Pedro Gonzalez-Alegre, M.D.
Affiliations: | University of Iowa, Iowa City, IA |
Google:
"Pedro Gonzalez-Alegre"Mean distance: 26716.5 (cluster 6)
Children
Sign in to add trainee| Adam Iliff | research assistant | 2006-2007 | University of Iowa |
| Kara L. Gordon | grad student | 2011 | University of Iowa |
| Ginny M. Harris | grad student | 2011 | University of Iowa |
| Janine N. Martin | grad student | 2011 | University of Iowa |
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Robbins NM, Ozmore JR, Winder TL, et al. (2020) A Novel SPAST/SPG4 Splice-Site Variant in a Family with Dominant Hereditary Spastic Paraplegia. Case Reports in Neurological Medicine. 2020: 7219514 |
| Gonzalez-Alegre P, Beauvais G, Martin J, et al. (2019) A novel transgenic mouse model to investigate the cell-autonomous effects of torsinA(ΔE) expression in striatal output neurons. Neuroscience |
| Hitti FL, Yang AI, Gonzalez-Alegre P, et al. (2019) Human gene therapy approaches for the treatment of Parkinson's disease: An overview of current and completed clinical trials. Parkinsonism & Related Disorders |
| Gonzalez-Alegre P. (2019) Advances in molecular and cell biology of dystonia: Focus on torsinA. Neurobiology of Disease. 127: 233-241 |
| Maguire JA, Gagne AL, Gonzalez-Alegre P, et al. (2018) Generation of Spinocerebellar Ataxia Type 2 induced pluripotent stem cell lines, CHOPi002-A and CHOPi003-A, from patients with abnormal CAG repeats in the coding region of the ATXN2 gene. Stem Cell Research. 34: 101361 |
| Beauvais G, Watson JL, Aguirre JA, et al. (2018) Efficient RNA interference-based knockdown of mutant torsinA reveals reversibility of PERK-eIF2α pathway dysregulation in DYT1 transgenic rats in vivo. Brain Research |
| Hitti FL, Gonzalez-Alegre P, Lucas TH. (2018) Gene Therapy for Neurological Disease: A Neurosurgical Review. World Neurosurgery |
| Zakirova Z, Fanutza T, Bonet J, et al. (2018) Mutations in THAP1/DYT6 reveal that diverse dystonia genes disrupt similar neuronal pathways and functions. Plos Genetics. 14: e1007169 |
| Mendizabal A, Ngo Vu AT, Thibault D, et al. (2017) Hospitalizations of Children with Huntington's Disease in the United States. Movement Disorders Clinical Practice. 4: 682-688 |
| Beauvais G, Rodriguez-Losada N, Ying L, et al. (2017) Exploring the Interaction Between eIF2α Dysregulation, Acute Endoplasmic Reticulum Stress and DYT1 Dystonia in the Mammalian Brain. Neuroscience |