Laparoscopic Anterior Lumbar Interbody Fusion von McLaughlin, Mark R, Comey, Christopher H, Haid, Regis W, Rodts, Gerald E, Erwood, Scott C, Smith, C Dan

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Pediatric Occipitocervical Arthrodesis: A Review of Current Options and Early Evaluation of a Rigid Internal Fixation Device von Schultz, Karl D., Joseph, Petronio, Regis, W Haid, Gerald, E Rodts, Scott, C Erwood, Joseph, Alexander, Christine, Narad

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Pediatric Occipitocervical Arthrodesis: A Review of Current Options and Early Evaluation of a Rigid Internal Fixation Device: 816 von Schultz, Karl D., Petronio, Joseph, Haid, Regis W, Rodts, Gerald E, Erwood, Scott C, Alexander, Joseph, Narad, Christine

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Neural Pathfinding on Uni- and Multidirectional Photopolymerized Micropatterns von Tuft, Bradley W, Xu, Linjing, White, Scott P, Seline, Alison E, Erwood, Andrew M, Hansen, Marlan R, Guymon, C. Allan

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Evaluation of the MODEMS Pain and Disability and Expectation Scale and a Short Form of This Scale von Morlock, Robert J., Ward, Richard, Nerenz, David, Benzel, Edward C., Dempsey, Peter, Erwood, Scott, Feil, Edward, Kalfas, Iain, Krauss, William, Nockels, Russ, Pfeifer, Bernard, Shaffrey, Christopher

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Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease von Carss, KJ, Arno, G, Erwood, M, Stephens, J, Sanchis-Juan, A, Hull, S, Megy, K, Grozeva, D, Dewhurst, E, Malka, S, Plagnol, V, Penkett, C, Stirrups, K, Rizzo, R, Wright, G, Josifova, D, Bitner-Glindzicz, M, Scott, RH, Clement, E, Allen, L, Armstrong, R, Brady, AF, Carmichael, J, Chitre, M, Henderson, RHH, Hurst, J, MacLaren, RE, Murphy, E, Paterson, J, Rosser, E, Thompson, DA, Wakeling, E, Ouwehand, WH, Michaelides, M, Moore, AT, Webster, AR, Raymond, FL

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Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease von Carss, KJ, Arno, G, Erwood, M, Stephens, J, Sanchis-Juan, A, Hull, S, Megy, K, Grozeva, D, Dewhurst, E, Malka, S, Plagnol, V, Penkett, C, Stirrups, K, Rizzo, R, Wright, G, Josifova, D, Bitner-Glindzicz, M, Scott, RH, Clement, E, Allen, L, Armstrong, R, Brady, AF, Carmichael, J, Chitre, M, Henderson, RHH, Hurst, J, MacLaren, RE, Murphy, E, Paterson, J, Rosser, E, Thompson, DA, Wakeling, E, Ouwehand, WH, Michaelides, M, Moore, AT, NIHR-BioResource Rare Diseases Consortium, Webster, AR, Raymond, FL

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Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease von Carss, KJ, Arno, G, Erwood, M, Stephens, J, Sanchis-Juan, A, Hull, S, Megy, K, Grozeva, D, Dewhurst, E, Malka, S, Plagnol, V, Penkett, C, Stirrups, K, Rizzo, R, Wright, G, Josifova, D, Bitner-Glindzicz, M, Scott, RH, Clement, E, Allen, L, Armstrong, R, Brady, AF, Carmichael, J, Chitre, M, Henderson, RHH, Hurst, J, MacLaren, RE, Murphy, E, Paterson, J, Rosser, E, Thompson, DA, Wakeling, E, Ouwehand, WH, Michaelides, M, Moore, AT, NIHR-BioResource Rare Diseases Consortium, Webster, AR, Raymond, FL

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