Zobrazeno 1 - 10
of 379
pro vyhledávání: '"Factor, SA"'
Autor:
Ciarochi, JA, Liu, J, Calhoun, V, Johnson, H, Misiura, M, Bockholt, HJ, Espinoza, FA, Caprihan, A, Plis, S, Turner, JA, Paulsen, JS, Long, JD, Johnson, HJ, Brashers-Krug, T, Danzer, P, Miller, A, Montross, K, Harrington, D, Westervelt, H, Aylward, E, Rao, S, Moser, DJ, Williams, J, Downing, N, Magnotta, VA, Vaidya, J, O Leary, D, Kim, EY, Kim, JI, Lourens, S, Zhang, Y, Lu, W, Erwin, C, Nance, M, Evans, J, Zschiegner, R, Chiu, E, Loi, S, Chua, P, Raymond, L, Ross, CA, Mallonee, WM, Samii, A, Jones, R, Barker, RA, McCusker, E, Loy, C, Orth, M, Süßmuth, S, Quaid, K, Guttman, M, Perlman, S, Geschwind, MD, Sha, S, Warner, T, Rosser, A, Marshall, F, Panegyres, P, Lee, J, Perlmutter, J, Miedzybrodzka, Z, Craufurd, D, Mazzoni, P, Marder, K, Kumar, R, Wheelock, V, Martin, W, Suchowersky, O, Ahmed, A, De Soriano, I, Shadrick, C, Preston, J, Goh, A, Antonopoulos, S, Komiti, A, Decolongon, J, Fan, M, Coleman, A, Varvaris, M, Ong, M, Yoritomo, N, Suter, G, Freney, EP, Macaraeg, A, Wood-Siverio, C, Factor, SA, Mason, S, Guzman, NV, Griffith, J, McMillan, J
This study assessed how BDNF (brain-derived neurotrophic factor) and other genes involved in its signaling influence brain structure and clinical functioning in pre-diagnosis Huntington’s disease (HD). Parallel independent component analysis (pICA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c33155136ae8c0931d45a171af69ae26
https://www.repository.cam.ac.uk/handle/1810/285331
https://www.repository.cam.ac.uk/handle/1810/285331
Autor:
Carvalho, JO, Long, JD, Westervelt, HJ, Smith, MM, Bruce, JM, Kim, JI, Mills, JA, Paulsen, JS, De Soriano, I, Shadrick, C, Miller, A, Chiu, E, Preston, J, Goh, A, Antonopoulos, S, Loi, S, Chua, P, Komiti, A, Raymond, L, Decolongon, J, Fan, M, Coleman, A, Ross, CA, Varvaris, M, Ong, M, Yoritomo, N, Mallonee, WM, Suter, G, Samii, A, Freney, EP, Macaraeg, A, Jones, R, Wood-Siverio, C, Factor, SA, Barker, RA, Mason, S, Guzman, NV, McCusker, E, Griffith, J, Loy, C, McMillan, J, Gunn, D, Orth, M, Süßmuth, S, Barth, K, Trautmann, S, Schwenk, D, Eschenbach, C, Quaid, K, Wesson, M, Wojcieszek, J, Guttman, M, Sheinberg, A, Law, A, Karmalkar, I, Perlman, S, Clemente, B, Geschwind, MD, Sha, S, Winer, J, Satris, G, Warner, T, Burrows, M, Rosser, A, Price, K, Hunt, S, Marshall, F, Chesire, A, Wodarski, M, Hickey, C, Panegyres, P, Lee, J, Tedesco, M, Maxwell, B, Perlmutter, J, Barton, S, Smith, S, Miedzybrodzka, Z, Rae, D, Vaughan, V, D'Alessandro, M, Craufurd, D, Bek, J, Howard, E, Mazzoni, P, Marder, K, Wasserman, P, Kumar, R, Erickson, D, Reeves, C, Nickels, B, Wheelock, V, Kjer, L, Martin, A, Farias, S
Publikováno v:
Carvalho, JO; Long, JD; Westervelt, HJ; Smith, MM; Bruce, JM; Kim, JI; et al.(2016). The impact of oculomotor functioning on neuropsychological performance in Huntington disease. Journal of Clinical and Experimental Neuropsychology, 38(2), 217-226. doi: 10.1080/13803395.2015.1101054. UCSF: Retrieved from: http://www.escholarship.org/uc/item/0nr7c12k
© 2016 Taylor & Francis. Huntington disease (HD) is a neurodegenerative condition with prominent motor (including oculomotor), cognitive, and psychiatric effects. While neuropsychological deficits are present in HD, motor impairments may impact perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::89d87b3fc601160badf850340166f423
http://www.escholarship.org/uc/item/0nr7c12k
http://www.escholarship.org/uc/item/0nr7c12k
Autor:
Musso, M, Westervelt, HJ, Long, JD, Morgan, E, Woods, SP, Smith, MM, Lu, W, Paulsen, JS, Cross, S, Ryan, P, Epping, EA, Chiu, E, Preston, J, Goh, A, Antonopoulos, S, Loi, S, Chua, P, Komiti, A, Raymond, L, Decolongon, J, Fan, M, Coleman, A, Ross, CA, Varvaris, M, Yoritomo, N, Mallonee, WM, Suter, G, Samii, A, Macaraeg, A, Jones, R, Wood-Siverio, C, Factor, SA, Barker, RA, Mason, S, Guzman, NV, McCusker, E, Griffith, J, Loy, C, Gunn, D, Orth, M, Süßmuth, S, Barth, K, Trautmann, S, Schwenk, D, Eschenbach, C, Quaid, K, Wesson, M, Wojcieszek, J, Guttman, M, Sheinberg, A, Karmalkar, I, Perlman, S, Clemente, B, Geschwind, MD, Sha, S, Satris, G, Warner, T, Burrows, M, Rosser, A, Price, K, Hunt, S, Marshall, F, Chesire, A, Wodarski, M, Hickey, C, Panegyres, P, Lee, J, Tedesco, M, Maxwell, B, Perlmutter, J, Barton, S, Smith, S, Miedzybrodzka, Z, Rae, D, D'Alessandro, M, Craufurd, D, Bek, J, Howard, E, Mazzoni, P, Marder, K, Wasserman, P, Kumar, R, Erickson, D, Nickels, B, Wheelock, V, Kjer, L, Martin, A, Farias, S, Suchowersky, O, Martin, W, King, P, Wieler, M, Sran, S, Ahmed, A, Rao, S, Reece, C
Publikováno v:
Musso, M; Westervelt, HJ; Long, JD; Morgan, E; Woods, SP; Smith, MM; et al.(2015). Intra-individual variability in prodromal Huntington disease and its relationship to genetic burden. Journal of the International Neuropsychological Society, 21(1), 8-21. doi: 10.1017/S1355617714001076. UCSF: Retrieved from: http://www.escholarship.org/uc/item/64s52036
© INS. The International Neuropsychological Society 2015. The current study sought to examine the utility of intra-individual variability (IIV) in distinguishing participants with prodromal Huntington disease (HD) from nongene-expanded controls. IIV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::d23dd8c8fac0e24327ed3d3840ecf159
http://www.escholarship.org/uc/item/64s52036
http://www.escholarship.org/uc/item/64s52036
Autor:
Kim, JI, Long, JD, Mills, JA, McCusker, E, Paulsen, JS, De Soriano, I, Shadrick, C, Miller, A, Chiu, E, Preston, J, Goh, A, Antonopoulos, S, Loi, S, Chua, P, Komiti, A, Raymond, L, Decolongon, J, Fan, M, Coleman, A, Ross, CA, Varvaris, M, Ong, M, Yoritomo, N, Mallonee, WM, Suter, G, Samii, A, Freney, EP, Macaraeg, A, Jones, R, Wood-Siverio, C, Factor, SA, Barker, RA, Mason, S, Guzman, NV, Griffith, J, Loy, C, McMillan, J, Gunn, D, Orth, M, Süßmuth, S, Barth, K, Trautmann, S, Schwenk, D, Eschenbach, C, Quaid, K, Wesson, M, Wojcieszek, J, Guttman, M, Sheinberg, A, Law, A, Karmalkar, I, Perlman, S, Clemente, B, Geschwind, MD, Sha, S, Winer, J, Satris, G, Warner, T, Burrows, M, Rosser, A, Price, K, Hunt, S, Marshall, F, Chesire, A, Wodarski, M, Hickey, C, Panegyres, P, Lee, J, Tedesco, M, Maxwell, B, Perlmutter, J, Barton, S, Smith, S, Miedzybrodzka, Z, Rae, D, Vaughan, V, D'Alessandro, M, Craufurd, D, Bek, J, Howard, E, Mazzoni, P, Marder, K, Wasserman, P, Kumar, R, Erickson, D, Reeves, C, Nickels, B, Wheelock, V, Kjer, L, Martin, A, Farias, S, Martin, W, Suchowersky, O, King, P, Wieler, M, Sran, S, Ahmed, A, Rao, S
Publikováno v:
Kim, JI; Long, JD; Mills, JA; McCusker, E; Paulsen, JS; De Soriano, I; et al.(2015). Multivariate clustering of progression profiles reveals different depression patterns in prodromal huntington disease. Neuropsychology, 29(6), 949-960. doi: 10.1037/neu0000199. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/89k3417q
Objective: Although Huntington disease (HD) is caused by an autosomal dominant mutation, its phenotypic presentation differs widely. Variability in clinical phenotypes of HD may reflect the existence of disease subtypes. This hypothesis was tested in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::0f0576da60b4b4d949b4469c0970b2ea
http://www.escholarship.org/uc/item/89k3417q
http://www.escholarship.org/uc/item/89k3417q
Autor:
Matsui, JT, Vaidya, JG, Wassermann, D, Kim, RE, Magnotta, VA, Johnson, HJ, Paulsen, JS, Isabella De Soriano, Shadrick, C, Miller, A, Edmond Chiu, Preston, J, Goh, A, Antonopoulos, S, Loi, S, Chua, P, Komiti, A, Lynn Raymond, Decolongon, J, Fan, M, Coleman, A, Christopher, AR, Varvaris, M, Ong, M, Yoritomo, N, Mallonee, WM, Suter, G, Samii, A, Freney, EP, Macaraeg, A, Jones, R, Wood-Siverio, C, Factor, SA, Barker, RA, Mason, S, Guzman, NV, McCusker, E, Griffith, J, Loy, C, McMillan, J, Gunn, D, Orth, M, Sübmuth, S, Barth, K, Trautmann, S, Schwenk, D, Eschenbach, C, Quaid, K, Wesson, M, Wojcieszek, J, Guttman, M, Sheinberg, A, Law, A, Karmalkar, I, Perlman, S, Clemente, B, Geschwind, MD, Sha, S, Winer, J, Satris, G, Warner, T, Burrows, M, Rosser, A, Price, K, Hunt, S, Marshall, F, Chesire, A, Wodarski, M, Hickey, C, Panegyres, P, Lee, J, Tedesco, M, Maxwell, B, Perlmutter, J, Barton, S, Smith, S, Miedzybrodzka, Z, Rae, D, Vaughan, V, D'Alessandro, M, Craufurd, D, Bek, J, Howard, E, Mazzoni, P, Marder, K, Wasserman, P, Kumar, R, Erickson, D, Reeves, C, Nickels, B, Wheelock, V, Kjer, L, Martin, A
Publikováno v:
Matsui, JT; Vaidya, JG; Wassermann, D; Kim, RE; Magnotta, VA; Johnson, HJ; et al.(2015). Prefrontal cortex white matter tracts in prodromal Huntington disease. Human Brain Mapping, 36(10), 3717-3732. doi: 10.1002/hbm.22835. UCSF: Retrieved from: http://www.escholarship.org/uc/item/3dg2h93m
© 2015 Wiley Periodicals, Inc. Huntington disease (HD) is most widely known for its selective degeneration of striatal neurons but there is also growing evidence for white matter (WM) deterioration. The primary objective of this research was to cond
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::d502ca7b136af3c9215810e454eb1029
http://www.escholarship.org/uc/item/3dg2h93m
http://www.escholarship.org/uc/item/3dg2h93m
Autor:
Long, JD, Paulsen, JS, Soriano, ID, Shadrick, C, Miller, A, Chiu, E, Preston, J, Goh, A, Antonopoulos, S, Loi, S, Chua, P, Komiti, A, Raymond, L, Decolongon, J, Fan, M, Coleman, A, Ross, CA, Varvaris, M, Ong, M, Yoritomo, N, Mallonee, WM, Suter, G, Samii, A, Freney, EP, Macaraeg, A, Jones, R, Wood-Siverio, C, Factor, SA, Barker, RA, Mason, S, Guzman, NV, McCusker, E, Griffith, J, Loy, C, McMillan, J, Gunn, D, Orth, M, Submuth, S, Barth, K, Trautmann, S, Schwenk, D, Eschenbach, C, Quaid, K, Wesson, M, Wojcieszek, J, Guttman, M, Sheinberg, A, Law, A, Karmalkar, I, Perlman, S, Clemente, B, Geschwind, MD, Sha, S, Winer, J, Satris, G, Warner, T, Burrows, M, Rosser, A, Price, K, Hunt, S, Marshall, F, Chesire, A, Wodarski, M, Hickey, C, Panegyres, P, Lee, J, Tedesco, M, Maxwell, B, Perlmutter, J, Barton, S, Smith, S, Miedzybrodzka, Z, Rae, D, Vaughan, V, D'Alessandro, M, Craufurd, D, Bek, J, Howard, E, Mazzoni, P, Marder, K, Wasserman, P, Kumar, R, Erickson, D, Reeves, C, Nickels, B, Wheelock, V, Kjer, L, Martin, A, Farias, S, Martin, W, Suchowersky, O, King, P, Wieler, M, Sran, S
Publikováno v:
Long, JD; Paulsen, JS; Soriano, ID; Shadrick, C; Miller, A; Chiu, E; et al.(2015). Multivariate prediction of motor diagnosis in Huntington's disease: 12 years of PREDICT-HD. Movement Disorders, 30(12), 1664-1672. doi: 10.1002/mds.26364. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/5040v01d
© 2015 The Authors. Background: It is well known in Huntington's disease that cytosine-adenine-guanine expansion and age at study entry are predictive of the timing of motor diagnosis. The goal of this study was to assess whether additional motor, i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::1a49c7dcdd5c41cd064fcd71e13b8007
http://www.escholarship.org/uc/item/5040v01d
http://www.escholarship.org/uc/item/5040v01d
Autor:
Mata, IF, Jang, Y, Kim, CH, Hanna, DS, Dorschner, MO, Samii, A, Agarwal, P, Roberts, JW, Klepitskaya, O, Shprecher, DR, Chung, KA, Factor, SA, Espay, AJ, Revilla, FJ, Higgins, DS, Litvan, I, Leverenz, JB, Yearout, D, Inca-Martinez, M, Martinez, E, Thompson, TR, Cholerton, BA, Hu, SC, Edwards, KL, Kim, KS, Zabetian, CP
Publikováno v:
Molecular neurodegeneration, vol 10, iss 1
Mata, IF; Jang, Y; Kim, CH; Hanna, DS; Dorschner, MO; Samii, A; et al.(2015). The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease. Molecular Neurodegeneration. doi: 10.1186/s13024-015-0045-4. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/6446j25p
Mata, IF; Jang, Y; Kim, CH; Hanna, DS; Dorschner, MO; Samii, A; et al.(2015). The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease. Molecular Neurodegeneration. doi: 10.1186/s13024-015-0045-4. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/6446j25p
© 2015 Mata et al. Objective: To identify the causal gene in a multi-incident U.S. kindred with Parkinson's disease (PD). Methods: We characterized a family with a classical PD phenotype in which 7 individuals (5 males and 2 females) were affected w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::922b058e17257b7ca4178113d935c656
https://escholarship.org/uc/item/6446j25p
https://escholarship.org/uc/item/6446j25p
Autor:
Kelly, VE, Johnson, CO, McGough, EL, Shumway-Cook, A, Horak, FB, Chung, KA, Espay, AJ, Revilla, FJ, Devoto, J, Wood-Siverio, C, Factor, SA, Cholerton, B, Edwards, KL, Peterson, AL, Quinn, JF, Montine, TJ, Zabetian, CP, Leverenz, JB
Publikováno v:
Parkinsonism & related disorders, vol 21, iss 7
IntroductionResearch suggests an association between global cognition and postural instability/gait disturbance (PIGD) in Parkinson disease (PD), but the relationship between specific cognitive domains and PIGD symptoms is not clear. This study exami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::75ffb3bcfa4bcae0eeb4d9737b39ce1d
https://escholarship.org/uc/item/1mw23628
https://escholarship.org/uc/item/1mw23628
Autor:
Srivatsal, S, Cholerton, B, Leverenz, JB, Wszolek, ZK, Uitti, RJ, Dickson, DW, Weintraub, D, Trojanowski, JQ, Van Deerlin, VM, Quinn, JF, Chung, KA, Peterson, AL, Factor, SA, Wood-Siverio, C, Goldman, JG, Stebbins, GT, Bernard, B, Ritz, B, Rausch, R, Espay, AJ, Revilla, FJ, Devoto, J, Rosenthal, LS, Dawson, TM, Albert, MS, Mata, IF, Hu, SC, Montine, KS, Johnson, C, Montine, TJ, Edwards, KL, Zhang, J, Zabetian, CP
Publikováno v:
Srivatsal, S; Cholerton, B; Leverenz, JB; Wszolek, ZK; Uitti, RJ; Dickson, DW; et al.(2015). Cognitive profile of LRRK2-related Parkinson's disease. Movement Disorders, 30(5), 728-733. doi: 10.1002/mds.26161. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/7ds270r7
Movement disorders : official journal of the Movement Disorder Society, vol 30, iss 5
Movement Disorders, vol 30, iss 5
Movement disorders : official journal of the Movement Disorder Society, vol 30, iss 5
Movement Disorders, vol 30, iss 5
© 2015 International Parkinson and Movement Disorder Society. Background: Increasing evidence suggests that genetic factors play a role in the variability associated with cognitive performance in Parkinson's disease (PD). Mutations in the LRRK2 gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::54973cdb1e6731dd5464c881543e15d1
http://www.escholarship.org/uc/item/7ds270r7
http://www.escholarship.org/uc/item/7ds270r7
Autor:
Kannarkat, GT, Cook, DA, Lee, J-K, Chang, J, Chung, J, Sandy, E, Paul, KC, Ritz, B, Bronstein, J, Factor, SA, Boss, JM, Tansey, MG
Publikováno v:
NPJ Parkinson's disease, vol 1, iss 1
Background/objectivesThe common non-coding single nucleotide polymorphism (SNP) rs3129882 in HLA-DRA is associated with risk for idiopathic Parkinson's disease (PD). The location of the SNP in the major histocompatibility complex class II (MHC-II) lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::08122ed340de31c71473176efa53421b
https://escholarship.org/uc/item/48r6x3tj
https://escholarship.org/uc/item/48r6x3tj