., Lowes, Linda P., Blomgren, Colleen, Milev, Evelin, Iodice, Mario, Pasternak, Amy, Chiu, Angela, Lehnert, Ilka, Claus, Nicole, Dieruf, Kathy A., Rolle, Enrica, Nicorici, Alina, Andres, Barbara, Hobbiebrunken, Elke, Roetmann, Gerda, Kern, Victoria, Civitello, Matthew, Vogt, Sibylle, Hayes, Melissa J., Scholtes, Cheryl, Lacroix, Catherine, Gunn, Tara, Warner, Sinead, Newman, Jennifer, Barp, Andrea, Kundrat, Katherine, Kovelman, Staci, Powers, Penny J., Guglieri, Michela

“…•Physiotherapy assessments, including FVC test, are reliable in a young DMD population (4–7 years of age); this is true if there is 30 days or more than 30…”
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A Longitudinal Study of Quantitative Muscle Strength and Functional Motor Ability in Ambulatory Boys with Duchenne Muscular Dystrophy by Buckon, Cathleen E, Sienko, Susan E, Fowler, Eileen G, Bagley, Anita M, Staudt, Loretta A, Sison-Williamson, Mitell, Heberer, Kent R, McDonald, Craig M, Sussman, Michael D

“…Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder, that is characterized by progressive muscle degeneration and loss of ambulation…”
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Are we being too ‘selective’ about motor control? by Fowler, Eileen, Staudt, Loretta

“…This commentary is on the review by Cahill‐Rowley and Rose on pages 522–528 of this issue…”
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Commentary on “Parent-Reported PEDI-CAT Mobility and Gross Motor Function in Infants With Cerebral Palsy” by Sargent, Barbara, Staudt, Loretta, Garg, Lindsey

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Commentary on “The Head Control Scale: Responsiveness and Concurrent Validity With the Alberta Infant Motor Scale” by Sargent, Barbara, Chang, Tracy Y., Staudt, Loretta

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Kinematic changes in gait in boys with Duchenne Muscular Dystrophy: Utility of the Gait Deviation Index, the Gait Profile Score and the Gait Variable Scores by Sienko, Susan, Buckon, Cathleen, Bagley, Anita, Fowler, Eileen, Heberer, Kent, Staudt, Loretta, Sison-Williamson, Mitell, McDonald, Craig, Sussman, Michael

“…Duchenne Muscular Dystrophy (DMD) is an X-linked muscle disorder caused by a mutation or deletion in the dystrophin gene. In boys with DMD, muscle weakness…”
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A Phase 2 Clinical Trial Evaluating the Safety and Efficacy of Delandistrogene Moxeparvovec (SRP-9001) in Patients with Duchenne Muscular Dystrophy (DMD) (S48.004) by Mendell, Jerry, Shieh, Perry, Sahenk, Zarife, Lehman, Kelly, Lowes, Linda, Reash, Natalie, Iammarino, Megan, Alfano, Lindsay, Sabo, Brenna, Woods, Jeremy, Skura, Christy, Mao, Howard, Staudt, Loretta, Potter, Rachael, Griffin, Danielle, Lewis, Sarah, Wang, Shufang, Singh, Tejdip, Rodino-Klapac, Louise

“…Abstract only…”
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Longitudinal changes in energy cost during walking in boys with Duchenne Muscular Dystrophy (DMD) by Sienko, Susan, Buckon, Cathleen E., Bagley, Anita, Staudt, Loretta, Fowler, Eileen, Heberer, Kent, Sison-Williamson, Mitell, McDonald, Craig, Sussman, Michael D.

“…•Boys with DMD have a decrease in velocity and an increase in energy cost with age.•NNcost and SMC-EC are less sensitive to changes in age over time than gross…”
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A Multicenter Randomized, Double-Blind, Placebo-Controlled, Gene-Delivery Clinical Trial of rAAVrh74.MHCK7.micro-dystrophin for Duchenne Muscular Dystrophy (4478) by Mendell, Jerry, Shieh, Perry, Sahenk, Zarife, Lehman, Kelly, Lowes, Linda, Miller, Natalie, Iammarino, Megan, Alfano, Lindsay, Woods, Jeremy, Skura, Christy, Mao, Howard, Staudt, Loretta, Potter, Rachael, Griffin, Danielle, Lewis, Sarah, Hu, Larry, Upadhyay, Sameer, Singh, Teji, Rodino-Klapac, Louise

“…Abstract only…”
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A Phase 2 Clinical Trial Evaluating the Safety and Efficacy of SRP-9001 for Treating Patients with Duchenne Muscular Dystrophy (S23.002) by Mendell, Jerry R., Shieh, Perry B., Sahenk, Zarife, Lehman, Kelly J., Lowes, Linda P., Reash, Natalie F., Iammarino, Megan A., Alfano, Lindsay N., Powers, Brenna, Woods, Jeremy D., Skura, Christy L., Mao, Howard C., Staudt, Loretta A., Potter, Rachael A., Griffin, Danielle A., Lewis, Sarah, Hu, Larry, Upadhyay, Sameer, Singh, Teji, Rodino-Klapac, Louise R.

“…Abstract only…”
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eP201: A phase 2 clinical trial evaluating the safety and efficacy of delandistrogene moxeparvovec for treating patients with Duchenne muscular dystrophy by O'Rourke, Erin, Mendell, Jerry, Shieh, Perry, Sahenk, Zarife, Lehman, Kelly, Lowes, Linda, Reash, Natalie, Iammarino, Megan, Alfano, Lindsay, Powers, Brenna, Woods, Jeremy, Skura, Christy, Mao, Howard, Staudt, Loretta, Potter, Rachael, Griffin, Danielle, Lewis, Sarah, Upadhyay, Sameer, Singh, Teji, Rodino-Klapac, Louise

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Hip kinetics during gait are clinically meaningful outcomes in young boys with Duchenne muscular dystrophy by Heberer, Kent, Fowler, Eileen, Staudt, Loretta, Sienko, Susan, Buckon, Cathleen E, Bagley, Anita, Sison-Williamson, Mitell, McDonald, Craig M, Sussman, Michael D

“…Highlights • This was the first natural history study of gait biomechanics in boys with DMD. • Peak hip moments and powers were inadequate in young boys with…”
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Spasticity in cerebral palsy and the selective posterior rhizotomy procedure by Peacock, W J, Staudt, L A

“…A review of the selective posterior rhizotomy procedure for reduction of spasticity in cerebral palsy is presented. The history of the procedure, selection of…”
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Can Quantitative Muscle Strength and Functional Motor Ability Differentiate the Influence of Age and Corticosteroids in Ambulatory Boys with Duchenne Muscular Dystrophy? by Buckon, Cathleen, Sienko, Susan, Bagley, Anita, Sison-Williamson, Mitell, Fowler, Eileen, Staudt, Loretta, Heberer, Kent, McDonald, Craig M, Sussman, Michael

“…In the absence of a curative treatment for Duchenne Muscular Dystrophy (DMD), corticosteroid therapy (prednisone, deflazacort) has been adopted as the standard…”
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