A randomized, double-blind comparison of two topical anesthesic formulations prior to electrodesiccation of dermatosis papulosa nigra by CARTER, Eric L, COPPOLA, Carol A, BARSANTI, Franco A

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Editorial by Zhan Chen Brian P. Coppola Carol A. Fierke

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A Randomized, Double-Blind Comparison of Two Topical Anesthesic Formulations Prior to Electrodesiccation of Dermatosis Papulosa Nigra: COMPARISON OF TWO TOPICAL ANESTHESIC FORMULAT... by CARTER, ERIC L., COPPOLA, CAROL A., BARSANTI, FRANCO A.

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A Randomized, Double‐Blind Comparison of Two Topical Anesthesic Formulations Prior to Electrodesiccation of Dermatosis Papulosa Nigra by CARTER, ERIC L., COPPOLA, CAROL A., BARSANTI, FRANCO A.

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A randomized, double-blind comparison of two topical anesthetic formulations prior to electrodesiccation of dermatosis papulosa nigra by Carter, Eric L, Coppola, Carol A, Barsanti, Franco A

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Fine-mapping of the human leukocyte antigen locus as a risk factor for Alzheimer disease: A case-control study by Steele, Natasha Z R, Carr, Jessie S, Bonham, Luke W, Geier, Ethan G, Damotte, Vincent, Miller, Zachary A, Desikan, Rahul S, Boehme, Kevin L, Mukherjee, Shubhabrata, Crane, Paul K, Kauwe, John S K, Kramer, Joel H, Miller, Bruce L, Coppola, Giovanni, Hollenbach, Jill A, Huang, Yadong, Yokoyama, Jennifer S

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Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies by Yu, Dongmei, Sul, Jae Hoon, Tsetsos, Fotis, Nawaz, Muhammad S, Huang, Alden Y, Zelaya, Ivette, Illmann, Cornelia, Osiecki, Lisa, Darrow, Sabrina M, Hirschtritt, Matthew E, Greenberg, Erica, Muller-Vahl, Kirsten R, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Sandor, Paul, Barr, Cathy L, Grados, Marco, Singer, Harvey S, Nöthen, Markus M, Hebebrand, Johannes, Hinney, Anke, King, Robert A, Fernandez, Thomas V, Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L, Rizzo, Renata, Lyon, Gholson J, McMahon, William M, Batterson, James R, Cath, Danielle C, Malaty, Irene A, Okun, Michael S, Berlin, Cheston, Woods, Douglas W, Lee, Paul C, Jankovic, Joseph, Robertson, Mary M, Gilbert, Donald L, Brown, Lawrence W, Coffey, Barbara J, Dietrich, Andrea, Hoekstra, Pieter J, Kuperman, Samuel, Zinner, Samuel H, Luðvigsson, Pétur, Sæmundsen, Evald, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Wagner, Michael, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N, Pato, Michele T, Knowles, James A, Roffman, Joshua L, Smoller, Jordan W, Buckner, Randy L, Willsey, A. Jeremy, Tischfield, Jay A, Heiman, Gary A, Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Cox, Nancy J, Pauls, David L, Freimer, Nelson B, Neale, Benjamin M, Davis, Lea K, Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A, Scharf, Jeremiah M

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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders by Tucker-Drob, Elliot M., Yu, Dongmei, Ge, Tian, Derks, Eske M., Keski-Rahkonen, Anna, Kirov, George, Asherson, Philip, Baldursson, Gísli, Bybjerg-Grauholm, Jonas, Churchhouse, Claire, Crosbie, Jennifer, Demontis, Ditte, Grove, Jakob, Martin, Joanna, McGough, James J., Pedersen, Carsten B., Poulsen, Jesper B., Rothenberger, Aribert, Schachar, Russell, Turley, Patrick, Arking, Dan E., Collins, Ryan L., Coon, Hilary, Delorme, Richard, Hope, Sigrun, Nyegaard, Mette, Pinto, Dalila, Qvist, Per, Talkowski, Michael E., Albani, Diego, Alda, Martin, Bass, Nicholas, Bauer, Michael, Cichon, Sven, Clarke, Toni-Kim, Czerski, Piotr M., Fischer, Sascha B., Frank, Josef, Goes, Fernando S., Holland, Dominic, Jones, Lisa A., Joachim, Oedegaard Ketil, Maaser, Anna, Malt, Ulrik F., McMahon, Francis J., Montgomery, Grant W., Myers, Richard M., Nöthen, Markus M., Perry, Amy, Vieta, Eduard, Aschauer, Harald, Bencko, Vladimir, Burghardt, Roland, Carlberg, Laura, Guo, Yiran, Klump, Kelly L., Le Hellard, Stephanie, Monteleone, Alessio Maria, Seitz, Jochen, Treasure, Janet, Wade, Tracey D., Wichmann, H-Erich, Woodside, D. Blake, Grabe, Hans J., Horn, Carsten, Penninx, Brenda WJH, Schulte, Eva C., Smith, Daniel J., Alexander, Madeline, Begemann, Martin, Campion, Dominique, Ehrenreich, Hannelore, Murphy, Kieran C., Riley, Brien, Sham, Pak C., van Os, Jim, Weiser, Mark, Brown, Lawrence W., Cheon, Keun-Ah, Denys, Damiaan, Gilbert, Donald L., Grados, Marco A., Ibanez-Gomez, Laura, King, Robert A., Leventhal, Bennett L., Okun, Michael S., Piras, Federica, Robertson, Mary, Samuels, Jack F., Spalletta, Gianfranco, Stein, Dan J., Stewart, S Evelyn, Storch, Eric A., Stranger, Barbara, Tübing, Jennifer, Visscher, Frank, Wagner, Michael, Santangelo, Susan L., Thornton, Laura M., Neale, Benjamin M.

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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome by Huang, Alden Y., Yu, Dongmei, Davis, Lea K., Sul, Jae Hoon, Tsetsos, Fotis, Ramensky, Vasily, Zelaya, Ivette, Ramos, Eliana Marisa, Osiecki, Lisa, Chen, Jason A., McGrath, Lauren M., Illmann, Cornelia, Sandor, Paul, Barr, Cathy L., Grados, Marco, Singer, Harvey S., Nöthen, Markus M., Hebebrand, Johannes, King, Robert A., Dion, Yves, Rouleau, Guy, Budman, Cathy L., Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Müller-Vahl, Kirsten R., Stuhrmann, Manfred, Aschauer, Harald, Stamenkovic, Mara, Schloegelhofer, Monika, Konstantinidis, Anastasios, Lyon, Gholson J., McMahon, William M., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Batterson, James R., Rizzo, Renata, Cath, Danielle C., Wolanczyk, Tomasz, Berlin, Cheston, Malaty, Irene A., Okun, Michael S., Woods, Douglas W., Rees, Elliott, Pato, Carlos N., Pato, Michele T., Knowles, James A., Posthuma, Danielle, Pauls, David L., Cox, Nancy J., Neale, Benjamin M., Freimer, Nelson B., Paschou, Peristera, Mathews, Carol A., Scharf, Jeremiah M., Coppola, Giovanni, Bruun, Ruth D., Chouinard, Sylvain, Darrow, Sabrina, Greenberg, Erica, Hirschtritt, Matthew E., Kurlan, Roger, Leckman, James F., Robertson, Mary M., Smit, Jan

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Comparing Methods to Constrain Future European Climate Projections Using a Consistent Framework by Brunner, Lukas, McSweeney, Carol, Ballinger, Andrew P., Befort, Daniel J., Benassi, Marianna, Booth, Ben, Coppola, Erika, de Vries, Hylke, Harris, Glen, Hegerl, Gabriele C., Knutti, Reto, Lenderink, Geert, Lowe, Jason, Nogherotto, Rita, O’Reilly, Chris, Qasmi, Saïd, Ribes, Aurélien, Stocchi, Paolo, Undorf, Sabine

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De Novo Coding Variants Are Strongly Associated with Tourette Disorder by Willsey, A. Jeremy, Yu, Dongmei, King, Robert A., Dietrich, Andrea, Xing, Jinchuan, Richer, Petra, Smith, Louw, Dong, Shan, Samocha, Kaitlin E., Bohnenpoll, Julia, Bromberg, Yana, Brown, Lawrence W., Cheon, Keun-Ah, Coffey, Barbara J., Deng, Li, Dong, Shan, Elzerman, Lonneke, Fernandez, Thomas V., Fründt, Odette, Garcia-Delgar, Blanca, Gedvilaite, Erika, Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heiman, Gary A., Heyman, Isobel, Hoekstra, Pieter J., Hong, Hyun Ju, Ibanez-Gomez, Laura, Kim, Young Key, Kim, Young-Shin, King, Robert A., Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Lamerz, Andreas, Ludolph, Andrea G., Lühr da Silva, Claudia, Madruga-Garrido, Marcos, Mir, Pablo, Münchau, Alexander, Murphy, Tara L., Nasello, Cara, Openneer, Thaïra J.C., Plessen, Kerstin J., Richer, Petra, Roessner, Veit, Sanders, Stephan, Smith, Louw, Song, Dong-Ho, State, Matthew W., Stolte, Anne Marie, Sun, Nawei, Tischfield, Jay A., Tübing, Jennifer, Visscher, Frank, Walker, Michael F., Wanderer, Sina, Wang, Shuoguo, Willsey, A. Jeremy, Woods, Martin, Xing, Jinchuan, Zhang, Yeting, Zhou, Anbo, Zinner, Samuel H., Batterson, James R., Berlin, Cheston, Bruun, Ruth D., Budman, Cathy L., Cath, Danielle C., Chouinard, Sylvain, Coppola, Giovanni, Cox, Nancy J., Darrow, Sabrina, Davis, Lea K., Freimer, Nelson B., Grados, Marco A., Hirschtritt, Matthew E., Illmann, Cornelia, Kurlan, Roger, Lyon, Gholson J., Malaty, Irene A., Mathews, Carol A., Neale, Benjamin M., Okun, Michael S., Osiecki, Lisa, Posthuma, Danielle, Ramensky, Vasily, Robertson, Mary M., Rouleau, Guy A., Sandor, Paul, Singer, Harvey S., Yu, Dongmei, Neale, Benjamin M., Coppola, Giovanni, Mathews, Carol A., Tischfield, Jay A., Scharf, Jeremiah M., State, Matthew W., Heiman, Gary A.

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Examining Ecological Constraints on the Intergenerational Transmission of Attachment Via Individual Participant Data Meta-analysis by Verhage, Marije L., Schuengel, Carlo, Bakermans-Kranenburg, Marian J., Roisman, Glenn I., Behrens, Kazuko Y., Mangelsdorf, Sarah, Brisch, Karl-Heinz, Fearon, R.M. Pasco, van IJzendoorn, Marinus H., Madigan, Sheri, Oosterman, Mirjam, Wong, Maria S., Priddis, Lynn E.

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Assessing observational constraints on future European climate in an out-of-sample framework by O’Reilly, Christopher H., Brunner, Lukas, Qasmi, Saïd, Nogherotto, Rita, Ballinger, Andrew P., Booth, Ben, Befort, Daniel J., Knutti, Reto, Schurer, Andrew P., Ribes, Aurélien, Weisheimer, Antje, Coppola, Erika, McSweeney, Carol

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Genome-Wide Association Study Points to Novel Locus for Gilles de la Tourette Syndrome by Jain, Pritesh, Yang, Zhiyu, Yu, Dongmei, Tumer, Zeynep, Hartmann, Andreas, Müller-Vahl, Kirsten R., Boomsma, Dorret I., Wolanczyk, Tomasz, Nemoda, Zsofia, Padmanabhuni, Shanmukha S., Grice, Dorothy, Glennon, Jeffrey, Stefansson, Hreinn, Stamatoyannopoulos, John A., Benaroya-Milshtein, Noa, Cardona, Francesco, Heyman, Isobel, Mir, Pablo, Munchau, Alexander, Plessen, Kerstin J., Roessner, Veit, Martino, Davide, Barr, Cathy L., Batterson, James R., Budman, Cathy L., Coppola, Giovanni, Darrow, Sabrina, Freimer, Nelson B., Grados, Marco A., Greenberg, Erica, Huang, Alden Y., Illmann, Cornelia, Kurlan, Roger, Leckman, James F., Malaty, Irene A., McMahon, William M., Neale, Benjamin M., Osiecki, Lisa, Rouleau, Guy A., Sul, Jae Hoon, Androutsos, Christos, Basha, Entela, Farkas, Luca, Janik, Piotr, Kapisyzi, Mira, Karagiannidis, Iordanis, Koumoula, Anastasia, Nagy, Peter, Puchala, Joanna, Szymanska, Urszula, Apter, Alan, Bodmer, Benjamin, Bognar, Emese, Buse, Judith, Fremer, Carolin, Garcia-Delgar, Blanca, Hagen, Annelieke, Hagstrøm, Julie, Madruga-Garrido, Marcos, Silvestri, Paola Rosaria, Skov, Liselotte, Steinberg, Tamar, Turner, Victoria L., Alexander, John, Aranyi, Tamas, Fan, Siyan, Forde, Natalie J., Gerasch, Sarah, Kanaan, Ahmad S., Möller, Harald E., Poelmans, Geert, Pouwels, Petra J.W., Rizzo, Francesca, Veltman, Dick J., van der Werf, Ysbrand D., Widomska, Joanna, Zilhäo, Nuno R., Brown, Lawrence W., Cheon, Keun-Ah, Fernandez, Thomas V., Kim, Eun-Joo, Kim, Young Key, Koh, Yun-Joo, Kook, Sodahm, Kuperman, Samuel, Maras, Athanasios, Murphy, Tara L., Shin, Eun-Young, Song, Dong-Ho, State, Matthew W., Visscher, Frank, Heiman, Gary A., Willsey, A. Jeremy, Dietrich, Andrea, Davis, Lea K., Crowley, James J., Scharf, Jeremiah M., Georgitsi, Marianthi, Hoekstra, Pieter J., Paschou, Peristera

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Collaborative Genome-Wide Association and Copy Number Variation Analysis of Tourette Syndrome by Scharf, Jeremiah, Yu, Dongmei, Huang, Alden, Tsetsos, Fotis, Paschou, Peristera, Coppola, Giovanni, Mathews, Carol

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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases by COPPOLA, Giovanni, CHINNATHAMBI, Subashchandrabose, LANE, Jessica R, KARYDAS, Anna M, KENET, Robert O, BIERNAT, Jacek, WANG, Li-San, COTMAN, Carl W, DECARLI, Charles S, LEVEY, Allan I, RINGMAN, John M, MENDEZ, Mario F, JIYONG LEE, Jason, CHUI, Helena C, LE BER, Isabelle, BRICE, Alexis, LUPTON, Michelle K, PREZA, Elisavet, LOVESTONE, Simon, POWELL, John, GRAFF-RADFORD, Neill, PETERSEN, Ronald C, BOEVE, Bradley F, DOMBROSKI, Beth A, LIPPA, Carol F, BIGIO, Eileen H, MACKENZIE, Ian, FINGER, Elizabeth, KERTESZ, Andrew, CASELLI, Richard J, GEARING, Marla, JUNCOS, Jorge L, GHETTI, Bernardino, SPINA, Salvatore, BAKER, Matt C, BORDELON, Yvette M, TOURTELLOTTE, Wallace W, FROSCH, Matthew P, VONSATTEL, Jean Paul G, ZAROW, Chris, BEACH, Thomas G, ALBIN, Roger L, LIEBERMAN, Andrew P, LEE, Virginia M, TROJANOWSKI, John Q, SOTO-ORTOLAZA, Alexandra I, VAN DEERLIN, Vivianna M, BIRD, Thomas D, GALASKO, Douglas R, MASLIAH, Eliezer, WHITE, Charles L, TRONCOSO, JuanC, HANNEQUIN, Didier, BOXER, Adam L, GESCHWIND, Michael D, KUMAR, Satish, LEE, Suzee E, KLEIN, Eric, HUANG, Alden Y, SEARS, Renee

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De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis by Wang, Sheng, Mandell, Jeffrey D., Kumar, Yogesh, Sun, Nawei, Nasello, Cara, Dong, Shan, Duhn, Clif, Zhao, Xin, Yang, Zhiyu, Padmanabhuni, Shanmukha S., Yu, Dongmei, King, Robert A., Dietrich, Andrea, Dahl, Niklas, Huang, Alden Y., Neale, Benjamin M., Mathews, Carol A., Abdulkadir, Mohamed, Arbelaez, Juan, Bodmer, Benjamin, Coffey, Barbara J., Deng, Li, Dietrich, Andrea, Duhn, Clif, Fernandez, Thomas V., Fremer, Carolin, Gilbert, Donald L., Grice, Dorothy E., Hagstrøm, Julie, Hedderly, Tammy, Heiman, Gary A., Hong, Hyun Ju, Huyser, Chaim, Kim, Eun-Joo, Kim, Young Key, Kim, Young-Shin, King, Robert A., Kuperman, Samuel, Mandell, Jeffrey D., Maras, Athanasios, Müller-Vahl, Kirsten, Münchau, Alexander, Nasello, Cara, Plessen, Kerstin J., Poisner, Hannah, Roessner, Veit, Sanders, Stephan J., Song, Jungeun, State, Matthew W., Tischfield, Jay A., Wanderer, Sina, Wang, Sheng, Willsey, A Jeremy, Xing, Jinchuan, Zhang, Yeting, Zhao, Xin, Zinner, Samuel H., Androutsos, Christos, Barta, Csaba, Farkas, Luca, Janik, Piotr, Karagiannidis, Iordanis, Koumoula, Anastasia, Nagy, Peter, Rizzo, Renata, Szymanska, Urszula, Tarnok, Zsanett, Tsironi, Vaia, Zekanowski, Cezary, Batterson, James R., Berlin, Cheston, Bruun, Ruth D., Budman, Cathy L., Chouinard, Sylvain, Coppola, Giovanni, Darrow, Sabrina, Dion, Yves, Freimer, Nelson B., Grados, Marco A., Hirschtritt, Matthew E., Kurlan, Roger, Lyon, Gholson J., Malaty, Irene A., MacMahon, William M., Neale, Benjamin M., Pauls, David L., Ramensky, Vasily, Robertson, Mary M., Scharf, Jeremiah M., Singer, Harvey S., Smit, Jan, Sul, Jae-Hoon, Yu, Dongmei, Fernandez, Thomas V., De Rubeis, Silvia, Xing, Jinchuan, Tischfield, Jay A., Paschou, Peristera, Willsey, A. Jeremy, State, Matthew W.

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Elevated common variant genetic risk for tourette syndrome in a densely-affected pedigree by Halvorsen, Matthew, Szatkiewicz, Jin, Mudgal, Poorva, Yu, Dongmei, Nordsletten, Ashley E., Mataix-Cols, David, Mathews, Carol A., Scharf, Jeremiah M., Mattheisen, Manuel, Robertson, Mary M., McQuillin, Andrew, Crowley, James J.

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Genome-Wide Association Study Meta-Analysis of 9619 Cases With Tic Disorders by Strom, Nora I., Halvorsen, Matthew W., Grove, Jakob, Ásbjörnsdóttir, Bergrún, Thorarensen, Ólafur, de Schipper, Elles, Bäckmann, Julia, Tian, Chao, Sul, Jae Hoon, Tsetsos, Fotis, Zelaya, Ivette, Osiecki, Lisa, Darrow, Sabrina M., Hirschtritt, Matthew E., Greenberg, Erica, Stuhrmann, Manfred, Dion, Yves, Rouleau, Guy, Aschauer, Harald, Stamenkovic, Mara, Schlögelhofer, Monika, Barr, Cathy L., Grados, Marco, Hinney, Anke, King, Robert A., Fernandez, Thomas V., Barta, Csaba, Tarnok, Zsanett, Nagy, Peter, Depienne, Christel, Worbe, Yulia, Hartmann, Andreas, Budman, Cathy L., Lyon, Gholson J., McMahon, William M., Batterson, James R., Malaty, Irene A., Okun, Michael S., Berlin, Cheston, Woods, Douglas W., Lee, Paul C., Jankovic, Joseph, Robertson, Mary M., Gilbert, Donald L., Brown, Lawrence W., Coffey, Barbara J., Hoekstra, Pieter J., Zinner, Samuel H., Luðvigsson, Pétur, Thorarensen, Ólafur, Atzmon, Gil, Barzilai, Nir, Moessner, Rainald, Ophoff, Roel, Pato, Carlos N., Knowles, James A., Buckner, Randy L., Willsey, Jeremy A., Tischfield, Jay A., Heiman, Gary A., Stefansson, Hreinn, Stefansson, Kári, Posthuma, Danielle, Pauls, David L., Freimer, Nelson B., Davis, Lea K., Paschou, Peristera, Coppola, Giovanni, Mathews, Carol A., Scharf, Jeremiah M., Agee, Michelle, Auton, Adam, Elson, Sarah L., Furlotte, Nicholas A., Hicks, Barry, Jewett, Ethan M., Jiang, Yunxuan, Kleinman, Aaron, Lin, Keng-Han, Litterman, Nadia K., McIntyre, Matthew H., McManus, Kimberly F., Mountain, Joanna L., Pitts, Steven J., Poznik, G. David, Sathirapongsasuti, J. Fah, Shelton, Janie F., Shringarpure, Suyash, Tung, Joyce Y., Wang, Xin, Als, Thomas Damm, Meier, Sandra M., Bybjerg-Grauholm, Jonas, Hougaard, David M., Werge, Thomas, Børglum, Anders D., Hinds, David A., Rück, Christian, Mataix-Cols, David, Mattheisen, Manuel

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Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C→T (Arg493X) mutation: an international initiative by Rademakers, Rosa, PhD, Baker, Matt, BSc, Gass, Jennifer, BS, Adamson, Jennifer, BS, Huey, Edward D, MD, Momeni, Parastoo, PhD, Spina, Salvatore, MD, Coppola, Giovanni, MD, Karydas, Anna M, BA, Stewart, Heather, PhD, Johnson, Nancy, PhD, Hsiung, Ging-Yuek, MD, Kelley, Brendan, MD, Kuntz, Karen, RN, Steinbart, Ellen, MA, Wood, Elisabeth McCarty, MS, Yu, Chang-En, PhD, Josephs, Keith, MD, Sorenson, Eric, MD, Womack, Kyle B, MD, Weintraub, Sandra, PhD, Pickering-Brown, Stuart M, PhD, Schofield, Peter R, DSc, Brooks, William S, MBBS, Van Deerlin, Vivianna M, MD, Snowden, Julie, PhD, Clark, Christopher M, MD, Kertesz, Andrew, MD, Boylan, Kevin, MD, Ghetti, Bernardino, MD, Neary, David, FRCP, Schellenberg, Gerard D, PhD, Beach, Thomas G, FRCPC, Mesulam, Marsel, MD, Mann, David, PhD, Grafman, Jordan, PhD, Mackenzie, Ian R, MD, Feldman, Howard, MD, Bird, Thomas, MD, Petersen, Ron, MD, Knopman, David, MD, Boeve, Bradley, MD, Geschwind, Dan H, MD, Miller, Bruce, MD, Wszolek, Zbigniew, MD, Lippa, Carol, MD, Bigio, Eileen H, MD, Dickson, Dennis, MD, Graff-Radford, Neill, FRCP, Hutton, Mike, PhD

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