Search Results - "Foust, K.D"

Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy by Mendell, Jerry R., Al-Zaidy, Samiah, Shell, Richard, Arnold, W. Dave, Rodino-Klapac, Louise R., Prior, Thomas W., Lowes, Linda, Alfano, Lindsay, Berry, Katherine, Church, Kathleen, Kissel, John T., Nagendran, Sukumar, L’Italien, James, Sproule, Douglas M., Wells, Courtney, Cardenas, Jessica A., Heitzer, Marjet D., Kaspar, Allan, Corcoran, Sarah, Braun, Lyndsey, Likhite, Shibi, Miranda, Carlos, Meyer, Kathrin, Foust, K.D., Burghes, Arthur H.M., Kaspar, Brian K.

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AVXS-101 Phase 1 gene therapy clinical trial in SMA Type 1: Interim data demonstrates improvements in supportive care use by Shell, Richard, Al-Zaidy, Samiah, Arnold, W. Dave, Rodino-Klapac, Louise, Prior, Thomas W, Lowes, Linda, Alfano, Lindsay, Berry, Katherine, Church, Kathleen, Kissel, John T, Nagendran, Sukumar, L'Italien, James, Sproule, Douglas M, Burghes, Arthur H.M, Foust, K.D, Meyer, Kathrin, Likhite, Shibi, Kaspar, Brian K, Mendell, Jerry R

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AVXS-101 Phase 1 gene therapy clinical trial in SMA Type 1: Event free survival and achievement of developmental milestones by Mendell, Jerry R, Al-Zaidy, Samiah, Shell, Richard, Arnold, W. David, Rodino-Klapac, Louise, Prior, Thomas W, Lowes, Linda, Alfano, Lindsay, Berry, Katherine, Church, Kathleen, Kissel, John T, Nagendran, Sukumar, L'Italien, James, Sproule, Douglas M, Cardenas, Jessica, Burghes, Arthur H.M, Foust, K.D, Meyer, Kathrin, Likhite, Shibi, Kaspar, Brian K

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Single-Dose Gene-Replacement Therapy for Spinal Muscular Atrophy by Mendell, Jerry R, Al-Zaidy, Samiah, Shell, Richard, Arnold, W. Dave, Rodino-Klapac, Louise R, Prior, Thomas W, Lowes, Linda, Alfano, Lindsay, Berry, Katherine, Church, Kathleen, Kissel, John T, Nagendran, Sukumar, L’Italien, James, Sproule, Douglas M, Wells, Courtney, Cardenas, Jessica A, Heitzer, Marjet D, Kaspar, Allan, Corcoran, Sarah, Braun, Lyndsey, Likhite, Shibi, Miranda, Carlos, Meyer, Kathrin, Foust, K.D, Burghes, Arthur H.M, Kaspar, Brian K

“…Fifteen children with spinal muscular atrophy type 1 received gene-replacement therapy with a single dose of adeno-associated virus containing SMN. In marked…”
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Intravascular AAV9 preferentially targets neonatal neurons and adult astrocytes by Foust, K.D

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Gene delivery to the spinal cord using MRI-guided focused ultrasound by Weber-Adrian, D, Thévenot, E, O'Reilly, M A, Oakden, W, Akens, M K, Ellens, N, Markham-Coultes, K, Burgess, A, Finkelstein, J, Yee, A J M, Whyne, C M, Foust, K D, Kaspar, B K, Stanisz, G J, Chopra, R, Hynynen, K, Aubert, I

“…Non-invasive gene delivery across the blood–spinal cord barrier (BSCB) remains a challenge for treatment of spinal cord injury and disease. Here, we…”
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