Cerebrospinal fluid, plasma, and saliva in the BioFIND study: Relationships among biomarkers and Parkinson's disease Features by Goldman, Jennifer G., Andrews, Howard, Amara, Amy, Naito, Anna, Alcalay, Roy N., Shaw, Leslie M., Taylor, Peggy, Xie, Tao, Tuite, Paul, Henchcliffe, Claire, Hogarth, Penelope, Frank, Samuel, Saint‐Hilaire, Marie‐Helene, Frasier, Mark, Arnedo, Vanessa, Reimer, Alyssa N., Sutherland, Margaret, Swanson‐Fischer, Christine, Gwinn, Katrina, Kang, Un Jung

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Exome Sequencing Reveals De Novo WDR45 Mutations Causing a Phenotypically Distinct, X-Linked Dominant Form of NBIA by Haack, Tobias B., Hogarth, Penelope, Kruer, Michael C., Gregory, Allison, Wieland, Thomas, Schwarzmayr, Thomas, Graf, Elisabeth, Sanford, Lynn, Meyer, Esther, Kara, Eleanna, Cuno, Stephan M., Harik, Sami I., Dandu, Vasuki H., Nardocci, Nardo, Zorzi, Giovanna, Dunaway, Todd, Tarnopolsky, Mark, Skinner, Steven, Frucht, Steven, Hanspal, Era, Schrander-Stumpel, Connie, Héron, Delphine, Mignot, Cyril, Garavaglia, Barbara, Bhatia, Kailash, Hardy, John, Strom, Tim M., Boddaert, Nathalie, Houlden, Henry H., Kurian, Manju A., Meitinger, Thomas, Prokisch, Holger, Hayflick, Susan J.

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MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder by Heimer, Gali, Kerätär, Juha M., Riley, Lisa G., Balasubramaniam, Shanti, Eyal, Eran, Pietikäinen, Laura P., Hiltunen, J. Kalervo, Marek-Yagel, Dina, Hamada, Jeffrey, Gregory, Allison, Rogers, Caleb, Hogarth, Penelope, Nance, Martha A., Shalva, Nechama, Veber, Alvit, Tzadok, Michal, Nissenkorn, Andreea, Tonduti, Davide, Renaldo, Florence, Bamshad, Michael J., Leal, Suzanne M., Nickerson, Deborah A., Anderson, Peter, Annable, Marcus, Blue, Elizabeth Marchani, Buckingham, Kati J., Chin, Jennifer, Chong, Jessica X., Cornejo, Rodolfo, Davis, Colleen P., Frazar, Christopher, He, Zongxiao, Jarvik, Gail P., Jimenez, Guillaume, Johanson, Eric, Kolar, Tom, Krauter, Stephanie A., Luksic, Daniel, Marvin, Colby T., McGee, Sean, McGoldrick, Daniel J., Patterson, Karynne, Perez, Marcos, Phillips, Sam W., Pijoan, Jessica, Robertson, Peggy D., Santos-Cortez, Regie, Shankar, Aditi, Slattery, Krystal, Shively, Kathryn M., Siegel, Deborah L., Smith, Joshua D., Tackett, Monica, Wang, Gao, Wegener, Marc, Weiss, Jeffrey M., Wernick, Riana I., Wheeler, Marsha M., Yi, Qian, Kraoua, Ichraf, Panteghini, Celeste, Valletta, Lorella, Garavaglia, Barbara, Cowley, Mark J., Gayevskiy, Velimir, Roscioli, Tony, Silberstein, Jonathon M., Hoffmann, Chen, Raas-Rothschild, Annick, Tiranti, Valeria, Anikster, Yair, Christodoulou, John, Kastaniotis, Alexander J., Ben-Zeev, Bruria, Hayflick, Susan J.

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Brain MRI Pattern Recognition in Neurodegeneration With Brain Iron Accumulation by Lee, Jae-Hyeok, Yun, Ji Young, Gregory, Allison, Hogarth, Penelope, Hayflick, Susan J

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4′‐Phosphopantetheine corrects CoA, iron, and dopamine metabolic defects in mammalian models of PKAN by Jeong, Suh Young, Hogarth, Penelope, Placzek, Andrew, Gregory, Allison M, Fox, Rachel, Zhen, Dolly, Hamada, Jeffrey, van der Zwaag, Marianne, Lambrechts, Roald, Jin, Haihong, Nilsen, Aaron, Cobb, Jared, Pham, Thao, Gray, Nora, Ralle, Martina, Duffy, Megan, Schwanemann, Leila, Rai, Puneet, Freed, Alison, Wakeman, Katrina, Woltjer, Randall L, Sibon, Ody CM, Hayflick, Susan J

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Sodium phenylbutyrate in Huntington's disease: A dose-finding study by Hogarth, Penelope, Lovrecic, Luca, Krainc, Dimitri

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Neurodegeneration with Brain Iron Accumulation: Diagnosis and Management by Hogarth, Penelope

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Immunohistochemical Method and Histopathology Judging for the Systemic Synuclein Sampling Study (S4) by Beach, Thomas G, Serrano, Geidy E, Kremer, Thomas, Canamero, Marta, Dziadek, Sebastian, Sade, Hadassah, Derkinderen, Pascal, Corbillé, Anne-Gaëlle, Letournel, Franck, Munoz, David G, White, Charles L, Schneider, Julie, Crary, John F, Sue, Lucia I, Adler, Charles H, Glass, Michael J, Intorcia, Anthony J, Walker, Jessica E, Foroud, Tatiana, Coffey, Christopher S, Ecklund, Dixie, Riss, Holly, Goßmann, Jennifer, König, Fatima, Kopil, Catherine M, Arnedo, Vanessa, Riley, Lindsey, Linder, Carly, Dave, Kuldip D, Jennings, Danna, Seibyl, John, Mollenhauer, Brit, Chahine, Lana

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The effect of deep brain stimulation randomized by site on balance in Parkinson's disease by St George, Rebecca J., Carlson-Kuhta, Patricia, Nutt, John G., Hogarth, Penelope, Burchiel, Kim J., Horak, Fay B.

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Effects of a NR2B selective NMDA glutamate antagonist, CP-101,606, on dyskinesia and parkinsonism by Nutt, John G., Gunzler, Steven A., Kirchhoff, Trish, Hogarth, Penelope, Weaver, Jerry L., Krams, Michael, Jamerson, Brenda, Menniti, Frank S., Landen, Jaren W.

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Autosomal dominant mitochondrial membrane protein‐associated neurodegeneration (MPAN) by Gregory, Allison, Lotia, Mitesh, Jeong, Suh Young, Fox, Rachel, Zhen, Dolly, Sanford, Lynn, Hamada, Jeff, Jahic, Amir, Beetz, Christian, Freed, Alison, Kurian, Manju A., Cullup, Thomas, Weijden, Marlous C. M., Nguyen, Vy, Setthavongsack, Naly, Garcia, Daphne, Krajbich, Victoria, Pham, Thao, Woltjer, Randy, George, Benjamin P., Minks, Kelly Q., Paciorkowski, Alexander R., Hogarth, Penelope, Jankovic, Joseph, Hayflick, Susan J.

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As iron goes, so goes disease? by Hayflick, Susan J, Hogarth, Penelope

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Transportation Innovation to Aid Parkinson Disease Trial Recruitment by Frank, Samuel, Berk, Sarah, Hernandez, Laura, Hogarth, Penelope, Shill, Holly A, Siddiqi, Bernadette, Simon, David K

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Safety and efficacy of deferiprone for pantothenate kinase-associated neurodegeneration: a randomised, double-blind, controlled trial and an open-label extension study by Klopstock, Thomas, Tricta, Fernando, Neumayr, Lynne, Karin, Ivan, Zorzi, Giovanna, Fradette, Caroline, Kmieć, Tomasz, Büchner, Boriana, Steele, Hannah E, Horvath, Rita, Chinnery, Patrick F, Basu, Anna, Küpper, Clemens, Neuhofer, Christiane, Kálmán, Bernadette, Dušek, Petr, Yapici, Zuhal, Wilson, Ian, Zhao, Feng, Zibordi, Federica, Nardocci, Nardo, Aguilar, Christine, Hayflick, Susan J, Spino, Michael, Blamire, Andrew M, Hogarth, Penelope, Vichinsky, Elliott

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The Parkinson Progression Marker Initiative (PPMI) by Marek, Kenneth, Jennings, Danna, Lasch, Shirley, Siderowf, Andrew, Tanner, Caroline, Simuni, Tanya, Coffey, Chris, Kieburtz, Karl, Flagg, Emily, Chowdhury, Sohini, Poewe, Werner, Mollenhauer, Brit, Klinik, Paracelsus-Elena, Sherer, Todd, Frasier, Mark, Meunier, Claire, Rudolph, Alice, Casaceli, Cindy, Seibyl, John, Mendick, Susan, Schuff, Norbert, Zhang, Ying, Toga, Arthur, Crawford, Karen, Ansbach, Alison, De Blasio, Pasquale, Piovella, Michele, Trojanowski, John, Shaw, Les, Singleton, Andrew, Hawkins, Keith, Eberling, Jamie, Brooks, Deborah, Russell, David, Leary, Laura, Factor, Stewart, Sommerfeld, Barbara, Hogarth, Penelope, Pighetti, Emily, Williams, Karen, Standaert, David, Guthrie, Stephanie, Hauser, Robert, Delgado, Holly, Jankovic, Joseph, Hunter, Christine, Stern, Matthew, Tran, Baochan, Leverenz, Jim, Baca, Marne, Frank, Sam, Thomas, Cathi-Ann, Richard, Irene, Deeley, Cheryl, Rees, Linda, Sprenger, Fabienne, Lang, Elisabeth, Shill, Holly, Obradov, Sanja, Fernandez, Hubert, Winters, Adrienna, Berg, Daniela, Gauss, Katharina, Galasko, Douglas, Fontaine, Deborah, Mari, Zoltan, Gerstenhaber, Melissa, Brooks, David, Malloy, Sophie, Barone, Paolo, Longo, Katia, Comery, Tom, Ravina, Bernard, Grachev, Igor, Gallagher, Kim, Collins, Michelle, Widnell, Katherine L., Ostrowizki, Suzanne, Fontoura, Paulo, Ho, Tony, Luthman, Johan, Brug, Marcel van der, Reith, Alastair D., Taylor, Peggy

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Abnormal Brain Iron Accumulation is a Rare Finding in Down Syndrome Regression Disorder by Gregory, Allison, Wilson, Jenny L., Hogarth, Penelope, Hayflick, Susan J.

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Bilateral Deep Brain Stimulation vs Best Medical Therapy for Patients With Advanced Parkinson Disease: A Randomized Controlled Trial by Weaver, Frances M, Follett, Kenneth, Stern, Matthew, Hur, Kwan, Harris, Crystal, Marks, William J, Rothlind, Johannes, Sagher, Oren, Reda, Domenic, Moy, Claudia S, Pahwa, Rajesh, Burchiel, Kim, Hogarth, Penelope, Lai, Eugene C, Duda, John E, Holloway, Kathryn, Samii, Ali, Horn, Stacy, Bronstein, Jeff, Stoner, Gatana, Heemskerk, Jill, Huang, Grant D, CSP 468 Study Group, for the

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Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectiona... by Simuni, Tanya, Uribe, Liz, Caspell-Garcia, Chelsea, Coffey, Christopher S, Siderowf, Andrew, Trojanowski, John Q, Shaw, Leslie M, Seibyl, John, Toga, Arthur W, Galasko, Doug, Tosun, Duygu, Poston, Kathleen, Weintraub, Daniel, Mollenhauer, Brit, Tanner, Caroline M, Kieburtz, Karl, Hutten, Samantha J, Bressman, Susan, Marek, Kenneth, Chowdhury, Sohini, Sherer, Todd, Casaceli, Cynthia, Dorsey, Ray, Wilson, Renee, Mahes, Sugi, Salerno, Christina, Crawford, Karen, Casalin, Paola, Malferrari, Giulia, Weisz, Mali Gani, Orr-Urtreger, Avi, Montine, Thomas, Baglieri, Chris, Russell, David, Giladi, Nir, Factor, Stewart, Hauser, Robert, Jankovic, Joseph, Saint-Hilaire, Marie, Richard, Irene, Shprecher, David, Brockmann, Katrina, Barone, Paolo, Espay, Alberto, Santiago, Anthony, Hu, Shu-Ching, Isaacson, Stuart, Corvol, Jean-Christophe, Ruiz Martinez, Javiar, Tolosa, Eduardo, Tai, Yen, Smejdir, Debra, Rees, Linda, Williams, Karen, Kausar, Farah, Richardson, Whitney, Willeke, Diana, Peacock, Shawnees, Sommerfeld, Barbara, Freed, Alison, Guthrie, Stephanie, Harrell, Leigh, Thomas, Cathi-Ann, James, Raymond, Zimmerman, Grace, Mule, Jennifer, Hilt, Ella, Ribb, Kori, Ainscough, Susan, Ranola, Madelaine, Mejia Santana, Helen, Moreno, Juliana, Raymond, Deborah, Carvajal, Lisbeth, Carvalo, Stephanie, Croitoru, Ioana, Garrido, Alicia, Payne, Laura Marie, Viswanth, Veena, Severt, Lawrence, Facheris, Maurizio, Cedarbaum, Jesse, Taylor, Peggy, Haider Sheikh, Zulfiqar, Fischer, Tanya, Sardi, Pablo, Forrat, Remi, Reith, Alastair, Ahlberg Hillert, Gabrielle, Saba, Barbara, Min, Chris, Umek, Robert, Mather, Joe, De Santi, Susan, Post, Anke, Boess, Frank, Taylor, Kirsten, Grachev, Igor, Muglia, Pierandrea, Merchant, Kaplana

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Cognitive performance and neuropsychiatric symptoms in early, untreated Parkinson's disease by Weintraub, Daniel, Simuni, Tanya, Caspell-Garcia, Chelsea, Coffey, Christopher, Lasch, Shirley, Siderowf, Andrew, Aarsland, Dag, Barone, Paolo, Burn, David, Chahine, Lama M., Eberling, Jamie, Espay, Alberto J., Foster, Eric D., Leverenz, James B., Litvan, Irene, Richard, Irene, Troyer, Matthew D., Hawkins, Keith A.

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Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study by Nalls, Mike A, PhD, McLean, Cory Y, PhD, Rick, Jacqueline, PhD, Eberly, Shirley, MS, Hutten, Samantha J, PhD, Gwinn, Katrina, MD, Sutherland, Margaret, PhD, Martinez, Maria, PhD, Heutink, Peter, PhD, Williams, Nigel M, PhD, Hardy, John, PhD, Gasser, Thomas, MD, Brice, Alexis, MD, Price, T Ryan, MS, Nicolas, Aude, PhD, Keller, Margaux F, PhD, Molony, Cliona, PhD, Gibbs, J Raphael, MS, Chen-Plotkin, Alice, MD, Suh, Eunran, PhD, Letson, Christopher, BS, Fiandaca, Massimo S, MD, Mapstone, Mark, PhD, Federoff, Howard J, MD, Noyce, Alastair J, MRCP, Morris, Huw, MD, Van Deerlin, Vivianna M, MD, Weintraub, Daniel, MD, Zabetian, Cyrus, MD, Hernandez, Dena G, MS, Lesage, Suzanne, PhD, Mullins, Meghan, BA, Conley, Emily Drabant, PhD, Northover, Carrie A M, PhD, Frasier, Mark, PhD, Marek, Ken, MD, Day-Williams, Aaron G, PhD, Stone, David J, PhD, Ioannidis, John P A, Prof, Singleton, Andrew B, Dr

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