Zobrazeno 1 - 10
of 184
pro vyhledávání: '"Geschwind, MD"'
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
Publikováno v:
AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Although prion diseases are generally thought to present as rapidly progressive dementias with survival of only a few months, the phenotypic spectrum for genetic prion diseases (gPrDs) is much broader. The majority have a rapid decline with short sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::bd1a07c6f07997116d8ea5cc536669ed
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=6803
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=6803
Autor:
Ljubenkov, PA, Geschwind, MD
Publikováno v:
Ljubenkov, PA; & Geschwind, MD. (2016). Dementia. SEMINARS IN NEUROLOGY, 36(4), 397-404. doi: 10.1055/s-0036-1585096. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/7nk8n5j1
Dementia often is defined as a progressive cognitive disturbance leading to a loss of independent function. Most clinicians are familiar with the typical pattern of amnestic Alzheimer's disease, the most common neurodegenerative presentation of demen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::919c7089004e45d59eb1e78ee6316222
http://www.escholarship.org/uc/item/7nk8n5j1
http://www.escholarship.org/uc/item/7nk8n5j1
Autor:
Geschwind, MD
Publikováno v:
Geschwind, MD. (2016). Deutetrabenazine for Treatment of Chorea in Huntington Disease. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 316(1), 33-35. doi: 10.1001/jama.2016.8011. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/3w49n1q7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::07e5c88357b1025d6474b8ce6bd294d3
http://www.escholarship.org/uc/item/3w49n1q7
http://www.escholarship.org/uc/item/3w49n1q7
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:
Watts, JC, Giles, K, Serban, A, Patel, S, Oehler, A, Bhardwaj, S, Guan, S, Greicius, MD, Miller, BL, Dearmond, SJ, Geschwind, MD, Prusiner, SB
Publikováno v:
Watts, JC; Watts, JC; Watts, JC; Giles, K; Giles, K; Serban, A; et al.(2015). Modulation of Creutzfeldt-Jakob disease prion propagation by the A224V mutation. Annals of Neurology. doi: 10.1002/ana.24463. UCSF: Retrieved from: http://www.escholarship.org/uc/item/7f3001jv
© 2015 American Neurological Association. Objective: Mutations in the gene encoding the prion protein (PrP) are responsible for approximately 10 to 15% of cases of prion disease in humans, including Creutzfeldt-Jakob disease (CJD). Here, we report o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::5732cb451549ad45dd788f81bbcad1e1
http://www.escholarship.org/uc/item/7f3001jv
http://www.escholarship.org/uc/item/7f3001jv