Alexander Disease: Diagnosis with MR Imaging von van der Knaap, Marjo S, Naidu, Sakkubai, Breiter, Steven N, Blaser, Susan, Stroink, Hans, Springer, Stephan, Begeer, Jacobus C, van Coster, Rudy, Barth, Peter G, Thomas, Neil H, Valk, Jacob, Powers, James M

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Land reform in Zimbabwe von Thomas, Neil H

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Congenital Titinopathy: Comprehensive characterization and pathogenic insights von Oates, Emily C., Jones, Kristi J., Donkervoort, Sandra, Charlton, Amanda, Brammah, Susan, Smith, John E., Ware, James S., Yau, Kyle S., Swanson, Lindsay C., Whiffin, Nicola, Peduto, Anthony J., Bournazos, Adam, Waddell, Leigh B., Farrar, Michelle A., Sampaio, Hugo A., Teoh, Hooi Ling, Lamont, Phillipa J., Mowat, David, Fitzsimons, Robin B., Corbett, Alastair J., Ryan, Monique M., O'Grady, Gina L., Sandaradura, Sarah A., Ghaoui, Roula, Joshi, Himanshu, Marshall, Jamie L., Nolan, Melinda A., Kaur, Simranpreet, Punetha, Jaya, Töpf, Ana, Harris, Elizabeth, Bakshi, Madhura, Genetti, Casie A., Marttila, Minttu, Werlauff, Ulla, Streichenberger, Nathalie, Pestronk, Alan, Mazanti, Ingrid, Pinner, Jason R., Vuillerot, Carole, Grosmann, Carla, Camacho, Ana, Mohassel, Payam, Leach, Meganne E., Foley, A. Reghan, Bharucha‐Goebel, Diana, Collins, James, Connolly, Anne M., Gilbreath, Heather R., Iannaccone, Susan T., Castro, Diana, Cummings, Beryl B., Webster, Richard I., Lazaro, Leïla, Vissing, John, Coppens, Sandra, Deconinck, Nicolas, Luk, Ho‐Ming, Thomas, Neil H., Foulds, Nicola C., Illingworth, Marjorie A., Ellard, Sian, McLean, Catriona A., Phadke, Rahul, Ravenscroft, Gianina, Witting, Nanna, Hackman, Peter, Richard, Isabelle, Cooper, Sandra T., Kamsteeg, Erik‐Jan, Hoffman, Eric P., Bushby, Kate, Straub, Volker, Udd, Bjarne, Ferreiro, Ana, North, Kathryn N., Clarke, Nigel F., Lek, Monkol, Beggs, Alan H., Bönnemann, Carsten G., MacArthur, Daniel G., Granzier, Henk, Davis, Mark R., Laing, Nigel G.

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Mutations in the gene for the E1β subunit: a novel cause of pyruvate dehydrogenase deficiency von BROWN, Ruth M, HEAD, Rosemary A, BOUBRIAK, Ivan I, LEONARD, James V, THOMAS, Neil H, BROWN, Garry K

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Correlation of SMNt and SMNc gene copy number with age of onset and survival in spinal muscular atrophy von Taylor, J E, Thomas, N H, Lewis, C M, Abbs, S J, Rodrigues, N R, Davies, K E, Mathew, C G

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FERTILITY AND POPULATION POLICY IN TWO COUNTIES IN CHINA 1980–1991 von THOMAS, NEIL H., AIPING, MU

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Diagnosis and management of Guillain–Barré syndrome von Thomas, Neil H.

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Identification of three novel frameshift mutations in patients with Friedreich's ataxia von POOK, MARK A, AL-MAHDAWI, SAHAR A H, THOMAS, NEIL H, APPLETON, RICHARD, NORMAN, ANDREW, MOUNTFORD, ROGER, CHAMBERLAIN, SUSAN

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Mutations in the gene for the E1beta subunit: a novel cause of pyruvate dehydrogenase deficiency von Brown, Ruth M, Head, Rosemary A, Boubriak, Ivan I, Leonard, James V, Thomas, Neil H, Brown, Garry K

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Mutations in the gene for the E1? subunit: a novel cause of pyruvate dehydrogenase deficiency von Brown, Ruth M, Head, Rosemary A, Boubriak, Ivan I, Leonard, James V, Thomas, Neil H, Brown, Garry K

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Storage times for Guthrie cards von Thomas, N. H.

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Muscular dystrophy and other muscle disorders von Thomas, Neil H., Dubowitz, Victor

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Beschichtungsdüse mit Schnellmontagemerkmalen von CILISKE, SCOTT L, THOMAS, NEIL H

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Coating die having quick assembly features von CILISKE SCOTT L.,THOMAS NEIL H

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COATING DIE HAVING QUICK ASSEMBLY FEATURES von CILISKE SCOTT L, THOMAS NEIL H

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COATING DIE HAVING QUICK ASSEMBLY FEATURES von CILISKE, SCOTT, L, THOMAS, NEIL, H

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Coating die having quick assembly features von CILISKE SCOTT L, THOMAS NEIL H

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Molecular studies of spinal muscular atrophy von Davies, Kay E., Thomas, Neil H., Daniels, Rachael J., Dubowitz, Victor

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APPARATUS AND METHOD FOR DISCHARGING SURGICAL DRAPE von ASMUS ROBERT A, SCHLEI DIETMAR, SHOR RITA M, THOMAS NEIL H, BAKER DENNIS L

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APPARATUS AND METHODS FOR DISPENSING SURGICAL DRAPES von SHOR, RITA M, BAKER, DENNIS L, SCHLEI, DIETMAR, ASMUS, ROBERT A, THOMAS, NEIL H

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