Intraoperative Flash Visual Evoked Potential Recording and Relationship to Visual Outcome von Houlden, David A., Turgeon, Chantal A., Amyot, Nathaniel S., Edem, Idara, Sinclair, John, Agbi, Charles, Polis, Thomas, Alkherayf, Fahad

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Early somatosensory evoked potential grades in comatose traumatic brain injury patients predict cognitive and functional outcome von Houlden, David A, Taylor, Amanda B, Feinstein, Anthony, Midha, Rajiv, Bethune, Allison J, Stewart, Craig P, Schwartz, Michael L

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Giant Somatosensory Evoked Potentials Coincident With Epileptiform Discharges in Acutely Comatose Patients von Houlden, David A., Boulos, Mark I., Murray, Brian J., Norton, Loretta, Young, G. Bryan

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Spinal Cord-Evoked Potentials and Muscle Responses Evoked by Transcranial Magnetic Stimulation in 10 Awake Human Subjects von Houlden, David A, Schwartz, Michael L, Tator, Charles H, Ashby, Peter, MacKay, William A

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Intraoperative flash VEPs are reproducible in the presence of low amplitude EEG von Houlden, David A., Turgeon, Chantal A., Polis, Thomas, Sinclair, John, Coupland, Stuart, Bourque, Pierre, Corsten, Martin, Kassam, Amin

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Optimal Intraoperative Somatosensory Evoked Potential Stimulus Intensity Can Be Determined by Nerve Action Potential Amplitude von Houlden, David A, Ubriaco, Gino, Stewart, Craig P, Robertson, Samantha L, Cohen, Meghan, Potapova, Ekaterina, Pirouzmand, Farhad

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Generalized peripheral nerve failure during thoracic spine surgery : A case report von BETHUNE, Allison J, HOULDEN, David A, SMITH, Terry S, YEE, Albert J, MIDHA, Rajiv, SINGRAKHIA, Manoj

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Giant Somatosensory Evoked Potentials Coincident With Epileptiform Discharges in Acutely Comatose Patients von Houlden, David A., Boulos, Mark I., Murray, Brian J., Norton, Loretta, Young, G. Bryan

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Neurogenic motor evoked potentials: role in brachial plexus surgery: Case report von Burkholder, Lee M., Houlden, David A., Midha, Rajiv, Weiss, Erin, Vennettilli, Marco

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Gender as a Predictor of Hearing Preservation Outcome in Acoustic Neuroma Surgery von Rowed, David W, Nedzelski, Julian M, Chen, Joseph M, Houlden, David A

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NEUROPHYSIOLOGIC DIAGNOSIS IN UNCOOPERATIVE TRAUMA PATIENTS: CONFOUNDING FACTORS von Houlden, David A., Schwartz, M. L., Klettke, K. A.

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Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications von Chelban, Viorica, Aksnes, Henriette, Maroofian, Reza, LaMonica, Lauren C., Seabra, Luis, Siggervåg, Anette, Devic, Perrine, Shamseldin, Hanan E., Vandrovcova, Jana, Murphy, David, Richard, Anne-Claire, Quenez, Olivier, Bonnevalle, Antoine, Zanetti, M. Natalia, Kaiyrzhanov, Rauan, Salpietro, Vincenzo, Efthymiou, Stephanie, Schottlaender, Lucia V., Morsy, Heba, Scardamaglia, Annarita, Tariq, Ambreen, Pagnamenta, Alistair T., Pennavaria, Ajia, Krogstad, Liv S., Bekkelund, Åse K., Caiella, Alessia, Glomnes, Nina, Brønstad, Kirsten M., Tury, Sandrine, Moreno De Luca, Andrés, Boland-Auge, Anne, Olaso, Robert, Deleuze, Jean-François, Anheim, Mathieu, Cretin, Benjamin, Vona, Barbara, Alajlan, Fahad, Abdulwahab, Firdous, Battini, Jean-Luc, İpek, Rojan, Bauer, Peter, Zifarelli, Giovanni, Gungor, Serdal, Kurul, Semra Hiz, Lochmuller, Hanns, Da’as, Sahar I., Fakhro, Khalid A., Gómez-Pascual, Alicia, Botía, Juan A., Wood, Nicholas W., Horvath, Rita, Ernst, Andreas M., Rothman, James E., McEntagart, Meriel, Crow, Yanick J., Alkuraya, Fowzan S., Nicolas, Gaël, Arnesen, Thomas, Houlden, Henry

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Cerebral small vessel disease-related protease HtrA1 processes latent TGF-β binding protein 1 and facilitates TGF-β signaling von Beaufort, Nathalie, Scharrer, Eva, Kremmer, Elisabeth, Lux, Vanda, Ehrmann, Michael, Huber, Robert, Houlden, Henry, Werring, David, Haffner, Christof, Dichgans, Martin

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Dapagliflozin in Patients with Chronic Kidney Disease von Heerspink, Hiddo J.L, Stefánsson, Bergur V, Correa-Rotter, Ricardo, Chertow, Glenn M, Greene, Tom, Hou, Fan-Fan, Mann, Johannes F.E, McMurray, John J.V, Lindberg, Magnus, Rossing, Peter, Sjöström, C. David, Toto, Roberto D, Langkilde, Anna-Maria, Wheeler, David C

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AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders von Salpietro, Vincenzo, Dixon, Christine L., Guo, Hui, Bello, Oscar D., Vandrovcova, Jana, Efthymiou, Stephanie, Maroofian, Reza, Heimer, Gali, Burglen, Lydie, Valence, Stephanie, Torti, Erin, Hacke, Moritz, Rankin, Julia, Tariq, Huma, Colin, Estelle, Procaccio, Vincent, Striano, Pasquale, Mankad, Kshitij, Lieb, Andreas, Chen, Sharon, Pisani, Laura, Bettencourt, Conceicao, Männikkö, Roope, Manole, Andreea, Brusco, Alfredo, Grosso, Enrico, Ferrero, Giovanni Battista, Armstrong-Moron, Judith, Gueden, Sophie, Bar-Yosef, Omer, Tzadok, Michal, Monaghan, Kristin G., Santiago-Sim, Teresa, Person, Richard E., Cho, Megan T., Willaert, Rebecca, Yoo, Yongjin, Chae, Jong-Hee, Quan, Yingting, Wu, Huidan, Wang, Tianyun, Bernier, Raphael A., Xia, Kun, Blesson, Alyssa, Jain, Mahim, Motazacker, Mohammad M., Jaeger, Bregje, Schneider, Amy L., Boysen, Katja, Muir, Alison M., Myers, Candace T., Gavrilova, Ralitza H., Gunderson, Lauren, Schultz-Rogers, Laura, Klee, Eric W., Dyment, David, Osmond, Matthew, Parellada, Mara, Llorente, Cloe, Gonzalez-Peñas, Javier, Carracedo, Angel, Van Haeringen, Arie, Ruivenkamp, Claudia, Nava, Caroline, Heron, Delphine, Nardello, Rosaria, Iacomino, Michele, Minetti, Carlo, Skabar, Aldo, Fabretto, Antonella, Raspall-Chaure, Miquel, Chez, Michael, Tsai, Anne, Fassi, Emily, Shinawi, Marwan, Constantino, John N., De Zorzi, Rita, Fortuna, Sara, Kok, Fernando, Keren, Boris, Bonneau, Dominique, Choi, Murim, Benzeev, Bruria, Zara, Federico, Mefford, Heather C., Scheffer, Ingrid E., Clayton-Smith, Jill, Macaya, Alfons, Rothman, James E., Eichler, Evan E., Kullmann, Dimitri M., Houlden, Henry

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Immediate detection of somatosensory evoked potential loss is necessary to prevent neurological deficits von Houlden, David

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Early onset cerebral amyloid angiopathy following childhood exposure to cadaveric dura von Banerjee, Gargi, Adams, Matthew E., Jaunmuktane, Zane, Alistair Lammie, G., Turner, Ben, Wani, Mushtaq, Sawhney, Inder M. S., Houlden, Henry, Mead, Simon, Brandner, Sebastian, Werring, David J.

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A novel RFC1 repeat motif (ACAGG) in two Asia-Pacific CANVAS families von Scriba, Carolin K., Beecroft, Sarah J., Clayton, Joshua S., Cortese, Andrea, Sullivan, Roisin, Yau, Wai Yan, Dominik, Natalia, Rodrigues, Miriam, Walker, Elizabeth, Dyer, Zoe, Wu, Teddy Y., Davis, Mark R., Chandler, David C., Weisburd, Ben, Houlden, Henry, Reilly, Mary M., Laing, Nigel G., Lamont, Phillipa J., Roxburgh, Richard H., Ravenscroft, Gianina

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GGC Repeat Expansion in NOTCH2NLC Is Rare in European Leukoencephalopathy von Yau, Wai Yan, Sullivan, Roisin, Chen, Zhongbo, Lynch, David S., Vandrovcova, Jana, Wood, Nicholas W., Houlden, Henry

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Recessive variants in SLC9A1 cause a syndrome of cerebellar ataxia, amelogenesis imperfecta and variable sensorineural hearing loss von Ceravolo, Giorgia, Pellerin, David, Maroofian, Reza, Houlden, Henry

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