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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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ACR Appropriateness Criteria [electronic resource] by
- Policeni, Bruno
- Corey, Amanda S
- Burns, Judah
- Conley, David B
- 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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Clinical and genetic features of cervical dystonia in a large multicenter cohort. [electronic resource] by
- LeDoux, Mark S
- 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
- Stover, Natividad P
Producer: 20160428
In:
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ACR Appropriateness Criteria [electronic resource] by
- Salmela, Michael B
- Mortazavi, Shabnam
- Jagadeesan, Bharathi D
- Broderick, Daniel F
- Burns, Judah
- Deshmukh, Tejaswini K
- 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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Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6. [electronic resource] by
- Xiao, Jianfeng
- 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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Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6. [electronic resource] by
- Xiao, Jianfeng
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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
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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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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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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
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Producer: 20171229
In:
Movement disorders : official journal of the Movement Disorder Society vol. 31
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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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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease. [electronic resource] by
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- 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
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Replication of association between ELAVL4 and Parkinson disease: the GenePD study. [electronic resource] by
- DeStefano, Anita L
- Latourelle, Jeanne
- Lew, Mark F
- Suchowersky, Oksana
- Klein, Christine
- Golbe, Lawrence I
- Mark, Margery H
- Growdon, John H
- Wooten, G Fredrick
- Watts, Ray
- Guttman, Mark
- Racette, Brad A
- Perlmutter, Joel S
- Marlor, Lynn
- Shill, Holly A
- Singer, Carlos
- Goldwurm, Stefano
- Pezzoli, Gianni
- Saint-Hilaire, Marie H
- Hendricks, Audrey E
- Gower, Adam
- Williamson, Sally
- Nagle, Michael W
- Wilk, Jemma B
- Massood, Tiffany
- Huskey, Karen W
- Baker, Kenneth B
- Itin, Ilia
- Litvan, Irene
- Nicholson, Garth
- Corbett, Alastair
- Nance, Martha
- Drasby, Edward
- Isaacson, Stuart
- Burn, David J
- Chinnery, Patrick F
- Pramstaller, Peter P
- Al-Hinti, Jomana
- Moller, Anette T
- Ostergaard, Karen
- Sherman, Scott J
- Roxburgh, Richard
- Snow, Barry
- Slevin, John T
- Cambi, Franca
- Gusella, James F
- Myers, Richard H
Producer: 20080730
In:
Human genetics vol. 124
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Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study. [electronic resource] by
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- Latourelle, Jeanne C
- MacDonald, Marcy E
- Lew, Mark F
- Suchowersky, Oksana
- Klein, Christine
- Golbe, Lawrence I
- Mark, Margery H
- Growdon, John H
- Wooten, G Frederick
- Watts, Ray L
- Guttman, Mark
- Racette, Brad A
- Perlmutter, Joel S
- Ahmed, Anwar
- Shill, Holly A
- Singer, Carlos
- Saint-Hilaire, Marie H
- Massood, Tiffany
- Huskey, Karen W
- DeStefano, Anita L
- Gillis, Tammy
- Mysore, Jayalakshmi
- Goldwurm, Stefano
- Pezzoli, Gianni
- Baker, Kenneth B
- Itin, Ilia
- Litvan, Irene
- Nicholson, Garth
- Corbett, Alastair
- Nance, Martha
- Drasby, Edward
- Isaacson, Stuart
- Burn, David J
- Chinnery, Patrick F
- Pramstaller, Peter P
- Al-Hinti, Jomana
- Moller, Anette T
- Ostergaard, Karen
- Sherman, Scott J
- Roxburgh, Richard
- Snow, Barry
- Slevin, John T
- Cambi, Franca
- Gusella, James F
- Myers, Richard H
Producer: 20090408
In:
Movement disorders : official journal of the Movement Disorder Society vol. 23
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The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study. [electronic resource] by
- Latourelle, Jeanne C
- Sun, Mei
- Lew, Mark F
- Suchowersky, Oksana
- Klein, Christine
- Golbe, Lawrence I
- Mark, Margery H
- Growdon, John H
- Wooten, G Frederick
- Watts, Ray L
- Guttman, Mark
- Racette, Brad A
- Perlmutter, Joel S
- Ahmed, Anwar
- Shill, Holly A
- Singer, Carlos
- Goldwurm, Stefano
- Pezzoli, Gianni
- Zini, Michela
- Saint-Hilaire, Marie H
- Hendricks, Audrey E
- Williamson, Sally
- Nagle, Michael W
- Wilk, Jemma B
- Massood, Tiffany
- Huskey, Karen W
- Laramie, Jason M
- DeStefano, Anita L
- Baker, Kenneth B
- Itin, Ilia
- Litvan, Irene
- Nicholson, Garth
- Corbett, Alastair
- Nance, Martha
- Drasby, Edward
- Isaacson, Stuart
- Burn, David J
- Chinnery, Patrick F
- Pramstaller, Peter P
- Al-hinti, Jomana
- Moller, Anette T
- Ostergaard, Karen
- Sherman, Scott J
- Roxburgh, Richard
- Snow, Barry
- Slevin, John T
- Cambi, Franca
- Gusella, James F
- Myers, Richard H
Producer: 20090518
In:
BMC medicine vol. 6
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218.
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A randomized, double-blind, placebo-controlled trial of coenzyme Q10 in Huntington disease. [electronic resource] by
- McGarry, Andrew
- McDermott, Michael
- Kieburtz, Karl
- de Blieck, Elisabeth A
- Beal, Flint
- Marder, Karen
- Ross, Christopher
- Shoulson, Ira
- Gilbert, Peter
- Mallonee, William M
- Guttman, Mark
- Wojcieszek, Joanne
- Kumar, Rajeev
- LeDoux, Mark S
- Jenkins, Mary
- Rosas, H Diana
- Nance, Martha
- Biglan, Kevin
- Como, Peter
- Dubinsky, Richard M
- Shannon, Kathleen M
- O'Suilleabhain, Padraig
- Chou, Kelvin
- Walker, Francis
- Martin, Wayne
- Wheelock, Vicki L
- McCusker, Elizabeth
- Jankovic, Joseph
- Singer, Carlos
- Sanchez-Ramos, Juan
- Scott, Burton
- Suchowersky, Oksana
- Factor, Stewart A
- Higgins, Donald S
- Molho, Eric
- Revilla, Fredy
- Caviness, John N
- Friedman, Joseph H
- Perlmutter, Joel S
- Feigin, Andrew
- Anderson, Karen
- Rodriguez, Ramon
- McFarland, Nikolaus R
- Margolis, Russell L
- Farbman, Eric S
- Raymond, Lynn A
- Suski, Valerie
- Kostyk, Sandra
- Colcher, Amy
- Seeberger, Lauren
- Epping, Eric
- Esmail, Sherali
- Diaz, Nancy
- Fung, Wai Lun Alan
- Diamond, Alan
- Frank, Samuel
- Hanna, Philip
- Hermanowicz, Neal
- Dure, Leon S
- Cudkowicz, Merit
Producer: 20170519
In:
Neurology vol. 88
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Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials. [electronic resource] by
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- Shoulson, Ira
- Kieburtz, Karl
- Oakes, David
- Kayson, Elise
- Shinaman, M Aileen
- Zhao, Hongwei
- Romer, Megan
- Young, Anne
- Hersch, Steven
- Penney, Jack
- Marder, Karen
- Paulsen, Jane
- Quaid, Kimberly
- Siemers, Eric
- Tanner, Caroline
- Mallonee, William
- Suter, Greg
- Dubinsky, Richard
- Gray, Carolyn
- Nance, Martha
- Bundlie, Scott
- Radtke, Dawn
- Kostyk, Sandra
- Baic, Corrine
- Caress, James
- Walker, Francis
- Hunt, Victoria
- O'Neill, Christine
- Chouinard, Sylvain
- Factor, Stewart
- Greenamyre, Timothy
- Wood-Siverio, Cathy
- Corey-Bloom, Jody
- Song, David
- Peavy, Guerry
- Moskowitz, Carol
- Wesson, Melissa
- Samii, Ali
- Bird, Thomas
- Lipe, Hillary
- Blindauer, Karen
- Marshall, Frederick
- Zimmerman, Carol
- Goldstein, Jody
- Rosas, Diana
- Novak, Peter
- Caviness, John
- Adler, Charles
- Duffy, Amy
- Wheelock, Vicki
- Tempkin, Teresa
- Richman, David
- Seeberger, Lauren
- Albin, Roger
- Chou, Kelvin L
- Racette, Brad
- Perlmutter, Joel S
- Perlman, Susan
- Bordelon, Yvette
- Martin, Wayne
- Wieler, Marguerite
- Leavitt, Blair
- Raymond, Lynn
- Decolongon, Joji
- Clarke, Lorne
- Jankovic, Joseph
- Hunter, Christine
- Hauser, Robert A
- Sanchez-Ramos, Juan
- Furtado, Sarah
- Suchowersky, Oksana
- Klimek, Mary Lou
- Guttman, Mark
- Sethna, Rustom
- Feigin, Andrew
- Cox, Marie
- Shannon, Barbara
- Percy, Alan
- Dure, Leon
- Harrison, Madaline
- Johnson, William
- Higgins, Donald
- Molho, Eric
- Nickerson, Constance
- Evans, Sharon
- Hobson, Douglas
- Singer, Carlos
- Galvez-Jimenez, Nestor
- Shannon, Kathleen
- Comella, Cynthia
- Ross, Christopher
- Saint-Hilaire, Marie H
- Testa, Claudia
- Rosenblatt, Adam
- Hogarth, Penelope
- Weiner, William
- Como, Peter
- Kumar, Rajeev
- Cotto, Candace
- Stout, Julie
- Brocht, Alicia
- Watts, Arthur
- Eberly, Shirley
- Weaver, Christine
- Foroud, Tatiana
- Gusella, James
- MacDonald, Marcy
- Myers, Richard
- Fahn, Stanley
- Shults, Clifford
Producer: 20160513
In:
JAMA neurology vol. 73
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A randomized clinical trial of high-dosage coenzyme Q10 in early Parkinson disease: no evidence of benefit. [electronic resource] by
- Beal, M Flint
- Oakes, David
- Shoulson, Ira
- Henchcliffe, Claire
- Galpern, Wendy R
- Haas, Richard
- Juncos, Jorge L
- Nutt, John G
- Voss, Tiffini Smith
- Ravina, Bernard
- Shults, Clifford M
- Helles, Karen
- Snively, Victoria
- Lew, Mark F
- Griebner, Brian
- Watts, Arthur
- Gao, Shan
- Pourcher, Emmanuelle
- Bond, Louisette
- Kompoliti, Katie
- Agarwal, Pinky
- Sia, Cherissa
- Jog, Mandar
- Cole, Linda
- Sultana, Munira
- Kurlan, Roger
- Richard, Irene
- Deeley, Cheryl
- Waters, Cheryl H
- Figueroa, Angel
- Arkun, Ani
- Brodsky, Matthew
- Ondo, William G
- Hunter, Christine B
- Jimenez-Shahed, Joohi
- Palao, Alicia
- Miyasaki, Janis M
- So, Julie
- Tetrud, James
- Reys, Liza
- Smith, Katharine
- Singer, Carlos
- Blenke, Anita
- Russell, David S
- Cotto, Candace
- Friedman, Joseph H
- Lannon, Margaret
- Zhang, Lin
- Drasby, Edward
- Kumar, Rajeev
- Subramanian, Thyagarajan
- Ford, Donna Stuppy
- Grimes, David A
- Cote, Diane
- Conway, Jennifer
- Siderowf, Andrew D
- Evatt, Marian Leslie
- Sommerfeld, Barbara
- Lieberman, Abraham N
- Okun, Michael S
- Rodriguez, Ramon L
- Merritt, Stacy
- Swartz, Camille Louise
- Martin, W R Wayne
- King, Pamela
- Stover, Natividad
- Guthrie, Stephanie
- Watts, Ray L
- Ahmed, Anwar
- Fernandez, Hubert H
- Winters, Adrienna
- Mari, Zoltan
- Dawson, Ted M
- Dunlop, Becky
- Feigin, Andrew S
- Shannon, Barbara
- Nirenberg, Melissa Jill
- Ogg, Mattson
- Ellias, Samuel A
- Thomas, Cathi-Ann
- Frei, Karen
- Bodis-Wollner, Ivan
- Glazman, Sofya
- Mayer, Thomas
- Hauser, Robert A
- Pahwa, Rajesh
- Langhammer, April
- Ranawaya, Ranjit
- Derwent, Lorelei
- Sethi, Kapil D
- Farrow, Buff
- Prakash, Rajan
- Litvan, Irene
- Robinson, Annette
- Sahay, Alok
- Gartner, Maureen
- Hinson, Vanessa K
- Markind, Samuel
- Pelikan, Melisa
- Perlmutter, Joel S
- Hartlein, Johanna
- Molho, Eric
- Evans, Sharon
- Adler, Charles H
- Duffy, Amy
- Lind, Marlene
- Elmer, Lawrence
- Davis, Kathy
- Spears, Julia
- Wilson, Stephanie
- Leehey, Maureen A
- Hermanowicz, Neal
- Niswonger, Shari
- Shill, Holly A
- Obradov, Sanja
- Rajput, Alex
- Cowper, Marilyn
- Lessig, Stephanie
- Song, David
- Fontaine, Deborah
- Zadikoff, Cindy
- Williams, Karen
- Blindauer, Karen A
- Bergholte, Jo
- Propsom, Clara Schindler
- Stacy, Mark A
- Field, Joanne
- Mihaila, Dragos
- Chilton, Mark
- Uc, Ergun Y
- Sieren, Jeri
- Simon, David K
- Kraics, Lauren
- Silver, Althea
- Boyd, James T
- Hamill, Robert W
- Ingvoldstad, Christopher
- Young, Jennifer
- Thomas, Karen
- Kostyk, Sandra K
- Wojcieszek, Joanne
- Pfeiffer, Ronald F
- Panisset, Michel
- Beland, Monica
- Reich, Stephen G
- Cines, Michelle
- Zappala, Nancy
- Rivest, Jean
- Zweig, Richard
- Lumina, L Pepper
- Hilliard, Colette Lynn
- Grill, Stephen
- Kellermann, Marye
- Tuite, Paul
- Rolandelli, Susan
- Kang, Un Jung
- Young, Joan
- Rao, Jayaraman
- Cook, Maureen M
- Severt, Lawrence
- Boyar, Karyn
Producer: 20140707
In:
JAMA neurology vol. 71
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