Deficient Platelet-Derived Nitric Oxide and Enhanced Hemostasis in Mice Lacking the NOSIII Gene von Freedman, Jane E, Sauter, Ryan, Battinelli, Elisabeth M, Ault, Kenneth, Knowles, Cathy, Huang, Paul L, Loscalzo, Joseph

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Genetic control of platelet activation in inbred mouse strains von Ault, K A, Knowles, C, Mitchell, J, Brown, C L, Schultz, K L, Beamer, W G

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An Audit of Stroke Patients Referred to a Special Needs Scheme von Knowles, Cathy, Woolman, Kate

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Abnormal platelet function and calcium handling in Dahl salt-hypertensive rats von YUN LI, ADACHI, Takeshi, BOLOTINA, Victoria M, KNOWLES, Cathy, AULT, Kenneth A, COHEN, Richard A

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Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines von Mavraki, Eleni, Labrum, Robyn, Sergeant, Kate, Alston, Charlotte L, Woodward, Cathy, Smith, Conrad, Knowles, Charlotte V Y, Patel, Yogen, Hodsdon, Philip, Baines, Jack P, Blakely, Emma L, Polke, James, Taylor, Robert W, Fratter, Carl

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Caught in the trap of PLC Lite: Essential steps needed for implementation of a true professional learning community von Riggins, Cathy, Knowles, Debbie

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Caught in the trap of PLC Lite: Essential steps needed for implementation of a true professional learning community von Riggins, Cathy, Knowles, Debbie

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Operative management and outcomes of gallbladder cancer in Australia: a multi-institutional, retrospective, observational cohort analysis von Santucci, Jordan, Hua, Cathy, Chong, Lynn, Lockie, Elizabeth, Lim, Justin, Lim, Sean, Zhou, Warren, Bradshaw, Luke

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Is Persistent Motor or Vocal Tic Disorder a Milder Form of Tourette Syndrome? von Claudio‐Campos, Karla, Stevens, Daniel, Koo, Sang‐Wahn, Valko, Alexa, Bienvenu, Oscar Joseph, Budman, Cathy B., Cath, Danielle C., Darrow, Sabrina, Geller, Daniel, Goes, Fernando S., Grados, Marco A., Greenberg, Benjamin D., Greenberg, Erica, Hirschtritt, Matthew E., Illmann, Cornelia, Ivankovic, Franjo, King, Robert A., Knowles, James A., Krasnow, Janice, Lee, Paul C., Lyon, Gholson J., McCracken, James T., Robertson, Mary M., Osiecki, Lisa, Riddle, Mark A., Rouleau, Guy, Sandor, Paul, Nestadt, Gerald, Samuels, Jack, Scharf, Jeremiah M., Mathews, Carol A.

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In Vivo Characterization of GSK256066, a High-Affinity Inhaled Phosphodiesterase 4 Inhibitor von Nials, Anthony T., Tralau-Stewart, Cathy J., Gascoigne, Michele H., Ball, Douglas I., Ranshaw, Lisa E., Knowles, Richard G.

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GSK256066, an Exceptionally High-Affinity and Selective Inhibitor of Phosphodiesterase 4 Suitable for Administration by Inhalation: In Vitro, Kinetic, and In Vivo Characterization von Tralau-Stewart, Cathy J., Williamson, Richard A., Nials, Anthony T., Gascoigne, Michele, Dawson, John, Hart, Graham J., Angell, Anthony D.R., Solanke, Yemisi E., Lucas, Fiona S., Wiseman, Joanne, Ward, Peter, Ranshaw, Lisa E., Knowles, Richard G.

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Genomewide suggestive linkage of opioid dependence to chromosome 14q von Lachman, Herbert M., Fann, Cathy S.J., Bartzis, Michael, Evgrafov, Oleg V., Rosenthal, Richard N., Nunes, Edward V., Miner, Christian, Santana, Maria, Gaffney, Jebediah, Riddick, Amy, Hsu, Chia-Lin, Knowles, James A.

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Adults with Rubinstein–Taybi syndrome von Stevens, Cathy A., Pouncey, Jill, Knowles, Darcy

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Phosphorylation of Rab11-FIP2 regulates polarity in MDCK cells von Lapierre, Lynne A, Avant, Kenya M, Caldwell, Cathy M, Oztan, Asli, Apodaca, Gerard, Knowles, Byron C, Roland, Joseph T, Ducharme, Nicole A, Goldenring, James R

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Maternal Black Race and Persistent Wheezing Illness in Former Extremely Low Gestational Age Newborns: Secondary Analysis of a Randomized Trial von Wai, Katherine C., Hibbs, Anna M., Steurer, Martina A., Black, Dennis M., Asselin, Jeanette M., Eichenwald, Eric C., Strong, Suzanne Hamilton, Immamura-Ching, Jill, Orfanos-Villalobos, Margaret, Williams, Cassandra, Durand, David J., Merrill, Jeffrey D., Horton, Dolia, Willard, April, Truog, William E., Gauldin, Cheryl, Holmes, Anne, Johnson, Patrice, Meinert, Kerrie, Reynolds, Anne Marie, Conway, Patrick, Leadersdorff, Michael, Orbank, Pam, Wynn, Karen, Steinhorn, Robin H., deUngria, Maria, Khan, Janine Yasmin, Hamann, Karin, Schau, Molly, Hopkins, Brad, Shariff, Jila, McGovern, Rose, Adelman, Jeff, Combs, Adrienne, Tjersland, Mary, Mayock, Dennis E., Howland, Elizabeth, Longoria, Jim, Meo, Holly, McDavid, Georgia, Burson, Katrina, Hinojosa, Richard, Johnson, Christopher, Martin, Sarah, Rogers, Shawna, Wright, Sharon, Hudak, Mark L., Barnette, Kimberly, Kellum, Amanda, Burcke, Michelle, Hayes, Christie, Chadwick, Stephanie, Howard, Danielle, Kennedy, Carla, O'Shea, T. Michael, Stefanescu, Beatrice, Brown, Patty, Bendel, Catherine M., Davern, Bridget, Mills, Marla, Ritter, Sharon, Wagner, Carol, Ryan, Rita M., Roberson, Jimmy, Mammel, Mark C., Lampland, Andrea, Meyers, Pat, Brey, Angela, Bendel-Stenzel, Ellen M., Mulrooney, Neil, Worwa, Cathy, Dixon, Pam, Ebert, Gerald, Hejl, Cathy, Maxwell, Molly, Dhanireddy, Ramasubbareddy, El Abiad, Mohammed T., Talati, Ajay, Dempsey, Sheila, Gammage, Kathy, Gower, Gayle, James, Kathy, LeNoue, Pam, Bell, Suzi, Bruton, Dawn, Beaulieu, Michelle, Williams, Richard, Barron-Nelson, Robin, Taylor, Shane, Lowe, Gary, Rogers, Elizabeth E., Chapin, Cheryl, Hamann, Karin, Kelley, Susan, Knowles, Karin, Newton, Nancy, Hietpas, Jean, Denton, Laurie, Palermo, Lisa, Wu, Lucy

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Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome von 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 A, Singer, Harvey S, Nöthen, Markus M, Hebebrand, Johannes, King, Robert A, Dion, Yves, Rouleau, Guy A, 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, Smit, Jan, The Tourette Syndrome Association International Consortium for Genetics (TSAICG), The Gilles de la Tourette Syndrome GWAS Replication Initiative (GGRI)

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Assessment of Discrepancies Between Follow-up Infarct Volume and 90-Day Outcomes Among Patients With Ischemic Stroke Who Received Endovascular Therapy von Ganesh, Aravind, Ospel, Johanna M, Menon, Bijoy K, Demchuk, Andrew M, McTaggart, Ryan A, Nogueira, Raul G, Poppe, Alexandre Y, Almekhlafi, Mohammed A, Hanel, Ricardo A, Thomalla, Götz, Holmin, Staffan, Puetz, Volker, van Adel, Brian A, Tarpley, Jason W, Tymianski, Michael, Hill, Michael D, Goyal, Mayank

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Mediation of Age and Thrombectomy Outcome by Neuroimaging Markers of Frailty in Patients With Stroke von Benali, Faysal, Singh, Nishita, Fladt, Joachim, Jaroenngarmsamer, Tanaporn, Bala, Fouzi, Ospel, Johanna M, Buck, Brian H, Dowlatshahi, Dar, Field, Thalia S, Hanel, Ricardo A, Peeling, Lissa, Tymianski, Michael, Hill, Michael D, Goyal, Mayank, Ganesh, Aravind

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Innovations in Practice: Adapting a specialized ADHD parenting programme for use with 'hard to reach' and 'difficult to treat' preschool children von McEwan, Fiona, Thompson, Margaret, Laver-Bradbury, Cathy, Jefferson, Harriet, Koerting, Johanna, Smith, Elizabeth, Knowles, Mark, McCann, Donna, Daley, David, Barton, Jo, Latter, Sue, Elsey, Helen, Sonuga-Barke, Edmund

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Adapting a specialized ADHD parenting programme for use with ‘hard to reach’ and ‘difficult to treat’ preschool children von McEwan, Fiona, Thompson, Margaret, Laver-Bradbury, Cathy, Jefferson, Harriet, Koerting, Johanna, Smith, Elizabeth, Knowles, Mark, McCann, Donna, Daley, David, Barton, Jo, Latter, Sue, Elsey, Helen, Sonuga-Barke, Edmund

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