Surgical Approaches to Diseases of the Orbital Apex von Leone, Charles R., Wissinger, John P.

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Lumbar spine lesion von WISSINGER, J. P, NAKAGAWA, H, IMANA, R, EL GINDI, S, REVERDIN, A

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Epidural steroids for cervical and lumbar radiculopathy von Pawl, Ronald P.

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Subdural hematoma von de Almeida, Gilberto Machado

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Proceedings: Chronic measurement of epidural pressure with an induction power oscillator transducer von Rylander, H G, Taylor, H L, Wissinger, J P, Story, J L

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Carpal tunnel syndrome von Mackinnon, Susan E.

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The use of dexamethasone in the control of cerebral oedema von Wissinger, J P, French, L A, Gillingham, F J

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Perspectives on the management of odontoid fracture von Wissinger, John Paul

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Transthoracic Approach for Pott's Disease von Richardson, J. David, Campbell, Donald L., Grover, Frederick L., Arom, Kit V., Wilkins, Kaye, Wissinger, John P., Trinkle, J. Kent

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Cerebrospinal fluid pseudocyst after anterior stabilization for cervical spine injury treated by ventricular drainage : Case report. Commentary von KALA, M, FEUER, H, WISSINGER, J. P

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A new method of acrylic cranioplasty. Commentary von SHERBURN, E. W, SILBERGELD, D. L, WISSINGER, J. P

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Gamma knife radiosurgery for trigeminal neuralgia: a study of predictors of success, efficacy, safety, and outcome at LSUHSC von Shaya, Mark, Jawahar, Ajay, Caldito, Gloria, Sin, Anthony, Willis, Brian K, Nanda, Anil

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An innovative approach for cranioplasty using hydroxyapatite cement. Commentary von DUJOVNY, M, AVILES, A, AGNER, C, CAREY, M. E, WISSINGER, J. P

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Brown-Sequard syndrome produced by cervical disc herniation : Case report and literature review. Commentary von RUMANA, C. S, BASKIN, D. S, WISSINGER, J. P, PAWL, R. P

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A long-term outcome study of 170 surgically treated patients with compressive cervical radiculopathy. Commentary von DAVIS, R. A, WIRTH, F. P, NAKAGAWA, H, CALATAYUD MALDONADO, V. D, BROCK, M, MEACHAM, W. F, WISSINGER, J. P, MILLER, C. A, SONNTAG, V. K. H

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Neurosurgical manpower needs : Achieving a balance. Commentary von HARRINGTON, T. R, KLINE, D. G, WISSINGER, J. P, FABI, R. A, NEBLETT, C. B, VANGILDER, J. C, VACCA, D. F, MANN, R. F, GOLDEN, P. F, MORTARA, R. H, SYPERT, G. W

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Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma von Bailey, Jessica N Cooke, Loomis, Stephanie J, Kang, Jae H, Allingham, R Rand, Gharahkhani, Puya, Khor, Chiea Chuen, Burdon, Kathryn P, Aschard, Hugues, Chasman, Daniel I, Igo, Robert P, Hysi, Pirro G, Glastonbury, Craig A, Ashley-Koch, Allison, Brilliant, Murray, Brown, Andrew A, Budenz, Donald L, Buil, Alfonso, Cheng, Ching-Yu, Choi, Hyon, Christen, William G, Curhan, Gary, De Vivo, Immaculata, Fingert, John H, Foster, Paul J, Fuchs, Charles, Gaasterland, Douglas, Gaasterland, Terry, Hewitt, Alex W, Hu, Frank, Hunter, David J, Khawaja, Anthony P, Lee, Richard K, Li, Zheng, Lichter, Paul R, Mackey, David A, McGuffin, Peter, Mitchell, Paul, Moroi, Sayoko E, Perera, Shamira A, Pepper, Keating W, Qi, Qibin, Realini, Tony, Richards, Julia E, Ridker, Paul M, Rimm, Eric, Ritch, Robert, Ritchie, Marylyn, Schuman, Joel S, Scott, William K, Singh, Kuldev, Sit, Arthur J, Song, Yeunjoo E, Tamimi, Rulla M, Topouzis, Fotis, Viswanathan, Ananth C, Verma, Shefali Setia, Vollrath, Douglas, Wang, Jie Jin, Weisschuh, Nicole, Wissinger, Bernd, Wollstein, Gadi, Wong, Tien Y, Yaspan, Brian L, Zack, Donald J, Zhang, Kang, Study, EPIC-Norfolk Eye, Weinreb, Robert N, Pericak-Vance, Margaret A, Small, Kerrin, Hammond, Christopher J, Aung, Tin, Liu, Yutao, Vithana, Eranga N, MacGregor, Stuart, Craig, Jamie E, Kraft, Peter, Howell, Gareth, Hauser, Michael A, Pasquale, Louis R, Haines, Jonathan L, Wiggs, Janey L

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CiliaCarta: An integrated and validated compendium of ciliary genes von van Dam, Teunis J P, Kennedy, Julie, van der Lee, Robin, de Vrieze, Erik, Wunderlich, Kirsten A, Rix, Suzanne, Dougherty, Gerard W, Lambacher, Nils J, Li, Chunmei, Jensen, Victor L, Leroux, Michel R, Hjeij, Rim, Horn, Nicola, Texier, Yves, Wissinger, Yasmin, van Reeuwijk, Jeroen, Wheway, Gabrielle, Knapp, Barbara, Scheel, Jan F, Franco, Brunella, Mans, Dorus A, van Wijk, Erwin, Képès, François, Slaats, Gisela G, Toedt, Grischa, Kremer, Hannie, Omran, Heymut, Szymanska, Katarzyna, Koutroumpas, Konstantinos, Ueffing, Marius, Nguyen, Thanh-Minh T, Letteboer, Stef J F, Oud, Machteld M, van Beersum, Sylvia E C, Schmidts, Miriam, Beales, Philip L, Lu, Qianhao, Giles, Rachel H, Szklarczyk, Radek, Russell, Robert B, Gibson, Toby J, Johnson, Colin A, Blacque, Oliver E, Wolfrum, Uwe, Boldt, Karsten, Roepman, Ronald, Hernandez-Hernandez, Victor, Huynen, Martijn A

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Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia von Kohl, Susanne, Zobor, Ditta, Chiang, Wei-Chieh, Weisschuh, Nicole, Staller, Jennifer, Menendez, Irene Gonzalez, Chang, Stanley, Beck, Susanne C, Garrido, Marina Garcia, Sothilingam, Vithiyanjali, Seeliger, Mathias W, Stanzial, Franco, Benedicenti, Francesco, Inzana, Francesca, Héon, Elise, Vincent, Ajoy, Beis, Jill, Strom, Tim M, Rudolph, Günther, Roosing, Susanne, Hollander, Anneke I den, Cremers, Frans P M, Lopez, Irma, Ren, Huanan, Moore, Anthony T, Webster, Andrew R, Michaelides, Michel, Koenekoop, Robert K, Zrenner, Eberhart, Kaufman, Randal J, Tsang, Stephen H, Wissinger, Bernd, Lin, Jonathan H

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A Nonsense Mutation in PDE6H Causes Autosomal-Recessive Incomplete Achromatopsia von Kohl, Susanne, Coppieters, Frauke, Meire, Françoise, Schaich, Simone, Roosing, Susanne, Brennenstuhl, Christina, Bolz, Sylvia, van Genderen, Maria M., Riemslag, Frans C.C., Lukowski, Robert, den Hollander, Anneke I., Cremers, Frans P.M., De Baere, Elfride, Hoyng, Carel B., Wissinger, Bernd

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