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Removal of high frequency contamination from motion estimates in single-band fMRI saves data without biasing functional connectivity. [electronic resource] by
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- Adeyemo, Babatunde
- Laumann, Timothy O
- Wig, Gagan S
- Kong, Tania S
- Gratton, Gabriele
- Fabiani, Monica
- Barch, Deanna M
- Tranel, Daniel
- Miranda-Dominguez, Oscar
- Fair, Damien A
- Dosenbach, Nico U F
- Snyder, Abraham Z
- Perlmutter, Joel S
- Petersen, Steven E
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Producer: 20210218
In:
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ACR Appropriateness Criteria Low Back Pain. [electronic resource] by
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- Fries, Ian Blair
- Harvey, H Benjamin
- Holly, Langston
- Hunt, Christopher H
- Jagadeesan, Bharathi D
- Kennedy, Tabassum A
- O'Toole, John E
- Perlmutter, Joel S
- Policeni, Bruno
- Rosenow, Joshua M
- Schroeder, Jason W
- Whitehead, Matthew T
- Cornelius, Rebecca S
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Producer: 20170830
In:
Journal of the American College of Radiology : JACR vol. 13
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203.
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A rare sequence variant in intron 1 of THAP1 is associated with primary dystonia. [electronic resource] by
- Vemula, Satya R
- Xiao, Jianfeng
- Zhao, Yu
- Bastian, Robert W
- Perlmutter, Joel S
- Racette, Brad A
- Paniello, Randal C
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Van Gerpen, Jay A
- Hedera, Peter
- Truong, Daniel D
- Blitzer, Andrew
- Rudzińska, Monika
- Momčilović, Dragana
- Jinnah, Hyder A
- Frei, Karen
- Pfeiffer, Ronald F
- LeDoux, Mark S
Producer: 20140617
In:
Molecular genetics & genomic medicine vol. 2
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204.
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Risk of spread in adult-onset isolated focal dystonia: a prospective international cohort study. [electronic resource] by
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- Sillau, Stefan H
- Pirio Richardson, Sarah
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- Junker, Johanna
- Brüggemann, Norbert
- Agarwal, Pinky
- Barbano, Richard L
- Espay, Alberto J
- Vizcarra, Joaquin A
- Klein, Christine
- Bäumer, Tobias
- Loens, Sebastian
- Reich, Stephen G
- Vidailhet, Marie
- Bonnet, Cecilia
- Roze, Emmanuel
- Jinnah, Hyder A
- Perlmutter, Joel S
Producer: 20200821
In:
Journal of neurology, neurosurgery, and psychiatry vol. 91
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205.
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Consensus-Based Attributes for Identifying Patients With Spasmodic Dysphonia and Other Voice Disorders. [electronic resource] by
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- Smith, Marshall E
- Blumin, Joel H
- Kalata, Carrie E
- Blindauer, Karen
- Johns, Michael
- Hapner, Edie
- Harmon, Archie
- Paniello, Randal
- Adler, Charles H
- Crujido, Lisa
- Lott, David G
- Bansberg, Stephen F
- Barone, Nicholas
- Drulia, Teresa
- Stebbins, Glenn
Producer: 20190930
In:
JAMA otolaryngology-- head & neck surgery vol. 144
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206.
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High-throughput mutational analysis of TOR1A in primary dystonia. [electronic resource] by
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- Bastian, Robert W
- Perlmutter, Joel S
- Racette, Brad A
- Tabbal, Samer D
- Karimi, Morvarid
- Paniello, Randal C
- Blitzer, Andrew
- Batish, Sat Dev
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Hedera, Peter
- Simon, David K
- Tarsy, Daniel
- Truong, Daniel D
- Frei, Karen P
- Pfeiffer, Ronald F
- Gong, Suzhen
- Zhao, Yu
- LeDoux, Mark S
Producer: 20090330
In:
BMC medical genetics vol. 10
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207.
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ACR Appropriateness Criteria [electronic resource] by
- Policeni, Bruno
- Corey, Amanda S
- Burns, Judah
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- Crowley, R Webster
- Harvey, H Benjamin
- Hoang, Jenny
- Hunt, Christopher H
- Jagadeesan, Bharathi D
- Juliano, Amy F
- Kennedy, Tabassum A
- Moonis, Gul
- Pannell, Jeffrey S
- Patel, Nandini D
- Perlmutter, Joel S
- Rosenow, Joshua M
- Schroeder, Jason W
- Whitehead, Mathew T
- Cornelius, Rebecca S
Producer: 20180404
In:
Journal of the American College of Radiology : JACR vol. 14
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208.
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Clinical and genetic features of cervical dystonia in a large multicenter cohort. [electronic resource] by
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- Vemula, Satya R
- Xiao, Jianfeng
- Thompson, Misty M
- Perlmutter, Joel S
- Wright, Laura J
- Jinnah, H A
- Rosen, Ami R
- Hedera, Peter
- Comella, Cynthia L
- Weissbach, Anne
- Junker, Johanna
- Jankovic, Joseph
- Barbano, Richard L
- Reich, Stephen G
- Rodriguez, Ramon L
- Berman, Brian D
- Chouinard, Sylvain
- Severt, Lawrence
- Agarwal, Pinky
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Producer: 20160428
In:
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209.
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ACR Appropriateness Criteria [electronic resource] by
- Salmela, Michael B
- Mortazavi, Shabnam
- Jagadeesan, Bharathi D
- Broderick, Daniel F
- Burns, Judah
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- Harvey, H Benjamin
- Hoang, Jenny
- Hunt, Christopher H
- Kennedy, Tabassum A
- Khalessi, Alexander A
- Mack, William
- Patel, Nandini D
- Perlmutter, Joel S
- Policeni, Bruno
- Schroeder, Jason W
- Setzen, Gavin
- Whitehead, Matthew T
- Cornelius, Rebecca S
- Corey, Amanda S
Producer: 20180328
In:
Journal of the American College of Radiology : JACR vol. 14
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210.
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Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6. [electronic resource] by
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- Bastian, Robert W
- Perlmutter, Joel S
- Racette, Brad A
- Tabbal, Samer D
- Karimi, Morvarid
- Paniello, Randal
- Blitzer, Andrew
- Batish, Sat Dev
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Van Gerpen, Jay A
- Hedera, Peter
- Simon, David K
- Tarsy, Daniel
- Truong, Daniel D
- Frei, Karen P
- Pfeiffer, Ronald F
- Gong, Suzhen
- LeDoux, Mark S
Producer: 20110506
In:
Human genetics vol. 127
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Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6. [electronic resource] by
- Xiao, Jianfeng
- Zhao, Y
- Bastian, Robert W
- Perlmutter, Joel S
- Racette, Brad A
- Tabbal, Samer D
- Karimi, Morvarid
- Paniello, Randal
- Blitzer, Andrew
- Batish, Sat Dev
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Van Gerpen, Jay A
- Hedera, Peter
- Simon, David K
- Tarsy, Daniel
- Truong, Daniel D
- Frei, Karen P
- Pfeiffer, Ronald F
- Gong, Suzhen
- LeDoux, Mark S
Producer: 20110506
In:
Human genetics vol. 127
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Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease. [electronic resource] by
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- Grupe, Andrew
- Rowland, Charles
- Holmans, Peter
- Segurado, Ricardo
- Abraham, Richard
- Jones, Lesley
- Catanese, Joseph
- Ross, David
- Mayo, Kevin
- Martinez, Maribel
- Hollingworth, Paul
- Goate, Alison
- Cairns, Nigel J
- Racette, Brad A
- Perlmutter, Joel S
- O'Donovan, Michael C
- Morris, John C
- Brayne, Carol
- Rubinsztein, David C
- Lovestone, Simon
- Thal, Leon J
- Owen, Michael J
- Williams, Julie
Producer: 20080314
In:
Human molecular genetics vol. 17
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213.
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Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6. [electronic resource] by
- Xiao, Jianfeng
- Zhao, Yu
- Bastian, Robert W
- Perlmutter, Joel S
- Racette, Brad A
- Tabbal, Samer D
- Karimi, Morvarid
- Paniello, Randal
- Blitzer, Andrew
- Batish, Sat Dev
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Van Gerpen, Jay A
- Hedera, Peter
- Simon, David K
- Tarsy, Daniel
- Truong, Daniel D
- Frei, Karen P
- Pfeiffer, Ronald F
- Gong, Suzhen
- LeDoux, Mark S
Producer: 20110506
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Human genetics vol. 127
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Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6. [electronic resource] by
- Xiao, Jianfeng
- Zhao, Yu
- Bastian, Robert W
- Perlmutter, Joel S
- Racette, Brad A
- Tabbal, Samer D
- Karimi, Morvarid
- Paniello, Randal
- Blitzer, Andrew
- Batish, Sat Dev
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Van Gerpen, Jay A
- Hedera, Peter
- Simon, David K
- Tarsy, Daniel
- Truong, Daniel D
- Frei, Karen P
- Pfeiffer, Ronald F
- Gong, Suzhen
- LeDoux, Mark S
Producer: 20110506
In:
Human genetics vol. 127
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The c.-237_236GA>TT THAP1 sequence variant does not increase risk for primary dystonia. [electronic resource] by
- Xiao, Jianfeng
- Zhao, Yu
- Bastian, Robert W
- Perlmutter, Joel S
- Racette, Brad A
- Tabbal, Samer D
- Karimi, Morvarid
- Paniello, Randal C
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Van Gerpen, Jay A
- Simon, David K
- Tarsy, Daniel
- Hedera, Peter
- Truong, Daniel D
- Frei, Karen P
- Blitzer, Andrew
- Rudzińska, Monika
- Pfeiffer, Ronald F
- Le, Carrie
- LeDoux, Mark S
Producer: 20110729
In:
Movement disorders : official journal of the Movement Disorder Society vol. 26
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216.
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Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6. [electronic resource] by
- Xiao, Jianfeng
- Zhao, Yu
- Bastian, Robert W
- Perlmutter, Joel S
- Racette, Brad A
- Tabbal, Samer D
- Karimi, Morvarid
- Paniello, Randal
- Blitzer, Andrew
- Batish, Sat Dev
- Wszolek, Zbigniew K
- Uitti, Ryan J
- Van Gerpen, Jay A
- Hedera, Peter
- Simon, David K
- Tarsy, Daniel
- Truong, Daniel D
- Frei, Karen P
- Pfeiffer, Ronald F
- Gong, Suzhen
- LeDoux, Mark S
Producer: 20110506
In:
Human genetics vol. 127
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217.
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Clinical and demographic characteristics related to onset site and spread of cervical dystonia. [electronic resource] by
- Norris, Scott A
- Jinnah, H A
- Espay, Alberto J
- Klein, Christine
- Brüggemann, Norbert
- Barbano, Richard L
- Malaty, Irene Andonia C
- Rodriguez, Ramon L
- Vidailhet, Marie
- Roze, Emmanuel
- Reich, Stephen G
- Berman, Brian D
- LeDoux, Mark S
- Richardson, Sarah Pirio
- Agarwal, Pinky
- Mari, Zoltan
- Ondo, William G
- Shih, Ludy C
- Fox, Susan H
- Berardelli, Alfredo
- Testa, Claudia M
- Cheng, Florence Ching-Fen
- Truong, Daniel
- Nahab, Fatta B
- Xie, Tao
- Hallett, Mark
- Rosen, Ami R
- Wright, Laura J
- Perlmutter, Joel S
Producer: 20171229
In:
Movement disorders : official journal of the Movement Disorder Society vol. 31
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218.
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Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study. [electronic resource] by
- Sun, Mei
- Latourelle, Jeanne C
- Wooten, G Frederick
- Lew, Mark F
- Klein, Christine
- Shill, Holly A
- Golbe, Lawrence I
- Mark, Margery H
- Racette, Brad A
- Perlmutter, Joel S
- Parsian, Abbas
- Guttman, Mark
- Nicholson, Garth
- Xu, Gang
- Wilk, Jemma B
- Saint-Hilaire, Marie H
- DeStefano, Anita L
- Prakash, Ranjana
- Williamson, Sally
- Suchowersky, Oksana
- Labelle, Nancy
- Growdon, John H
- Singer, Carlos
- Watts, Ray L
- Goldwurm, Stefano
- Pezzoli, Gianni
- Baker, Kenneth B
- Pramstaller, Peter P
- Burn, David J
- Chinnery, Patrick F
- Sherman, Scott
- Vieregge, Peter
- Litvan, Irene
- Gillis, Tammy
- MacDonald, Marcy E
- Myers, Richard H
- Gusella, James F
Producer: 20060726
In:
Archives of neurology vol. 63
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219.
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Genome-wide association study reveals genetic risk underlying Parkinson's disease. [electronic resource] by
- Simón-Sánchez, Javier
- Schulte, Claudia
- Bras, Jose M
- Sharma, Manu
- Gibbs, J Raphael
- Berg, Daniela
- Paisan-Ruiz, Coro
- Lichtner, Peter
- Scholz, Sonja W
- Hernandez, Dena G
- Krüger, Rejko
- Federoff, Monica
- Klein, Christine
- Goate, Alison
- Perlmutter, Joel
- Bonin, Michael
- Nalls, Michael A
- Illig, Thomas
- Gieger, Christian
- Houlden, Henry
- Steffens, Michael
- Okun, Michael S
- Racette, Brad A
- Cookson, Mark R
- Foote, Kelly D
- Fernandez, Hubert H
- Traynor, Bryan J
- Schreiber, Stefan
- Arepalli, Sampath
- Zonozi, Ryan
- Gwinn, Katrina
- van der Brug, Marcel
- Lopez, Grisel
- Chanock, Stephen J
- Schatzkin, Arthur
- Park, Yikyung
- Hollenbeck, Albert
- Gao, Jianjun
- Huang, Xuemei
- Wood, Nick W
- Lorenz, Delia
- Deuschl, Günther
- Chen, Honglei
- Riess, Olaf
- Hardy, John A
- Singleton, Andrew B
- Gasser, Thomas
Producer: 20100105
In:
Nature genetics vol. 41
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220.
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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. [electronic resource] by
- Nalls, Mike A
- Pankratz, Nathan
- Lill, Christina M
- Do, Chuong B
- Hernandez, Dena G
- Saad, Mohamad
- DeStefano, Anita L
- Kara, Eleanna
- Bras, Jose
- Sharma, Manu
- Schulte, Claudia
- Keller, Margaux F
- Arepalli, Sampath
- Letson, Christopher
- Edsall, Connor
- Stefansson, Hreinn
- Liu, Xinmin
- Pliner, Hannah
- Lee, Joseph H
- Cheng, Rong
- Ikram, M Arfan
- Ioannidis, John P A
- Hadjigeorgiou, Georgios M
- Bis, Joshua C
- Martinez, Maria
- Perlmutter, Joel S
- Goate, Alison
- Marder, Karen
- Fiske, Brian
- Sutherland, Margaret
- Xiromerisiou, Georgia
- Myers, Richard H
- Clark, Lorraine N
- Stefansson, Kari
- Hardy, John A
- Heutink, Peter
- Chen, Honglei
- Wood, Nicholas W
- Houlden, Henry
- Payami, Haydeh
- Brice, Alexis
- Scott, William K
- Gasser, Thomas
- Bertram, Lars
- Eriksson, Nicholas
- Foroud, Tatiana
- Singleton, Andrew B
Producer: 20150115
In:
Nature genetics vol. 46
Availability: No items available.
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