Spectrum of Mutations in the Batten Disease Gene, CLN3 von Munroe, Patricia B., Mitchison, Hannah M., O'Rawe, Angela M., Anderson, John W., Boustany, Rose-Mary, Lerner, Terry J., Taschner, Peter E.M., Vos, Nanneke de, Breuning, Martijn H., Gardiner, R. Mark, Mole, Sara E.

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Delayed classic and protracted phenotypes of compound heterozygous juvenile neuronal ceroid lipofuscinosis von LAURONEN, L, MUNROE, P. B, KIRVESKARI, E, SANTAVUORI, P, JÄRVELÄ, I, AUTTI, T, MITCHISON, H. M, O'RAWE, A. M, GARDINER, R. M, MOLE, S. E, PURANEN, J, HÄKKINEN, A.-M

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Mutations in the Palmitoyl-Protein Thioesterase Gene (PPT; CLN1) Causing Juvenile Neuronal Ceroid Lipofuscinosis with Granular Osmiophilic Deposits von Mitchison, Hannah M., Hofmann, Sandra L., Becerra, Carlos H. R., Munroe, Patricia B., Lake, Brian D., Crow, Yanick J., Stephenson, John B. P., Williams, Ruth E., Hofman, Irene L., Taschner, Peter E. M., Martin, Jean-Jacques, Philippart, Michel, Andermann, Eva, Andermann, Frederick, Mole, Sara E., Gardiner, R. Mark, O'Rawe, Angela M.

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Rapid diagnostic test for the major mutation underlying Batten disease von Järvelä, I, Mitchison, H M, Munroe, P B, O'Rawe, A M, Mole, S E, Syvänen, A C

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Batten disease gene, CLN3 : linkage disequilibrium mapping in the Finnish population, and analysis of European haplotypes von MITCHISON, H. M, O'RAWE, A. M, SANDKUIJL, L. A, SANTAVUORI, P, DE VOS, N, BREUNING, M. H, MOLE, S. E, GARDINER, R. M, JÄRVELÄ, I. E, TASCHNER, P. E. M

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Genomic Structure and Complete Nucleotide Sequence of the Batten Disease Gene,CLN3 von Mitchison, Hannah M., Munroe, Patricia B., O'Rawe, Angela M., Taschner, Peter E.M., de Vos, Nanneke, Kremmidiotis, Gabriel, Lensink, Ingrid, Munk, A.Christine, D'Arigo, Kenneth L, Anderson, John W., Lerner, Terry J., Moyzis, Robert K., Callen, David F., Breuning, Martijn H., Doggett, Norman A., Gardiner, R.Mark, Mole, Sara E.

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YAC and Cosmid Contigs Spanning the Batten Disease (CLN3) Region at 16p12.1–p11.2 von JÄRVELÄ, IRMA E., MITCHISON, HANNAH M., O'RAWE, ANGELA M., MUNROE, PATRICIA B., TASCHNER, PETER E.M., DEVOS, NANNEKE, LERNER, TERRY J., D'ARIGO, KEN L., CALLEN, DAVID F., THOMPSON, ANDREW D., KNIGHT, MAREE, MARRONE, BABETTA L., MUNDT, MARK O., MEINCKE, LINDA, BREUNING, MARTIJN H., GARDINER, MARK R., DOGGETT, NORMAN A., MOLE, SARA E.

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Genetic Mapping of the Batten Disease Locus (CLN3) to the Interval D16S288-D16S383 by Analysis of Haplotypes and Allelic Association von Mitchison, Hannah M., Taschner, Peter E.M., O'Rawe, Angela M., de Vos, Nanneke, Phillips, Hilary A., Thompson, Andrew D., Kozman, Helen M., Haines, Jonathan L., Schlumpf, Karen, D'Arigo, Kenneth, Boustany, Rose-Mary N., Callen, David F., Breuning, Martijn H., Gardiner, R.Mark, Mole, Sara E., Lerner, Terry J.

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Structure of the CLN3 Gene and Predicted Structure, Location and Function of CLN3 Protein von Mitchison, Hannah M., Taschner, P. E., Kremmidiotis, C., Callen, D. F., Doggett, N. A., Lemer, T. J., Janes, R. B., Wallace, B. A., Munroe, Patricia B., O'Rawe, Angela M., Gardiner, R. M., Mole, Sara E.

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Refined localization of the Batten disease gene (CLN3) by haplotype and linkage disequilibrium mapping to D16S288-D16S383 and exclusion from this region of a variant form of Batten... von Mitchison, H. M., O'Rawe, A. M., Lerner, T. J., Taschner, P. E. M., Schlumpf, K., D'Arigo, K., de Vos, N., Gormally, E., Phillips, H. A., Thompson, A. D., Haines, J. L., Hart, Y. M., Andermann, E., Callen, D. F., Breuning, M. H., Gardiner, R. M., Mole, S. E.

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Strategy for Mutation Detection in CLN3: Characterisation of Two Finnish Mutations von Munroe, Patricia B., O'Rawe, Angela M., Mitchison, Hannah M., Järvelä, Irma E., Santavuori, Pirkko, Lerner, Terry J., Taschner, P. E., Gardiner, R. M., Mole, Sara E.

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Nutritional aspects in cystic fibrosis : Advances in cystic fibrosis : Gastrointestinal and nutritional aspects von DODGE, J. A, O'RAWE, A. M

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Nutritional aspects in cystic fibrosis von Dodge, J A, O'Rawe, A M

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Isolation of a novel gene underlying batten disease, CLN3 von Lerner, Terry J, Boustany, Rose-Mary N, Anderson, John W, D'Arigo, Kenneth L, Schlumpf, Karen, Buckler, Alan J, Gusella, James F, Haines, Jonathan L

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Cellular-resolution optogenetics reveals attenuation-by-suppression in visual cortical neurons von LaFosse, Paul K, Zhou, Zhishang, O'Rawe, Jonathan F, Friedman, Nina G, Scott, Victoria M, Deng, Yanting, Histed, Mark H

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TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations von O’Rawe, Jason A., Wu, Yiyang, Dörfel, Max J., Rope, Alan F., Au, P.Y. Billie, Parboosingh, Jillian S., Moon, Sungjin, Kousi, Maria, Kosma, Konstantina, Smith, Christopher S., Tzetis, Maria, Schuette, Jane L., Hufnagel, Robert B., Prada, Carlos E., Martinez, Francisco, Orellana, Carmen, Crain, Jonathan, Caro-Llopis, Alfonso, Oltra, Silvestre, Monfort, Sandra, Jiménez-Barrón, Laura T., Swensen, Jeffrey, Ellingwood, Sara, Smith, Rosemarie, Fang, Han, Ospina, Sandra, Stegmann, Sander, Den Hollander, Nicolette, Mittelman, David, Highnam, Gareth, Robison, Reid, Yang, Edward, Faivre, Laurence, Roubertie, Agathe, Rivière, Jean-Baptiste, Monaghan, Kristin G., Wang, Kai, Davis, Erica E., Katsanis, Nicholas, Kalscheuer, Vera M., Wang, Edith H., Metcalfe, Kay, Kleefstra, Tjitske, Innes, A. Micheil, Kitsiou-Tzeli, Sophia, Rosello, Monica, Keegan, Catherine E., Lyon, Gholson J.

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Music therapy for children and adolescents with behavioural and emotional problems: a randomised controlled trial von Porter, Sam, McConnell, Tracey, McLaughlin, Katrina, Lynn, Fiona, Cardwell, Christopher, Braiden, Hannah‐Jane, Boylan, Jackie, Holmes, Valerie, Rogan, Sheelagh, Clinician, Lead, Diamond, Karen, Allen, Julie, Reilly, Ciara, Davidson, Fiona, McDowell, Clíona, Boyd, Ruth, Oldfield, Amelia, Mullowney, M., Downes, C., Jack, K., Cresswell, M., Wilson, J., Gardner, C., Patterson, F., Gboloo‐Teye, D, McClatchey, L., Wilson, J., Gribbon, M., Kamat, M., Kehoe, A., Slack, T., Welsh, J., Nelson, J., Lawlor, K., McKenna, A., O'Rawe, A., Rowan, V., Sharvin, M., Bann, B., McQuillan, M., Spratt, A., Gill, P., Rankin, G., Lehmann, K., Boyd, H., Kierans, A., Carney, J., Haridas, M., Cormack, E., Morrow, A., Browne, H., McShane, C., Hurley, S., Welsh, J., McGurgan, M., O'Neill, S., Campbell, M., Corrigan, N., Maxwell, L., Fitzsimmons, L., McMahon, E., McGibbon, A., Short, M., Cummings, J., McGuire, C., Fulton, K., McKenna, S., Mercer, F., Mullin, A., Heale, A.

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Virtual Reality as a Travel Promotional Tool: Insights from a Consumer Travel Fair von Gibson, Alex, O’Rawe, Mary

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Amplified cortical neural responses as animals learn to use novel activity patterns von Akitake, Bradley, Douglas, Hannah M., LaFosse, Paul K., Beiran, Manuel, Deveau, Ciana E., O’Rawe, Jonathan, Li, Anna J., Ryan, Lauren N., Duffy, Samuel P., Zhou, Zhishang, Deng, Yanting, Rajan, Kanaka, Histed, Mark H.

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A case of subependymal giant cell astrocytoma without tuberous sclerosis complex and review of the literature von O’Rawe, Michael, Chandran, Arjun S., Joshi, Stuti, Simonin, Alexandre, Dyke, Jason M., Lee, Sharon

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