Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sheryl Osborne"'
Autor:
Waldy San Sebastian, Adrian P Kells, John Bringas, Lluis Samaranch, Piotr Hadaczek, Agnieszka Ciesielska, Michael J Macayan, Phillip J Pivirotto, John Forsayeth, Sheryl Osborne, J Fraser Wright, Foad Green, Gregory Heller, Krystof S Bankiewicz
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 1, Iss C (2014)
Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare, autosomal-recessive neurological disorder caused by mutations in the DDC gene that leads to an inability to synthesize catecholamines and serotonin. As a result, patients suffer comprom
Externí odkaz:
https://doaj.org/article/6808879212064f8090e19ab0d9b2d62a
Autor:
Robert H. Baloh, J. Patrick Johnson, Pablo Avalos, Peggy Allred, Soshana Svendsen, Genevieve Gowing, Kristina Roxas, Amanda Wu, Becky Donahue, Sheryl Osborne, George Lawless, Brandon Shelley, Koral Wheeler, Carolyn Prina, Dana Fine, Tami Kendra-Romito, Haniah Stokes, Vicki Manoukian, Abirami Muthukumaran, Leslie Garcia, Maria G. Bañuelos, Marlesa Godoy, Catherine Bresee, Hong Yu, Doniel Drazin, Lindsey Ross, Robert Naruse, Harish Babu, Eric A. Macklin, Ashley Vo, Ashraf Elsayegh, Warren Tourtellotte, Marcel Maya, Matthew Burford, Frank Diaz, Chirag G. Patil, Richard A. Lewis, Clive N. Svendsen
Publikováno v:
Nature Medicine. 28:1813-1822
Amyotrophic lateral sclerosis (ALS) involves progressive motor neuron loss, leading to paralysis and death typically within 3–5 years of diagnosis. Dysfunctional astrocytes may contribute to disease and glial cell line-derived neurotrophic factor (
Autor:
John Forsayeth, Lluis Samaranch, Gregory Heller, Piotr Hadaczek, Waldy San Sebastian, Sheryl Osborne, J. Fraser Wright, Adrian P. Kells, John Bringas, Agnieszka Ciesielska, Michael Macayan, Foad Green, Phillip Pivirotto, Krystof S. Bankiewicz
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 1, Iss C (2014)
San Sebastian, W; Kells, AP; Bringas, J; Samaranch, L; Hadaczek, P; Ciesielska, A; et al.(2014). Safety and tolerability of MRI-guided infusion of AAV2-hAADC into the mid-brain of nonhuman primate. MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT, 1. doi: 10.1038/mtm.2014.49. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/6d30b5xg
Molecular Therapy. Methods & Clinical Development
San Sebastian, W; Kells, AP; Bringas, J; Samaranch, L; Hadaczek, P; Ciesielska, A; et al.(2014). Safety and tolerability of MRI-guided infusion of AAV2-hAADC into the mid-brain of nonhuman primate. MOLECULAR THERAPY-METHODS & CLINICAL DEVELOPMENT, 1. doi: 10.1038/mtm.2014.49. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/6d30b5xg
Molecular Therapy. Methods & Clinical Development
Aromatic L-amino acid decarboxylase (AADC) deficiency is a rare, autosomal-recessive neurological disorder caused by mutations in the DDC gene that leads to an inability to synthesize catecholamines and serotonin. As a result, patients suffer comprom